US20120184007A1

US20120184007A1 - Engineered microorganisms with enhanced fermentation activity

Info

Publication number: US20120184007A1
Application number: US13/382,903
Authority: US
Inventors: Stephen Picataggio; Kirsty Anne Lily Salmon; Jose Miguel Laplaza
Original assignee: Verdezyne Inc
Current assignee: Verdezyne Inc
Priority date: 2009-07-09
Filing date: 2010-07-09
Publication date: 2012-07-19
Also published as: CA2767361A1; US20110229959A1; US20110165661A1; WO2011006126A3; WO2011006136A2; US20110224416A1; BRPI1011934A2; IN2012DN00568A; AP3766A; WO2011006136A3; CA2767259A1; US8114974B2; US20120184020A1; ZA201200506B; US20110165660A1; WO2011006126A2; US8227236B2; AP2012006105A0; BRPI1011934A8; US8093037B2

Abstract

Provided herein are genetically modified microorganisms that have enhanced fermentation activity, and methods for making and using such microorganisms.

Description

RELATED PATENT APPLICATION(S)

This patent application is a national stage of international patent application no. PCT/2010/041607 filed Jul. 9, 2010, entitled ENGINEERED MICROORGANISMS WITH ENHANCED FERMENTATION ACTIVITY, naming Stephen Picataggio, Kirsty Anne Lily Salmon, and Jose Miguel LaPlaza as inventors, and designated by Attorney Docket No. VRD-1002-PC2, which claims the benefit of U.S. provisional patent application No. 61/224,430 filed on Jul. 9, 2009, entitled USE OF ENGINEERED MICROORGANISMS WITH ENHANCED FERMENTATION ACTIVITY, naming Stephen Picataggio as inventor and designated by Attorney Docket No. VRD-1002-PV; claims the benefit of U.S. provisional patent application No. 61/316,780 filed on Mar. 23, 2010, entitled USE OF ENGINEERED MICROORGANISMS WITH ENHANCED FERMENTATION ACTIVITY, naming Stephen Picataggio as inventor and designated by Attorney Docket No. VRD-1002-PV2; and claims the benefit of U.S. provisional patent application No. 61/334,097 filed on May 12, 2010, entitled ENGINEERED MICROORGANISMS WITH ENHANCED FERMENTATION ACTIVITY, naming Stephen Picataggio as inventor and designated by Attorney Docket No. VRD-1002-PV3. The entire contents of the foregoing patent applications are incorporated herein by reference, including, without limitation, all text, tables and drawings.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Feb. 10, 2012, is named VRD12US2.txt and is 410,500 bytes in size.

FIELD

The technology relates in part to genetically modified microorganisms that have enhanced fermentation activity, and methods for making and using such microorganisms.

BACKGROUND

Microorganisms employ various enzyme-driven biological pathways to support their own metabolism and growth. A cell synthesizes native proteins, including enzymes, in vivo from deoxyribonucleic acid (DNA). DNA first is transcribed into a complementary ribonucleic acid (RNA) that comprises a ribonucleotide sequence encoding the protein. RNA then directs translation of the encoded protein by interaction with various cellular components, such as ribosomes. The resulting enzymes participate as biological catalysts in pathways involved in production of molecules utilized or secreted by the organism.
These pathways can be exploited for the harvesting of the naturally produced products. The pathways also can be altered to increase production or to produce different products that may be commercially valuable. Advances in recombinant molecular biology methodology allow researchers to isolate DNA from one organism and insert it into another organism, thus altering the cellular synthesis of enzymes or other proteins. Such genetic engineering can change the biological pathways within the host organism, causing it to produce a desired product. Microorganic industrial production can minimize the use of caustic chemicals and production of toxic byproducts, thus providing a “clean” source for certain products.

SUMMARY

Provided herein are engineered microorganisms having enhanced fermentation activity. In certain non-limiting embodiments, such microorganisms are capable of generating a target product with enhanced fermentation efficiency by, for example, (i) preferentially utilizing a particular glycolysis pathway, which increases yield of a target product, upon a change in fermentation conditions; (ii) reducing cell division rates upon a change in fermentation conditions, thereby diverting nutrients towards production of a target product; (iii) having the ability to readily metabolize five-carbon sugars; and/or (iv) having the ability to readily metabolize carbon dioxide; and combinations of the foregoing. In some embodiments, a target product is ethanol or succinic acid.
Thus, provided in certain embodiments are engineered microorganisms that comprise: (a) a functional Embden-Meyerhoff glycolysis pathway that metabolizes six-carbon sugars under aerobic fermentation conditions, and (b) a genetic modification that reduces an Embden-Meyerhoff glycolysis pathway member activity upon exposure of the engineered microorganism to anaerobic fermentation conditions, whereby the engineered microorganisms preferentially metabolize six-carbon sugars by the Enter-Doudoroff pathway under the anaerobic fermentation conditions. In some embodiments, the genetic modification is insertion of a promoter into genomic DNA in operable linkage with a polynucleotide that encodes the Embden-Meyerhoff glycolysis pathway member activity. In certain embodiments, the genetic modification is provision of a heterologous promoter polynucleotide in operable linkage with a polynucleotide that encodes the Embden-Meyerhoff glycolysis pathway member activity. In some embodiments, the genetic modification is a deletion or disruption of a polynucleotide that encodes, or regulates production of, the Embden-Meyerhoff glycolysis pathway member, and the microorganism comprises a heterologous nucleic acid that includes a polynucleotide encoding the Embden-Meyerhoff glycolysis pathway member operably linked to a polynucleotide that down-regulates production of the member under anaerobic fermentation conditions. In certain embodiments, the Embden-Meyerhoff glycolysis pathway member activity is a phosphofructokinase activity. In some embodiments, the activity of one or more (e.g., 2, 3, 4, 5 or more) pathway members in an EM pathway is reduced or removed to undetectable levels.
Also provided in some embodiments are engineered microorganisms that comprise a genetic modification that inhibits cell division upon exposure to a change in fermentation conditions, where: the genetic modification comprises introduction of a heterologous promoter operably linked to a polynucleotide encoding a polypeptide that regulates the cell cycle of the microorganism; and the promoter activity is altered by the change in fermentation conditions. Provided also in certain embodiments are engineered microorganisms that comprise a genetic modification that inhibits cell division and/or cell proliferation upon exposure of the microorganisms to a change in fermentation conditions. In certain embodiments, the genetic modification inhibits cell division, inhibits cell proliferation, inhibits the cell cycle and/or induces cell cycle arrest. In some embodiments, the change in fermentation conditions is a switch to anaerobic fermentation conditions, and in certain embodiments, the change in fermentation conditions is a switch to an elevated temperature. In some embodiments, the polypeptide that regulates the cell cycle has thymidylate synthase activity. In certain embodiments, the promoter activity is reduced by the change in fermentation conditions. In some embodiments, the genetic modification is a temperature sensitive mutation.
Provided also in some embodiments are methods for manufacturing a target product produced by an engineered microorganism, which comprise: (a) culturing an engineered microorganism described herein under aerobic conditions; and (b) culturing the engineered microorganism after (a) under anaerobic conditions, whereby the engineered microorganism produces the target product. Also provided in some embodiments are methods for producing a target product by an engineered microorganism, which comprise: (a) culturing an engineered microorganism described herein under a first set of fermentation conditions; and (b) culturing the engineered microorganism after (a) under a second set of fermentation conditions different than the first set of fermentation conditions, whereby the second set of fermentation conditions inhibits cell division and/or cell proliferation of the engineered microorganism. In certain embodiments, the target product is ethanol or succinic acid. In some embodiments, the host microorganism from which the engineered microorganism is produced does not produce a detectable amount of the target product. In certain embodiments, the culture conditions comprise fermentation conditions, comprise introduction of biomass, comprise introduction of a six-carbon sugar (e.g., glucose), and/or comprise introduction of a five-carbon sugar (e.g., xylulose, xylose); or combinations of the foregoing. In some embodiments, the target product is produced with a yield of greater than about 0.3 grams per gram of glucose added, and in certain embodiments, a method comprises purifying the target product from the cultured microorganisms. In some embodiments, a method comprises modifying the target product, thereby producing modified target product. In certain embodiments, a method comprises placing the cultured microorganisms, the target product or the modified target product in a container, and in certain embodiments, a method comprises shipping the container. In some embodiments, the second set of fermentation conditions comprises an elevated temperature as compared to the temperature in the first set of fermentation conditions. In certain embodiments, the genetic modification inhibits the cell cycle of the engineered microorganism upon exposure to the second set of fermentation conditions. In some embodiments, the genetic modification inhibits cell proliferation, inhibits cell division, inhibits the cell cycle and/or induces cell cycle arrest upon exposure to the second set of fermentation conditions. In certain embodiments, the genetic modification inhibits thymidylate synthase activity upon exposure to the change in fermentation conditions, and sometimes the genetic modification comprises a temperature sensitive mutation.
Also provided in certain embodiments are methods for manufacturing an engineered microorganism, which comprise: (a) introducing a genetic modification to a host microorganism that reduces an Embden-Meyerhoff glycolysis pathway member activity upon exposure of the engineered microorganism to anaerobic conditions; and (b) selecting for engineered microorganisms that (i) metabolize six-carbon sugars by the Embden-Meyerhoff glycolysis pathway under aerobic fermentation conditions, and (ii) preferentially metabolize six-carbon sugars by the Enter-Doudoroff pathway under the anaerobic fermentation conditions. In some embodiments, the genetic modification is insertion of a promoter into genomic DNA in operable linkage with a polynucleotide that encodes the Embden-Meyerhoff glycolysis pathway member activity. The genetic modification sometimes is provision of a heterologous promoter polynucleotide in operable linkage with a polynucleotide that encodes the Embden-Meyerhoff glycolysis pathway member activity. In certain embodiments, the genetic modification is a deletion or disruption of a polynucleotide that encodes, or regulates production of, the Embden-Meyerhoff glycolysis pathway member, and the microorganism comprises a heterologous nucleic acid that includes a polynucleotide encoding the Embden-Meyerhoff glycolysis pathway member operably linked to a polynucleotide that down-regulates production of the member under anaerobic fermentation conditions. In some embodiments, the Embden-Meyerhoff glycolysis pathway member activity is a phosphofructokinase activity. In certain embodiments, the activity of one or more (e.g., 2, 3, 4, 5 or more) pathway members in an EM pathway is reduced or removed to undetectable levels. Provided also in some embodiments are methods for manufacturing an engineered microorganism, which comprise: (a) introducing a genetic modification to a host microorganism that inhibits cell division upon exposure to a change in fermentation conditions, thereby producing engineered microorganisms; and (b) selecting for engineered microorganisms with inhibited cell division upon exposure of the engineered microorganisms to the change in fermentation conditions. In certain embodiments, the change in fermentation conditions comprises a change to anaerobic fermentation conditions. The change in fermentation conditions sometimes comprises a change to an elevated temperature. In some embodiments, the genetic modification inhibits the cell cycle of the engineered microorganism upon exposure to the change in fermentation conditions. The genetic modification sometimes inhibits cell division, inhibits the cell cycle, inhibits cell proliferation and/or induces cell cycle arrest upon exposure to the change in fermentation conditions. In some embodiments, the genetic modification inhibits thymidylate synthase activity upon exposure to the change in fermentation conditions, and in certain embodiments, the genetic modification comprises a temperature sensitive mutation.
In certain embodiments pertaining to engineered microorganisms, and methods of making or using such microorganisms, the microorganism comprises a genetic modification that adds or alters a five-carbon sugar metabolic activity. In some embodiments, the microorganism comprises a genetic alteration that adds or alters xylose isomerase activity. In certain embodiments, the microorganism comprises a genetic alteration that adds or alters five-carbon sugar transporter activity, and sometimes the transporter activity is a transporter facilitator activity or an active transporter activity. In some embodiments, the microorganism comprises a genetic alteration that adds or alters carbon dioxide fixation activity, and sometimes the genetic alteration that adds or alters phosphoenolpyruvate (PEP) carboxylase activity. In certain embodiments, the microorganism comprises a genetic modification that reduces or removes an alcohol dehydrogenase 2 activity. In some embodiments the microorganism is an engineered yeast, such as a Saccharomyces yeast (e.g., S. cerevisiae), for example.
Additional embodiments can be found in Example 29: Examples of the embodiments. Certain embodiments are described further in the following description, examples, claims and drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

The drawings illustrate embodiments of the technology and are not limiting. For clarity and ease of illustration, the drawings are not made to scale and, in some instances, various aspects may be shown exaggerated or enlarged to facilitate an understanding of particular embodiments.

FIG. 1 depicts a metabolic pathway that produces ethanol as by product of cellular respiration. The solid lines represent activities present in the Embden-Meyerhoff pathway (e.g., aerobic respiration). Dashed lines represent activities associated with the Entner-Doudoroff pathway (e.g., anaerobic respiration). One or both pathways often can be operational in a microorganism. The level of activity of each pathway can vary from organism to organism. The arrow from FBP (e.g., Fructose-1,6-bisphosphate, also referred to as F-1,6-BP) to G3P (e.g., glcyeraldehyde-3-phosphate), illustrates wild type levels of conversion of FBP to two molecules of G3P. In the embodiments shown in FIGS. 2, 3 and 5 a smaller arrow from FBP to G3P is illustrated, indicating reduced or no conversion of FBP to G3P. The reduction in conversion of FBP to G3P illustrated in FIGS. 2, 3 and 5 is a result of the reduction or elimination of the previous activity that converts fructose-6-phosphate (F6P) to FBP (e.g., the activity of PFK).

FIG. 2 depicts an engineered metabolic pathway that can be used to produce ethanol more efficiently in a host microorganism in which the pathway has been engineered. The solid lines in FIGS. 2-5 represent the metabolic pathway naturally found in a host organism (e.g., Saccharomyces cerevisiae, for example). The dashed lines in FIGS. 2-5 represent a novel activity or pathway engineered into a microorganism to allow increased ethanol production efficiency. In FIG. 2 the activity of an enzyme in the Embden-Meyerhoff pathway, phosphofructokinase (e.g., PFK) is permanently or temporarily reduced or eliminated. The inactivation is shown as the “X” in FIG. 2. Disruption of the activity of PFK serves to inactivate the Embden-Meyerhoff pathway (EM pathway). To allow cells to survive with a non-functional PFK, two activities from the Entner-Doudoroff pathway (ED pathway) have been introduced into a host organism engineered with the reduced or non-functional EM pathway. The introduced activities allow survival with an inactivated EM pathway in addition to increased efficiency of ethanol production.

FIG. 3 depicts an engineered metabolic pathway that can be used to produce ethanol using xylose as a carbon source by introducing the activity into a microorganism. The engineered microorganism can convert xylose to xylulose in a single reaction using the introduced xylose isomerase activity. Xylulose then can be fermented to ethanol by entering the EM pathway. Engineered microorganisms also can use the increased efficiency of ethanol production associated with inactivation of the EM pathway and introduction of activities of the ED pathway, shown in FIG. 2 and discussed below. The ability to utilize xylose efficiently (e.g., concurrently with six-carbon sugars or prior to the depletion of six-carbon sugars) can be provided by the introduction of the novel activity, xylose isomerase.

FIG. 4 depicts an engineered metabolic pathway that can be used to increase the efficiency of ethanol production (and other products) by introducing the ability to fix atmospheric carbon dioxide into a microorganism. The engineered microorganism can incorporate or fix atmospheric carbon dioxide into organic molecules using the introduced phosphoenolpyruvate carboxylase activity. Carbon dioxide incorporated in this manner can be used as an additional carbon source that can increase production of many organic molecules, including ethanol. Non-limiting examples of other products whose production can benefit from carbon fixation include; pyruvate, oxaloacetate, glyceraldehyde-3-phosphate and the like. The pathway depicted in FIG. 4 illustrates the introduction of the novel carbon dioxide fixation activity in the background of a fully functional EM pathway, and an introduced ED pathway. It is understood the introduction of the carbon fixation activity can benefit microorganisms that have no other modifications to any metabolic pathways. It also is understood that microorganism modified in one, or multiple, other metabolic pathways can benefit from the introduction of a carbon fixation activity.

FIG. 5 shows a combination of some engineered metabolic pathways described herein. The combination of engineered metabolic pathways shown in FIG. 5 can provide significant increases in the production of ethanol (or other products) when compared to the wild type organism or organisms lacking one, two, three or more of the modifications. Other combinations of engineered metabolic pathways not shown in FIG. 5 are possible, including but not limited to, combinations including increased alcohol tolerance, modified alcohol dehydrogenase 2 activity and/or modified thymidylate synthase activity, as described herein. Therefore, FIG. 5 also illustrates an embodiment of a method for generating an engineered microorganism with the ability to produce a greater amount of target product comprising expressing one or more genetically modified activities, described herein, in a host organism that produces the desired target (e.g., ethanol, pyruvate, oxaloacetate and the like, for example) via one or more metabolic pathways. In some embodiments, the combination of metabolic pathways includes those depicted in FIG. 5 in addition to combinations including one, two or three of the following activities; increased alcohol tolerance, modified alcohol dehydrogenase 2 activity and modified thymidylate synthase activity.

FIG. 6 shows DNA and amino acid sequence alignments for the nucleotide sequences of EDA (FIG. 6A (SEQ ID NOS 266-269, respectively, in order of appearance), 6B (SEQ ID NOS 270-273, respectively, in order of appearance)) and EDD (FIG. 6C (SEQ ID NOS 454-457, respectively, in order of appearance), 6D (SEQ ID NOS 458-461, respectively, in order of appearance)) genes from Zymomonas mobilis (native and optimized) and Escherichia coli.

FIG. 7 shows a representative western blot used to detect the presence of an enzyme associated with an activity described herein.

FIGS. 8A and 8B show representative Western blots used to detect levels of various exogenous EDD and EDA gene combinations expressed in a host organism. Experimental conditions and results are described in Example 9.

FIG. 9 graphically displays the relative activities of the various EDD/EDA combinations generated as described in Example 10.

FIG. 10 graphically represents the fermentation efficiency of engineered yeast strains carrying exogenous EDD/EDA gene combinations. Vector=p426GPD/p425GPD; EE=EDD-E. coli/EDA-E. coli, EP=EDD-E. coli/EDA-PAO1; PE=EDD-PAO1/EDA-E. coli, PP=EDD-PAO1/EDA-PAO1. Experimental conditions and results are described in Example 11. FIGS. 11A and 11B graphically illustrate fermentation data (e.g., cell growth, glucose usage and ethanol production) for engineered yeast strains generated as described herein. FIG. 11A illustrates the fermentation data for engineered strain BF428 (BY4742 with vector controls), and FIG. 11B illustrates the fermentation data for engineered strain BF591 (BY4742 with EDD-PAO1/EDA-PAO1). Experimental conditions and results are described in Example 12.

FIGS. 12A and 12B graphically illustrate fermentation data for engineered yeast strains described herein. FIG. 12A illustrates the fermentation data for engineered strain BF738 (BY4742 tal1 with vector controls p426GPD and p425GPD). FIG. 12B illustrates the fermentation data for engineered strain BF741 (BY4742 tal1 with plasmids pBF290 (EDD-PAO1) and pBF292 (EDA-PAO1). Experimental conditions and results are described in Example 13.

FIGS. 13A and 13B graphically illustrate fermentation data for engineered yeast strains as described herein. FIG. 13A illustrates the fermentation data for BF740 grown on 2% dextrose, and FIG. 13B illustrates the fermentation data for BF743 grown on 2% dextrose. Strain descriptions, experimental conditions and results are described in Example 14. FIG. 14 graphically illustrates the results of coupled assay kinetics for single plasmid and two plasmid edd/eda expression vector systems. Vector construction and experimental conditions are described in Example 16.

FIG. 15 shows a western blot of E. coli crude extract illustrated the presence of the EDD protein at the expected size. Lane 1 is a standard size ladder (Novex Sharp standard), Lane 2 is 1 μg BF1055 cell lysate, Lane 3 is 10 μg BF1055 cell lysate, Lane 4 is 1.5 μg BF1706 cell lysate, Lane 5 is 15 μg BF1706 cell lysate. Experimental methods and results are described in Example 22. FIG. 16 graphically illustrates the results of activity evaluations of EDA genes expressed in yeast. Experimental methods and results are described in Example 22.

DETAILED DESCRIPTION

Ethanol is a two carbon, straight chain, primary alcohol that can be produced from fermentation (e.g., cellular respiration processes) or as a by-product of petroleum refining. Ethanol has widespread use in medicine, consumables, and in industrial processes where it often is used as an essential solvent and a precursor, or feedstock, for the synthesis of other products (e.g., ethyl halides, ethyl esters, diethyl ether, acetic acid, ethyl amines and to a lesser extent butadiene, for example). The largest use of ethanol, worldwide, is as a motor fuel and fuel additive. Greater than 90% of the cars produced world wide can run efficiently on hydrous ethanol (e.g., 95% ethanol and 5% water). Ethanol also is commonly used for production of heat and light.
World production of ethanol exceeds 50 gigaliters (e.g., 1.3×10¹⁰US gallons), with 69% of the world supply coming from Brazil and the United States. The United States fuel ethanol industry is based largely on corn biomass. The use of corn biomass for ethanol production may not yield a positive net energy gain, and further has the potential of diverting land that could be used for food production into ethanol production. It is possible that cellulosic crops may displace corn as the main fuel crop for producing bio-ethanol. Non-limiting examples of cellulosic crops and waste materials include switchgrass and wood pulp waste from paper production and wood milling industries.
Biomass produced in the paper pulping and wood milling industries contains both 5 and six-carbon sugars. Use of this wasted biomass could allow production of significant amounts of bio-fuels and products, while reducing the use of land that could be used for food production. Predominant forms of sugars in the biomass produced in wood and paper pulping and wood milling industries are glucose and xylose.
Provided herein are methods for producing ethanol, ethanol derivatives and/or conjugates and other organic chemical intermediates (e.g., pyruvate, acetaldehyde, glyceraldehyde-3-phospate, and the like) using biological systems. Such production systems may have significantly less environmental impact and could be economically competitive with current manufacturing systems. Thus, provided herein are methods for manufacturing ethanol and other organic chemical intermediates by engineered microorganisms. In some embodiments microorganisms are engineered to contain at least one heterologous gene encoding an enzyme, where the enzyme is a member of a novel pathway engineered into the microorganism. In certain embodiments, an organism may be selected for elevated activity of a native enzyme.
Genetically engineered microorganisms described herein produce organic molecules for industrial uses. The organisms are designed to be “feedstock flexible” in that they can use five-carbon sugars (e.g., pentose sugars such as xylose, for example), six-carbon sugars (e.g., hexose sugars such as glucose or fructose, for example) or both as carbon sources. Further, the organisms described herein have been designed to be highly efficient in their use of hexose sugars to produce desired organic molecules. To that end, the microorganisms described herein are “pathway flexible” such that the microorganisms are able to direct hexose sugars primarily to either (i) the traditional glycolysis pathway (the Embden-Meyerhoff pathway) thereby generating ATP energy for cell growth and division at certain times, or (ii) a separate glycolytic pathway (the Entner-Doudoroff pathway) thereby producing significant levels of pyruvic acid, a key 3-carbon intermediate for producing many desired industrial organic molecules.
Pathway selection in the microorganism can be directed via one or more environmental switches such as a temperature change, oxygen level change, addition or subtraction of a component of the culture medium, or combinations thereof. The metabolic pathway flexibility of microorganisms described herein allow the microorganisms to efficiently use hexose sugars, which ultimately can lead to microorganisms capable of producing a greater amount of industrial chemical product per gram of feedstock as compared with conventional microorganisms (e.g., the organism from which the engineered organism was generated, for example). In some embodiments, the metabolic pathway flexibility of the engineered microorganisms described herein is generated by adding or increasing metabolic activities associated with the Entner-Doudoroff pathway. In certain embodiments the metabolic activities added are phosphogluconate dehydratase (e.g., EDD gene), 2-keto-3-deoxygluconate-6-phosphate aldolase (e.g., EDA gene) or both.
A number of industrially useful microorganisms (e.g., microorganisms used in fermentation processes, yeast for example), metabolize xylose inefficiently or are incapable of metabolizing xylose. Many organisms that can metabolize xylose do so only after all glucose and/or other six-carbon sugars have been depleted. The microorganisms described herein have been engineered to efficiently utilize five-carbon sugars (e.g., xylose, for example) as an alternative or additional source of carbon, concurrently with and/or prior to six-carbon sugar usage, by the incorporation of a heterologous nucleic acid (e.g., gene) encoding a xylose isomerase, in some embodiments, Xylose isomerase converts the five-carbon sugar xylose to xylulose. Xylulose can ultimately be converted to pyruvic acid or to ethanol through metabolism via the Embden-Meyerhoff or Entner-Doudoroff pathways.
Many non-photosynthetic organisms are not capable of incorporating inorganic atmospheric carbon into organic carbon compounds, via carbon fixation pathways, to any appreciable degree, or at all.
Often, microorganisms used in industrial fermentation process also are incapable of significant carbon fixation. The ability to incorporate atmospheric carbon dioxide, or carbon dioxide waste from respiration in fermentation processes, can increase the amount of industrial chemical product produced per gram of feedstock, in certain embodiments. Thus, the microorganisms described herein also can be modified to add or increase the ability to incorporate carbon from carbon dioxide into industrial chemical products, in some embodiments. In certain embodiments, the microorganisms described herein are engineered to express enzymes such as phosphoenolpyruvate carboxylase (“PEP” carboxylase) and/or ribulose 1,5-bis-phosphate carboxylase (“Rubisco”), thus allowing the use of carbon dioxide as an additional source of carbon.
A particularly useful industrial chemical product produced by fermentation is ethanol. Ethanol is an end product of cellular respiration and is produced from acetaldehyde by an alcohol dehydrogenase activity (e.g., by an enzyme like alcohol dehydrogenase 1 or ADH1, for example). However, ethanol can readily be converted back to acetaldehyde by the action of the enzyme alcohol dehydrogenase 2 (e.g., ADH2), thus lowering the yield of ethanol produced. In some embodiments, microorganisms described herein are modified to reduce or eliminate the activity of ADH2, to allow increased yields of ethanol. In certain embodiments, the engineered microorganisms described herein also are modified to have a higher tolerance to alcohol, thus enabling even higher yields of alcohol as a fermentation product without inhibition of cellular processes due to increased levels of alcohol in the growth medium.

Microorganisms

A microorganism selected often is suitable for genetic manipulation and often can be cultured at cell densities useful for industrial production of a target product. A microorganism selected often can be maintained in a fermentation device.
The term “engineered microorganism” as used herein refers to a modified microorganism that includes one or more activities distinct from an activity present in a microorganism utilized as a starting point (hereafter a “host microorganism”). An engineered microorganism includes a heterologous polynucleotide in some embodiments, and in certain embodiments, an engineered organism has been subjected to selective conditions that alter an activity, or introduce an activity, relative to the host microorganism. Thus, an engineered microorganism has been altered directly or indirectly by a human being. A host microorganism sometimes is a native microorganism, and at times is a microorganism that has been engineered to a certain point.
In some embodiments an engineered microorganism is a single cell organism, often capable of dividing and proliferating. A microorganism can include one or more of the following features: aerobe, anaerobe, filamentous, non-filamentous, monoploid, dipoid, auxotrophic and/or non-auxotrophic. In certain embodiments, an engineered microorganism is a prokaryotic microorganism (e.g., bacterium), and in certain embodiments, an engineered microorganism is a non-prokaryotic microorganism. In some embodiments, an engineered microorganism is a eukaryotic microorganism (e.g., yeast, fungi, amoeba).
Any suitable yeast may be selected as a host microorganism, engineered microorganism or source for a heterologous polynucleotide. Yeast include, but are not limited to, Yarrowia yeast (e.g., Y. lipolytica (formerly classified as Candida lipolytica)), Candida yeast (e.g., C. revkaufi, C. pulcherrima, C. tropicalis, C. utilis), Rhodotorula yeast (e.g., R. glutinus, R. graminis), Rhodosporidium yeast (e.g., R. toruloides), Saccharomyces yeast (e.g., S. cerevisiae, S. bayanus, S. pastorianus, S. carlsbergensis), Cryptococcus yeast, Trichosporon yeast (e.g., T. pullans, T. cutaneum), Pichia yeast (e.g., P. pastoris) and Lipomyces yeast (e.g., L. starkeyii, L. lipoferus). In some embodiments, a yeast is a S. cerevisiae strain including, but not limited to, YGR240CBY4742 (ATCC accession number 4015893) and BY4742 (ATCC accession number 201389). In some embodiments, a yeast is a Y. lipolytica strain that includes, but is not limited to, ATCC20362, ATCC8862, ATCC18944, ATCC20228, ATCC76982 and LGAM S(7)1 strains (Papanikolaou S., and Aggelis G., Bioresour. Technol. 82(1):43-9 (2002)). In certain embodiments, a yeast is a C. tropicalis strain that includes, but is not limited to, ATCC20336, ATCC20913, SU-2 (ura3−/ura3−), ATCC20962, H5343 (beta oxidation blocked; U.S. Pat. No. 5,648,247) strains.
Any suitable fungus may be selected as a host microorganism, engineered microorganism or source for a heterologous polynucleotide. Non-limiting examples of fungi include, but are not limited to, Aspergillus fungi (e.g., A. parasiticus, A. nidulans), Thraustochytrium fungi, Schizochytrium fungi and Rhizopus fungi (e.g., R. arrhizus, R. oryzae, R. nigricans), Orpinomyces or Piromyces. In some embodiments, a fungus is an A. parasiticus strain that includes, but is not limited to, strain ATCC24690, and in certain embodiments, a fungus is an A. nidulans strain that includes, but is not limited to, strain ATCC38163.
Any suitable prokaryote may be selected as a host microorganism, engineered microorganism or source for a heterologous polynucleotide. A Gram negative or Gram positive bacteria may be selected. Examples of bacteria include, but are not limited to, Bacillus bacteria (e.g., B. subtilis, B. megaterium, B. stearothermophilus), Bacteroides bacteria (e.g., Bacteroides uniformis, Bacteroides thetaiotaomicron), Clostridium bacteria (e.g., C. phytofermentans, C. thermohydrosulfuricum, C. cellulyticum (H10)), Acinetobacter bacteria, Norcardia baceteria, Lactobacillus bacterial (e.g., Lactobacillus pentosus), Xanthobacter bacteria, Escherichia bacteria (e.g., E. coli (e.g., strains DH10B, Stb12, DH5-alpha, DB3, DB3.1), DB4, DB5, JDP682 and ccdA-over (e.g., U.S. application Ser. No. 09/518,188))), Streptomyces bacteria (e.g., Streptomyces rubiginosus, Streptomyces murinus), Erwinia bacteria, Klebsiella bacteria, Serratia bacteria (e.g., S. marcessans), Pseudomonas bacteria (e.g., P. aeruginosa), Salmonella bacteria (e.g., S. typhimurium, S. typhi), Thermus bacteria (e.g., Thermus thermophilus), and Thermotoga bacteria (e.g., Thermotoga maritiima, Thermotoga neopolitana) and Ruminococcus (e.g., Ruminococcus environmental samples, Ruminococcus albus, Ruminococcus bromii, Ruminococcus callidus, Ruminococcus flavefaciens, Ruminococcus gauvreauii, Ruminococcus gnavus, Ruminococcus lactaris, Ruminococcus obeum, Ruminococcus sp., Ruminococcus sp. 14531, Ruminococcus sp. 15975, Ruminococcus sp. 16442, Ruminococcus sp. 18P13, Ruminococcus sp. 25F6, Ruminococcus sp. 25F7, Ruminococcus sp. 25F8, Ruminococcus sp. 4_—1_—47FAA, Ruminococcus sp. 5, Ruminococcus sp. 5_—1_—39BFAA, Ruminococcus sp. 7L75, Ruminococcus sp. 8_—1_—37FAA, Ruminococcus sp. 9SE51, Ruminococcus sp. C36, Ruminococcus sp. CB10, Ruminococcus sp. CB3, Ruminococcus sp. CCUG 37327 A, Ruminococcus sp. CE2, Ruminococcus sp. CJ60, Ruminococcus sp. CJ63, Ruminococcus sp. CO1, Ruminococcus sp. CO12, Ruminococcus sp. CO22, Ruminococcus sp. CO27, Ruminococcus sp. CO28, Ruminococcus sp. CO34, Ruminococcus sp. CO41, Ruminococcus sp. CO47, Ruminococcus sp. CO7, Ruminococcus sp. CS1, Ruminococcus sp. CS6, Ruminococcus sp. DJF_VR52, Ruminococcus sp. DJF_VR66, Ruminococcus sp. DJF_VR67, Ruminococcus sp. DJF_VR70k1, Ruminococcus sp. DJF_VR87, Ruminococcus sp. Eg2, Ruminococcus sp. Egf, Ruminococcus sp. END-1, Ruminococcus sp. FD1, Ruminococcus sp. GM2/1, Ruminococcus sp. ID1, Ruminococcus sp. ID8, Ruminococcus sp. K-1, Ruminococcus sp. KKA Seq234, Ruminococcus sp. M-1, Ruminococcus sp. M10, Ruminococcus sp. M22, Ruminococcus sp. M23, Ruminococcus sp. M6, Ruminococcus sp. M73, Ruminococcus sp. M76, Ruminococcus sp. MLG080-3, Ruminococcus sp. NML 00-0124, Ruminococcus sp. Pei041, Ruminococcus sp. SC101, Ruminococcus sp. SC103, Ruminococcus sp. Siijpesteijn 1948, Ruminococcus sp. WAL 17306, Ruminococcus sp. YE281, Ruminococcus sp. YE58, Ruminococcus sp. YE71, Ruminococcus sp. ZS2-15, Ruminococcus torques). Bacteria also include, but are not limited to, photosynthetic bacteria (e.g., green non-sulfur bacteria (e.g., Choroflexus bacteria (e.g., C. aurantiacus), Chloronema bacteria (e.g., C. gigateum)), green sulfur bacteria (e.g., Chlorobium bacteria (e.g., C. limicola), Pelodictyon bacteria (e.g., P. luteolum), purple sulfur bacteria (e.g., Chromatium bacteria (e.g., C. okenii)), and purple non-sulfur bacteria (e.g., Rhodospirillum bacteria (e.g., R. rubrum), Rhodobacter bacteria (e.g., R. sphaeroides, R. capsulatus), and Rhodomicrobium bacteria (e.g., R. vanellii)).
Cells from non-microbial organisms can be utilized as a host microorganism, engineered microorganism or source for a heterologous polynucleotide. Examples of such cells, include, but are not limited to, insect cells (e.g., Drosophila (e.g., D. melanogaster), Spodoptera (e.g., S. frugiperda Sf9 or Sf21 cells) and Trichoplusa (e.g., High-Five cells); nematode cells (e.g., C. elegans cells); avian cells; amphibian cells (e.g., Xenopus laevis cells); reptilian cells; and mammalian cells (e.g., NIH3T3, 293, CHO, COS, VERO, C127, BHK, Per-C6, Bowes melanoma and HeLa cells).
Microorganisms or cells used as host organisms or source for a heterologous polynucleotide are commercially available. Microorganisms and cells described herein, and other suitable microorganisms and cells are available, for example, from Invitrogen Corporation, (Carlsbad, Calif.), American Type Culture Collection (Manassas, Va.), and Agricultural Research Culture Collection (NRRL; Peoria, Ill.).
Host microorganisms and engineered microorganisms may be provided in any suitable form. For example, such microorganisms may be provided in liquid culture or solid culture (e.g., agar-based medium), which may be a primary culture or may have been passaged (e.g., diluted and cultured) one or more times. Microorganisms also may be provided in frozen form or dry form (e.g., lyophilized). Microorganisms may be provided at any suitable concentration.

Six-Carbon Sugar Metabolism and Activities

Six-carbon or hexose sugars can be metabolized using one of two pathways in many organisms. One pathway, the Embden-Meyerhoff pathway (EM pathway), operates primarily under aerobic (e.g., oxygen rich) conditions. The other pathway, the Entner-Doudoroff pathway (ED pathway), operates primarily under anaerobic (e.g., oxygen poor) conditions, producing pyruvate that can be converted to lactic acid. Lactic acid can be further metabolized upon a return to appropriate conditions. The EM pathway produces two ATP for each six-carbon sugar metabolized, as compared to one ATP produced for each six-carbon sugar metabolized in the ED pathway. Thus the ED pathway yields ethanol more efficiently than the EM pathway with respect to a given amount of input carbon, as seen by the lower net energy yield. However, yeast preferentially use the EM pathway for metabolism of six-carbon sugars, thereby preferentially using the pathway that yields more energy and less desired product.
The following steps and enzymatic activities metabolize six-carbon sugars via the EM pathway. Six-carbon sugars (glucose, sucrose, fructose, hexose and the like) are converted to glucose-6-phosphate by hexokinase or glucokinase (e.g., HXK or GLK, respectively). Glucose-6-phosphate can be converted to fructose-6-phosphate by phosphoglucoisomerase (e.g., PGI). Fructose-6-phosphate can be converted to fructose-1,6-bisphosphate by phosphofructokinase (e.g., PFK). Fructose-1,6-bisphosphate (F1,6BP) represents a key intermediate in the metabolism of six-carbon sugars, as the next enzymatic reaction converts the six-carbon sugar into two 3 carbon sugars. The reaction is catalyzed by fructose bisphosphate aldolase and yields a mixture of dihydroxyacetone phosphate (DHAP) and glyceraldehyde-3-phosphate (G-3-P). The mixture of the two 3 carbon sugars is preferentially converted to glyceraldehyde-3-phosphate by the action of triosephosphate isomerase. G-3-P is converted is converted to 1,3-diphosphoglycerate (1,3-DPG) by glyceraldehyde-3-phosphate dehydrogenase (GLD). 1,3-DPG is converted to 3-phosphoglycerate (3-P-G by phosphoglycerate kinase (PGK). 3-P-G is converted to 2-phosphoglycerate (2-P-G) by phophoglycero mutase (GPM). 2-P-G is converted to phosphoenolpyruvate (PEP) by enolase (ENO). PEP is converted to pyruvate (PYR) by pyruvate kinase (PYK). PYR is converted to acetaldehyde by pyruvate dicarboxylase (PDC). Acetaldehyde is converted to ethanol by alcohol dehydrogenase 1 (ADH1).
Many enzymes in the EM pathway are reversible. The enzymes in the EM pathway that are not reversible, and provide a useful activity with which to control six-carbon sugar metabolism, via the EM pathway, include, but are not limited to phosphofructokinase and alcohol dehydrogenase. In some embodiments, reducing or eliminating the activity of phosphofructokinase may inactivate the EM pathway. Engineering microorganisms with modified activities in PFK and/or ADH may yield increased product output as compared to organisms with the wild type activities, in certain embodiments. In some embodiments, modifying a reverse activity (e.g., the enzyme responsible for catalyzing the reverse activity of ADH, for example) may also yield an increase in product yield by reducing or eliminating the back conversion of products by the backwards reaction. The activity which catalyzes the conversion of ethanol to acetaldehyde is alcohol dehydrogenase 2 (ADH2). Reducing or eliminating the activity of ADH2 can increase the yield of ethanol per unit of carbon input due to the inactivation of the conversion of ethanol to acetaldehyde, in certain embodiments. In addition to enzyme activities that are not reversible, certain reversible activities also can be used to control six-carbon sugar metabolism via the EM pathway, in some embodiments. A non-limiting example of a reversible enzymatic activity that can be utilized to control six-carbon sugar metabolism includes phosphoglucose isomerase (PGI).
A microorganism may be engineered to include or regulate one or more activities in the Embden-Meyerhoff pathway, for example. In some embodiments, one or more of these activities may be altered such that the activity or activities can be increased or decreased according to a change in environmental conditions. In certain embodiments, one or more of the activities (e.g., PGI, PFK or ADH2) can be altered to allow regulated control and an alternative pathway for more efficient carbon metabolism can be provided (e.g., one or more activities from the ED pathway, for example). An engineered organism with the EM pathway under regulatable control and a novel or enhanced ED pathway would be useful for producing significantly more ethanol or other end product from a given amount of input feedstock. The term “activity” as used herein refers to the functioning of a microorganism's natural or engineered biological pathways to yield various products including ethanol and its precursors. Ethanol (or other product) producing activity can be provided by any non-mammalian source in certain embodiments. Such sources include, without limitation, eukaryotes such as yeast and fungi and prokaryotes such as bacteria. In some embodiments, the activity of one or more (e.g., 2, 3, 4, 5 or more) pathway members in an EM pathway is reduced or removed to undetectable levels.
An engineered microorganism may, in some embodiments, preferentially metabolize six-carbon sugars via the ED pathway as opposed to the EM pathway under certain conditions. Such engineered microorganisms may metabolize about 60% or more of the available six-carbon sugars via the ED pathway (e.g., about 62%, 64%, 66%, 68%, 70%, 72%, 74%, 76%, 78%, 80%, 82%, 84%, 86%, 88%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%, or greater than any one of the foregoing), and such fraction of the available six-carbon sugars are not metabolized by the EM pathway, under certain conditions. A microorganism may metabolize six-carbon sugars substantially via the ED pathway, and not the EM pathway, in certain embodiments (e.g., 99% or greater, or 100%, of the available six-carbon sugars are metabolized via the ED pathway). A six-carbon sugar is deemed as being metabolized via a particular pathway when the sugar is converted to end metabolites of the pathway, and not intermediate metabolites only, of the particular pathway. A microorganism may preferentially metabolize certain sugars under the ED pathway after a certain time after the microorganism is exposed to a certain set of conditions (e.g., there may be a time delay after a microorganism is exposed to a certain set of conditions before the microorganism preferentially metabolizes sugars by the ED pathway).
Certain novel activities involved in the metabolism of six-carbon sugars by the ED pathway can be engineered into a desired yeast strain to increase the efficiency of ethanol (or other products) production. Yeast do not have an activity that converts 6-phophogluconate to 2-keto-3-deoxy-6-p-gluconate or an activity that converts 2-keto-3-deoxy-6-p-gluconate to pyruvate. Addition of these activities to engineered yeast can allow the engineered microorganisms to increase fermentation efficiency by allowing yeast to ferment ethanol under anaerobic condition without having to use the EM pathway and expend additional energy. Therefore, by providing novel activities associated with converting 6-phophogluconate to 2-keto-3-deoxy-6-p-gluconate and 2-keto-3-deoxy-6-p-gluconate to pyruvate, the engineered microorganism can benefit by producing ethanol more efficiently, with respect to a given amount of input carbon, than by using the native EM pathway.
Bacteria often have enzymatic activities that confer the ability to anaerobically metabolize six-carbon sugars to ethanol. These activities are associated with the ED pathway and include, but are not limited to, phosphogluconate dehydratase (e.g., the EDD gene, for example), and 2-keto-3-deoxygluconate-6-phosphate aldolase (e.g., the EDA gene, for example). Phosphogluconate dehydratase converts 6-phophogluconate to 2-keto-3-deoxy-6-p-gluconate. 2-keto-3-deoxygluconate-6-phosphate aldolase converts 2-keto-3-deoxy-6-p-gluconate to pyruvate. In some embodiments, these activities can be introduced into a host organism to generate an engineered microorganism which gains the ability to use the ED pathway to produce ethanol more efficiently than the non-engineered starting organism, by virtue of the lower net energy yield by the ED pathway. A microorganism may be engineered to include or regulate one or more activities in the Entner-Doudoroff pathway. In some embodiments, one or more of these activities may be altered such that the activity or activities can be increased or decreased according to a change in environmental conditions. Nucleic acid sequences encoding Embden-Meyerhoff pathway and Entner-Doudoroff pathway activities can be obtained from any suitable organism (e.g., plants, bacteria, and other microorganisms, for example) and any of these activities can be used herein with the proviso that the nucleic acid sequence is naturally active in the chosen microorganism when expressed, or can be altered or modified to be active.
Yeast also can have endogenous or heterologous enzymatic activities that enable the organism to anaerobically metabolize six carbon sugars. Saccharomyces cerevisiae used in fermentation often convert glucose-6-phospate (G-6-P) to fructose-6-phosphate (F-6-P) via phosphoglucose isomerase (EC 5.3.1.9), up to 95% of G-6-P is converted to F-6-P in this manner for example. Only a minor proportion of G-6-P is converted to 6-phophoglucono-lactone (6-PGL) by an alternative enzyme, glucose-6-phosphate dehydrogenase (EC 1.1.1.49). Yeast engineered to carry both Entner-Doudoroff (ED) and Embden-Meyerhoff (EM) pathways often covert sugars to ethanol using the EM pathway preferentially. Inactivation of one or more activities in the EM pathway can result in conversion of sugars to ethanol using the ED pathway preferentially, in some embodiments.
Phosphoglucose isomerase (EC 5.3.1.9) catalyzes the reversible interconversion of glucose-6-phosphate and fructose-6-phosphate. Phosphoglucose isomerase is encoded by the PGI1 gene in S. cerevisiae. The proposed mechanism for sugar isomerization involves several steps and is thought to occur via general acid/base catalysis. Since glucose 6-phosphate and fructose 6-phosphate exist predominantly in their cyclic forms, PGI is believed to catalyze first the opening of the hexose ring to yield the straight chain form of the substrates. Glucose 6-phosphate and fructose 6-phosphate then undergo isomerization via formation of a cis-enediol intermediate with the double bond located between C-1 and C-2. Phosphoglucose isomerase sometimes also is referred to as glucose-6-phosphate isomerase or phosphohexose isomerase.
PGI is involved in different pathways in different organisms. In some higher organisms PGI is involved in glycolysis, and in mammals PGI also is involved in gluconeogenesis. In plants PGI is involved in carbohydrate biosynthesis, and in some bacteria PGI provides a gateway for fructose into the Entner-Doudoroff pathway. PGI also is known as neuroleukin (a neurotrophic factor that mediates the differentiation of neurons), autocrine motility factor (a tumor-secreted cytokine that regulates cell motility), differentiation and maturation mediator and myofibril-bound serine proteinase inhibitor, and has different roles inside and outside the cell. In the cytoplasm, PGI catalyses the second step in glycolysis, while outside the cell it serves as a nerve growth factor and cytokine. PGI activity is involved in cell cycle progression and completion of the gluconeogenic events of sporulation in S. cerevisiae.
In certain embodiments, phosphoglucose isomerase activity is altered in an engineered microorganism. In some embodiments phosphoglucose isomerase activity is decreased or disrupted in an engineered microorganism. In certain embodiments, decreasing or disrupting phosphoglucose isomerase activity may be desirable to decrease or eliminate the isomerization of glucose-6-phosphate to fructose-6-phosphate, thereby increasing the proportion of glucose-6-phosphate converted to gluconolactone-6-phosphate by the activity encoded by ZWF1 (e.g., glucose-6-phosphate dehydrogenase). Increased levels of gluconolactone-6-phosphate can be further metabolized and thereby improve fermentation of sugar to ethanol via activities in the Entner-Doudoroff pathway, even in the presence of the enzymes comprising the Embden-Meyerhoff pathway. Decreased or disrupted phosphoglucose isomerase (EC 5.3.1.9) activity in yeast may be achieved by any suitable method, or as described herein. Non-limiting examples of methods suitable for decreasing or disrupting the activity of phosphoglucose isomerase include use of a regulated promoter, use of a weak constitutive promoter, disruption of one of the two copies of the gene in a diploid yeast, disruption of both copies of the gene in a diploid yeast, expression of an anti-sense nucleic acid, expression of an siRNA, over expression of a negative regulator of the endogenous promoter, alteration of the activity of an endogenous or heterologous gene, use of a heterologus gene with lower specific activity, the like or combinations thereof. In some embodiments, a gene used to knockout one activity can also introduce or increase another activity. PGI1 genes may be native to S. cerevisiae, or may be obtained from a heterologous source.
Glucose-6-phosphate dehydrogenase (EC 1.1.1.49) catalyzes the first step of the pentose phosphate pathway, and is encoded by the S. cerevisiae gene, zwf1. The reaction for the first step in the PPP pathway is;
D-glucose 6-phosphate+NADP⁺=D-glucono-1,5-lactone 6-phosphate+NADPH+H⁺
This reaction is irreversible and rate-limiting for efficient fermentation of sugar via the Entner-Doudoroff pathway. The enzyme regenerates NADPH from NADP+ and is important both for maintaining cytosolic levels of NADPH and protecting yeast against oxidative stress. Zwf1p expression in yeast is constitutive, and the activity is inhibited by NADPH such that processes that decrease the cytosolic levels of NADPH stimulate the oxidative branch of the pentose phosphate pathway. Amplification of glucose-6-phosphate dehydrogenase activity in yeast may be desirable to increase the proportion of glucose-6-phosphate converted to 6-phosphoglucono-lactone and thereby improve fermentation of sugar to ethanol via the Entner-Doudoroff pathway, even in the presence of the enzymes comprising the Embden-Meyerhoff pathway.
Glucose-6-phosphate dehydrogenase (EC 1.1.1.49) activity in yeast may be amplified by over-expression of the zwf1 gene by any suitable method. Non-limiting examples of methods suitable to amplify or over express zwf1 include amplifying the number of ZWF1 genes in yeast following transformation with a high-copy number plasmid (e.g., such as one containing a 2 uM origin of replication), integration of multiple copies of ZWF1 into the yeast genome, over-expression of the ZWF1 gene directed by a strong promoter, the like or combinations thereof. The ZWF1 gene may be native to S. cerevisiae, or it may be obtained from a heterologous source. 6-phosphogluconolactonase (EC 3.1.1.31) catalyzes the second step of the ED (e.g., pentose phosphate pathway), and is encoded by S. cerevisiae genes SOL3 and SOL4. The reaction for the second step of the pentose phosphate pathway is;
6-phospho-D-glucono-1,5-lactone+H2O=6-phospho-D-gluconate
Amplification of 6-phosphogluconolactonase activity in yeast may be desirable to increase the proportion of 6-phospho-D-glucono-1,5-lactone converted to 6-phospho-D-gluconate and thereby improve fermentation of sugar to ethanol via the Entner-Doudoroff pathway, even in the presence of the enzymes comprising the Embden-Meyerhoff pathway. For example, over expression of SOL3 is known to increase the rate of carbon source utilization to result in faster growth on xylose than wild type.
The Saccharomyces cerevisiae SOL protein family includes Sol3p and Sol4p. Both localize predominantly in the cytosol, exhibit 6-phosphogluconolactonase activity and function in the pentose phosphate pathway. 6-phosphogluconolactonase (EC 3.1.1.31) activity in yeast may be amplified by over-expression of the SOL3 and/or SOL4 gene(s) by any suitable method. Non-limiting examples of methods to amplify or over express SOL3 and SOL4 include increasing the number of SOL3 and/or SOL4 genes in yeast by transformation with a high-copy number plasmid, integration of multiple copies of SOL3 and/or SOL4 gene(s) into the yeast genome, over-expression of the SOL3 and/or SOL4 gene(s) directed by a strong promoter, the like or combinations thereof. The SOL3 and/or SOL4 gene(s) may be native to S. cerevisiae, or may be obtained from a heterologous source. For example, Sol3p and Sol4p have similarity to each other, and to Candida albicans Sol1p, Schizosaccharomyces pombe Sol1p, human PGLS which is associated with 6-phosphogluconolactonase deficiency, and human H6PD which is associated with cortisone reductase deficiency. Sol3p and Sol4p are also similar to the 6-phosphogluconolactonases in bacteria (Pseudomonas aeruginosa) and eukaryotes (Drosophila melanogaster, Arabidopsis thaliana, and Trypanosoma brucei), to the glucose-6-phosphate dehydrogenase enzymes from bacteria (Mycobacterium leprae) and eukaryotes (Plasmodium falciparum and rabbit liver microsomes), and have regions of similarity to proteins of the Nag family, including human GNPI and Escherichia coli NagB.
Phosphogluconate dehydrogenase (EC:1.1.1.44) catalyzes the second oxidative reduction of NADP+ to NADPH in the cytosolic oxidative branch of the pentose phosphate pathway, and is encoded by the S. cerevisiae genes GND1 and GND2. GND1 encodes the major isoform of the enzyme accounting for up to 80% of phosphogluconate dehydrogenase activity, while GND2 encodes the minor isoform of the enzyme. Phosphogluconate dehydrogenase sometimes also is referred to as phosphogluconic acid dehydrogenase, 6-phosphogluconic dehydrogenase, 6-phosphogluconic carboxylase, 6-phosphogluconate dehydrogenase (decarboxylating), and 6-phospho-D-gluconate dehydrogenase. Phosphogluconate dehydrogenase belongs to the family of oxidoreductases, specifically those acting on the CH—OH group of donor with NAD⁺ or NADP⁺ as the acceptor. The reaction for the second oxidative reduction of NADP+ to NADPH in the cytosolic oxidative branch of the pentose phosphate pathway is;
6-phospho-D-gluconate+NADP
D-ribulose 5-phosphate+CO₂+NADPH
Decreasing the level of 6-phosphogluconolactonase activity in yeast may be desirable to decrease the proportion of 6-phospho-D-gluconate converted to D-ribulose 5-phosphate thereby increasing the levels of the intermediate gluconate-6-phosphate available for conversion to 6-dehydro-3-deoxy-gluconate-6-phosphate, in some embodiments involving engineered microorganisms including increased EDA and EDD activities, thereby improving fermentation of sugar to ethanol via the Entner-Doudoroff pathway, even in the presence of the enzymes comprising the Embden-Meyerhoff pathway.
Decreasing or disrupting 6-phosphogluconolactonase activity in yeast may be achieved by any suitable method, or as described herein. Non-limiting examples of methods suitable for decreasing the activity of 6-phosphogluconate dehydrogenase include use of a regulated promoter, use of a weak constitutive promoter, disruption of one of the two copies of the gene in a diploid yeast (e.g., partial gene knockout), disrupting both copies of the gene in a diploid yeast (e.g., complete gene knockout) expression of an anti-sense nucleic acid, expression of an siRNA, over expression of a negative regulator of the endogenous promoter, alteration of the activity of an endogenous or heterologous gene, use of a heterologus gene with lower specific activity, the like or combinations thereof. In some embodiments, a gene used to knockout one activity can also introduce or increase another activity. GND1 and/or GND2 gene(s) may be native to S. cerevisiae, or may be obtained from a heterologous source. For example, S. cerevisiae GND1 and GND2 have similarity to each other, and to the phosphogluconate dehydrogenase nucleotide sequences of Candida parapsilosis, Cryptococcus neoformans and humans.

Five-Carbon Sugar Metabolism and Activities

As noted above, five-carbon sugars are the second most predominant form of sugars in lignocelluosic waste biomass produced in wood pulp and wood milling industries. Furthermore, xylose is the second most abundant carbohydrate in nature. However, the conversion of biomass to energy (e.g., ethanol, for example) has not proven economically attractive because many organisms cannot metabolize hemicellulose. Biomass and waste biomass contain both cellulose and hemicellulose. Many industrially applicable organisms can metabolize five-carbon sugars (e.g., xylose, pentose and the like), but may do so at low efficiency, or may not begin metabolizing five-carbon sugars until all six-carbon sugars have been depleted from the growth medium. Many yeast and fungus grow slowly on xylose and other five-carbon sugars. Some yeast, such as S. cerevisiae do not naturally use xylose, or do so only if there are no other carbon sources. An engineered microorganism (e.g., yeast, for example) that could grow rapidly on xylose and provide ethanol and/or other products as a result of fermentation of xylose can be useful due to the ability to use a feedstock source that is currently underutilized while also reducing the need for petrochemicals.
The pentose phosphate pathway (PPP), which is a biochemical route for xylose metabolism, is found in virtually all cellular organisms where it provides D-ribose for nucleic acid biosynthesis, D-erythrose 4-phosphate for the synthesis of aromatic amino acids and NADPH for anabolic reactions. The PPP is thought of as having two phases. The oxidative phase converts the hexose, D-glucose 6P, into the pentose, D-ribulose 5P, plus CO2 and NADPH. The non-oxidative phase converts D-ribulose 5P into D-ribose 5P, D-xylulose 5P, D-sedoheptulose 7P, D-erythrose 4P, D-fructose 6P and D-glyceraldehyde 3P. D-Xylose and L-arabinose enter the PPP through D-xylulose.
Certain organisms (e.g., yeast, filamentous fungus and other eukaryotes, for example) require two or more activities to convert xylose to a usable from that can be metabolized in the pentose phosphate pathway. The activities are a reduction and an oxidation carried out by xylose reductase (XYL1) and xylitol dehydrogenase (XYL2), respectively. Xylose reductase converts D-xylose to xylitol. Xylitol dehydrogenase converts xylitol to D-xylulose. The use of these activities sometimes can inhibit cellular function due to cofactor and metabolite imbalances.
Some organisms (e.g., certain bacteria, for example) require only one activity, xylose isomerase (xylA). Xylose isomerase converts xylose directly to xylulose. Xylulose can then be converted to xylulose-5-phosphate by xylulose kinase. Phosphorylation of xylulose then allows the five-carbon sugar to be further converted by transketolase (e.g., TKL1/TKL2) to enter the EM pathway for further metabolism at either fructose-6-phosphate or glyceraldehyde-3-phosphate. In some embodiments, where the EM pathway is inactivated, five-carbon sugars enter the EM pathway and are further converted for use by the ED pathway. Therefore, engineering a microorganism with xylose isomerase activity may allow rapid growth on xylose when compared to the non-engineered microorganism, while avoiding cofactor and metabolite imbalances.
A microorganism may be engineered to include or regulate one or more activities in a five-carbon sugar metabolism pathway (e.g., pentose phosphate pathway, for example). In some embodiments, an engineered microorganism can comprise a xylose isomerase activity. In some embodiments, the xylose isomerase activity may be altered such that the activity can be increased or decreased according to a change in environmental conditions. Nucleic acid sequences encoding xylose isomerase activities can be obtained from any suitable bacteria (e.g., Piromyces, Orpinomyces, Bacteroides thetaiotaomicron, Clostridium phytofermentans, Thermus thermophilus and Ruminococcus (e.g., R. flavefaciens) and any of these activities can be used herein with the proviso that the nucleic acid sequence is naturally active in the chosen microorganism when expressed, or can be altered or modified to be active.

Carbon Dioxide Metabolism and Activities

Microorganisms grown in fermentors often are grown under anaerobic conditions, with limited or no gas exchange. Therefore the atmosphere inside fermentors sometimes is carbon dioxide rich. Unlike photosynthetic organisms, many microorganisms suitable for use in industrial fermentation processes do not incorporate atmospheric carbon (e.g., CO₂) to any significant degree, or at all. Thus, to ensure that increasing levels of carbon dioxide do not inhibit cell growth and the fermentation process, methods to remove carbon dioxide from the interior of fermentors can be useful.
Photosynthetic organisms make use of atmospheric carbon by incorporating the carbon available in carbon dioxide into organic carbon compounds by a process known as carbon fixation. The activities responsible for a photosynthetic organism's ability to fix carbon dioxide include phosphoenolpyruvate carboxylase (e.g., PEP carboxylase) or ribulose 1,5-bis-phosphate carboxylase (e.g., Rubisco). PEP carboxylase catalyzes the addition of carbon dioxide to phosphoenolpyruvate to generate the four-carbon compound oxaloacetate. Oxaloacetate can be used in other cellular processes or be further converted to yield several industrially useful products (e.g., malate, succinate, citrate and the like). Rubisco catalyzes the addition of carbon dioxide and ribulose-1,5-bisphosphate to generate 2 molecules of 3-phosphoglycerate. 3-phosphoglycerate can be further converted to ethanol via cellular fermentation or used to produce other commercially useful products. Nucleic acid sequences encoding PEP carboxylase and Rubisco activities can be obtained from any suitable organism (e.g., plants, bacteria, and other microorganisms, for example) and any of these activities can be used herein with the proviso that the nucleic acid sequence is either naturally active in the chosen microorganism when expressed, or can be altered or modified to be active.

Examples of Altered Activities

In some embodiments, engineered microorganisms can include modifications to one or more (e.g., 1, 2, 3, 4, 5, 6 or all) of the following activities: phosphofructokinase activity (PFK1 A subunit, PFK2 B subunit), phosphogluconate dehydratase activity (EDD), 2-keto-3-deoxygluconate-6-phosphate aldolase activity (EDA), xylose isomerase activity (xylA), phosphoenolpyruvate carboxylase activity (PEP carboxylase), alcohol dehydrogenase 2 activity (ADH2), thymidylate synthase activity, phosphoglucose isomerase activity (PGI1), transaldolase activity (TAL1), transketolase activity (TKL1, TKL2), 6-phosphogluconolactonase activity (SOL3, SOL4), Glucose-6-phosphate dehydrogenase activity (ZWF1), 6-phosphogluconate dehydrogenase (decarboxylating) activity (GND1, GND2), galactose permease activity (GAL2), high affinity glucose transport activity (HXT7), glucose/xylose transport activity (GXS1, GXF1) and combinations of the foregoing.
The term “phosphofructokinase activity” as used herein refers to conversion of fructose-6-phosphate to fructose-1,6-bisphosphate. Phosphofructokinase activity may be provided by an enzyme that includes one or two subunits (referred to hereafter as “subunit A” and/or “subunit B”).
The term “inactivating the Embden-Meyerhoff pathway” as used herein refers to reducing or eliminating the activity of one or more activities in the Embden-Meyerhoff pathway, including but not limited to phosphofructokinase activity. In some embodiments, the phosphofructokinase activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the phosphofructokinase activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of phosphofructokinase activity can have sequences partially or substantially complementary to sequences described herein. Presence or absence of the amount of phosphofructokinase activity can be detected by any suitable method known in the art, including requiring a five-carbon sugar carbon source or a functional Entner-Doudoroff pathway for growth. Inactivation of the Embden-Meyerhoff pathway is described in further detail below. As referred to herein, “substantially complementary” with respect to sequences refers to nucleotide sequences that will hybridize with each other. The stringency of the hybridization conditions can be altered to tolerate varying amounts of sequence mismatch. Included are regions of counterpart, target and capture nucleotide sequences 55% or more, 56% or more, 57% or more, 58% or more, 59% or more, 60% or more, 61% or more, 62% or more, 63% or more, 64% or more, 65% or more, 66% or more, 67% or more, 68% or more, 69% or more, 70% or more, 71% or more, 72% or more, 73% or more, 74% or more, 75% or more, 76% or more, 77% or more, 78% or more, 79% or more, 80% or more, 81% or more, 82% or more, 83% or more, 84% or more, 85% or more, 86% or more, 87% or more, 88% or more, 89% or more, 90% or more, 91% or more, 92% or more, 93% or more, 94% or more, 95% or more, 96% or more, 97% or more, 98% or more or 99% or more complementary to each other.
The term “phosphogluconate dehydratase activity” as used herein refers to conversion of 6-phophogluconate to 2-keto-3-deoxy-6-p-gluconate. The phosphogluconate dehydratase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring phosphogluconate dehydratase activity can be obtained from a number of sources, including Zymomonas mobilis and Escherichia coli. Examples of an amino acid sequence of a polypeptide having phosphogluconate dehydratase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of phosphogluconate dehydratase activity can be detected by any suitable method known in the art, including western blot analysis.
The term “2-keto-3-deoxygluconate-6-phosphate aldolase activity” as used herein refers to conversion of 2-keto-3-deoxy-6-p-gluconate to pyruvate. The 2-keto-3-deoxygluconate-6-phosphate aldolase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring 2-keto-3-deoxygluconate-6-phosphate aldolase activity can be obtained from a number of sources, including Zymomonas mobilis and Escherichia coli. Examples of an amino acid sequence of a polypeptide having 2-keto-3-deoxygluconate-6-phosphate aldolase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of 2-keto-3-deoxygluconate-6-phosphate aldolase activity can be detected by any suitable method known in the art, including western blot analysis.
The term “xylose isomerase activity” as used herein refers to conversion of xylose to xylulose. The xylose isomerase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring xylose isomerase activity can be obtained from a number of sources, including Piromyces, Orpinomyces, Bacteroides (e.g., B. thetaiotaomicron, B. uniformis, B. stercoris), Clostrialies (e.g., Clostrialies BVAB3), Clostridium (e.g., C. phytofermentans, C. thermohydrosulfuricum, C. cellulyticum), Thermus thermophilus, Eschericia coli, Streptomyces (e.g., S. rubiginosus, S. murinus), Bacillus stearothermophilus, Lactobacillus pentosus, Thermotoga (e.g., T. maritime, T. neopolitana) and Ruminococcus (e.g., Ruminococcus environmental samples, Ruminococcus albus, Ruminococcus bromii, Ruminococcus callidus, Ruminococcus flavefaciens, Ruminococcus gauvreauii, Ruminococcus gnavus, Ruminococcus lactaris, Ruminococcus obeum, Ruminococcus sp., Ruminococcus sp. 14531, Ruminococcus sp. 15975, Ruminococcus sp. 16442, Ruminococcus sp. 18P13, Ruminococcus sp. 25F6, Ruminococcus sp. 25F7, Ruminococcus sp. 25F8, Ruminococcus sp. 4_—1_—47FAA, Ruminococcus sp. 5, Ruminococcus sp. 5_—1_—39BFAA, Ruminococcus sp. 7L75, Ruminococcus sp. 8_—1_—37FAA, Ruminococcus sp. 9SE51, Ruminococcus sp. C36, Ruminococcus sp. CB10, Ruminococcus sp. CB3, Ruminococcus sp. CCUG 37327 A, Ruminococcus sp. CE2, Ruminococcus sp. CJ60, Ruminococcus sp. CJ63, Ruminococcus sp. CO1, Ruminococcus sp. CO12, Ruminococcus sp. CO22, Ruminococcus sp. CO27, Ruminococcus sp. CO28, Ruminococcus sp. CO34, Ruminococcus sp. CO41, Ruminococcus sp. CO47, Ruminococcus sp. CO7, Ruminococcus sp. CS1, Ruminococcus sp. CS6, Ruminococcus sp. DJF_VR52, Ruminococcus sp. DJF_VR66, Ruminococcus sp. DJF_VR67, Ruminococcus sp. DJF_VR70k1, Ruminococcus sp. DJF_VR87, Ruminococcus sp. Eg2, Ruminococcus sp. Egf, Ruminococcus sp. END-1, Ruminococcus sp. FD1, Ruminococcus sp. GM2/1, Ruminococcus sp. ID1, Ruminococcus sp. ID8, Ruminococcus sp. K-1, Ruminococcus sp. KKA Seq234, Ruminococcus sp. M-1, Ruminococcus sp. M10, Ruminococcus sp. M22, Ruminococcus sp. M23, Ruminococcus sp. M6, Ruminococcus sp. M73, Ruminococcus sp. M76, Ruminococcus sp. MLG080-3, Ruminococcus sp. NML 00-0124, Ruminococcus sp. Pei041, Ruminococcus sp. SC101, Ruminococcus sp. SC103, Ruminococcus sp. Siijpesteijn 1948, Ruminococcus sp. WAL 17306, Ruminococcus sp. YE281, Ruminococcus sp. YE58, Ruminococcus sp. YE71, Ruminococcus sp. ZS2-15, Ruminococcus torques). Examples of an amino acid sequence of a polypeptide having xylose isomerase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of xylose isomerase activity can be detected by any suitable method known in the art, including western blot analysis.
The term “phosphoenolpyruvate carboxylase activity” as used herein refers to the addition of carbon dioxide to phosphoenolpyruvate to generate the four-carbon compound oxaloacetate. The phosphoenolpyruvate carboxylase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring phosphoenolpyruvate carboxylase activity can be obtained from a number of sources, including Zymomonas mobilis. Examples of an amino acid sequence of a polypeptide having phosphoenolpyruvate carboxylase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of xylose isomerase activity can be detected by any suitable method known in the art.
The term “alcohol dehydrogenase 2 activity” as used herein refers to conversion of ethanol to acetaldehyde, which is the reverse of the forward action catalyzed by alcohol dehydrogenase 1. The term “inactivation of the conversion of ethanol to acetaldehyde” refers to a reduction or elimination in the activity of alcohol dehydrogenase 2. Reducing or eliminating the activity of alcohol dehydrogenase 2 activity can lead to an increase in ethanol production. In some embodiments, the alcohol dehydrogenase 2 activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the alcohol dehydrogenase 2 activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of alcohol dehydrogenase 2 can have sequences partially or substantially complementary to nucleic acid sequences that encode alcohol dehydrogenase 2 activity. Presence or absence of the amount of alcohol dehydrogenase 2 activity can be detected by any suitable method known in the art, including inability to grown in media with ethanol as the sole carbon source.
The term “thymidylate synthase activity” as used herein refers to a reductive methylation, where deoxyuridine monophosphate (dUMP) and N5,N10-methylene tetrahydrofolate are together used to generate thymidine monophosphate (dTMP), yielding dihydrofolate as a secondary product. The term “temporarily inactivate thymidylate synthase activity” refers to a temporary reduction or elimination in the activity of thymidylate synthase when the modified organism is shifted to a non-permissive temperature. The activity can return to normal upon return to a permissive temperature. Temporarily inactivating thymidylate synthase uncouples cell growth from cell division while under the non permissive temperature. This inactivation in turn allows the cells to continue fermentation without producing biomass and dividing, thus increasing the yield of product produced during fermentation.
In some embodiments, the thymidylate synthase activity can be temporarily reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. Nucleic acid sequences conferring temperature sensitive thymidylate synthase activity can be obtained from S. cerevisiae strain 172066 (accession number 208583). The cdc21 mutation in S. cerevisiae strain 172066 has a point mutation at position G139S relative to the initiating methionine. Examples of nucleotide sequences used to PCR amplify the polynucleotide encoding the temperature sensitive polypeptide, are presented below in tables. Presence, absence or amount of thymidylate synthase activity can be detected by any suitable method known in the art, including growth arrest at the non-permissive temperature.
Thymidylate synthase is one of many polypeptides that regulate the cell cycle. The cell cycle may be inhibited in engineered microorganisms under certain conditions (e.g., temperature shift, dissolved oxygen shift), which can result in inhibited or reduced cell proliferation, inhibited or reduced cell division, and sometimes cell cycle arrest (collectively “cell cycle inhibition”). Upon exposure to triggering conditions, a microorganism may display cell cycle inhibition after a certain time after the microorganism is exposed to the triggering conditions (e.g., there may be a time delay after a microorganism is exposed to a certain set of conditions before the microorganism displays cell cycle inhibition). Where cell cycle inhibition results in reduced cell proliferation, cell proliferation rates may be reduced by about 50% or greater, for example (e.g., reduced by about 52%, 54%, 56%, 58%, 60%, 62%, 64%, 66%, 68%, 70%, 72%, 74%, 76%, 78%, 80%, 82%, 84%, 86%, 88%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%, or greater than any one of the foregoing). Where cell cycle inhibition results a reduced number of cells undergoing cell division, the rate of cell division may be reduced by about 50% or greater, for example (e.g., the number of cells undergoing division is reduced by about 52%, 54%, 56%, 58%, 60%, 62%, 64%, 66%, 68%, 70%, 72%, 74%, 76%, 78%, 80%, 82%, 84%, 86%, 88%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%, or greater than any one of the foregoing). Where cell cycle inhibition results in cell cycle arrest, cells may be arrested at any stage of the cell cycle (e.g., resting G₀phase, interphase (e.g., G₁, S, G₂phases), mitosis (e.g., prophase, prometaphase, metaphase, anaphase, telophase)) and different percentages of cells in a population can be arrested at different stages of the cell cycle.
The term “phosphoglucose isomerase activity” as used herein refers to the conversion of glucose-6-phosphate to fructose-6-phosphate. The term “inactivation of the conversion of glucose-6-phosphate to fructose-6-phosphate” refers to a reduction or elimination in the activity of phosphoglucose isomerase. Reducing or eliminating the activity of phosphoglucose isomerase activity can lead to an increase in ethanol production. In some embodiments, the phosphoglucose isomerase activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the phosphoglucose isomerase activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of phosphoglucose isomerase can have sequences partially or substantially complementary to nucleic acid sequences that encode phosphoglucose isomerase activity. Presence or absence of the amount of phosphoglucose isomerase activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “glucose-6-phosphate dehydrogenase activity” as used herein refers to conversion of glucose-6-phosphate to gluconolactone-6-phosphate coupled with the generation of NADPH. The glucose-6-phosphate dehydrogenase aldolase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring glucose-6-phosphate dehydrogenase activity can be obtained from a number of sources, including, but not limited to S. cerevisiae Examples of a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of glucose-6-phosphate dehydrogenase activity can be detected by any suitable method known in the art, including western blot analysis.
The term “6-phosphogluconolactonase activity” as used herein refers to conversion of gluconolactone-6-phosphate to gluconate-6-phosphate. The 6-phosphogluconolactonase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring 6-phosphogluconolactonase activity can be obtained from a number of sources, including, but not limited to S. cerevisiae. Examples of an amino acid sequence of a polypeptide having 6-phosphogluconolactonase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in tables. Presence, absence or amount of 6-phosphogluconolactonase activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “6-phosphogluconate dehydrogenase (decarboxylating) activity” as used herein refers to the conversion of gluconate-6-phosphate to ribulose-5-phosphate. The term “inactivation of the conversion of gluconate-6-phosphate to ribulose-5-phosphate” refers to a reduction or elimination in the activity of 6-phosphogluconate dehydrogenase. Reducing or eliminating the activity of 6-phosphogluconate dehydrogenase (decarboxylating) activity can lead to an increase in ethanol production. In some embodiments, the 6-phosphogluconate dehydrogenase (decarboxylating) activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the 6-phosphogluconate dehydrogenase (decarboxylating) activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of 6-phosphogluconate dehydrogenase (decarboxylating) can have sequences partially or substantially complementary to nucleic acid sequences that encode 6-phosphogluconate dehydrogenase (decarboxylating) activity. Presence or absence of the amount of 6-phosphogluconate dehydrogenase (decarboxylating) activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “transketolase activity” as used herein refers to conversion of xylulose-5-phosphate and ribose-5-phosphate to sedoheptulose-7-phosphate and glyceraldehyde-3-phosphate. The transketolase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring transketolase activity can be obtained from a number of sources, including, but not limited to S. cerevisiae, Kluyveromyces, Pichia, Escherichia, Bacillus, Ruminococcus, Schizosaccharomyces, and Candida. Examples of an amino acid sequence of a polypeptide having transketolase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in the examples. The term “inactivation of the conversion of xylulose-5-phosphate and ribose-5-phosphate to sedoheptulose-7-phosphate and glyceraldehyde-3-phosphate” refers to a reduction or elimination in the activity of transketolase. Reducing or eliminating the activity of transketolase activity can lead to an increase in ethanol production. In some embodiments, the transketolase activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the transketolase activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of transketolase can have sequences partially or substantially complementary to nucleic acid sequences that encode transketolase activity. Presence, absence or amount of transketolase activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “transaldolase activity” as used herein refers to conversion of sedoheptulose 7-phosphate and glyceraldehyde 3-phosphate to erythrose 4-phosphate and fructose 6-phosphate.
The transaldolase activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring transaldolase activity can be obtained from a number of sources, including, but not limited to S. cerevisiae, Kluyveromyces, Pichia, Escherichia, Bacillus, Ruminococcus, Schizosaccharomyces, and Candida. Examples of an amino acid sequence of a polypeptide having transaldolase activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in the examples. The term “inactivation of the conversion of sedoheptulose 7-phosphate and glyceraldehyde 3-phosphate to erythrose 4-phosphate and fructose 6-phosphate” refers to a reduction or elimination in the activity of transaldolase. Reducing or eliminating the activity of transaldolase activity can lead to an increase in ethanol production. In some embodiments, the transaldolase activity can be reduced or eliminated by introduction of an untranslated RNA molecule (e.g., antisense RNA, RNAi, and the like, for example). In certain embodiments, the untranslated RNA is encoded by a heterologous nucleotide sequence introduced to a host microorganism.
In some embodiments, the transaldolase activity can be temporarily or permanently reduced or eliminated by genetic modification, as described below. In certain embodiments, the genetic modification renders the activity responsive to changes in the environment. In some embodiments, the genetic modification disrupts synthesis of a functional nucleic acid encoding the activity or produces a nonfunctional polypeptide or protein. Nucleic acid sequences that can be used to reduce or eliminate the activity of transaldolase can have sequences partially or substantially complementary to nucleic acid sequences that encode transaldolase activity. Presence, absence or amount of transaldolase activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “galactose permease activity” as used herein refers to the import of galactose into a cell or organism by an activity that transports galactose across cell membranes. The galactose permease activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring galactose permease activity can be obtained from a number of sources, including, but not limited to S. cerevisiae, Candida albicans, Debaryomyces hansenii, Schizosaccharomyces pombe, Arabidopsis thaliana, and Colwellia psychrerythraea. Examples of an amino acid sequence of a polypeptide having galactose permease activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in the Examples. Presence, absence or amount of galactose permease activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The term “glucose/xylose transport activity” as used herein refers to the import of glucose and/or xylose into a cell or organism by an activity that transports glucose and/or xylose across cell membranes. The glucose/xylose transport activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring glucose/xylose transport activity can be obtained from a number of sources, including, but not limited to Pichia yeast, Saccharomyces cerevisiae, Candida albicans, Debaryomyces hansenii, Schizosaccaromyces pombe. Examples of an amino acid sequence of a polypeptide having glucose/xylose transport activity, and a nucleotide sequence of a polynucleotide that encodes the polypeptide, are presented below in the Examples. Presence, absence or amount of glucose/xylose transport activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
The terms “high affinity glucose transport activity” and “hexose transport activity” as used herein refer to the import of glucose and other hexose sugars into a cell or organism by an activity that transports glucose and other hexose sugars across cell membranes. The high affinity glucose transport activity or hexose transport activity can be provided by a polypeptide. In some embodiments, the polypeptide is encoded by a heterologous nucleotide sequence introduced to a host microorganism. Nucleic acid sequences conferring high affinity glucose transport activity or hexose transport activity can be obtained from a number of sources, including, but not limited to S. cerevisiae, Pichia yeast, Candida albicans, Debaryomyces hansenii, Schizosaccaromyces pombe. Presence, absence or amount of glucose/xylose transport activity can be detected by any suitable method known in the art, including nucleic acid based analysis and western blot analysis.
Activities described herein can be modified to generate microorganisms engineered to allow a method of independently regulating or controlling (e.g., ability to independently turn on or off, or increase or decrease, for example) six-carbon sugar metabolism, five-carbon sugar metabolism, atmospheric carbon metabolism (e.g., carbon dioxide fixation) or combinations thereof. In some embodiments, regulated control of a desired activity can be the result of a genetic modification. In certain embodiments, the genetic modification can be modification of a promoter sequence. In some embodiments the modification can increase of decrease an activity encoded by a gene operably linked to the promoter element. In certain embodiments, the modification to the promoter element can add or remove a regulatory sequence. In some embodiments the regulatory sequence can respond to a change in environmental or culture conditions. Non-limiting examples of culture conditions that could be used to regulate an activity in this manner include, temperature, light, oxygen, salt, metals and the like. Additional methods for altering an activity by modification of a promoter element are given below.
In some embodiments, the genetic modification can be to an ORF. In certain embodiments, the modification of the ORF can increase or decrease expression of the ORF. In some embodiments modification of the ORF can alter the efficiency of translation of the ORF. In certain embodiments, modification of the ORF can alter the activity of the polypeptide or protein encoded by the ORF. Additional methods for altering an activity by modification of an ORF are given below.
In some embodiments, the genetic modification can be to an activity associated with cell division (e.g., cell division cycle or CDC activity, for example). In certain embodiments the cell division cycle activity can be thymidylate synthase activity. In certain embodiments, regulated control of cell division can be the result of a genetic modification. In some embodiments, the genetic modification can be to a nucleic acid sequence that encodes thymidylate synthase. In certain embodiments, the genetic modification can temporarily inactivate thymidylate synthase activity by rendering the activity temperature sensitive (e.g., heat resistant, heat sensitive, cold resistant, cold sensitive and the like).
In some embodiments, the genetic modification can modify a promoter sequence operably linked to a gene encoding an activity involved in control of cell division. In some embodiments the modification can increase of decrease an activity encoded by a gene operably linked to the promoter element. In certain embodiments, the modification to the promoter element can add or remove a regulatory sequence. In some embodiments the regulatory sequence can respond to a change in environmental or culture conditions. Non-limiting examples of culture conditions that could be used to regulate an activity in this manner include, temperature, light, oxygen, salt, metals and the like. In some embodiments, an engineered microorganism comprising one or more activities described above or below can be used in to produce ethanol by inhibiting cell growth and cell division by use of a temperature sensitive cell division control activity while allowing cellular fermentation to proceed, thereby producing a significant increase in ethanol yield when compared to the native organism.

Polynucleotides and Polypeptides

A nucleic acid (e.g., also referred to herein as nucleic acid reagent, target nucleic acid, target nucleotide sequence, nucleic acid sequence of interest or nucleic acid region of interest) can be from any source or composition, such as DNA, cDNA, gDNA (genomic DNA), RNA, siRNA (short inhibitory RNA), RNAi, tRNA or mRNA, for example, and can be in any form (e.g., linear, circular, supercoiled, single-stranded, double-stranded, and the like). A nucleic acid can also comprise DNA or RNA analogs (e.g., containing base analogs, sugar analogs and/or a non-native backbone and the like). It is understood that the term “nucleic acid” does not refer to or infer a specific length of the polynucleotide chain, thus polynucleotides and oligonucleotides are also included in the definition. Deoxyribonucleotides include deoxyadenosine, deoxycytidine, deoxyguanosine and deoxythymidine. For RNA, the uracil base is uridine.
A nucleic acid sometimes is a plasmid, phage, autonomously replicating sequence (ARS), centromere, artificial chromosome, yeast artificial chromosome (e.g., YAC) or other nucleic acid able to replicate or be replicated in a host cell. In certain embodiments a nucleic acid can be from a library or can be obtained from enzymatically digested, sheared or sonicated genomic DNA (e.g., fragmented) from an organism of interest. In some embodiments, nucleic acid subjected to fragmentation or cleavage may have a nominal, average or mean length of about 5 to about 10,000 base pairs, about 100 to about 1,000 base pairs, about 100 to about 500 base pairs, or about 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000 or 10000 base pairs. Fragments can be generated by any suitable method in the art, and the average, mean or nominal length of nucleic acid fragments can be controlled by selecting an appropriate fragment-generating procedure by the person of ordinary skill. In some embodiments, the fragmented DNA can be size selected to obtain nucleic acid fragments of a particular size range.
Nucleic acid can be fragmented by various methods known to the person of ordinary skill, which include without limitation, physical, chemical and enzymic processes. Examples of such processes are described in U.S. Patent Application Publication No. 20050112590 (published on May 26, 2005, entitled “Fragmentation-based methods and systems for sequence variation detection and discovery,” naming Van Den Boom et al.). Certain processes can be selected by the person of ordinary skill to generate non-specifically cleaved fragments or specifically cleaved fragments. Examples of processes that can generate non-specifically cleaved fragment sample nucleic acid include, without limitation, contacting sample nucleic acid with apparatus that expose nucleic acid to shearing force (e.g., passing nucleic acid through a syringe needle; use of a French press); exposing sample nucleic acid to irradiation (e.g., gamma, x-ray, UV irradiation; fragment sizes can be controlled by irradiation intensity); boiling nucleic acid in water (e.g., yields about 500 base pair fragments) and exposing nucleic acid to an acid and base hydrolysis process.
Nucleic acid may be specifically cleaved by contacting the nucleic acid with one or more specific cleavage agents. The term “specific cleavage agent” as used herein refers to an agent, sometimes a chemical or an enzyme that can cleave a nucleic acid at one or more specific sites. Specific cleavage agents often will cleave specifically according to a particular nucleotide sequence at a particular site. Examples of enzymic specific cleavage agents include without limitation endonucleases (e.g., DNase (e.g., DNase I, II); RNase (e.g., RNase E, F, H, P); Cleavase™ enzyme; Taq DNA polymerase; E. coli DNA polymerase I and eukaryotic structure-specific endonucleases; murine FEN-1 endonucleases; type I, II or III restriction endonucleases such as Acc I, Afl III, Alu I, Alw44 I, Apa I, Asn I, Ava I, Ava II, BamH I, Ban II, Bcl I, Bgl I. Bgl II, Bln I, Bsm I, BssH II, BstE II, Cfo I, Cla I, Dde I, Dpn I, Dra I, EclX I, EcoR I, EcoR I, EcoR II, EcoR V, Hae II, Hae II, Hind III, Hind III, Hpa I, Hpa II, Kpn I, Ksp I, Mlu I, MluN I, Msp I, Nci I, Nco I, Nde I, Nde II, Nhe I, Not I, Nru I, Nsi I, Pst I, Pvu I, Pvu II, Rsa I, Sac I, Sal I, Sau3A I, Sca I, ScrF I, Sfi I, Sma I, Spe I, Sph I, Ssp I, Stu I, Sty I, Swa I, Taq I, Xba I, Xho I); glycosylases (e.g., uracil-DNA glycolsylase (UDG), 3-methyladenine DNA glycosylase, 3-methyladenine DNA glycosylase II, pyrimidine hydrate-DNA glycosylase, FaPy-DNA glycosylase, thymine mismatch-DNA glycosylase, hypoxanthine-DNA glycosylase, 5-Hydroxymethyluracil DNA glycosylase (HmUDG), 5-Hydroxymethylcytosine DNA glycosylase, or 1,N6-etheno-adenine DNA glycosylase); exonucleases (e.g., exonuclease III); ribozymes, and DNAzymes. Sample nucleic acid may be treated with a chemical agent, or synthesized using modified nucleotides, and the modified nucleic acid may be cleaved. In non-limiting examples, sample nucleic acid may be treated with (i) alkylating agents such as methylnitrosourea that generate several alkylated bases, including N3-methyladenine and N3-methylguanine, which are recognized and cleaved by alkyl purine DNA-glycosylase; (ii) sodium bisulfite, which causes deamination of cytosine residues in DNA to form uracil residues that can be cleaved by uracil N-glycosylase; and (iii) a chemical agent that converts guanine to its oxidized form, 8-hydroxyguanine, which can be cleaved by formamidopyrimidine DNA N-glycosylase. Examples of chemical cleavage processes include without limitation alkylation, (e.g., alkylation of phosphorothioate-modified nucleic acid); cleavage of acid lability of P3′-N5′-phosphoroamidate-containing nucleic acid; and osmium tetroxide and piperidine treatment of nucleic acid.
As used herein, the term “complementary cleavage reactions” refers to cleavage reactions that are carried out on the same nucleic acid using different cleavage reagents or by altering the cleavage specificity of the same cleavage reagent such that alternate cleavage patterns of the same target or reference nucleic acid or protein are generated. In certain embodiments, nucleic acids of interest may be treated with one or more specific cleavage agents (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more specific cleavage agents) in one or more reaction vessels (e.g., nucleic acid of interest is treated with each specific cleavage agent in a separate vessel).
A nucleic acid suitable for use in the embodiments described herein sometimes is amplified by any amplification process known in the art (e.g., PCR, RT-PCR and the like). Nucleic acid amplification may be particularly beneficial when using organisms that are typically difficult to culture (e.g., slow growing, require specialize culture conditions and the like). The terms “amplify”, “amplification”, “amplification reaction”, or “amplifying” as used herein, refer to any in vitro processes for multiplying the copies of a target sequence of nucleic acid. Amplification sometimes refers to an “exponential” increase in target nucleic acid. However, “amplifying” as used herein can also refer to linear increases in the numbers of a select target sequence of nucleic acid, but is different than a one-time, single primer extension step. In some embodiments, a limited amplification reaction, also known as pre-amplification, can be performed. Pre-amplification is a method in which a limited amount of amplification occurs due to a small number of cycles, for example 10 cycles, being performed. Pre-amplification can allow some amplification, but stops amplification prior to the exponential phase, and typically produces about 500 copies of the desired nucleotide sequence(s). Use of pre-amplification may also limit inaccuracies associated with depleted reactants in standard PCR reactions.
In some embodiments, a nucleic acid reagent sometimes is stably integrated into the chromosome of the host organism, or a nucleic acid reagent can be a deletion of a portion of the host chromosome, in certain embodiments (e.g., genetically modified organisms, where alteration of the host genome confers the ability to selectively or preferentially maintain the desired organism carrying the genetic modification). Such nucleic acid reagents (e.g., nucleic acids or genetically modified organisms whose altered genome confers a selectable trait to the organism) can be selected for their ability to guide production of a desired protein or nucleic acid molecule. When desired, the nucleic acid reagent can be altered such that codons encode for (i) the same amino acid, using a different tRNA than that specified in the native sequence, or (ii) a different amino acid than is normal, including unconventional or unnatural amino acids (including detectably labeled amino acids). As described herein, the term “native sequence” refers to an unmodified nucleotide sequence as found in its natural setting (e.g., a nucleotide sequence as found in an organism).
A nucleic acid or nucleic acid reagent can comprise certain elements often selected according to the intended use of the nucleic acid. Any of the following elements can be included in or excluded from a nucleic acid reagent. A nucleic acid reagent, for example, may include one or more or all of the following nucleotide elements: one or more promoter elements, one or more 5′ untranslated regions (5′UTRs), one or more regions into which a target nucleotide sequence may be inserted (an “insertion element”), one or more target nucleotide sequences, one or more 3′ untranslated regions (3′UTRs), and one or more selection elements. A nucleic acid reagent can be provided with one or more of such elements and other elements may be inserted into the nucleic acid before the nucleic acid is introduced into the desired organism. In some embodiments, a provided nucleic acid reagent comprises a promoter, 5′UTR, optional 3′UTR and insertion element(s) by which a target nucleotide sequence is inserted (i.e., cloned) into the nucleotide acid reagent. In certain embodiments, a provided nucleic acid reagent comprises a promoter, insertion element(s) and optional 3′UTR, and a 5′ UTR/target nucleotide sequence is inserted with an optional 3′UTR. The elements can be arranged in any order suitable for expression in the chosen expression system (e.g., expression in a chosen organism, or expression in a cell free system, for example), and in some embodiments a nucleic acid reagent comprises the following elements in the 5′ to 3′ direction: (1) promoter element, 5′UTR, and insertion element(s); (2) promoter element, 5′UTR, and target nucleotide sequence; (3) promoter element, 5′UTR, insertion element(s) and 3′UTR; and (4) promoter element, 5′UTR, target nucleotide sequence and 3′UTR.
A promoter element typically is required for DNA synthesis and/or RNA synthesis. A promoter element often comprises a region of DNA that can facilitate the transcription of a particular gene, by providing a start site for the synthesis of RNA corresponding to a gene. Promoters generally are located near the genes they regulate, are located upstream of the gene (e.g., 5′ of the gene), and are on the same strand of DNA as the sense strand of the gene, in some embodiments.
A promoter often interacts with a RNA polymerase. A polymerase is an enzyme that catalyses synthesis of nucleic acids using a preexisting nucleic acid reagent. When the template is a DNA template, an RNA molecule is transcribed before protein is synthesized. Enzymes having polymerase activity suitable for use in the present methods include any polymerase that is active in the chosen system with the chosen template to synthesize protein. In some embodiments, a promoter (e.g., a heterologous promoter) also referred to herein as a promoter element, can be operably linked to a nucleotide sequence or an open reading frame (ORF). Transcription from the promoter element can catalyze the synthesis of an RNA corresponding to the nucleotide sequence or ORF sequence operably linked to the promoter, which in turn leads to synthesis of a desired peptide, polypeptide or protein. The term “operably linked” as used herein with respect to promoters refers to a nucleic acid sequence (e.g., a coding sequence) present on the same nucleic acid molecule as a promoter element and whose expression is under the control of said promoter element.
Promoter elements sometimes exhibit responsiveness to regulatory control. Promoter elements also sometimes can be regulated by a selective agent. That is, transcription from promoter elements sometimes can be turned on, turned off, up-regulated or down-regulated, in response to a change in environmental, nutritional or internal conditions or signals (e.g., heat inducible promoters, light regulated promoters, feedback regulated promoters, hormone influenced promoters, tissue specific promoters, oxygen and pH influenced promoters, promoters that are responsive to selective agents (e.g., kanamycin) and the like, for example). Promoters influenced by environmental, nutritional or internal signals frequently are influenced by a signal (direct or indirect) that binds at or near the promoter and increases or decreases expression of the target sequence under certain conditions.
Non-limiting examples of selective or regulatory agents that can influence transcription from a promoter element used in embodiments described herein include, without limitation, (1) nucleic acid segments that encode products that provide resistance against otherwise toxic compounds (e.g., antibiotics); (2) nucleic acid segments that encode products that are otherwise lacking in the recipient cell (e.g., essential products, tRNA genes, auxotrophic markers); (3) nucleic acid segments that encode products that suppress the activity of a gene product; (4) nucleic acid segments that encode products that can be readily identified (e.g., phenotypic markers such as antibiotics (e.g., β-lactamase), β-galactosidase, green fluorescent protein (GFP), yellow fluorescent protein (YFP), red fluorescent protein (RFP), cyan fluorescent protein (CFP), and cell surface proteins); (5) nucleic acid segments that bind products that are otherwise detrimental to cell survival and/or function; (6) nucleic acid segments that otherwise inhibit the activity of any of the nucleic acid segments described in Nos. 1-5 above (e.g., antisense oligonucleotides); (7) nucleic acid segments that bind products that modify a substrate (e.g., restriction endonucleases); (8) nucleic acid segments that can be used to isolate or identify a desired molecule (e.g., specific protein binding sites); (9) nucleic acid segments that encode a specific nucleotide sequence that can be otherwise non-functional (e.g., for PCR amplification of subpopulations of molecules); (10) nucleic acid segments that, when absent, directly or indirectly confer resistance or sensitivity to particular compounds; (11) nucleic acid segments that encode products that either are toxic or convert a relatively non-toxic compound to a toxic compound (e.g., Herpes simplex thymidine kinase, cytosine deaminase) in recipient cells; (12) nucleic acid segments that inhibit replication, partition or heritability of nucleic acid molecules that contain them; and/or (13) nucleic acid segments that encode conditional replication functions, e.g., replication in certain hosts or host cell strains or under certain environmental conditions (e.g., temperature, nutritional conditions, and the like). In some embodiments, the regulatory or selective agent can be added to change the existing growth conditions to which the organism is subjected (e.g., growth in liquid culture, growth in a fermentor, growth on solid nutrient plates and the like for example).
In some embodiments, regulation of a promoter element can be used to alter (e.g., increase, add, decrease or substantially eliminate) the activity of a peptide, polypeptide or protein (e.g., enzyme activity for example). For example, a microorganism can be engineered by genetic modification to express a nucleic acid reagent that can add a novel activity (e.g., an activity not normally found in the host organism) or increase the expression of an existing activity by increasing transcription from a homologous or heterologous promoter operably linked to a nucleotide sequence of interest (e.g., homologous or heterologous nucleotide sequence of interest), in certain embodiments. In some embodiments, a microorganism can be engineered by genetic modification to express a nucleic acid reagent that can decrease expression of an activity by decreasing or substantially eliminating transcription from a homologous or heterologous promoter operably linked to a nucleotide sequence of interest, in certain embodiments.
In some embodiments the activity can be altered using recombinant DNA and genetic techniques known to the artisan. Methods for engineering microorganisms are further described herein. Tables herein provide non-limiting lists of yeast promoters that are up-regulated by oxygen, yeast promoters that are down-regulated by oxygen, yeast transcriptional repressors and their associated genes, DNA binding motifs as determined using the MEME sequence analysis software. Potential regulator binding motifs can be identified using the program MEME to search intergenic regions bound by regulators for overrepresented sequences. For each regulator, the sequences of intergenic regions bound with p-values less than 0.001 were extracted to use as input for motif discovery. The MEME software was run using the following settings: a motif width ranging from 6 to 18 bases, the “zoops” distribution model, a 6th order Markov background model and a discovery limit of 20 motifs. The discovered sequence motifs were scored for significance by two criteria: an E-value calculated by MEME and a specificity score. The motif with the best score using each metric is shown for each regulator. All motifs presented are derived from datasets generated in rich growth conditions with the exception of a previously published dataset for epitope-tagged Gal4 grown in galactose
In some embodiments, the altered activity can be found by screening the organism under conditions that select for the desired change in activity. For example, certain microorganisms can be adapted to increase or decrease an activity by selecting or screening the organism in question on a media containing substances that are poorly metabolized or even toxic. An increase in the ability of an organism to grow a substance that is normally poorly metabolized would result in an increase in the growth rate on that substance, for example. A decrease in the sensitivity to a toxic substance might be manifested by growth on higher concentrations of the toxic substance, for example. Genetic modifications that are identified in this manner sometimes are referred to as naturally occurring mutations or the organisms that carry them can sometimes be referred to as naturally occurring mutants. Modifications obtained in this manner are not limited to alterations in promoter sequences. That is, screening microorganisms by selective pressure, as described above, can yield genetic alterations that can occur in non-promoter sequences, and sometimes also can occur in sequences that are not in the nucleotide sequence of interest, but in a related nucleotide sequences (e.g., a gene involved in a different step of the same pathway, a transport gene, and the like). Naturally occurring mutants sometimes can be found by isolating naturally occurring variants from unique environments, in some embodiments.
In addition to the regulated promoter sequences, regulatory sequences, and coding polynucleotides provided herein, a nucleic acid reagent may include a polynucleotide sequence 70% or more identical to the foregoing (or to the complementary sequences). That is, a nucleotide sequence that is at least 70% or more, 71% or more, 72% or more, 73% or more, 74% or more, 75% or more, 76% or more, 77% or more, 78% or more, 79% or more, 80% or more, 81% or more, 82% or more, 83% or more, 84% or more, 85% or more, 86% or more, 87% or more, 88% or more, 89% or more, 90% or more, 91% or more, 92% or more, 93% or more, 94% or more, 95% or more, 96% or more, 97% or more, 98% or more, or 99% or more identical to a nucleotide sequence described herein can be utilized. The term “identical” as used herein refers to two or more nucleotide sequences having substantially the same nucleotide sequence when compared to each other. One test for determining whether two nucleotide sequences or amino acids sequences are substantially identical is to determine the percent of identical nucleotide sequences or amino acid sequences shared.
Calculations of sequence identity can be performed as follows. Sequences are aligned for optimal comparison purposes (e.g., gaps can be introduced in one or both of a first and a second amino acid or nucleic acid sequence for optimal alignment and non-homologous sequences can be disregarded for comparison purposes). The length of a reference sequence aligned for comparison purposes is sometimes 30% or more, 40% or more, 50% or more, often 60% or more, and more often 70% or more, 80% or more, 90% or more, or 100% of the length of the reference sequence. The nucleotides or amino acids at corresponding nucleotide or polypeptide positions, respectively, are then compared among the two sequences. When a position in the first sequence is occupied by the same nucleotide or amino acid as the corresponding position in the second sequence, the nucleotides or amino acids are deemed to be identical at that position. The percent identity between the two sequences is a function of the number of identical positions shared by the sequences, taking into account the number of gaps, and the length of each gap, introduced for optimal alignment of the two sequences.
Comparison of sequences and determination of percent identity between two sequences can be accomplished using a mathematical algorithm. Percent identity between two amino acid or nucleotide sequences can be determined using the algorithm of Meyers & Miller, CABIOS 4: 11-17 (1989), which has been incorporated into the ALIGN program (version 2.0), using a PAM120 weight residue table, a gap length penalty of 12 and a gap penalty of 4. Also, percent identity between two amino acid sequences can be determined using the Needleman & Wunsch, J. Mol. Biol. 48: 444-453 (1970) algorithm which has been incorporated into the GAP program in the GCG software package (available at the http address www.gcg.com), using either a Blossum 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6, or 4 and a length weight of 1, 2, 3, 4, 5, or 6. Percent identity between two nucleotide sequences can be determined using the GAP program in the GCG software package (available at http address www.gcg.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70, or 80 and a length weight of 1, 2, 3, 4, 5, or 6. A set of parameters often used is a Blossum 62 scoring matrix with a gap open penalty of 12, a gap extend penalty of 4, and a frameshift gap penalty of 5.
Sequence identity can also be determined by hybridization assays conducted under stringent conditions. As use herein, the term “stringent conditions” refers to conditions for hybridization and washing. Stringent conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y., 6.3.1-6.3.6 (1989). Aqueous and non-aqueous methods are described in that reference and either can be used. An example of stringent hybridization conditions is hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45° C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 50° C. Another example of stringent hybridization conditions are hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45° C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 55° C. A further example of stringent hybridization conditions is hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45° C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 60° C. Often, stringent hybridization conditions are hybridization in 6× sodium chloride/sodium citrate (SSC) at about 45° C., followed by one or more washes in 0.2×SSC, 0.1% SDS at 65° C. More often, stringency conditions are 0.5M sodium phosphate, 7% SDS at 65° C., followed by one or more washes at 0.2×SSC, 1% SDS at 65° C.
As noted above, nucleic acid reagents may also comprise one or more 5′ UTR's, and one or more 3′UTR's. A 5′ UTR may comprise one or more elements endogenous to the nucleotide sequence from which it originates, and sometimes includes one or more exogenous elements. A 5′ UTR can originate from any suitable nucleic acid, such as genomic DNA, plasmid DNA, RNA or mRNA, for example, from any suitable organism (e.g., virus, bacterium, yeast, fungi, plant, insect or mammal). The artisan may select appropriate elements for the 5′ UTR based upon the chosen expression system (e.g., expression in a chosen organism, or expression in a cell free system, for example). A 5′ UTR sometimes comprises one or more of the following elements known to the artisan: enhancer sequences (e.g., transcriptional or translational), transcription initiation site, transcription factor binding site, translation regulation site, translation initiation site, translation factor binding site, accessory protein binding site, feedback regulation agent binding sites, Pribnow box, TATA box, −35 element, E-box (helix-loop-helix binding element), ribosome binding site, replicon, internal ribosome entry site (IRES), silencer element and the like. In some embodiments, a promoter element may be isolated such that all 5′ UTR elements necessary for proper conditional regulation are contained in the promoter element fragment, or within a functional subsequence of a promoter element fragment.
A 5′UTR in the nucleic acid reagent can comprise a translational enhancer nucleotide sequence.
A translational enhancer nucleotide sequence often is located between the promoter and the target nucleotide sequence in a nucleic acid reagent. A translational enhancer sequence often binds to a ribosome, sometimes is an 18S rRNA-binding ribonucleotide sequence (i.e., a 40S ribosome binding sequence) and sometimes is an internal ribosome entry sequence (IRES). An IRES generally forms an RNA scaffold with precisely placed RNA tertiary structures that contact a 40S ribosomal subunit via a number of specific intermolecular interactions. Examples of ribosomal enhancer sequences are known and can be identified by the artisan (e.g., Mignone et al., Nucleic Acids Research 33: D141-D146 (2005); Paulous et al., Nucleic Acids Research 31: 722-733 (2003); Akbergenov et al., Nucleic Acids Research 32: 239-247 (2004); Mignone et al., Genome Biology 3(3): reviews0004.1-0001.10 (2002); Gallie, Nucleic Acids Research 30: 3401-3411 (2002); Shaloiko et al., http address www.interscience.wiley.com, DOI: 10.1002/bit.20267; and Gallie et al., Nucleic Acids Research 15: 3257-3273 (1987)).
A translational enhancer sequence sometimes is a eukaryotic sequence, such as a Kozak consensus sequence or other sequence (e.g., hydroid polyp sequence, GenBank accession no. U07128). A translational enhancer sequence sometimes is a prokaryotic sequence, such as a Shine-Dalgarno consensus sequence. In certain embodiments, the translational enhancer sequence is a viral nucleotide sequence. A translational enhancer sequence sometimes is from a 5′ UTR of a plant virus, such as Tobacco Mosaic Virus (TMV), Alfalfa Mosaic Virus (AMV); Tobacco Etch Virus (ETV); Potato Virus Y (PVY); Turnip Mosaic (poty) Virus and Pea Seed Borne Mosaic Virus, for example. In certain embodiments, an omega sequence about 67 bases in length from TMV is included in the nucleic acid reagent as a translational enhancer sequence (e.g., devoid of guanosine nucleotides and includes a 25 nucleotide long poly (CAA) central region).
A 3′ UTR may comprise one or more elements endogenous to the nucleotide sequence from which it originates and sometimes includes one or more exogenous elements. A 3′ UTR may originate from any suitable nucleic acid, such as genomic DNA, plasmid DNA, RNA or mRNA, for example, from any suitable organism (e.g., a virus, bacterium, yeast, fungi, plant, insect or mammal). The artisan can select appropriate elements for the 3′ UTR based upon the chosen expression system (e.g., expression in a chosen organism, for example). A 3′ UTR sometimes comprises one or more of the following elements known to the artisan: transcription regulation site, transcription initiation site, transcription termination site, transcription factor binding site, translation regulation site, translation termination site, translation initiation site, translation factor binding site, ribosome binding site, replicon, enhancer element, silencer element and polyadenosine tail. A 3′ UTR often includes a polyadenosine tail and sometimes does not, and if a polyadenosine tail is present, one or more adenosine moieties may be added or deleted from it (e.g., about 5, about 10, about 15, about 20, about 25, about 30, about 35, about 40, about 45 or about 50 adenosine moieties may be added or subtracted).
In some embodiments, modification of a 5′ UTR and/or a 3′ UTR can be used to alter (e.g., increase, add, decrease or substantially eliminate) the activity of a promoter. Alteration of the promoter activity can in turn alter the activity of a peptide, polypeptide or protein (e.g., enzyme activity for example), by a change in transcription of the nucleotide sequence(s) of interest from an operably linked promoter element comprising the modified 5′ or 3′ UTR. For example, a microorganism can be engineered by genetic modification to express a nucleic acid reagent comprising a modified 5′ or 3′ UTR that can add a novel activity (e.g., an activity not normally found in the host organism) or increase the expression of an existing activity by increasing transcription from a homologous or heterologous promoter operably linked to a nucleotide sequence of interest (e.g., homologous or heterologous nucleotide sequence of interest), in certain embodiments. In some embodiments, a microorganism can be engineered by genetic modification to express a nucleic acid reagent comprising a modified 5′ or 3′ UTR that can decrease the expression of an activity by decreasing or substantially eliminating transcription from a homologous or heterologous promoter operably linked to a nucleotide sequence of interest, in certain embodiments.
A nucleotide reagent sometimes can comprise a target nucleotide sequence. A “target nucleotide sequence” as used herein encodes a nucleic acid, peptide, polypeptide or protein of interest, and may be a ribonucleotide sequence or a deoxyribonucleotide sequence.
A target nucleic acid sometimes can comprise a chimeric nucleic acid (or chimeric nucleotide sequence), which can encode a chimeric protein (or chimeric amino acid sequence). The term “chimeric” as used herein refers to a nucleic acid or nucleotide sequence, or encoded product thereof, containing sequences from two or more different sources. Any suitable source can be selected, including, but not limited to, a sequence from a nucleic acid, nucleotide sequence, ribosomal nucleic acid, RNA, DNA, regulatory nucleotide sequence (e.g., promoter, URL, enhancer, repressor and the like), coding nucleic acid, gene, nucleic acid linker, nucleic acid tag, amino acid sequence, peptide, polypeptide, protein, chromosome, and organism. A chimeric molecule can include a sequence of contiguous nucleotides or amino acids from a source including, but not limited to, a virus, prokaryote, eukaryote, genus, species, homolog, ortholog, paralog and isozyme, nucleic acid linkers, nucleic acid tags, the like and combinations thereof). A chimeric molecule can be generated by placing in juxtaposition fragments of related or unrelated nucleic acids, nucleotide sequences or DNA segments, in some embodiments. In certain embodiments the nucleic acids, nucleotide sequences or DNA segments can be native or wild type sequences, mutant sequences or engineered sequences (completely engineered or engineered to a point, for example).
In some embodiments, a chimera includes about 1, 2, 3, 4 or 5 sequences (e.g., contiguous nucleotides, contiguous amino acids) from one organism and 1, 2, 3, 4 or 5 sequences (e.g., contiguous nucleotides, contiguous amino acids) from another organism. The organisms sometimes are a microbe, such as a bacterium (e.g., gram positive, gram negative), yeast or fungus (e.g., aerobic fungus, anaerobic fungus), for example. In some embodiments, the organisms are bacteria, the organisms are yeast or the organisms are fungi (e.g., different species), and sometimes one organism is a bacterium or yeast and another is a fungus. A chimeric molecule may contain up to about 99% of sequences from one organism (e.g., about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97, 98, 99%) and the balance percentage from one or more other organisms. In certain embodiments, a chimeric molecule includes altered codons (in the case of a chimeric nucleic acid) and one or more mutations (e.g., point mutations, nucleotide substitutions, amino acid substitutions).
A chimera sometimes is the result of recombination between two or more nucleic acids, nucleotide sequences or genes, and sometimes is the result of genetic manipulation (e.g., designed and/or generated by the hand of a human being). Any suitable nucleic acid or nucleotide sequence and method for combining nucleic acids or nucleotide sequences can be used to generate a chimeric nucleic acid or nucleotide sequence. Non-limiting examples of nucleic acid and nucleotide sequence sources and methods for generating chimeric nucleic acids and nucleotide sequences are presented herein.
In some embodiments, fragments used to generate a chimera can be juxtaposed as units (e.g., nucleic acid from the sources are combined end to end and not interspersed. In embodiments where a chimera includes one stretch of contiguous nucleotides for each organism, nucleotide sequence combinations can be noted as DNA source 1 DNA source 2 or DNA source 1/DNA source 2/DNA source 3, the like and combinations thereof, for example. In certain embodiments, fragments used to generate a chimera can be juxtaposed such that one or more fragments from one or more sources can be interspersed with other fragments used to generate the chimera (e.g., DNA source 1/DNA source 2/DNA source 1/DNA source 3/DNA source 2/DNA source 1). In some embodiments, the nucleotide sequence length of the fragments used to generate a chimera can be in the range from about 5 base pairs to about 5,000 base pairs (e.g., about 5 base pairs (bp), about 10 bp, about 15 bp, about 20 bp, about 25 bp, about 30 bp, about 35 bp, about 40 bp, about 45 bp, about 50 bp, about 55 bp, about 60 bp, about bp, about 65 bp, about 70 bp, about 75 bp, about 80 bp, about 85 bp, about 90 bp, about 95 bp, about 100 bp, about 125 bp, about 150 bp, about 175 bp, about 200 bp, about 250 bp, about 300 bp, about 350 bp, about 400 bp, about 450 bp, about 500 bp, about 550 bp, about 600 bp, about 650 bp, about 700 bp, about 750 bp, about 800 bp, about 850 bp, about 900 bp, about 950 bp, about 1000 bp, about 1500 bp, about 2000 bp, about 2500 bp, about 3000 bp, about 3500 bp, about 4000 bp, about 4500 bp, or about 5000 bp).
In certain embodiments, a chimeric nucleic acid or nucleotide sequence encodes the same activity as the activity encoded by the source nucleic acids or nucleotide sequences. In some embodiments, a chimeric nucleic acid or nucleotide sequence has a similar or the same activity, but the amount of the activity, or kinetics of the activity, are altered (e.g., increased, decreased). In certain embodiments, a chimeric nucleic acid or nucleotide sequence encodes a different activity, and in some embodiments a chimeric nucleic acid or nucleotide sequences encodes a chimeric activity (e.g., a combination of two or more activities).
A target nucleic acid sometimes is an untranslated ribonucleic acid and sometimes is a translated ribonucleic acid. An untranslated ribonucleic acid may include, but is not limited to, a small interfering ribonucleic acid (siRNA), a short hairpin ribonucleic acid (shRNA), other ribonucleic acid capable of RNA interference (RNAi), an antisense ribonucleic acid, or a ribozyme. A translatable target nucleotide sequence (e.g., a target ribonucleotide sequence) sometimes encodes a peptide, polypeptide or protein, which are sometimes referred to herein as “target peptides,” “target polypeptides” or “target proteins.”
Any peptides, polypeptides or proteins, or an activity catalyzed by one or more peptides, polypeptides or proteins may be encoded by a target nucleotide sequence and may be selected by a person of ordinary skill in the art. Representative proteins include enzymes (e.g., phosphofructokinase activity, phosphogluconate dehydratase activity, 2-keto-3-deoxygluconate-6-phosphate aldolase activity, xylose isomerase activity, phosphoenolpyruvate carboxylase activity, alcohol dehydrogenase 2 activity and thymidylate synthase activity and the like, for example), antibodies, serum proteins (e.g., albumin), membrane bound proteins, hormones (e.g., growth hormone, erythropoietin, insulin, etc.), cytokines, etc., and include both naturally occurring and exogenously expressed polypeptides. Representative activities (e.g., enzymes or combinations of enzymes which are functionally associated to provide an activity) include phosphofructokinase activity, phosphogluconate dehydratase activity, 2-keto-3-deoxygluconate-6-phosphate aldolase activity, xylose isomerase activity, phosphoenolpyruvate carboxylase activity, alcohol dehydrogenase 2 activity and thymidylate synthase activity and the like for example. The term “enzyme” as used herein refers to a protein which can act as a catalyst to induce a chemical change in other compounds, thereby producing one or more products from one or more substrates.
Specific polypeptides (e.g., enzymes) useful for embodiments described herein are listed hereafter. The term “protein” as used herein refers to a molecule having a sequence of amino acids linked by peptide bonds. This term includes fusion proteins, oligopeptides, peptides, cyclic peptides, polypeptides and polypeptide derivatives, whether native or recombinant, and also includes fragments, derivatives, homologs, and variants thereof. A protein or polypeptide sometimes is of intracellular origin (e.g., located in the nucleus, cytosol, or interstitial space of host cells in vivo) and sometimes is a cell membrane protein in vivo. In some embodiments (described above, and in further detail below in Engineering and Alteration Methods), a genetic modification can result in a modification (e.g., increase, substantially increase, decrease or substantially decrease) of a target activity.
A translatable nucleotide sequence generally is located between a start codon (AUG in ribonucleic acids and ATG in deoxyribonucleic acids) and a stop codon (e.g., UAA (ochre), UAG (amber) or UGA (opal) in ribonucleic acids and TAA, TAG or TGA in deoxyribonucleic acids), and sometimes is referred to herein as an “open reading frame” (ORF). A nucleic acid reagent sometimes comprises one or more ORFs. An ORF may be from any suitable source, sometimes from genomic DNA, mRNA, reverse transcribed RNA or complementary DNA (cDNA) or a nucleic acid library comprising one or more of the foregoing, and is from any organism species that contains a nucleic acid sequence of interest, protein of interest, or activity of interest. Non-limiting examples of organisms from which an ORF can be obtained include bacteria, yeast, fungi, human, insect, nematode, bovine, equine, canine, feline, rat or mouse, for example.
A nucleic acid reagent sometimes comprises a nucleotide sequence adjacent to an ORF that is translated in conjunction with the ORF and encodes an amino acid tag. The tag-encoding nucleotide sequence is located 3′ and/or 5′ of an ORF in the nucleic acid reagent, thereby encoding a tag at the C-terminus or N-terminus of the protein or peptide encoded by the ORF. Any tag that does not abrogate in vitro transcription and/or translation may be utilized and may be appropriately selected by the artisan. Tags may facilitate isolation and/or purification of the desired ORF product from culture or fermentation media.
A tag sometimes specifically binds a molecule or moiety of a solid phase or a detectable label, for example, thereby having utility for isolating, purifying and/or detecting a protein or peptide encoded by the ORF. In some embodiments, a tag comprises one or more of the following elements: FLAG (e.g., DYKDDDDKG (SEQ ID NO: 29)), V5 (e.g., GKPIPNPLLGLDST (SEQ ID NO: 30)), c-MYC (e.g., EQKLISEEDL (SEQ ID NO: 31)), HSV (e.g., QPELAPEDPED (SEQ ID NO: 32)), influenza hemaglutinin, HA (e.g., YPYDVPDYA (SEQ ID NO: 33)), VSV-G (e.g., YTDIEMNRLGK (SEQ ID NO: 34)), bacterial glutathione-S-transferase, maltose binding protein, a streptavidin- or avidin-binding tag (e.g., pcDNA™6 BioEase™ Gateway® Biotinylation System (Invitrogen)), thioredoxin, β-galactosidase, VSV-glycoprotein, a fluorescent protein (e.g., green fluorescent protein or one of its many color variants (e.g., yellow, red, blue)), a polylysine or polyarginine sequence, a polyhistidine sequence (e.g., His6 (SEQ ID NO: 35)) or other sequence that chelates a metal (e.g., cobalt, zinc, copper), and/or a cysteine-rich sequence that binds to an arsenic-containing molecule. In certain embodiments, a cysteine-rich tag comprises the amino acid sequence CC-Xn-CC (SEQ ID NO: 36), wherein X is any amino acid and n is 1 to 3, and the cysteine-rich sequence sometimes is CCPGCC (SEQ ID NO: 37). In certain embodiments, the tag comprises a cysteine-rich element and a polyhistidine element (e.g., CCPGCC (SEQ ID NO: 37) and His6 (SEQ ID NO: 35)).
A tag often conveniently binds to a binding partner. For example, some tags bind to an antibody (e.g., FLAG) and sometimes specifically bind to a small molecule. For example, a polyhistidine tag specifically chelates a bivalent metal, such as copper, zinc and cobalt; a polylysine or polyarginine tag specifically binds to a zinc finger; a glutathione S-transferase tag binds to glutathione; and a cysteine-rich tag specifically binds to an arsenic-containing molecule. Arsenic-containing molecules include LUMIO™ agents (Invitrogen, California), such as FlAsH™ (EDT2[4′,5′-bis(1,3,2-dithioarsolan-2-yl)fluorescein-(1,2-ethanedithiol)2]) and ReAsH reagents (e.g., U.S. Pat. No. 5,932,474 to Tsien et al., entitled “Target Sequences for Synthetic Molecules;” U.S. Pat. No. 6,054,271 to Tsien et al., entitled “Methods of Using Synthetic Molecules and Target Sequences;” U.S. Pat. Nos. 6,451,569 and 6,008,378; published U.S. Patent Application 2003/0083373, and published PCT Patent Application WO 99/21013, all to Tsien et al. and all entitled “Synthetic Molecules that Specifically React with Target Sequences”). Such antibodies and small molecules sometimes are linked to a solid phase for convenient isolation of the target protein or target peptide.
A tag sometimes comprises a sequence that localizes a translated protein or peptide to a component in a system, which is referred to as a “signal sequence” or “localization signal sequence” herein. A signal sequence often is incorporated at the N-terminus of a target protein or target peptide, and sometimes is incorporated at the C-terminus. Examples of signal sequences are known to the artisan, are readily incorporated into a nucleic acid reagent, and often are selected according to the organism in which expression of the nucleic acid reagent is performed. A signal sequence in some embodiments localizes a translated protein or peptide to a cell membrane. Examples of signal sequences include, but are not limited to, a nucleus targeting signal (e.g., steroid receptor sequence and N-terminal sequence of SV40 virus large T antigen); mitochondrial targeting signal (e.g., amino acid sequence that forms an amphipathic helix); peroxisome targeting signal (e.g., C-terminal sequence in YFG from S. cerevisiae); and a secretion signal (e.g., N-terminal sequences from invertase, mating factor alpha, PHO5 and SUC2 in S. cerevisiae; multiple N-terminal sequences of B. subtilis proteins (e.g., Tjalsma et al., Microbiol. Molec. Biol. Rev. 64: 515-547 (2000)); alpha amylase signal sequence (e.g., U.S. Pat. No. 6,288,302); pectate lyase signal sequence (e.g., U.S. Pat. No. 5,846,818); precollagen signal sequence (e.g., U.S. Pat. No. 5,712,114); OmpA signal sequence (e.g., U.S. Pat. No. 5,470,719); Iam beta signal sequence (e.g., U.S. Pat. No. 5,389,529); B. brevis signal sequence (e.g., U.S. Pat. No. 5,232,841); and P. pastoris signal sequence (e.g., U.S. Pat. No. 5,268,273)).
A tag sometimes is directly adjacent to the amino acid sequence encoded by an ORF (i.e., there is no intervening sequence) and sometimes a tag is substantially adjacent to an ORF encoded amino acid sequence (e.g., an intervening sequence is present). An intervening sequence sometimes includes a recognition site for a protease, which is useful for cleaving a tag from a target protein or peptide. In some embodiments, the intervening sequence is cleaved by Factor Xa (e.g., recognition site I (E/D)GR), thrombin (e.g., recognition site LVPRGS (SEQ ID NO: 38)), enterokinase (e.g., recognition site DDDDK (SEQ ID NO: 39)), TEV protease (e.g., recognition site ENLYFQG (SEQ ID NO: 40)) or PreScission™ protease (e.g., recognition site LEVLFQGP (SEQ ID NO: 41)), for example.
An intervening sequence sometimes is referred to herein as a “linker sequence,” and may be of any suitable length selected by the artisan. A linker sequence sometimes is about 1 to about 20 amino acids in length, and sometimes about 5 to about 10 amino acids in length. The artisan may select the linker length to substantially preserve target protein or peptide function (e.g., a tag may reduce target protein or peptide function unless separated by a linker), to enhance disassociation of a tag from a target protein or peptide when a protease cleavage site is present (e.g., cleavage may be enhanced when a linker is present), and to enhance interaction of a tag/target protein product with a solid phase. A linker can be of any suitable amino acid content, and often comprises a higher proportion of amino acids having relatively short side chains (e.g., glycine, alanine, serine and threonine).
A nucleic acid reagent sometimes includes a stop codon between a tag element and an insertion element or ORF, which can be useful for translating an ORF with or without the tag. Mutant tRNA molecules that recognize stop codons (described above) suppress translation termination and thereby are designated “suppressor tRNAs.” Suppressor tRNAs can result in the insertion of amino acids and continuation of translation past stop codons (e.g., U.S. Patent Application No. 60/587,583, filed Jul. 14, 2004, entitled “Production of Fusion Proteins by Cell-Free Protein Synthesis,”; Eggertsson, et al., (1988) Microbiological Review 52(3):354-374, and Engleerg-Kukla, et al. (1996) in Escherichia coli and Salmonella Cellular and Molecular Biology, Chapter 60, pps 909-921, Neidhardt, et al. eds., ASM Press, Washington, D.C.). A number of suppressor tRNAs are known, including but not limited to, supE, supP, supD, supF and supZ suppressors, which suppress the termination of translation of the amber stop codon; supB, gIT, supL, supN, supC and supM suppressors, which suppress the function of the ochre stop codon and glyT, trpT and Su-9 suppressors, which suppress the function of the opal stop codon. In general, suppressor tRNAs contain one or more mutations in the anti-codon loop of the tRNA that allows the tRNA to base pair with a codon that ordinarily functions as a stop codon. The mutant tRNA is charged with its cognate amino acid residue and the cognate amino acid residue is inserted into the translating polypeptide when the stop codon is encountered. Mutations that enhance the efficiency of termination suppressors (i.e., increase stop codon read-through) have been identified. These include, but are not limited to, mutations in the uar gene (also known as the prfA gene), mutations in the ups gene, mutations in the sueA, sueB and sueC genes, mutations in the rpsD (ramA) and rpsE (spcA) genes and mutations in the rplL gene.
Thus, a nucleic acid reagent comprising a stop codon located between an ORF and a tag can yield a translated ORF alone when no suppressor tRNA is present in the translation system, and can yield a translated ORF-tag fusion when a suppressor tRNA is present in the system. Suppressor tRNA can be generated in cells transfected with a nucleic acid encoding the tRNA (e.g., a replication incompetent adenovirus containing the human tRNA-Ser suppressor gene can be transfected into cells, or a YAC containing a yeast or bacterial tRNA suppressor gene can be transfected into yeast cells, for example). Vectors for synthesizing suppressor tRNA and for translating ORFs with or without a tag are available to the artisan (e.g., Tag-On-Demand™ kit (Invitrogen Corporation, California); Tag-On-Demand™ Suppressor Supernatant Instruction Manual, Version B, 6 Jun. 2003, at http address www.invitrogen.com/content/sfs/manuals/tagondemand_supernatant_man.pdf; Tag-On-Demand™ Gateway® Vector Instruction Manual, Version B, 20 June, 2003 at http address www.invitrogen.com/content/sfs/manuals/tagondemand_vectors_man.pdf; and Capone et al., Amber, ochre and opal suppressor tRNA genes derived from a human serine tRNA gene. EMBO J. 4:213, 1985).
Any convenient cloning strategy known in the art may be utilized to incorporate an element, such as an ORF, into a nucleic acid reagent. Known methods can be utilized to insert an element into the template independent of an insertion element, such as (1) cleaving the template at one or more existing restriction enzyme sites and ligating an element of interest and (2) adding restriction enzyme sites to the template by hybridizing oligonucleotide primers that include one or more suitable restriction enzyme sites and amplifying by polymerase chain reaction (described in greater detail herein). Other cloning strategies take advantage of one or more insertion sites present or inserted into the nucleic acid reagent, such as an oligonucleotide primer hybridization site for PCR, for example, and others described hereafter. In some embodiments, a cloning strategy can be combined with genetic manipulation such as recombination (e.g., recombination of a nucleic acid reagent with a nucleic acid sequence of interest into the genome of the organism to be modified, as described further below). In some embodiments, the cloned ORF(s) can produce (directly or indirectly) a desired product, by engineering a microorganism with one or more ORFs of interest, which microorganism comprises one or more altered activities selected from the group consisting of phosphofructokinase activity, phosphogluconate dehydratase activity, 2-keto-3-deoxygluconate-6-phosphate aldolase activity, xylose isomerase activity, phosphoenolpyruvate carboxylase activity, alcohol dehydrogenase 2 activity, sugar transport activity, phosphoglucoisomerase activity, transaldolase activity, transketolase activity, glucose-6-phosphate dehydrogenase activity, 6-phosphogluconolactonase activity, 6-phosphogluconate dehydrogenase (decarboxylating) activity, and thymidylate synthase activity.
In some embodiments, the nucleic acid reagent includes one or more recombinase insertion sites. A recombinase insertion site is a recognition sequence on a nucleic acid molecule that participates in an integration/recombination reaction by recombination proteins. For example, the recombination site for Cre recombinase is IoxP, which is a 34 base pair sequence comprised of two 13 base pair inverted repeats (serving as the recombinase binding sites) flanking an 8 base pair core sequence (e.g., FIG. 1 of Sauer, B., Curr. Opin. Biotech. 5:521-527 (1994)). Other examples of recombination sites include attB, attP, attL, and attR sequences, and mutants, fragments, variants and derivatives thereof, which are recognized by the recombination protein A Int and by the auxiliary proteins integration host factor (IHF), FIS and excisionase (Xis) (e.g., U.S. Pat. Nos. 5,888,732; 6,143,557; 6,171,861; 6,270,969; 6,277,608; and 6,720,140; U.S. patent application Ser. No. 09/517,466, filed Mar. 2, 2000, and 09/732,914, filed Aug. 14, 2003, and in U.S. patent publication no. 2002-0007051-A1; Landy, Curr. Opin. Biotech. 3:699-707 (1993)).
Examples of recombinase cloning nucleic acids are in Gateway® systems (Invitrogen, California), which include at least one recombination site for cloning a desired nucleic acid molecules in vivo or in vitro. In some embodiments, the system utilizes vectors that contain at least two different site-specific recombination sites, often based on the bacteriophage lambda system (e.g., att1 and att2), and are mutated from the wild-type (att0) sites. Each mutated site has a unique specificity for its cognate partner att site (i.e., its binding partner recombination site) of the same type (for example attB1 with attP1, or attL1 with attR1) and will not cross-react with recombination sites of the other mutant type or with the wild-type att0 site. Different site specificities allow directional cloning or linkage of desired molecules thus providing desired orientation of the cloned molecules. Nucleic acid fragments flanked by recombination sites are cloned and subcloned using the Gateway® system by replacing a selectable marker (for example, ccdB) flanked by att sites on the recipient plasmid molecule, sometimes termed the Destination Vector. Desired clones are then selected by transformation of a ccdB sensitive host strain and positive selection for a marker on the recipient molecule. Similar strategies for negative selection (e.g., use of toxic genes) can be used in other organisms such as thymidine kinase (TK) in mammals and insects.
A recombination system useful for engineering yeast is outlined briefly. The system makes use of the ura3 gene (e.g., for S. cerevisiae and C. albicans, for example) or ura4 and ura5 genes (e.g., for S. pombe, for example) and toxicity of the nucleotide analogue 5-Fluoroorotic acid (5-FOA). The ura3 or ura4 and ura5 genes encode orotine-5′-monophosphate (OMP) dicarboxylase. Yeast with an active ura3 or ura4 and ura5 gene (phenotypically Ura+) convert 5-FOA to fluorodeoxyuridine, which is toxic to yeast cells. Yeast carrying a mutation in the appropriate gene(s) or having a knock out of the appropriate gene(s) can grow in the presence of 5-FOA, if the media is also supplemented with uracil.
A nucleic acid engineering construct can be made which may comprise the URA3 gene or cassette (for S. cerevisiae), flanked on either side by the same nucleotide sequence in the same orientation. The ura3 cassette comprises a promoter, the ura3 gene and a functional transcription terminator. Target sequences which direct the construct to a particular nucleic acid region of interest in the organism to be engineered are added such that the target sequences are adjacent to and abut the flanking sequences on either side of the ura3 cassette. Yeast can be transformed with the engineering construct and plated on minimal media without uracil. Colonies can be screened by PCR to determine those transformants that have the engineering construct inserted in the proper location in the genome. Checking insertion location prior to selecting for recombination of the ura3 cassette may reduce the number of incorrect clones carried through to later stages of the procedure. Correctly inserted transformants can then be replica plated on minimal media containing 5-FOA to select for recombination of the ura3 cassette out of the construct, leaving a disrupted gene and an identifiable footprint (e.g., nucleic acid sequence) that can be use to verify the presence of the disrupted gene. The technique described is useful for disrupting or “knocking out” gene function, but also can be used to insert genes or constructs into a host organisms genome in a targeted, sequence specific manner. Further detail will be described below in the engineering section and in the example section.
In certain embodiments, a nucleic acid reagent includes one or more topoisomerase insertion sites. A topoisomerase insertion site is a defined nucleotide sequence recognized and bound by a site-specific topoisomerase. For example, the nucleotide sequence 5′-(C/T)CCTT-3′ is a topoisomerase recognition site bound specifically by most poxvirus topoisomerases, including vaccinia virus DNA topoisomerase I. After binding to the recognition sequence, the topoisomerase cleaves the strand at the 3′-most thymidine of the recognition site to produce a nucleotide sequence comprising 5′-(C/T)CCTT-PO₄-TOPO, a complex of the topoisomerase covalently bound to the 3′ phosphate via a tyrosine in the topoisomerase (e.g., Shuman, J. Biol. Chem. 266:11372-11379, 1991; Sekiguchi and Shuman, Nucl. Acids Res. 22:5360-5365, 1994; U.S. Pat. No. 5,766,891; PCT/US95/16099; and PCT/US98/12372). In comparison, the nucleotide sequence 5′-GCAACTT-3′ is a topoisomerase recognition site for type IA E. coli topoisomerase III. An element to be inserted often is combined with topoisomerase-reacted template and thereby incorporated into the nucleic acid reagent (e.g., http address www.invitrogen.com/downloads/F-13512_Topo_Flyer.pdf; http address at world wide web uniform resource locator invitrogen.com/content/sfs/brochures/710_—021849%20_B_TOPOCloning_bro.pdf; TOPO TA Cloning® Kit and Zero Blunt® TOPO® Cloning Kit product information).
A nucleic acid reagent sometimes contains one or more origin of replication (ORI) elements. In some embodiments, a template comprises two or more ORIs, where one functions efficiently in one organism (e.g., a bacterium) and another functions efficiently in another organism (e.g., a eukaryote, like yeast for example). In some embodiments, an ORI may function efficiently in one species (e.g., S. cerevisiae, for example) and another ORI may function efficiently in a different species (e.g., S. pombe, for example). A nucleic acid reagent also sometimes includes one or more transcription regulation sites.
A nucleic acid reagent can include one or more selection elements (e.g., elements for selection of the presence of the nucleic acid reagent, and not for activation of a promoter element which can be selectively regulated). Selection elements often are utilized using known processes to determine whether a nucleic acid reagent is included in a cell. In some embodiments, a nucleic acid reagent includes two or more selection elements, where one functions efficiently in one organism and another functions efficiently in another organism. Examples of selection elements include, but are not limited to, (1) nucleic acid segments that encode products that provide resistance against otherwise toxic compounds (e.g., antibiotics); (2) nucleic acid segments that encode products that are otherwise lacking in the recipient cell (e.g., essential products, tRNA genes, auxotrophic markers); (3) nucleic acid segments that encode products that suppress the activity of a gene product; (4) nucleic acid segments that encode products that can be readily identified (e.g., phenotypic markers such as antibiotics (e.g., β-lactamase), β-galactosidase, green fluorescent protein (GFP), yellow fluorescent protein (YFP), red fluorescent protein (RFP), cyan fluorescent protein (CFP), and cell surface proteins); (5) nucleic acid segments that bind products that are otherwise detrimental to cell survival and/or function; (6) nucleic acid segments that otherwise inhibit the activity of any of the nucleic acid segments described in Nos. 1-5 above (e.g., antisense oligonucleotides); (7) nucleic acid segments that bind products that modify a substrate (e.g., restriction endonucleases); (8) nucleic acid segments that can be used to isolate or identify a desired molecule (e.g., specific protein binding sites); (9) nucleic acid segments that encode a specific nucleotide sequence that can be otherwise non-functional (e.g., for PCR amplification of subpopulations of molecules); (10) nucleic acid segments that, when absent, directly or indirectly confer resistance or sensitivity to particular compounds; (11) nucleic acid segments that encode products that either are toxic or convert a relatively non-toxic compound to a toxic compound (e.g., Herpes simplex thymidine kinase, cytosine deaminase) in recipient cells; (12) nucleic acid segments that inhibit replication, partition or heritability of nucleic acid molecules that contain them; and/or (13) nucleic acid segments that encode conditional replication functions, e.g., replication in certain hosts or host cell strains or under certain environmental conditions (e.g., temperature, nutritional conditions, and the like).
A nucleic acid reagent is of any form useful for in vivo transcription and/or translation. A nucleic acid sometimes is a plasmid, such as a supercoiled plasmid, sometimes is a yeast artificial chromosome (e.g., YAC), sometimes is a linear nucleic acid (e.g., a linear nucleic acid produced by PCR or by restriction digest), sometimes is single-stranded and sometimes is double-stranded. A nucleic acid reagent sometimes is prepared by an amplification process, such as a polymerase chain reaction (PCR) process or transcription-mediated amplification process (TMA). In TMA, two enzymes are used in an isothermal reaction to produce amplification products detected by light emission (see, e.g., Biochemistry 1996 Jun. 25; 35(25):8429-38 and http address world wide web uniform resource locator devicelink.com/ivdt/archive/00/11/007.html). Standard PCR processes are known (e.g., U.S. Pat. Nos. 4,683,202; 4,683,195; 4,965,188; and 5,656,493), and generally are performed in cycles. Each cycle includes heat denaturation, in which hybrid nucleic acids dissociate; cooling, in which primer oligonucleotides hybridize; and extension of the oligonucleotides by a polymerase (i.e., Taq polymerase). An example of a PCR cyclical process is treating the sample at 95° C. for 5 minutes; repeating forty-five cycles of 95° C. for 1 minute, 59° C. for 1 minute, 10 seconds, and 72° C. for 1 minute 30 seconds; and then treating the sample at 72° C. for 5 minutes. Multiple cycles frequently are performed using a commercially available thermal cycler. PCR amplification products sometimes are stored for a time at a lower temperature (e.g., at 4° C.) and sometimes are frozen (e.g., at −20° C.) before analysis.
In some embodiments, a nucleic acid reagent, protein reagent, protein fragment reagent or other reagent described herein is isolated or purified. The term “isolated” as used herein refers to material removed from its original environment (e.g., the natural environment if it is naturally occurring, or a host cell if expressed exogenously), and thus is altered “by the hand of man” from its original environment. The term “purified” as used herein with reference to molecules does not refer to absolute purity. Rather, “purified” refers to a substance in a composition that contains fewer substance species in the same class (e.g., nucleic acid or protein species) other than the substance of interest in comparison to the sample from which it originated. “Purified,” if a nucleic acid or protein for example, refers to a substance in a composition that contains fewer nucleic acid species or protein species other than the nucleic acid or protein of interest in comparison to the sample from which it originated. Sometimes, a protein or nucleic acid is “substantially pure,” indicating that the protein or nucleic acid represents at least 50% of protein or nucleic acid on a mass basis of the composition. Often, a substantially pure protein or nucleic acid is at least 75% on a mass basis of the composition, and sometimes at least 95% on a mass basis of the composition.

Engineering and Alteration Methods

Methods and compositions (e.g., nucleic acid reagents) described herein can be used to generate engineered microorganisms. As noted above, the term “engineered microorganism” as used herein refers to a modified organism that includes one or more activities distinct from an activity present in a microorganism utilized as a starting point for modification (e.g., host microorganism or unmodified organism). Engineered microorganisms typically arise as a result of a genetic modification, usually introduced or selected for, by one of skill in the art using readily available techniques. Non-limiting examples of methods useful for generating an altered activity include, introducing a heterologous polynucleotide (e.g., nucleic acid or gene integration, also referred to as “knock in”), removing an endogenous polynucleotide, altering the sequence of an existing endogenous nucleic acid sequence (e.g., site-directed mutagenesis), disruption of an existing endogenous nucleic acid sequence (e.g., knock outs and transposon or insertion element mediated mutagenesis), selection for an altered activity where the selection causes a change in a naturally occurring activity that can be stably inherited (e.g., causes a change in a nucleic acid sequence in the genome of the organism or in an epigenetic nucleic acid that is replicated and passed on to daughter cells), PCR-based mutagenesis, and the like. The term “mutagenesis” as used herein refers to any modification to a nucleic acid (e.g., nucleic acid reagent, or host chromosome, for example) that is subsequently used to generate a product in a host or modified organism. Non-limiting examples of mutagenesis include, deletion, insertion, substitution, rearrangement, point mutations, suppressor mutations and the like. Mutagenesis methods are known in the art and are readily available to the artisan. Non-limiting examples of mutagenesis methods are described herein and can also be found in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
The term “genetic modification” as used herein refers to any suitable nucleic acid addition, removal or alteration that facilitates production of a target product (e.g., phosphogluconate dehydratase activity, 2-keto-3-deoxygluconate-6-phosphate aldolase activity, xylose isomerase activity, or phosphoenolpyruvate carboxylase activity, for example). in an engineered microorganism. Genetic modifications include, without limitation, insertion of one or more nucleotides in a native nucleic acid of a host organism in one or more locations, deletion of one or more nucleotides in a native nucleic acid of a host organism in one or more locations, modification or substitution of one or more nucleotides in a native nucleic acid of a host organism in one or more locations, insertion of a non-native nucleic acid into a host organism (e.g., insertion of an autonomously replicating vector), and removal of a non-native nucleic acid in a host organism (e.g., removal of a vector).
The term “heterologous polynucleotide” as used herein refers to a nucleotide sequence not present in a host microorganism in some embodiments. In certain embodiments, a heterologous polynucleotide is present in a different amount (e.g., different copy number) than in a host microorganism, which can be accomplished, for example, by introducing more copies of a particular nucleotide sequence to a host microorganism (e.g., the particular nucleotide sequence may be in a nucleic acid autonomous of the host chromosome or may be inserted into a chromosome). A heterologous polynucleotide is from a different organism in some embodiments, and in certain embodiments, is from the same type of organism but from an outside source (e.g., a recombinant source).
The term “altered activity” as used herein refers to an activity in an engineered microorganism that is added or modified relative to the host microorganism (e.g., added, increased, reduced, inhibited or removed activity). An activity can be altered by introducing a genetic modification to a host microorganism that yields an engineered microorganism having added, increased, reduced, inhibited or removed activity.
An added activity often is an activity not detectable in a host microorganism. An increased activity generally is an activity detectable in a host microorganism that has been increased in an engineered microorganism. An activity can be increased to any suitable level for production of a target product (e.g., adipic acid, 6-hydroxyhexanoic acid), including but not limited to less than 2-fold (e.g., about 10% increase to about 99% increase; about 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% increase), 2-fold, 3-fold, 4-fold, 5-fold, 6-fold, 7-fold, 8-fold, 9-fold, of 10-fold increase, or greater than about 10-fold increase. A reduced or inhibited activity generally is an activity detectable in a host microorganism that has been reduced or inhibited in an engineered microorganism. An activity can be reduced to undetectable levels in some embodiments, or detectable levels in certain embodiments. An activity can be decreased to any suitable level for production of a target product (e.g., adipic acid, 6-hydroxyhexanoic acid), including but not limited to less than 2-fold (e.g., about 10% decrease to about 99% decrease; about 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% decrease), 2-fold, 3-fold, 4-fold, 5-fold, 6-fold, 7-fold, 8-fold, 9-fold, of 10-fold decrease, or greater than about 10-fold decrease.
An altered activity sometimes is an activity not detectable in a host organism and is added to an engineered organism. An altered activity also may be an activity detectable in a host organism and is increased in an engineered organism. An activity may be added or increased by increasing the number of copies of a polynucleotide that encodes a polypeptide having a target activity, in some embodiments. In certain embodiments an activity can be added or increased by inserting into a host microorganism a heterologous polynucleotide that encodes a polypeptide having the added activity. In certain embodiments, an activity can be added or increased by inserting into a host microorganism a heterologous polynucleotide that is (i) operably linked to another polynucleotide that encodes a polypeptide having the added activity, and (ii) up regulates production of the polynucleotide. Thus, an activity can be added or increased by inserting or modifying a regulatory polynucleotide operably linked to another polynucleotide that encodes a polypeptide having the target activity. In certain embodiments, an activity can be added or increased by subjecting a host microorganism to a selective environment and screening for microorganisms that have a detectable level of the target activity. Examples of a selective environment include, without limitation, a medium containing a substrate that a host organism can process and a medium lacking a substrate that a host organism can process.
An altered activity sometimes is an activity detectable in a host organism and is reduced, inhibited or removed (i.e., not detectable) in an engineered organism. An activity may be reduced or removed by decreasing the number of copies of a polynucleotide that encodes a polypeptide having a target activity, in some embodiments. In some embodiments, an activity can be reduced or removed by (i) inserting a polynucleotide within a polynucleotide that encodes a polypeptide having the target activity (disruptive insertion), and/or (ii) removing a portion of or all of a polynucleotide that encodes a polypeptide having the target activity (deletion or knock out, respectively). In certain embodiments, an activity can be reduced or removed by inserting into a host microorganism a heterologous polynucleotide that is (i) operably linked to another polynucleotide that encodes a polypeptide having the target activity, and (ii) down regulates production of the polynucleotide. Thus, an activity can be reduced or removed by inserting or modifying a regulatory polynucleotide operably linked to another polynucleotide that encodes a polypeptide having the target activity.
An activity also can be reduced or removed by (i) inhibiting a polynucleotide that encodes a polypeptide having the activity or (ii) inhibiting a polynucleotide operably linked to another polynucleotide that encodes a polypeptide having the activity. A polynucleotide can be inhibited by a suitable technique known in the art, such as by contacting an RNA encoded by the polynucleotide with a specific inhibitory RNA (e.g., RNAi, siRNA, ribozyme). An activity also can be reduced or removed by contacting a polypeptide having the activity with a molecule that specifically inhibits the activity (e.g., enzyme inhibitor, antibody). In certain embodiments, an activity can be reduced or removed by subjecting a host microorganism to a selective environment and screening for microorganisms that have a reduced level or removal of the target activity.
In some embodiments, an untranslated ribonucleic acid, or a cDNA can be used to reduce the expression of a particular activity or enzyme. For example, a microorganism can be engineered by genetic modification to express a nucleic acid reagent that reduces the expression of an activity by producing an RNA molecule that is partially or substantially homologous to a nucleic acid sequence of interest which encodes the activity of interest. The RNA molecule can bind to the nucleic acid sequence of interest and inhibit the nucleic acid sequence from performing its natural function, in certain embodiments. In some embodiments, the RNA may alter the nucleic acid sequence of interest which encodes the activity of interest in a manner that the nucleic acid sequence of interest is no longer capable of performing its natural function (e.g., the action of a ribozyme for example).
In certain embodiments, nucleotide sequences sometimes are added to, modified or removed from one or more of the nucleic acid reagent elements, such as the promoter, 5′UTR, target sequence, or 3′UTR elements, to enhance, potentially enhance, reduce, or potentially reduce transcription and/or translation before or after such elements are incorporated in a nucleic acid reagent. In some embodiments, one or more of the following sequences may be modified or removed if they are present in a 5′UTR: a sequence that forms a stable secondary structure (e.g., quadruplex structure or stem loop stem structure (e.g., EMBL sequences X12949, AF274954, AF139980, AF152961, S95936, U194144, AF116649 or substantially identical sequences that form such stem loop stem structures)); a translation initiation codon upstream of the target nucleotide sequence start codon; a stop codon upstream of the target nucleotide sequence translation initiation codon; an ORF upstream of the target nucleotide sequence translation initiation codon; an iron responsive element (IRE) or like sequence; and a 5′ terminal oligopyrimidine tract (TOP, e.g., consisting of 5-15 pyrimidines adjacent to the cap). A translational enhancer sequence and/or an internal ribosome entry site (IRES) sometimes is inserted into a 5′UTR (e.g., EMBL nucleotide sequences J04513, X87949, M95825, M12783, AF025841, AF013263, AF006822, M17169, M13440, M22427, D14838 and M17446 and substantially identical nucleotide sequences).
An AU-rich element (ARE, e.g., AUUUA repeats) and/or splicing junction that follows a non-sense codon sometimes is removed from or modified in a 3′UTR. A polyadenosine tail sometimes is inserted into a 3′UTR if none is present, sometimes is removed if it is present, and adenosine moieties sometimes are added to or removed from a polyadenosine tail present in a 3′UTR. Thus, some embodiments are directed to a process comprising: determining whether any nucleotide sequences that increase, potentially increase, reduce or potentially reduce translation efficiency are present in the elements, and adding, removing or modifying one or more of such sequences if they are identified. Certain embodiments are directed to a process comprising: determining whether any nucleotide sequences that increase or potentially increase translation efficiency are not present in the elements, and incorporating such sequences into the nucleic acid reagent.
In some embodiments, an activity can be altered by modifying the nucleotide sequence of an ORF. An ORF sometimes is mutated or modified (for example, by point mutation, deletion mutation, insertion mutation, PCR based mutagenesis and the like) to alter, enhance or increase, reduce, substantially reduce or eliminate the activity of the encoded protein or peptide. The protein or peptide encoded by a modified ORF sometimes is produced in a lower amount or may not be produced at detectable levels, and in other embodiments, the product or protein encoded by the modified ORF is produced at a higher level (e.g., codons sometimes are modified so they are compatible with tRNA's preferentially used in the host organism or engineered organism). To determine the relative activity, the activity from the product of the mutated ORF (or cell containing it) can be compared to the activity of the product or protein encoded by the unmodified ORF (or cell containing it).
In some embodiments, an ORF nucleotide sequence sometimes is mutated or modified to alter the triplet nucleotide sequences used to encode amino acids (e.g., amino acid codon triplets, for example). Modification of the nucleotide sequence of an ORF to alter codon triplets sometimes is used to change the codon found in the original sequence to better match the preferred codon usage of the organism in which the ORF or nucleic acid reagent will be expressed. For example, the codon usage, and therefore the codon triplets encoded by a nucleic acid sequence from bacteria may be different from the preferred codon usage in eukaryotes like yeast or plants. Preferred codon usage also may be different between bacterial species. In certain embodiments an ORF nucleotide sequences sometimes is modified to eliminate codon pairs and/or eliminate mRNA secondary structures that can cause pauses during translation of the mRNA encoded by the ORF nucleotide sequence. Translational pausing sometimes occurs when nucleic acid secondary structures exist in an mRNA, and sometimes occurs due to the presence of codon pairs that slow the rate of translation by causing ribosomes to pause. In some embodiments, the use of lower abundance codon triplets can reduce translational pausing due to a decrease in the pause time needed to load a charged tRNA into the ribosome translation machinery. Therefore, to increase transcriptional and translational efficiency in bacteria (e.g., where transcription and translation are concurrent, for example) or to increase translational efficiency in eukaryotes (e.g., where transcription and translation are functionally separated), the nucleotide sequence of a nucleotide sequence of interest can be altered to better suit the transcription and/or translational machinery of the host and/or genetically modified microorganism. In certain embodiment, slowing the rate of translation by the use of lower abundance codons, which slow or pause the ribosome, can lead to higher yields of the desired product due to an increase in correctly folded proteins and a reduction in the formation of inclusion bodies.
Codons can be altered and optimized according to the preferred usage by a given organism by determining the codon distribution of the nucleotide sequence donor organism and comparing the distribution of codons to the distribution of codons in the recipient or host organism. Techniques described herein (e.g., site directed mutagenesis and the like) can then be used to alter the codons accordingly. Comparisons of codon usage can be done by hand, or using nucleic acid analysis software commercially available to the artisan.
Modification of the nucleotide sequence of an ORF also can be used to correct codon triplet sequences that have diverged in different organisms. For example, certain yeast (e.g., C. tropicalis and C. maltosa) use the amino acid triplet CUG (e.g., CTG in the DNA sequence) to encode serine. CUG typically encodes leucine in most organisms. In order to maintain the correct amino acid in the resultant polypeptide or protein, the CUG codon must be altered to reflect the organism in which the nucleic acid reagent will be expressed. Thus, if an ORF from a bacterial donor is to be expressed in either Candida yeast strain mentioned above, the heterologous nucleotide sequence must first be altered or modified to the appropriate leucine codon. Therefore, in some embodiments, the nucleotide sequence of an ORF sometimes is altered or modified to correct for differences that have occurred in the evolution of the amino acid codon triplets between different organisms. In some embodiments, the nucleotide sequence can be left unchanged at a particular amino acid codon, if the amino acid encoded is a conservative or neutral change in amino acid when compared to the originally encoded amino acid.
In some embodiments, an activity can be altered by modifying translational regulation signals, like a stop codon for example. A stop codon at the end of an ORF sometimes is modified to another stop codon, such as an amber stop codon described above. In some embodiments, a stop codon is introduced within an ORF, sometimes by insertion or mutation of an existing codon. An ORF comprising a modified terminal stop codon and/or internal stop codon often is translated in a system comprising a suppressor tRNA that recognizes the stop codon. An ORF comprising a stop codon sometimes is translated in a system comprising a suppressor tRNA that incorporates an unnatural amino acid during translation of the target protein or target peptide. Methods for incorporating unnatural amino acids into a target protein or peptide are known, which include, for example, processes utilizing a heterologous tRNA/synthetase pair, where the tRNA recognizes an amber stop codon and is loaded with an unnatural amino acid (e.g., World Wide Web URL iupac.org/news/prize/2003/wang.pdf).
Depending on the portion of a nucleic acid reagent (e.g., Promoter, 5′ or 3′ UTR, ORI, ORF, and the like) chosen for alteration (e.g., by mutagenesis, introduction or deletion, for example) the modifications described above can alter a given activity by (i) increasing or decreasing feedback inhibition mechanisms, (ii) increasing or decreasing promoter initiation, (iii) increasing or decreasing translation initiation, (iv) increasing or decreasing translational efficiency, (v) modifying localization of peptides or products expressed from nucleic acid reagents described herein, or (vi) increasing or decreasing the copy number of a nucleotide sequence of interest, (vii) expression of an anti-sense RNA, RNAi, siRNA, ribozyme and the like. In some embodiments, alteration of a nucleic acid reagent or nucleotide sequence can alter a region involved in feedback inhibition (e.g., 5′ UTR, promoter and the like). A modification sometimes is made that can add or enhance binding of a feedback regulator and sometimes a modification is made that can reduce, inhibit or eliminate binding of a feedback regulator.
In certain embodiments, alteration of a nucleic acid reagent or nucleotide sequence can alter sequences involved in transcription initiation (e.g., promoters, 5′ UTR, and the like). A modification sometimes can be made that can enhance or increase initiation from an endogenous or heterologous promoter element. A modification sometimes can be made that removes or disrupts sequences that increase or enhance transcription initiation, resulting in a decrease or elimination of transcription from an endogenous or heterologous promoter element.
In some embodiments, alteration of a nucleic acid reagent or nucleotide sequence can alter sequences involved in translational initiation or translational efficiency (e.g., 5′ UTR, 3′ UTR, codon triplets of higher or lower abundance, translational terminator sequences and the like, for example). A modification sometimes can be made that can increase or decrease translational initiation, modifying a ribosome binding site for example. A modification sometimes can be made that can increase or decrease translational efficiency. Removing or adding sequences that form hairpins and changing codon triplets to a more or less preferred codon are non-limiting examples of genetic modifications that can be made to alter translation initiation and translation efficiency.
In certain embodiments, alteration of a nucleic acid reagent or nucleotide sequence can alter sequences involved in localization of peptides, proteins or other desired products (e.g., adipic acid, for example). A modification sometimes can be made that can alter, add or remove sequences responsible for targeting a polypeptide, protein or product to an intracellular organelle, the periplasm, cellular membranes, or extracellularly. Transport of a heterologous product to a different intracellular space or extracellularly sometimes can reduce or eliminate the formation of inclusion bodies (e.g., insoluble aggregates of the desired product).
In some embodiments, alteration of a nucleic acid reagent or nucleotide sequence can alter sequences involved in increasing or decreasing the copy number of a nucleotide sequence of interest. A modification sometimes can be made that increases or decreases the number of copies of an ORF stably integrated into the genome of an organism or on an epigenetic nucleic acid reagent. Non-limiting examples of alterations that can increase the number of copies of a sequence of interest include, adding copies of the sequence of interest by duplication of regions in the genome (e.g., adding additional copies by recombination or by causing gene amplification of the host genome, for example), cloning additional copies of a sequence onto a nucleic acid reagent, or altering an ORI to increase the number of copies of an epigenetic nucleic acid reagent. Non-limiting examples of alterations that can decrease the number of copies of a sequence of interest include, removing copies of the sequence of interest by deletion or disruption of regions in the genome, removing additional copies of the sequence from epigenetic nucleic acid reagents, or altering an ORI to decrease the number of copies of an epigenetic nucleic acid reagent.
In certain embodiments, increasing or decreasing the expression of a nucleotide sequence of interest can also be accomplished by altering, adding or removing sequences involved in the expression of an anti-sense RNA, RNAi, siRNA, ribozyme and the like. The methods described above can be used to modify expression of anti-sense RNA, RNAi, siRNA, ribozyme and the like.
Engineered microorganisms can be prepared by altering, introducing or removing nucleotide sequences in the host genome or in stably maintained epigenetic nucleic acid reagents, as noted above. The nucleic acid reagents use to alter, introduce or remove nucleotide sequences in the host genome or epigenetic nucleic acids can be prepared using the methods described herein or available to the artisan.
Nucleic acid sequences having a desired activity can be isolated from cells of a suitable organism using lysis and nucleic acid purification procedures available in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. or with commercially available cell lysis and DNA purification reagents and kits. In some embodiments, nucleic acids used to engineer microorganisms can be provided for conducting methods described herein after processing of the organism containing the nucleic acid. For example, the nucleic acid of interest may be extracted, isolated, purified or amplified from a sample (e.g., from an organism of interest or culture containing a plurality of organisms of interest, like yeast or bacteria for example). The term “isolated” as used herein refers to nucleic acid removed from its original environment (e.g., the natural environment if it is naturally occurring, or a host cell if expressed exogenously), and thus is altered “by the hand of man” from its original environment. An isolated nucleic acid generally is provided with fewer non-nucleic acid components (e.g., protein, lipid) than the amount of components present in a source sample. A composition comprising isolated sample nucleic acid can be substantially isolated (e.g., about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or greater than 99% free of non-nucleic acid components). The term “purified” as used herein refers to sample nucleic acid provided that contains fewer nucleic acid species than in the sample source from which the sample nucleic acid is derived. A composition comprising sample nucleic acid may be substantially purified (e.g., about 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or greater than 99% free of other nucleic acid species). The term “amplified” as used herein refers to subjecting nucleic acid of a cell, organism or sample to a process that linearly or exponentially generates amplicon nucleic acids having the same or substantially the same nucleotide sequence as the nucleotide sequence of the nucleic acid in the sample, or portion thereof. As noted above, the nucleic acids used to prepare nucleic acid reagents as described herein can be subjected to fragmentation or cleavage.
Amplification of nucleic acids is sometimes necessary when dealing with organisms that are difficult to culture. Where amplification may be desired, any suitable amplification technique can be utilized. Non-limiting examples of methods for amplification of polynucleotides include, polymerase chain reaction (PCR); ligation amplification (or ligase chain reaction (LCR)); amplification methods based on the use of Q-beta replicase or template-dependent polymerase (see US Patent Publication Number US20050287592); helicase-dependant isothermal amplification (Vincent et al., “Helicase-dependent isothermal DNA amplification”. EMBO reports 5 (8): 795-800 (2004)); strand displacement amplification (SDA); thermophilic SDA nucleic acid sequence based amplification (3SR or NASBA) and transcription-associated amplification (TAA). Non-limiting examples of PCR amplification methods include standard PCR, AFLP-PCR, Allele-specific PCR, Alu-PCR, Asymmetric PCR, Colony PCR, Hot start PCR, Inverse PCR (IPCR), In situ PCR (ISH), Intersequence-specific PCR (ISSR-PCR), Long PCR, Multiplex PCR, Nested PCR, Quantitative PCR, Reverse Transcriptase PCR(RT-PCR), Real Time PCR, Single cell PCR, Solid phase PCR, combinations thereof, and the like. Reagents and hardware for conducting PCR are commercially available.
Protocols for conducting the various type of PCR listed above are readily available to the artisan. PCR conditions can be dependent upon primer sequences, target abundance, and the desired amount of amplification, and therefore, one of skill in the art may choose from a number of PCR protocols available (see, e.g., U.S. Pat. Nos. 4,683,195 and 4,683,202; and PCR Protocols: A Guide to Methods and Applications, Innis et al., eds, 1990. PCR often is carried out as an automated process with a thermostable enzyme. In this process, the temperature of the reaction mixture is cycled through a denaturing region, a primer-annealing region, and an extension reaction region automatically. Machines specifically adapted for this purpose are commercially available. A non-limiting example of a PCR protocol that may be suitable for embodiments described herein is, treating the sample at 95° C. for 5 minutes; repeating forty-five cycles of 95° C. for 1 minute, 59° C. for 1 minute, 10 seconds, and 72° C. for 1 minute 30 seconds; and then treating the sample at 72° C. for 5 minutes. Additional PCR protocols are described in the example section. Multiple cycles frequently are performed using a commercially available thermal cycler. Suitable isothermal amplification processes known and selected by the person of ordinary skill in the art also may be applied, in certain embodiments. In some embodiments, nucleic acids encoding polypeptides with a desired activity can be isolated by amplifying the desired sequence from an organism having the desired activity using oligonucleotides or primers designed based on sequences described herein
Amplified, isolated and/or purified nucleic acids can be cloned into the recombinant DNA vectors described in Figures herein or into suitable commercially available recombinant DNA vectors. Cloning of nucleic acid sequences of interest into recombinant DNA vectors can facilitate further manipulations of the nucleic acids for preparation of nucleic acid reagents, (e.g., alteration of nucleotide sequences by mutagenesis, homologous recombination, amplification and the like, for example). Standard cloning procedures (e.g., enzymic digestion, ligation, and the like) are readily available to the artisan and can be found in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
In some embodiments, nucleic acid sequences prepared by isolation or amplification can be used, without any further modification, to add an activity to a microorganism and thereby generate a genetically modified or engineered microorganism. In certain embodiments, nucleic acid sequences prepared by isolation or amplification can be genetically modified to alter (e.g., increase or decrease, for example) a desired activity. In some embodiments, nucleic acids, used to add an activity to an organism, sometimes are genetically modified to optimize the heterologous polynucleotide sequence encoding the desired activity (e.g., polypeptide or protein, for example). The term “optimize” as used herein can refer to alteration to increase or enhance expression by preferred codon usage. The term optimize can also refer to modifications to the amino acid sequence to increase the activity of a polypeptide or protein, such that the activity exhibits a higher catalytic activity as compared to the “natural” version of the polypeptide or protein.
Nucleic acid sequences of interest can be genetically modified using methods known in the art. Mutagenesis techniques are particularly useful for small scale (e.g., 1, 2, 5, 10 or more nucleotides) or large scale (e.g., 50, 100, 150, 200, 500, or more nucleotides) genetic modification. Mutagenesis allows the artisan to alter the genetic information of an organism in a stable manner, either naturally (e.g., isolation using selection and screening) or experimentally by the use of chemicals, radiation or inaccurate DNA replication (e.g., PCR mutagenesis). In some embodiments, genetic modification can be performed by whole scale synthetic synthesis of nucleic acids, using a native nucleotide sequence as the reference sequence, and modifying nucleotides that can result in the desired alteration of activity. Mutagenesis methods sometimes are specific or targeted to specific regions or nucleotides (e.g., site-directed mutagenesis, PCR-based site-directed mutagenesis, and in vitro mutagenesis techniques such as transplacement and in vivo oligonucleotide site-directed mutagenesis, for example). Mutagenesis methods sometimes are non-specific or random with respect to the placement of genetic modifications (e.g., chemical mutagenesis, insertion element (e.g., insertion or transposon elements) and inaccurate PCR based methods, for example).
Site directed mutagenesis is a procedure in which a specific nucleotide or specific nucleotides in a DNA molecule are mutated or altered. Site directed mutagenesis typically is performed using a nucleic acid sequence of interest cloned into a circular plasmid vector. Site-directed mutagenesis requires that the wild type sequence be known and used a platform for the genetic alteration. Site-directed mutagenesis sometimes is referred to as oligonucleotide-directed mutagenesis because the technique can be performed using oligonucleotides which have the desired genetic modification incorporated into the complement a nucleotide sequence of interest. The wild type sequence and the altered nucleotide are allowed to hybridize and the hybridized nucleic acids are extended and replicated using a DNA polymerase. The double stranded nucleic acids are introduced into a host (e.g., E. coli, for example) and further rounds of replication are carried out in vivo. The transformed cells carrying the mutated nucleic acid sequence are then selected and/or screened for those cells carrying the correctly mutagenized sequence. Cassette mutagenesis and PCR-based site-directed mutagenesis are further modifications of the site-directed mutagenesis technique. Site-directed mutagenesis can also be performed in vivo (e.g., transplacement “pop-in pop-out”, In vivo site-directed mutagenesis with synthetic oligonucleotides and the like, for example).
PCR-based mutagenesis can be performed using PCR with oligonucleotide primers that contain the desired mutation or mutations. The technique functions in a manner similar to standard site-directed mutagenesis, with the exception that a thermocycler and PCR conditions are used to replace replication and selection of the clones in a microorganism host. As PCR-based mutagenesis also uses a circular plasmid vector, the amplified fragment (e.g., linear nucleic acid molecule) containing the incorporated genetic modifications can be separated from the plasmid containing the template sequence after a sufficient number of rounds of thermocycler amplification, using standard electrophorectic procedures. A modification of this method uses linear amplification methods and a pair of mutagenic primers that amplify the entire plasmid. The procedure takes advantage of the E. coli Dam methylase system which causes DNA replicated in vivo to be sensitive to the restriction endonucleases DpnI. PCR synthesized DNA is not methylated and is therefore resistant to DpnI. This approach allows the template plasmid to be digested, leaving the genetically modified, PCR synthesized plasmids to be isolated and transformed into a host bacteria for DNA repair and replication, thereby facilitating subsequent cloning and identification steps. A certain amount of randomness can be added to PCR-based sited directed mutagenesis by using partially degenerate primers.
Recombination sometimes can be used as a tool for mutagenesis. Homologous recombination allows the artisan to specifically target regions of known sequence for insertion of heterologous nucleotide sequences using the host organisms natural DNA replication and repair enzymes. Homologous recombination methods sometimes are referred to as “pop in pop out” mutagenesis, transplacement, knock out mutagenesis or knock in mutagenesis. Integration of a nucleic acid sequence into a host genome is a single cross over event, which inserts the entire nucleic acid reagent (e.g., pop in). A second cross over event excises all but a portion of the nucleic acid reagent, leaving behind a heterologous sequence, often referred to as a “footprint” (e.g., pop out). Mutagenesis by insertion (e.g., knock in) or by double recombination leaving behind a disrupting heterologous nucleic acid (e.g., knock out) both server to disrupt or “knock out” the function of the gene or nucleic acid sequence in which insertion occurs. By combining selectable markers and/or auxotrophic markers with nucleic acid reagents designed to provide the appropriate nucleic acid target sequences, the artisan can target a selectable nucleic acid reagent to a specific region, and then select for recombination events that “pop out” a portion of the inserted (e.g., “pop in”) nucleic acid reagent.
Such methods take advantage of nucleic acid reagents that have been specifically designed with known target nucleic acid sequences at or near a nucleic acid or genomic region of interest. Popping out typically leaves a “foot print” of left over sequences that remain after the recombination event. The left over sequence can disrupt a gene and thereby reduce or eliminate expression of that gene. In some embodiments, the method can be used to insert sequences, upstream or downstream of genes that can result in an enhancement or reduction in expression of the gene. In certain embodiments, new genes can be introduced into the genome of a host organism using similar recombination or “pop in” methods. An example of a yeast recombination system using the ura3 gene and 5-FOA were described briefly above and further detail is presented herein.
A method for modification is described in Alani et al., “A method for gene disruption that allows repeated use of URA3 selection in the construction of multiply disrupted yeast strains”, Genetics 116(4):541-545 August 1987. The original method uses a Ura3 cassette with 1000 base pairs (bp) of the same nucleotide sequence cloned in the same orientation on either side of the URA3 cassette. Targeting sequences of about 50 bp are added to each side of the construct. The double stranded targeting sequences are complementary to sequences in the genome of the host organism. The targeting sequences allow site-specific recombination in a region of interest. The modification of the original technique replaces the two 1000 bp sequence direct repeats with two 200 bp direct repeats. The modified method also uses 50 bp targeting sequences. The modification reduces or eliminates recombination of a second knock out into the 1000 bp repeat left behind in a first mutagenesis, therefore allowing multiply knocked out yeast. Additionally, the 200 bp sequences used herein are uniquely designed, self-assembling sequences that leave behind identifiable footprints. The technique used to design the sequences incorporate design features such as low identity to the yeast genome, and low identity to each other. Therefore a library of the self-assembling sequences can be generated to allow multiple knockouts in the same organism, while reducing or eliminating the potential for integration into a previous knockout.
As noted above, the URA3 cassette makes use of the toxicity of 5-FOA in yeast carrying a functional URA3 gene. Uracil synthesis deficient yeast are transformed with the modified URA3 cassette, using standard yeast transformation protocols, and the transformed cells are plated on minimal media minus uracil. In some embodiments, PCR can be used to verify correct insertion into the region of interest in the host genome, and certain embodiments the PCR step can be omitted. Inclusion of the PCR step can reduce the number of transformants that need to be counter selected to “pop out” the URA3 cassette. The transformants (e.g., all or the ones determined to be correct by PCR, for example) can then be counter-selected on media containing 5-FOA, which will select for recombination out (e.g., popping out) of the URA3 cassette, thus rendering the yeast ura3 deficient again, and resistant to 5-FOA toxicity. Targeting sequences used to direct recombination events to specific regions are presented herein. A modification of the method described above can be used to integrate genes in to the chromosome, where after recombination a functional gene is left in the chromosome next to the 200 bp footprint.
In some embodiments, other auxotrophic or dominant selection markers can be used in place of URA3 (e.g., an auxotrophic selectable marker), with the appropriate change in selection media and selection agents. Auxotrophic selectable markers are used in strains deficient for synthesis of a required biological molecule (e.g., amino acid or nucleoside, for example). Non-limiting examples of additional auxotrophic markers include; HIS3, TRP1, LEU2, LEU2-d, and LYS2. Certain auxotrophic markers (e.g., URA3 and LYS2) allow counter selection to select for the second recombination event that pops out all but one of the direct repeats of the recombination construct. HIS3 encodes an activity involved in histidine synthesis. TRP1 encodes an activity involved in tryptophan synthesis. LEU2 encodes an activity involved in leucine synthesis. LEU2-d is a low expression version of LEU2 that selects for increased copy number (e.g., gene or plasmid copy number, for example) to allow survival on minimal media without leucine. LYS2 encodes an activity involved in lysine synthesis, and allows counter selection for recombination out of the LYS2 gene using alpha-amino adipate (α-amino adipate).
Dominant selectable markers are useful because they also allow industrial and/or prototrophic strains to be used for genetic manipulations. Additionally, dominant selectable markers provide the advantage that rich medium can be used for plating and culture growth, and thus growth rates are markedly increased. Non-limiting examples of dominant selectable markers include; Tn903 kan^r, Cm^r, Hyg^r, CUP1, and DHFR. Tn903 kan^rencodes an activity involved in kanamycin antibiotic resistance (e.g., typically neomycin phosphotransferase II or NPTII, for example). Cm^rencodes an activity involved in chloramphenicol antibiotic resistance (e.g., typically chloramphenicol acetyl transferase or CAT, for example). Hyg^rencodes an activity involved in hygromycin resistance by phosphorylation of hygromycin B (e.g., hygromycin phosphotransferase, or HPT). CUP1 encodes an activity involved in resistance to heavy metal (e.g., copper, for example) toxicity. DHFR encodes a dihydrofolate reductase activity which confers resistance to methotrexate and sulfanilamde compounds.
In contrast to site-directed or specific mutagenesis, random mutagenesis does not require any sequence information and can be accomplished by a number of widely different methods. Random mutagenesis often is used to generate mutant libraries that can be used to screen for the desired genotype or phenotype. Non-limiting examples of random mutagenesis include; chemical mutagenesis, UV-induced mutagenesis, insertion element or transposon-mediated mutagenesis, DNA shuffling, error-prone PCR mutagenesis, and the like.
Chemical mutagenesis often involves chemicals like ethyl methanesulfonate (EMS), nitrous acid, mitomycin C, N-methyl-N-nitrosourea (MNU), diepoxybutane (DEB), 1, 2, 7, 8-diepoxyoctane (DEO), methyl methane sulfonate (MMS), N-methyl-N′-nitro-N-nitrosoguanidine (MNNG), 4-nitroquinoline 1-oxide (4-NQO), 2-methyloxy-6-chloro-9(3-[ethyl-2-chloroethyl]-aminopropylamino)-acridinedihydrochloride (ICR-170), 2-amino purine (2AP), and hydroxylamine (HA), provided herein as non-limiting examples. These chemicals can cause base-pair substitutions, frameshift mutations, deletions, transversion mutations, transition mutations, incorrect replication, and the like. In some embodiments, the mutagenesis can be carried out in vivo. Sometimes the mutagenic process involves the use of the host organisms DNA replication and repair mechanisms to incorporate and replicate the mutagenized base or bases.
Another type of chemical mutagenesis involves the use of base-analogs. The use of base-analogs cause incorrect base pairing which in the following round of replication is corrected to a mismatched nucleotide when compared to the starting sequence. Base analog mutagenesis introduces a small amount of non-randomness to random mutagenesis, because specific base analogs can be chose which can be incorporated at certain nucleotides in the starting sequence. Correction of the mispairing typically yields a known substitution. For example, Bromo-deoxyuridine (BrdU) can be incorporated into DNA and replaces T in the sequence. The host DNA repair and replication machinery can sometime correct the defect, but sometimes will mispair the BrdU with a G. The next round of replication then causes a G-C transversion from the original A-T in the native sequence.
Ultra violet (UV) induced mutagenesis is caused by the formation of thymidine dimers when UV light irradiates chemical bonds between two adjacent thymine residues. Excision repair mechanism of the host organism correct the lesion in the DNA, but occasionally the lesion is incorrectly repaired typically resulting in a C to T transition.
Insertion element or transposon-mediated mutagenesis makes use of naturally occurring or modified naturally occurring mobile genetic elements. Transposons often encode accessory activities in addition to the activities necessary for transposition (e.g., movement using a transposase activity, for example). In many examples, transposon accessory activities are antibiotic resistance markers (e.g., see Tn903 kan^rdescribed above, for example). Insertion elements typically only encode the activities necessary for movement of the nucleic acid sequence. Insertion element and transposon mediated mutagenesis often can occur randomly, however specific target sequences are known for some transposons. Mobile genetic elements like IS elements or Transposons (Tn) often have inverted repeats, direct repeats or both inverted and direct repeats flanking the region coding for the transposition genes. Recombination events catalyzed by the transposase cause the element to remove itself from the genome and move to a new location, leaving behind a portion of an inverted or direct repeat. Classic examples of transposons are the “mobile genetic elements” discovered in maize. Transposon mutagenesis kits are commercially available which are designed to leave behind a 5 codon insert (e.g., Mutation Generation System kit, Finnzymes, World Wide Web URL finnzymes.us, for example). This allows the artisan to identify the insertion site, without fully disrupting the function of most genes.
DNA shuffling is a method which uses DNA fragments from members of a mutant library and reshuffles the fragments randomly to generate new mutant sequence combinations. The fragments are typically generated using DNaseI, followed by random annealing and re-joining using self priming PCR. The DNA overhanging ends, from annealing of random fragments, provide “primer” sequences for the PCR process. Shuffling can be applied to libraries generated by any of the above mutagenesis methods.
Error prone PCR and its derivative rolling circle error prone PCR uses increased magnesium and manganese concentrations in conjunction with limiting amounts of one or two nucleotides to reduce the fidelity of the Taq polymerase. The error rate can be as high as 2% under appropriate conditions, when the resultant mutant sequence is compared to the wild type starting sequence. After amplification, the library of mutant coding sequences must be cloned into a suitable plasmid.
Although point mutations are the most common types of mutation in error prone PCR, deletions and frameshift mutations are also possible. There are a number of commercial error-prone PCR kits available, including those from Stratagene and Clontech (e.g., World Wide Web URL strategene.com and World Wide Web URL clontech.com, respectively, for example). Rolling circle error-prone PCR is a variant of error-prone PCR in which wild-type sequence is first cloned into a plasmid, the whole plasmid is then amplified under error-prone conditions.
As noted above, organisms with altered activities can also be isolated using genetic selection and screening of organisms challenged on selective media or by identifying naturally occurring variants from unique environments. For example, 2-Deoxy-D-glucose is a toxic glucose analog. Growth of yeast on this substance yields mutants that are glucose-deregulated. A number of mutants have been isolated using 2-Deoxy-D-glucose including transport mutants, and mutants that ferment glucose and galactose simultaneously instead of glucose first then galactose when glucose is depleted. Similar techniques have been used to isolate mutant microorganisms that can metabolize plastics (e.g., from landfills), petrochemicals (e.g., from oil spills), and the like, either in a laboratory setting or from unique environments.
Similar methods can be used to isolate naturally occurring mutations in a desired activity when the activity exists at a relatively low or nearly undetectable level in the organism of choice, in some embodiments. The method generally consists of growing the organism to a specific density in liquid culture, concentrating the cells, and plating the cells on various concentrations of the substance to which an increase in metabolic activity is desired. The cells are incubated at a moderate growth temperature, for 5 to 10 days. To enhance the selection process, the plates can be stored for another 5 to 10 days at a low temperature. The low temperature sometimes can allow strains that have gained or increased an activity to continue growing while other strains are inhibited for growth at the low temperature. Following the initial selection and secondary growth at low temperature, the plates can be replica plated on higher or lower concentrations of the selection substance to further select for the desired activity.
A native, heterologous or mutagenized polynucleotide can be introduced into a nucleic acid reagent for introduction into a host organism, thereby generating an engineered microorganism. Standard recombinant DNA techniques (restriction enzyme digests, ligation, and the like) can be used by the artisan to combine the mutagenized nucleic acid of interest into a suitable nucleic acid reagent capable of (i) being stably maintained by selection in the host organism, or (ii) being integrating into the genome of the host organism. As noted above, sometimes nucleic acid reagents comprise two replication origins to allow the same nucleic acid reagent to be manipulated in bacterial before final introduction of the final product into the host organism (e.g., yeast or fungus for example). Standard molecular biology and recombinant DNA methods available to one of skill in the art can be found in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
Nucleic acid reagents can be introduced into microorganisms using various techniques. Non-limiting examples of methods used to introduce heterologous nucleic acids into various organisms include; transformation, transfection, transduction, electroporation, ultrasound-mediated transformation, particle bombardment and the like. In some instances the addition of carrier molecules (e.g., bis-benzimdazolyl compounds, for example, see U.S. Pat. No. 5,595,899) can increase the uptake of DNA in cells typically though to be difficult to transform by conventional methods. Conventional methods of transformation are readily available to the artisan and can be found in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.

Culture, Production and Process Methods

Engineered microorganisms often are cultured under conditions that optimize yield of a target molecule. A non-limiting example of such a target molecule is ethanol. Culture conditions often can alter (e.g., add, optimize, reduce or eliminate, for example) activity of one or more of the following activities: phosphofructokinase activity, phosphogluconate dehydratase activity, 2-keto-3-deoxygluconate-6-phosphate aldolase activity, xylose isomerase activity, phosphoenolpyruvate carboxylase activity, alcohol dehydrogenase 2 activity and thymidylate synthase activities. In general, conditions that may be optimized include the type and amount of carbon source, the type and amount of nitrogen source, the carbon-to-nitrogen ratio, the oxygen level, growth temperature, pH, length of the biomass production phase, length of target product accumulation phase, and time of cell harvest.
The term “fermentation conditions” as used herein refers to any culture conditions suitable for maintaining a microorganism (e.g., in a static or proliferative state). Fermentation conditions can include several parameters, including without limitation, temperature, oxygen content, nutrient content (e.g., glucose content), pH, agitation level (e.g., revolutions per minute), gas flow rate (e.g., air, oxygen, nitrogen gas), redox potential, cell density (e.g., optical density), cell viability and the like. A change in fermentation conditions (e.g., switching fermentation conditions) is an alteration, modification or shift of one or more fermentation parameters. For example, one can change fermentation conditions by increasing or decreasing temperature, increasing or decreasing pH (e.g., adding or removing an acid, a base or carbon dioxide), increasing or decreasing oxygen content (e.g., introducing air, oxygen, carbon dioxide, nitrogen) and/or adding or removing a nutrient (e.g., one or more sugars or sources of sugar, biomass, vitamin and the like), or combinations of the foregoing. Examples of fermentation conditions are described herein. Aerobic conditions often comprise greater than about 50% dissolved oxygen (e.g., about 52%, 54%, 56%, 58%, 60%, 62%, 64%, 66%, 68%, 70%, 72%, 74%, 76%, 78%, 80%, 82%, 84%, 86%, 88%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99%, or greater than any one of the foregoing). Anaerobic conditions often comprise less than about 50% dissolved oxygen (e.g., about 1%, 2%, 4%, 6%, 8%, 10%, 12%, 14%, 16%, 18%, 20%, 22%, 24%, 26%, 28%, 30%, 32%, 34%, 36%, 38%, 40%, 42%, 44%, 46%, 48%, or less than any one of the foregoing).
Culture media generally contain a suitable carbon source. Carbon sources may include, but are not limited to, monosaccharides (e.g., glucose, fructose, xylose), disaccharides (e.g., lactose, sucrose), oligosaccharides, polysaccharides (e.g., starch, cellulose, hemicellulose, other lignocellulosic materials or mixtures thereof), sugar alcohols (e.g., glycerol), and renewable feedstocks (e.g., cheese whey permeate, cornsteep liquor, sugar beet molasses, barley malt). Carbon sources also can be selected from one or more of the following non-limiting examples: linear or branched alkanes (e.g., hexane), linear or branched alcohols (e.g., hexanol), fatty acids (e.g., about 10 carbons to about 22 carbons), esters of fatty acids, monoglycerides, diglycerides, triglycerides, phospholipids and various commercial sources of fatty acids including vegetable oils (e.g., soybean oil) and animal fats. A carbon source may include one-carbon sources (e.g., carbon dioxide, methanol, formaldehyde, formate and carbon-containing amines) from which metabolic conversion into key biochemical intermediates can occur. It is expected that the source of carbon utilized may encompass a wide variety of carbon-containing sources and will only be limited by the choice of the engineered microorganism(s).
Nitrogen may be supplied from an inorganic (e.g., (NH.sub.4).sub.2SO.sub.4) or organic source (e.g., urea or glutamate). In addition to appropriate carbon and nitrogen sources, culture media also can contain suitable minerals, salts, cofactors, buffers, vitamins, metal ions (e.g., Mn.sup.+2, Co.sup.+2, Zn.sup.+2, Mg.sup.+2) and other components suitable for culture of microorganisms. Engineered microorganisms sometimes are cultured in complex media (e.g., yeast extract-peptone-dextrose broth (YPD)). In some embodiments, engineered microorganisms are cultured in a defined minimal media that lacks a component necessary for growth and thereby forces selection of a desired expression cassette (e.g., Yeast Nitrogen Base (DIFCO Laboratories, Detroit, Mich.)). Culture media in some embodiments are common commercially prepared media, such as Yeast Nitrogen Base (DIFCO Laboratories, Detroit, Mich.). Other defined or synthetic growth media may also be used and the appropriate medium for growth of the particular microorganism are known.
A variety of host organisms can be selected for the production of engineered microorganisms. Non-limiting examples include yeast and fungi. In specific embodiments, yeast are cultured in YPD media (10 g/L Bacto Yeast Extract, 20 g/L Bacto Peptone, and 20 g/L Dextrose). Filamentous fungi, in particular embodiments, are grown in CM (Complete Medium) containing 10 g/L Dextrose, 2 g/L Bacto Peptone, 1 g/L Bacto Yeast Extract, 1 g/L Casamino acids, 50 mL/L 20× Nitrate Salts (120 g/L NaNO₃, 10.4 g/L KCl, 10.4 g/L MgSO₄.7H₂O, 1 mL/L 1000× Trace Elements (22 g/L ZnSO₄.7H₂O, 11 g/L H₃BO₃, 5 g/L MnCl₂.7H₂O, 5 g/L FeSO₄.7H₂O, 1.7 g/L CoCl₂.6H₂O, 1.6 g/L CuSO₄.5H₂O, 1.5 g/L Na₂MoO₄.2H₂O, and 50 g/L Na₄EDTA), and 1 mL/L Vitamin Solution (100 mg each of Biotin, pyridoxine, thiamine, riboflavin, p-aminobenzoic acid, and nicotinic acid in 100 mL water).
A suitable pH range for the fermentation often is between about pH 4.0 to about pH 8.0, where a pH in the range of about pH 5.5 to about pH 7.0 sometimes is utilized for initial culture conditions. Culturing may be conducted under aerobic or anaerobic conditions, where microaerobic conditions sometimes are maintained. A two-stage process may be utilized, where one stage promotes microorganism proliferation and another state promotes production of target molecule. In a two-stage process, the first stage may be conducted under aerobic conditions (e.g., introduction of air and/or oxygen) and the second stage may be conducted under anaerobic conditions (e.g., air or oxygen are not introduced to the culture conditions).
A variety of fermentation processes may be applied for commercial biological production of a target product. In some embodiments, commercial production of a target product from a recombinant microbial host is conducted using a batch, fed-batch or continuous fermentation process, for example.
A batch fermentation process often is a closed system where the media composition is fixed at the beginning of the process and not subject to further additions beyond those required for maintenance of pH and oxygen level during the process. At the beginning of the culturing process the media is inoculated with the desired organism and growth or metabolic activity is permitted to occur without adding additional sources (i.e., carbon and nitrogen sources) to the medium. In batch processes the metabolite and biomass compositions of the system change constantly up to the time the culture is terminated. In a typical batch process, cells proceed through a static lag phase to a high-growth log phase and finally to a stationary phase, wherein the growth rate is diminished or halted. Left untreated, cells in the stationary phase will eventually die.
A variation of the standard batch process is the fed-batch process, where the carbon source is continually added to the fermentor over the course of the fermentation process. Fed-batch processes are useful when catabolite repression is apt to inhibit the metabolism of the cells or where it is desirable to have limited amounts of carbon source in the media at any one time. Measurement of the carbon source concentration in fed-batch systems may be estimated on the basis of the changes of measurable factors such as pH, dissolved oxygen and the partial pressure of waste gases (e.g., CO.sub.2). Batch and fed-batch culturing methods are known in the art. Examples of such methods may be found in Thomas D. Brock in Biotechnology: A Textbook of Industrial Microbiology, 2.sup.nd ed., (1989) Sinauer Associates Sunderland, Mass. and Deshpande, Mukund V., Appl. Biochem. Biotechnol., 36:227 (1992).
In continuous fermentation process a defined media often is continuously added to a bioreactor while an equal amount of culture volume is removed simultaneously for product recovery. Continuous cultures generally maintain cells in the log phase of growth at a constant cell density. Continuous or semi-continuous culture methods permit the modulation of one factor or any number of factors that affect cell growth or end product concentration. For example, an approach may limit the carbon source and allow all other parameters to moderate metabolism. In some systems, a number of factors affecting growth may be altered continuously while the cell concentration, measured by media turbidity, is kept constant. Continuous systems often maintain steady state growth and thus the cell growth rate often is balanced against cell loss due to media being drawn off the culture. Methods of modulating nutrients and growth factors for continuous culture processes, as well as techniques for maximizing the rate of product formation, are known and a variety of methods are detailed by Brock, supra.
In various embodiments ethanol may be purified from the culture media or extracted from the engineered microorganisms. Culture media may be tested for ethanol concentration and drawn off when the concentration reaches a predetermined level. Detection methods are known in the art, including but not limited to the use of a hydrometer and infrared measurement of vibrational frequency of dissolved ethanol using the CH band at 2900 cm⁻¹. Ethanol may be present at a range of levels as described herein.
A target product sometimes is retained within an engineered microorganism after a culture process is completed, and in certain embodiments, the target product is secreted out of the microorganism into the culture medium. For the latter embodiments, (i) culture media may be drawn from the culture system and fresh medium may be supplemented, and/or (ii) target product may be extracted from the culture media during or after the culture process is completed. Engineered microorganisms may be cultured on or in solid, semi-solid or liquid media. In some embodiments media is drained from cells adhering to a plate. In certain embodiments, a liquid-cell mixture is centrifuged at a speed sufficient to pellet the cells but not disrupt the cells and allow extraction of the media, as known in the art. The cells may then be resuspended in fresh media. Target product may be purified from culture media according to methods known in the art.
In certain embodiments, target product is extracted from the cultured engineered microorganisms. The microorganism cells may be concentrated through centrifugation at speed sufficient to shear the cell membranes. In some embodiments, the cells may be physically disrupted (e.g., shear force, sonication) or chemically disrupted (e.g., contacted with detergent or other lysing agent). The phases may be separated by centrifugation or other method known in the art and target product may be isolated according to known methods.
Commercial grade target product sometimes is provided in substantially pure form (e.g., 90% pure or greater, 95% pure or greater, 99% pure or greater or 99.5% pure or greater). In some embodiments, target product may be modified into any one of a number of downstream products. For example, ethanol may be derivatized or further processed to produce ethyl halides, ethyl esters, diethyl ether, acetic acid, ethyl amines, butadiene, solvents, food flavorings, distilled spirits and the like.
Target product may be provided within cultured microbes containing target product, and cultured microbes may be supplied fresh or frozen in a liquid media or dried. Fresh or frozen microbes may be contained in appropriate moisture-proof containers that may also be temperature controlled as necessary. Target product sometimes is provided in culture medium that is substantially cell-free. In some embodiments target product or modified target product purified from microbes is provided, and target product sometimes is provided in substantially pure form. In certain embodiments, ethanol can be provided in anhydrous or hydrous forms. Ethanol may be transported in a variety of containers including pints, quarts, liters, gallons, drums (e.g., 10 gallon or 55 gallon, for example) and the like.
In certain embodiments, a target product (e.g., ethanol, succinic acid) is produced with a yield of about 0.30 grams of target product, or greater, per gram of glucose added during a fermentation process (e.g., about 0.31 grams of target product per gram of glucose added, or greater; about 0.32 grams of target product per gram of glucose added, or greater; about 0.33 grams of target product per gram of glucose added, or greater; about 0.34 grams of target product per gram of glucose added, or greater; about 0.35 grams of target product per gram of glucose added, or greater; about 0.36 grams of target product per gram of glucose added, or greater; about 0.37 grams of target product per gram of glucose added, or greater; about 0.38 grams of target product per gram of glucose added, or greater; about 0.39 grams of target product per gram of glucose added, or greater; about 0.40 grams of target product per gram of glucose added, or greater; about 0.41 grams of target product per gram of glucose added, or greater; 0.42 grams of target product per gram of glucose added, or greater; 0.43 grams of target product per gram of glucose added, or greater; 0.44 grams of target product per gram of glucose added, or greater; 0.45 grams of target product per gram of glucose added, or greater; 0.46 grams of target product per gram of glucose added, or greater; 0.47 grams of target product per gram of glucose added, or greater; 0.48 grams of target product per gram of glucose added, or greater; 0.49 grams of target product per gram of glucose added, or greater; 0.50 grams of target product per gram of glucose added, or greater; 0.51 grams of target product per gram of glucose added, or greater; 0.52 grams of target product per gram of glucose added, or greater; 0.53 grams of target product per gram of glucose added, or greater; 0.54 grams of target product per gram of glucose added, or greater; 0.55 grams of target product per gram of glucose added, or greater; 0.56 grams of target product per gram of glucose added, or greater; 0.57 grams of target product per gram of glucose added, or greater; 0.58 grams of target product per gram of glucose added, or greater; 0.59 grams of target product per gram of glucose added, or greater; 0.60 grams of target product per gram of glucose added, or greater; 0.61 grams of target product per gram of glucose added, or greater; 0.62 grams of target product per gram of glucose added, or greater; 0.63 grams of target product per gram of glucose added, or greater; 0.64 grams of target product per gram of glucose added, or greater; 0.65 grams of target product per gram of glucose added, or greater; 0.66 grams of target product per gram of glucose added, or greater; 0.67 grams of target product per gram of glucose added, or greater; 0.68 grams of target product per gram of glucose added, or greater; 0.69 or 0.70 grams of target product per gram of glucose added or greater). In some embodiments, 0.45 grams of target product per gram of glucose added, or greater, is produced during the fermentation process.

EXAMPLES

The examples set forth below illustrate certain embodiments and do not limit the technology.
Certain examples set forth below utilize standard recombinant DNA and other biotechnology protocols known in the art. Many such techniques are described in detail in Maniatis, T., E. F. Fritsch and J. Sambrook (1982) Molecular Cloning: a Laboratory Manual; Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y. DNA mutagenesis can be accomplished using the Stratagene (San Diego, Calif.) “QuickChange” kit according to the manufacturer's instructions, or by one of the other types of mutagenesis described above.

Example 1

Activation of the Entner-Doudoroff Pathway in Yeast Cells

Genomic DNA from Zymomonas mobilis (ZM4) was obtained from the American Type Culture Collection (ATCC accession number 31821 D-5). The genes encoding phosphogluconate dehydratase EC 4.2.1.12 (referred to as “edd”) and 2-keto-3-deoxygluconate-6-phosphate aldolase EC 4.2.1.14 (referred to as “eda”) were isolated from the ZM4 genomic DNA using the following oligonucleotides:

The ZM4 eda gene:

(SEQ ID No: 1)

5′-aactgactagtaaaaaaatgcgtgatatcgattcc-3′

(SEQ ID No: 2)

5′-agtaactcgagctactaggcaacagcagcgcgcttg-3′

The ZM4 edd gene:

(SEQ ID NO: 3)

5′-aactgactagtaaaaaaatgactgatctgcattcaacg-3′

(SEQ ID NO: 4)

5′-agtaactcgagctactagataccggcacctgcatatattgc-3′

E. coli genomic DNA was prepared using Qiagen DNeasy blood and tissue kit according to the manufacture's protocol. The E. coli edd and eda constructs were isolated from E. coli genomic DNA using the following oligonucleotides:

The E. coli eda gene:

(SEQ ID NO: 5)

5′-aactgactagtaaaaaaatgaaaaactggaaaacaagtgcag

aatc-3′

(SEQ ID NO: 6)

5′-agtaactcgagctactacagcttagcgccttctacagcttcacg-3′

The E. coli edd gene:

(SEQ ID NO: 7)

5′-aactgactagtaaaaaaatgaatccacaattgttacgcgtaacaaa

tcg-3′

(SEQ ID NO: 8)

5′agtaactcgagctactaaaaagtgatacaggttgcgccctgttcgg

cac-3′

All oligonucleotides set forth above were purchased from Integrated DNA technologies (“IDT”, Coralville, Iowa). These oligonucleotides were designed to incorporate a SpeI restriction endonuclease cleavage site upstream and a XhoI restriction endonuclease cleavage site downstream of the edd and eda gene constructs such that these sites could be used to clone these genes into yeast expression vectors p426GPD (ATCC accession number 87361) and p425GPD (ATCC accession number 87359). In addition to incorporating restriction endonuclease cleavage sites, the forward oligonucleotides were designed to incorporate six consecutive AAAAAA nucleotides immediately upstream of the ATG initiation codon. This ensured that there was a conserved kozak sequence important for efficient translation initiation in yeast.
Cloning the edd and eda genes from ZM4 and E. coli genomic DNA was accomplished using the following procedure: About 100 ng of ZM4 or E. coli genomic DNA, 1 μM of the oligonucleotide primer set listed above, 2.5 U of PfuUltra High-Fidelity DNA polymerase (Stratagene), 300 μM dNTPs (Roche), and 1×PfuUltra reaction buffer was mixed in a final reaction volume of 50 μl. A BIORAD DNA Engine Tetrad 2 Peltier thermal cycler was used for the PCR reactions and the following cycle conditions were used: 5 min denaturation step at 95° C., followed by 30 cycles of 20 sec at 95° C., 20 sec at 55° C., and 1 min at 72° C., and a final step of 5 min at 72° C.
In an attempt to maximize expression of the ZM4 edd and eda genes in yeast, two different approaches were undertaken to optimize the ZM4 edd and eda genes. The first approach was to remove translational pauses from the polynucleotide sequence by designing the gene to incorporate only codons that are preferred in yeast. This optimization is referred to as the “hot rod” optimization. In the second approach, translational pauses which are present in the native organism gene sequence are matched in the heterologous expression host organism by substituting the codon usage pattern of that host organism. This optimization is referred to as the “matched” optimization. The final gene and protein sequences for edd and eda from the ZM4 native, hot rod (HR) and matched versions, as well as the E. coli native are shown in FIG. 6.
Certain sequences in FIG. 6 are presented at the end of this Example 1. The matched version of ZM4 edd and ZM4 eda genes were synthesized by IDT, and the hot rod version was constructed using methods described in Larsen et al. (Int. J. Bioinform. Res. Appl; 2008:4[3]; 324-336).
Each version of each edd and eda gene was inserted into the yeast expression vector p426GPD (GPD promoter, 2 micron, URA3) (ATCC accession number 87361) between the SpeI and XhoI cloning sites. Each version of the eda gene was also inserted into the SpeI and XhoI sites of the yeast expression vector p425GPD (GPD promoter, 2 micron, LEU3) (ATCC accession number 87359). For each edd and eda version, 3′ His tagged and non tagged p426 GPD constructs were made. Please refer to table 1 for all oligonucleotides used for PCR amplification of edd and eda constructs for cloning into p425 and p426 GPD vectors. All cloning procedures were conducted according to standard cloning procedures described by Maniatis et al.
Each edd and eda p426GPD construct was transformed into Saccharomyces cerevisiae strain BY4742 (MATalpha his3delta1 leu2delta0 lys2delta0 ura3delta0) (ATCC accession number 201389). This strain has a deletion of the his3 gene, an imidazoleglycerol-phosphate dehydratase which catalyzes the sixth step in histidine biosynthesis; a deletion of leu2 gene, a beta-isopropylmalate dehydrogenase which catalyzes the third step in the leucine biosynthesis pathway; a deletion of the lys2 gene, an alpha aminoadipate reductase which catalyzes the fifth step in biosynthesis of lysine; and a deletion of the ura3 gene, an orotidine-5′-phosphate decarboxylase which catalyzes the sixth enzymatic step in the de novo biosynthesis of pyrimidines. The genotype of BY4742 makes it an auxotroph for histidine, leucine, lysine and uracil.
Transformation of the p426GPD plasmids containing an edd or an eda variant gene into yeast strain BY4742 was accomplished using the Zymo Research frozen-EZ yeast transformation II kit according to the manufacturer's protocol. The transformed BY4742 cells were selected by growth on a synthetic dextrose medium (SD) (0.67% yeast nitrogen base-2% dextrose) containing complete amino acids minus uracil (Krackeler Scientific Inc). Plates were incubated at about 30° C. for about 48 hours. Transformant colonies for each edd and eda variant were inoculated onto 5 ml of SD minus uracil medium and cells were grown at about 30° C. and shaken at about 250 rpm for about 24 hours. Cells were harvested by centrifugation at 1000×g for about 5 minutes, after which protein crude extract was prepared with Y-PER Plus (Thermo Scientific) according to the manufacturer's instructions. Whole cell extract protein concentrations were determined using the Coomassie Plus Protein Assay (Thermo Scientific) according to the manufacturer's directions. For each edd and eda variant His-tagged construct, about 10 μg of soluble and insoluble fractions were loaded on 4-12% NuPAGE Novex Bis-Tris protein gels (Invitrogen) and proteins were analyzed by western using anti-(His)₆mouse monoclonal antibody (‘(His)₆’ disclosed as SEQ ID NO: 35) (Abcam) and HRP-conjugated secondary antibody (Abcam). Supersignal West Pico Chemiluminescent substrate (Thermo Scientific) was used for western detection according to manufacturer's instructions. All edd variants showed expression in both soluble and insoluble fractions whereas only the E. coli eda variant showed expression in the soluble fraction.
In order to confirm that edd and eda variants were functional in yeast, the combined edd and eda activities were assayed by the formation of pyruvate, coupled to the NADH-dependent activity of lactate dehydrogenase. Transformation of combined edd (in p426GPD) and edd (in p425GPD) constructs was accomplished with the Zymo Research frozen-EZ yeast transformation II kit based on manufacturer's protocol. As a negative control, p425GPD and p426GPD vectors were also transformed into BY4742. Transformants (16 different combinations total including the variant edd and eda combinations plus vector controls) were selected on synthetic dextrose medium (SD) (0.67% yeast nitrogen base-2% dextrose) containing complete amino acids minus uracil and leucine. Transformants of edd and eda variant combinations were inoculated onto 5 ml of SD minus uracil and leucine and cells were grown at about 30° C. in shaker flasks at about 250 rpm for about 24 hours. Fresh overnight culture was used to inoculate about 100 ml of (SD media minus uracil and leucine containing about 0.01 g ergosterol/L and about 400 μl of Tween80) to an initial inoculum OD_600nmof about 0.1 and grown anaerobically at about 30° C. for approximately 14 hours until cells reached an OD_600nmof 3-4. The cells were centrifuged at about 3000 g for about 10 minutes. The cells were then washed with 25 ml deionized H₂O and centrifuged at 3000 g for 10 min. the cells were resuspended at about 2 ml/g of cell pellet) in lysis buffer (50 mM TrisCl pH7, 10 mM MgCl ₂1× Calbiochem protease inhibitor cocktail set III). Approximately 900 μl of glass beads were added and cells were lysed by vortexing at maximum speed for 4×30 seconds. Cell lysate was removed from the glass beads, placed into fresh tubes and spun at about 10,000 g for about 10 minutes at about 4° C. The supernatant containing whole cell extract (WCE) was transferred to a fresh tube. WCE protein concentrations were measured using the Coomassie Plus Protein Assay (Thermo Scientific) according to the manufacturer's directions. A total of about 750 μg of WCE was used for the edd and eda coupled assay. For this assay, about 750 μg of WCE was mixed with about 2 mM 6-phosphogluconate and about 4.5 U lactate dehydrogenase in a final volume of about 400 μl. A total of about 100 μl of NADH was added to this reaction to a final molarity of about 0.3 mM, and NADH oxidation was monitored for about 10 minutes at about 340 nM using a DU800 spectrophotometer.

ZM4 HR EDA GENE

(SEQ ID NO: 42)

ATGAGAGACATTGATTCTGTTATGAGATTGGCTCCAGTTATGCCAGTCTT

TGGTTAAGAAGATATAGCTGATGCTAAGCCAATTGCTGAGGCTTTGGTTG

CTGGTGGTTTAAATGTTTTGGAAGTTACATTGAGAACTCCATGTGCTTTG

GAAGCTATTAAAATTATGAAGGAAGTTCCAGGTGCTGTTGTTGGTGCTGG

TACTGTTTTAAACGCTAAAATGTTGGATCAAGCTCAAGAAGCTGGTTGTG

AGTTCTTTGTATCACCAGGTTTGACTGCTGATTTGGGAAAACATGCTGTT

GCTCAAAAAGCGGCTCTTCTACCAGGGGTTGCTAATGCTGCTGATGTTAT

GTTGGGATTGGATTTGGGTTTGGATAGATTTAAATTCTTCCCAGCTGAAA

ATATAGGTGGTTTGCCAGCTTTAAAATCTATGGCTTCTGTTTTTAGACAA

GTTAGATTTTGTCCAACTGGAGGAATTACTCCGACTTCTGCTCCAAAATA

TTTGGAAAATCCATCTATTTTGTGTGTTGGTGGTTCTTGGGTTGTTCCAG

CGGGTAAACCAGATGTTGCGAAAATTACTGCTTTGGCTAAAGAGGCTTCA

GCTTTTAAAAGAGCTGCTGTGGCGTAG

ZM4 HR EDD GENE

(SEQ ID NO: 43)

ATGACGGATTTGCATTCAACTGTTGAGAAAGTAACTGCTAGAGTAATTGA

AAGATCAAGGGAAACTAGAAAGGCTTATTTGGATTTGATACAATATGAGA

GGGAAAAAGGTGTTGATAGACCAAATTTGTCTTGTTCTAATTTGGCTCAT

GGTTTTGCTGCTATGAATGGTGATAAACCAGCTTTGAGAGATTTTAATAG

AATGAATATAGGTGTAGTTACTTCTTATAATGATATGTTGTCTGCTCATG

AACCATATTATAGATATCCAGAACAAATGAAGGTTTTTGCTCGTGAAGTT

GGTGCTACAGTTCAAGTTGCTGGTGGTGTTCCTGCAATGTGTGATGGTGT

TACTCAAGGTCAACCAGGTATGGAAGAATCTTTGTTTTCCAGAGATGTAA

TTGCTTTGGCTACATCTGTTTCATTGTCTCACGGAATGTTTGAAGGTGCT

GCATTGTTGGGAATTTGTGATAAAATTGTTCCAGGTTTGTTGATGGGTGC

TTTGAGGTTCGGTCATTTGCCAACTATTTTGGTTCCATCTGGTCCAATGA

CTACTGGAATCCCAAATAAAGAAAAGATTAGAATTAGACAATTGTATGCT

CAAGGAAAAATTGGTCAAAAGGAATTGTTGGATATGGAAGCTGCCTGTTA

TCATGCTGAAGGTACTTGTACTTTTTATGGTACTGCTAACACTAATCAGA

TGGTTATGGAAGTTTTGGGTTTGCACATGCCAGGTAGTGCATTCGTTACT

CCAGGTACTCCACTGAGACAGGCTTTGACTAGAGCTGCTGTTCATAGAGT

TGCAGAGTTGGGTTGGAAAGGTGATGATTATAGACCTTTGGGTAAAATTA

TTGATGAGAAATCTATTGTTAATGCTATTGTTGGTTTGTTAGCTACAGGT

GGTTCTACAAATCATACAATGCATATTCCGGCCATAGCTAGAGCAGCAGG

GGTTATAGTTAATTGGAATGATTTTCATGATTTGTCTGAAGTTGTTCCAT

TGATTGCTAGAATTTATCCAAATGGTCCTAGAGATATAAATGAATTTCAA

AATGCAGGAGGAATGGCTTATGTAATTAAAGAATTGTTGAGTGCGAATTT

GTTAAATAGAGATGTTACTACTATTGCTAAAGGAGGGATAGAAGAATATG

CTAAAGCTCCAGCTCTGAACGATGCGGGTGAATTGGTGTGGAAACCGGCT

GGCGAACCTGGGGACGACACAATTTTGAGACCAGTATCTAATCCATTTGC

TAAAGATGGTGGTTTGCGTCTCTTGGAAGGTAATTTGGGTAGAGCAATGT

ATAAGGCTTCTGCTGTAGATCCAAAATTCTGGACTATTGAAGCTCCCGTT

AGAGTTTTCTCTGATCAAGATGATGTTCAAAAGGCTTTTAAAGCAGGCGA

GTTAAATAAAGATGTTATAGTTGTTGTTAGATTTCAAGGTCCTCGTGCTA

ATGGTATGCCTGAATTGCATAAGTTGACTCCTGCGCTAGGCGTATTGCAA

GATAATGGTTATAAGGTTGCTTTAGTTACTGATGGTAGAATGTCTGGTGC

AACTGGTAAAGTACCGGTGGCTCTGCATGTTTCACCAGAGGCTTTAGGAG

GTGGGGCGATTGGCAAGTTGAGAGATGGCGATATAGTTAGAATTTCTGTT

GAAGAAGGTAAATTAGAGGCTCTTGTCCCCGCCGACGAGTGGAATGCTAG

ACCACATGCTGAGAAGCCCGCTTTTAGACCTGGTACTGGGAGAGAATTGT

TTGACATTTTTAGACAAAACGCTGCTAAGGCTGAGGATGGTGCAGTTGCA

ATTTATGCTGGGGCAGGGATCTAG

ZM4 MATCHED EDA GENE

(SEQ ID NO: 44)

ATGAGGGATATTGATAGTGTGATGAGGTTAGCCCCTGTTATGCCTGTTCT

CGTTATTGAAGATATTGCAGATGCCAAACCTATTGCCGAAGCACTCGTTG

CAGGTGGTCTAAACGTTCTAGAAGTGACACTAAGGACTCCTTGTGCACTA

GAAGCTATTAAGATTATGAAGGAAGTTCCTGGTGCTGTTGTTGGTGCTGG

TACAGTTCTAAACGCCAAAATGCTCGACCAGGCACAAGAAGCAGGTTGCG

AATTTTTCGTTTCACCTGGTCTAACTGCCGACCTCGGAAAGCACGCAGTT

GCTCAAAAAGCCGCATTACTACCCGGTGTTGCAAATGCAGCAGATGTGAT

GCTAGGTCTAGACCTAGGTCTAGATAGGTTCAAGTTCTTCCCTGCCGAAA

ACATTGGTGGTCTACCTGCTCTAAAGAGTATGGCATCAGTTTTCAGGCAA

GTTAGGTTCTGCCCTACTGGAGGTATAACTCCTACAAGTGCACCTAAATA

TCTAGAAAACCCTAGTATTCTATGCGTTGGTGGTTCATGGGTTGTTCCTG

CCGGAAAACCCGATGTTGCCAAAATTACAGCCCTCGCAAAAGAAGCAAGT

GCATTCAAGAGGGCAGCAGTTGCTTAG

ZM4 MATCHED EDD GENE

(SEQ ID NO: 45)

ATGACGGATCTACATAGTACAGTGGAGAAGGTTACTGCCAGGGTTATTGA

AAGGAGTAGGGAAACTAGGAAGGCATATCTAGATTTAATTCAATATGAGA

GGGAAAAAGGAGTGGACAGGCCCAACCTAAGTTGTAGCAACCTAGCACAT

GGATTCGCCGCAATGAATGGTGACAAGCCCGCATTAAGGGACTTCAACAG

GATGAATATTGGAGTTGTGACGAGTTACAACGATATGTTAAGTGCACATG

AACCCTATTATAGGTATCCTGAGCAAATGAAGGTGTTTGCAAGGGAAGTT

GGAGCCACAGTTCAAGTTGCTGGTGGAGTGCCTGCAATGTGCGATGGTGT

GACTCAGGGTCAACCTGGAATGGAAGAATCCCTATTTTCAAGGGATGTTA

TTGCATTAGCAACTTCAGTTTCATTATCACATGGTATGTTTGAAGGGGCA

GCTCTACTCGGTATATGTGACAAGATTGTTCCTGGTCTACTAATGGGAGC

ACTAAGGTTTGGTCACCTACCTACTATTCTAGTTCCCAGTGGACCTATGA

CAACGGGTATACCTAACAAAGAAAAAATTAGGATTAGGCAACTCTATGCA

CAAGGTAAAATTGGACAAAAAGAACTACTAGATATGGAAGCCGCATGCTA

CCATGCAGAAGGTACTTGCACTTTCTATGGTACAGCCAACACTAACCAGA

TGGTTATGGAAGTTCTCGGTCTACATATGCCCGGTAGTGCCTTTGTTACT

CCTGGTACTCCTCTCAGGCAAGCACTAACTAGGGCAGCAGTGCATAGGGT

TGCAGAATTAGGTTGGAAGGGAGACGATTATAGGCCTCTAGGTAAAATTA

TTGACGAAAAAAGTATTGTTAATGCAATTGTTGGTCTATTAGCCACTGGT

GGTAGTACTAACCATACGATGCATATTCCTGCTATTGCAAGGGCAGCAGG

TGTTATTGTTAACTGGAATGACTTCCATGATCTATCAGAAGTTGTTCCTT

TAATTGCTAGGATTTACCCTAATGGACCTAGGGACATTAACGAATTTCAA

AATGCCGGAGGAATGGCATATGTTATTAAGGAACTACTATCAGCAAATCT

ACTAAACAGGGATGTTACAACTATTGCTAAGGGAGGTATAGAAGAATACG

CTAAGGCACCTGCCCTAAATGATGCAGGAGAATTAGTTTGGAAGCCCGCA

GGAGAACCTGGTGATGACACTATTCTAAGGCCTGTTTCAAATCCTTTCGC

CAAAGATGGAGGTCTAAGGCTCTTAGAAGGTAACCTAGGAAGGGCCATGT

ACAAGGCTAGCGCCGTTGATCCTAAATTCTGGACTATTGAAGCCCCTGTT

AGGGTTTTCTCAGACCAGGACGATGTTCAAAAAGCCTTCAAGGCAGGAGA

ACTAAACAAAGACGTTATTGTTGTTGTTAGGTTCCAAGGACCTAGGGCCA

ACGGTATGCCTGAATTACATAAGCTAACTCCTGCATTAGGTGTTCTACAA

GATAATGGATACAAAGTTGCATTAGTGACGGATGGTAGGATGAGTGGTGC

AACTGGTAAAGTTCCTGTTGCATTACATGTTTCACCCGAAGCACTAGGAG

GTGGTGCTATTGGTAAACTTAGGGATGGAGATATTGTTAGGATTAGTGTT

GAAGAAGGAAAACTTGAAGCACTCGTTCCCGCAGATGAGTGGAATGCAAG

GCCTCATGCAGAAAAACCTGCATTCAGGCCTGGGACTGGGAGGGAATTAT

TTGATATTTTCAGGCAAAATGCAGCAAAAGCAGAAGACGGTGCCGTTGCC

ATCTATGCCGGTGCTGGTATATAG

Example 2

Inactivation of the Embden-Meyerhof Pathway in Yeast

Saccharomyces cerevisiae strain YGR240CBY4742 was obtained from the ATCC (accession number 4015893). This strain is genetically identical to S. cerevisiae strain BY4742, except that YGR420C, the gene encoding the PFK1 enzyme, which is the alpha subunit of heterooctameric phosphofructokinase, has been deleted. A DNA construct designed to delete the gene encoding the PFK2 enzyme via homologous recombination was prepared. This construct substituted the gene encoding HIS3 (imidazoleglycerol-phosphate dehydratase, an enzyme required for synthesis of histidine) for the PFK2 gene. The DNA construct comprised, in the 5′ to 3′ direction, 100 bases of the 5′ end of the open reading frame of PFK2, followed by the HIS3 promoter, HIS3 open reading frame, HIS3 terminator, and 100 bp of the 3′ end of the PFK2 open reading frame.
This construct was prepared by two rounds of PCR. In the first round, about 100 ng of BY4742 genomic DNA was used as a template. The genomic DNA was prepared from cells using the Zymo Research Yeastar kit according to the manufacturer's instructions. PCR was performed using the following primers:

(SEQ ID NO: 9)

5′-tgcatattccgttcaatcttataaagctgccatagatttttacacc

aagtcgttttaagagcttggtgagcgcta-3′

(SEQ ID NO: 10)

5′-cttgccagtgaatgacctttggcattctcatggaaacttcagttt

catagtcgagttcaagagaaaaaaaaagaa-3′

The PCR reaction conditions were the same as those set forth in Example 1 for preparing the edd and eda genes.
For the second round of PCR, approximately 1 μl of the first PCR product was used as a template. The second round of PCR reaction was performed with the following primer set:

(SEQ ID NO: 11)

5′-atgactgttactactccttttgtgaatggtacttcttattgtaccg

tcactgcatattccgttcaatcttataaa-3′

(SEQ ID NO: 12)

5′-ttaatcaactctctttcttccaaccaaatggtcagcaatgagtct

ggtagcttgccagtgaatgacctttggcat-3′

PCR conditions for this reaction were the same as for the first reaction immediately above. The final PCR product was separated by agarose gel electrophoresis, excised, and purified using MP Biomedicals Geneclean II kit according to the manufacturer's instructions.
Approximately 2 μg of the purified DNA was used for transformation of the yeast strain YGR240CBY4742 by lithium acetate procedure as described by Shiestl and Gietz with an additional recovery step added after the heat shock step. Essentially after heat shock, cells were centrifuged at 500×g for 2 min and resuspended in 1 ml of YP-Ethanol (1% yeast extract-2% peptone-2% ethanol) and incubated at 30° C. for 2 hours prior to plating on selective media containing SC-Ethanol (0.67% yeast nitrogen base-2% ethanol) containing complete amino acids minus histidine. The engineered transformant strain referred to as YGR420CBY4742ΔPFK2 has PFK1 and PFK2 genes deleted and is an auxotroph for leucine, uracil and lysine.
The YGR420CBY4742ΔPFK2 strain was used for transformation of the combination of edd-p426 GPD (edd variants in p426 GPD) and eda-p425 GPD (eda variants in p425 GPD) variant constructs. A total of 16 combinations of edd-p426 GPD and eda-p425 GPD variant constructs were tested. Each combination was transformed into YGR420CBY4742ΔPFK2. For all transformation, 1 μg of edd-p426 GPD and 1 μg of eda-p425 GPD was used. All transformants from each edd-p426 GPD and eda-p425 GPD construct combination were selected on SC-Ethanol (0.67% yeast nitrogen base-2% ethanol) containing complete amino acids minus uracil and leucine.
To confirm that the edd and eda variants are functional in yeast, a complementation test for growth of YGR420CBY4742ΔPFK2 strain on YPD (1% yeast extract-2% peptone-2% dextrose) and YPGluconate (1% yeast extract-2% peptone-2% gluconate) was performed. Viable colonies of edd-p426 GPD and eda-p425 GPD variant construct combinations grown on SC-Ethanol minus uracil and leucine were patched to plates containing SC-ethanol minus uracil and leucine and incubated at 30° C. for 48 hrs. These patches were used to inoculate 5 ml of YPD media to an initial inoculum OD_600nmof 0.1 and the cells were grown anaerobically at 30° C. for 3 to 7 days.

Example 3

Preparation of Carbon Dioxide Fixing Yeast Cells

Total genomic DNA from Zymomonas mobilis was obtained from ATCC (ATCC Number 31821). The Z. mobilis gene encoding the enzyme phosphoenolpyruvate carboxylase (“PEP carboxylase”) was isolated from this genomic DNA and cloned using PCR amplification. PCR was performed in a total volume of about 50 micro-liters in the presence of about 20 nanograms of Z. mobilis genomic DNA, about 0.2 mM of 5′ forward primer, about 0.2 mM of 3′ reverse primer, about 0.2 mM of dNTP, about 1 micro-liter of pfu UltraII DNA polymerase (Stratagene, La Jolla, Calif.), and 1×PCR buffer (Stratagene, La Jolla, Calif.). PCR was carried out in a thermocycler using the following program: Step One “95° C. for 10 minutes” for 1 cycle, followed by Step Two “95° C. for 20 seconds, 65° C. for 30 seconds, and 72° C. for 45 seconds” for 35 cycles, followed by Step Three “72° C. for 5 minutes” for 1 cycle, and then Step Four “4° C. Hold” to stop the reaction. The primers for the PCR reaction were:

(SEQ ID NO: 13)

5′GACTAACTGAACTAGTAAAAAAATGACCAAGCCGCGCACAATTAA

TCAG-3′

(SEQ ID NO: 14)

5′AAGTGAGTAACTCGAGTTATTAACCGCTGTTGCGAAGTGCCGT

CGC-3′

The DNA sequence of native Z. Mobilis PEP carboxylase is set forth as SEQ ID NO:20.
The cloned gene was inserted into the vector pGPD426 (ATCC Number: 87361) in between the SpeI and XhoI sites. The final plasmid containing the PEP carboxylase gene was named pGPD426 PEPC.
Separately, a similar plasmid, referred to as pGPD426 N-his PEPC was constructed to insert a six-histidine tag (SEQ ID NO: 35) at the N-terminus of the PEPC sequence for protein expression verification in yeast. This plasmid was constructed using two rounds of PCR to extend the 5′ end of the PEPC gene to incorporate a six-histidine tag (SEQ ID NO: 35) at the N-terminus of the PEPC protein. The two 5′ forward primers used sequentially were:

(SEQ ID NO: 15)

5′ATGTCTCATCATCATCATCATCATACCAAGCCGCGCACAATTAAT

CAGAAC-3′

and

(SEQ ID NO: 16)

5′GACTAACTGAACTAGTAAAAAAATGTCTCATCATCATCATCATCAT

ACCAAG-3′

The same 3′ primer was used as described above. The PCR was performed in a total volume of about 50 micro-liters in the presence of about 20 nanograms of Z Mobilis PEP carboxylase polynucleotide, about 0.2 mM of 5′ forward primer, about 0.2 mM of 3′ reverse primer, about 0.2 mM of dNTP, about 1 micro-liter of pfu UltraII DNA polymerase (Stratagene, La Jolla, Calif.), and 1×PCR buffer (Stratagene, La Jolla, Calif.). The PCR was carried out in a thermocycler using the following program: Step One “95° C. for 10 minutes” for 1 cycle, followed by Step Two “95° C. for 20 seconds, 65° C. for 30 seconds, and 72° C. for 45 seconds” for 35 cycles, followed Step Three “72° C. for 5 minutes” for 1 cycle, and then Step Four “4° C. Hold” to stop the reaction.
To increase protein expression level of Z. Mobilis PEP carboxylase in yeast, the PEPC coding sequence was optimized to incorporate frequently used codons obtained from yeast glycolytic genes. The resulting PEP carboxylase amino acid sequence remains identical to the wild type.
The codon optimized PEP carboxylase DNA sequence was ordered from IDT and was inserted into the vector pGPD426 at the SpeI and XhoI site. The final plasmid containing the codon optimized PEP carboxylase gene was named pGPD426 PEPC_opti. A similar plasmid, named pGPD426 N-his PEPC_opti was constructed to insert a six-histidine tag (SEQ ID NO: 35) at the N-terminus of the optimized PEPC gene for protein expression verification in yeast.
To construct pGPD426 N-his PEPC_opti, two rounds of PCR were performed to extend the 5′ end of the codon optimized PEPC gene to incorporate the six-histidine tag (SEQ ID NO: 35) at the N-terminus of the PEPC protein. Two 5′ forward primers used in sequential order were:

(SEQ ID NO: 17)

5′ATGTCTCATCATCATCATCATCATATGACCAAGCCAAGAACTATTA

ACCAAAACCC-3′

and

(SEQ ID NO: 18)

5′GACTAACTGAACTAGTAAAAAAATGTCTCATCATCATCATCATCA

TATGACCAAGCCAAG

3′

The 3′ reverse primer sequence used for both PCR reactions was:

(SEQ ID NO: 19)

5′AAGTGAGTAACTCGAGTTATTAACCGGAGTTTCTCAAAGCAGTAGCG

ATAG3′

Both PCR reactions were performed in a total volume of about 50 micro-liters in the presence of about 20 nanograms of the codon optimized PEP carboxylase polynucleotide, about 0.2 mM of 5′ forward primer, about 0.2 mM of 3′ reverse primer, about 0.2 mM of dNTP, about 1 micro-liter of pfu UltraII DNA polymerase (Stratagene, La Jolla, Calif.), and 1×PCR buffer (Stratagene, La Jolla, Calif.). PCR reactions were carried out in a thermocycler using the following program: Step One “95° C. for 10 minutes” for 1 cycle, followed by Step Two “95° C. for 20 seconds, 65° C. for 30 seconds, and 72° C. for 45 seconds” for 35 cycles, followed Step Three “72° C. for 5 minutes” for 1 cycle, and then Step Four “4° C. Hold” to stop the reaction.
Saccharomyces cerevisiae strain BY4742 was cultured in YPD medium to an OD of about 1.0, and then prepared for transformation using the Frozen-EZ Yeast Transformation II kit (Zymo Research, Orange, Calif.) and following the manufacturer's instructions. Approximately 500 micrograms of each plasmid was added to the cells, and transformation was accomplished by addition of PEG solution (“Solution 3” in the Frozen-EZ Yeast Transformation II kit) and incubation at about 30° C. for an hour. After transformation, the cells were plated on synthetic complete medium (described in Example IV below) minus uracil (sc-ura) medium, grown for about 48 hours at about 30° C., and transformants were selected based on auxotrophic complementation.
Following a similar procedure, the same plasmids were individually transformed using the procedure described above into the following yeast mutant strains: YKR097W (ATCC Number 4016013, APCK, in the phosphoenolpyruvate carboxykinase gene is deleted), YGL062W (ATCC Number 4014429, ΔPYC1, in which the pyruvate carboxylase 1 gene is deleted), and YBR218C (ATCC Number 4013358, ΔPYC2, in which the pyruvate carboxylase 2 gene is deleted).
The transformed yeast cells were grown aerobically in a shake flask in synthetic complete medium minus uracil (see Example IV) containing 1% glucose to mid-log phase (an OD of 2.0). The mid-log phase cultures were then used to inoculate a fresh culture (in sc-ura medium with 1% glucose) to an initial OD of 0.1 at which time the cultures were then grown anaerobically in a serum bottle. Culture samples were drawn periodically to monitor the level of glucose consumption and ethanol production.


DNA sequence of the native Z. mobilis PEP carboxylase gene (SEQ ID NO: 20):
ACTAGTAAAAAAATGACCAAGCCGCGCACAATTAATCAGAACCCAGACCTTCGCTATTTTGGT

AACCTGCTCGGTCAGGTTATTAAGGAACAAGGCGGAGAGTCTTTATTCAACCAGATCGAGCAA

ATTCGCTCTGCCGCGATTAGACGCCATCGGGGTATTGTTGACAGCACCGAGCTAAGTTCTCG

CTTAGCCGATCTCGACCTTAATGACATGTTCTCTTTTGCACATGCCTTTTTGCTGTTTTCAATG

CTGGCCAATTTGGCTGATGATCGTCAGGGAGATGCCCTTGATCCTGATGCCAATATGGCAAGT

GCCCTTAAGGACATAAAAGCCAAAGGCGTCAGTCAGCAGGCGATCATTGATATGATCGACAAA

GCCTGCATTGTGCCTGTTCTGACAGCACATCCGACCGAAGTCCGTCGGAAAAGTATGCTTGA

CCATTATAATCGCATTGCAGGTTTAATGCGGTTAAAAGATGCTGGACAAACGGTGACCGAAGA

TGGTCTTCCGATCGAAGATGCGTTAATCCAGCAAATCACGATATTATGGCAGACTCGTCCGCT

CATGCTGCAAAAGCTGACCGTGGCTGATGAAATCGAAACTGCCCTGTCTTTCTTAAGAGAAAC

TTTTCTGCCTGTTCTGCCCCAGATTTATGCAGAATGGGAAAAATTGCTTGGTAGTTCTATTCCA

AGCTTTATCAGACCTGGTAATTGGATTGGTGGTGACCGTGACGGTAACCCCAATGTCAATGCC

GATACGATCATGCTGTCTTTGAAGCGCAGCTCGGAAACGGTATTGACGGATTATCTCAACCGT

CTTGATAAACTGCTTTCCAACCTTTCGGTCTCAACCGATATGGTTTCGGTATCCGATGATATTC

TACGTCTAGCCGATAAAAGTGGTGACGATGCTGCGATCCGTGCGGATGAACCTTATCGTCGT

GCCTTAAATGGTATTTATGACCGTTTAGCCGCTACCTATCGTCAGATCGCCGGTCGCAACCCT

TCGCGCCCAGCCTTGCGTTCTGCAGAAGCCTATAAACGGCCTCAAGAATTGCTGGCTGATTT

GAAGACCTTGGCCGAAGGCTTGGGTAAATTGGCAGAAGGTAGTTTTAAGGCATTGATCCGTTC

GGTTGAAACCTTTGGTTTCCATTTGGCCACCCTCGATCTGCGTCAGAATTCGCAGGTTCATGA

AAGAGTTGTCAATGAACTGCTACGGACAGCCACCGTTGAAGCCGATTATTTATCTCTATCGGA

AGAAGATCGCGTTAAGCTGTTAAGACGGGAATTGTCGCAGCCGCGGACTCTATTCGTTCCGC

GCGCCGATTATTCCGAAGAAACGCGTTCTGAACTTGATATTATTCAGGCAGCAGCCCGCGCC

CATGAAATTTTTGGCCCTGAATCCATTACGACTTATTTGATTTCGAATGGCGAAAGCATTTCCG

ATATTCTGGAAGTCTATTTGCTTTTGAAAGAAGCAGGGCTGTATCAAGGGGGTGCTAAGCCAA

AAGCGGCGATTGAAGCTGCGCCTTTATTCGAGACGGTGGCCGATCTTGAAAATGCGCCAAAG

GTCATGGAGGAATGGTTCAAGCTGCCTGAAGCGCAAGCCATTGCAAAGGCACATGGCGTTCA

GGAAGTGATGGTTGGCTATTCTGACTCCAATAAGGACGGCGGATATCTGACCTCGGTTTGGG

GTCTTTATAAGGCTTGCCTCGCTTTGGTGCCGATTTTTGAGAAAGCCGGTGTACCGATCCAGT

TTTTCCATGGACGGGGTGGTTCCGTTGGTCGCGGTGGTGGTTCCAACTTTAATGCCATTCTGT

CGCAGCCAGCCGGAGCCGTCAAAGGGCGTATCCGTTATACAGAACAGGGTGAAGTCGTGGC

GGCCAAATATGGCACCCATGAAAGCGCTATTGCCCATCTGGATGAGGCCGTAGCGGCGACTT

TGATTACGTCTTTGGAAGCACCGACCATTGTCGAGCCAGAGTTTAGTCGTTACCGTAAGGCCT

TGGATCAGATCTCAGATTCAGCTTTCCAGGCCTATCGCCAATTGGTCTATGGAACGAAGGGCT

TCCGTAAATTCTTTAGTGAATTTACGCCTTTGCCGGAAATTGCCCTGTTAAAGATCGGGTCACG

CCCACCTAGCCGCAAAAAATCCGACCGGATTGAAGATCTACGCGCTATTCCTTGGGTGTTTAG

CTGGTCTCAAGTTCGAGTCATGTTACCCGGTTGGTTCGGTTTCGGTCAGGCTTTATATGACTT

TGAAGATACCGAGCTGTTACAGGAAATGGCAAGCCGTTGGCCGTTTTTCCGCACGACTATTCG

GAATATGGAACAGGTGATGGCACGTTCCGATATGACGATCGCCAAGCATTATCTGGCCTTGGT

TGAGGATCAGACAAATGGTGAGGCTATCTATGATTCTATCGCGGATGGCTGGAATAAAGGTTG

TGAAGGTCTGTTAAAGGCAACCCAGCAGAATTGGCTGTTGGAACGCTTTCCGGCGGTTGATA

ATTCGGTGCAGATGCGTCGGCCTTATCTGGAACCGCTTAATTACTTACAGGTCGAATTGCTGA

AGAAATGGCGGGGAGGTGATACCAACCCGCATATCCTCGAATCTATTCAGCTGACAATCAATG

CCATTGCGACGGCACTTCGCAACAGCGGTTAATAACTCGAG

DNA sequence of the codon optimized PEP carboxylase gene (SEQ ID NO: 21):
ACTAGTAAAAAAATGACCAAGCCAAGAACTATTAACCAAAACCCAGACTTGAGATACTTCGGTA

ACTTGTTGGGTCAAGTTATCAAGGAACAAGGTGGTGAATCTTTGTTCAACCAAATTGAACAAAT

CAGATCCGCTGCTATTAGAAGACACAGAGGTATCGTCGACTCTACCGAATTGTCCTCTAGATT

GGCTGACTTGGACTTGAACGACATGTTCTCCTTCGCTCACGCTTTCTTGTTGTTCTCTATGTTG

GCTAACTTGGCTGACGACAGACAAGGTGACGCTTTGGACCCAGACGCTAACATGGCTTCCGC

TTTGAAGGACATTAAGGCTAAGGGTGTTTCTCAACAAGCTATCATTGACATGATCGACAAGGC

TTGTATTGTCCCAGTTTTGACTGCTCACCCAACCGAAGTCAGAAGAAAGTCCATGTTGGACCA

CTACAACAGAATCGCTGGTTTGATGAGATTGAAGGACGCTGGTCAAACTGTTACCGAAGACG

GTTTGCCAATTGAAGACGCTTTGATCCAACAAATTACTATCTTGTGGCAAACCAGACCATTGAT

GTTGCAAAAGTTGACTGTCGCTGACGAAATTGAAACCGCTTTGTCTTTCTTGAGAGAAACTTTC

TTGCCAGTTTTGCCACAAATCTACGCTGAATGGGAAAAGTTGTTGGGTTCCTCTATTCCATCCT

TCATCAGACCAGGTAACTGGATTGGTGGTGACAGAGACGGTAACCCAAACGTCAACGCTGAC

ACCATCATGTTGTCTTTGAAGAGATCCTCTGAAACTGTTTTGACCGACTACTTGAACAGATTGG

ACAAGTTGTTGTCCAACTTGTCTGTCTCCACTGACATGGTTTCTGTCTCCGACGACATTTTGAG

ATTGGCTGACAAGTCTGGTGACGACGCTGCTATCAGAGCTGACGAACCATACAGAAGAGCTT

TGAACGGTATTTACGACAGATTGGCTGCTACCTACAGACAAATCGCTGGTAGAAACCCATCCA

GACCAGCTTTGAGATCTGCTGAAGCTTACAAGAGACCACAAGAATTGTTGGCTGACTTGAAGA

CTTTGGCTGAAGGTTTGGGTAAGTTGGCTGAAGGTTCCTTCAAGGCTTTGATTAGATCTGTTG

AAACCTTCGGTTTCCACTTGGCTACTTTGGACTTGAGACAAAACTCCCAAGTCCACGAAAGAG

TTGTCAACGAATTGTTGAGAACCGCTACTGTTGAAGCTGACTACTTGTCTTTGTCCGAAGAAG

ACAGAGTCAAGTTGTTGAGAAGAGAATTGTCTCAACCAAGAACCTTGTTCGTTCCAAGAGCTG

ACTACTCCGAAGAAACTAGATCTGAATTGGACATCATTCAAGCTGCTGCTAGAGCTCACGAAA

TCTTCGGTCCAGAATCCATTACCACTTACTTGATCTCTAACGGTGAATCCATTTCTGACATCTT

GGAAGTCTACTTGTTGTTGAAGGAAGCTGGTTTGTACCAAGGTGGTGCTAAGCCAAAGGCTG

CTATTGAAGCTGCTCCATTGTTCGAAACCGTTGCTGACTTGGAAAACGCTCCAAAGGTCATGG

AAGAATGGTTCAAGTTGCCAGAAGCTCAAGCTATCGCTAAGGCTCACGGTGTTCAAGAAGTCA

TGGTTGGTTACTCCGACTCTAACAAGGACGGTGGTTACTTGACTTCCGTCTGGGGTTTGTACA

AGGCTTGTTTGGCTTTGGTTCCAATTTTCGAAAAGGCTGGTGTCCCAATCCAATTCTTCCACG

GTAGAGGTGGTTCTGTTGGTAGAGGTGGTGGTTCCAACTTCAACGCTATTTTGTCTCAACCAG

CTGGTGCTGTCAAGGGTAGAATCAGATACACCGAACAAGGTGAAGTTGTCGCTGCTAAGTAC

GGTACTCACGAATCCGCTATTGCTCACTTGGACGAAGCTGTTGCTGCTACCTTGATCACTTCT

TTGGAAGCTCCAACCATTGTCGAACCAGAATTCTCCAGATACAGAAAGGCTTTGGACCAAATC

TCTGACTCCGCTTTCCAAGCTTACAGACAATTGGTTTACGGTACTAAGGGTTTCAGAAAGTTCT

TCTCTGAATTCACCCCATTGCCAGAAATTGCTTTGTTGAAGATCGGTTCCAGACCACCATCTAG

AAAGAAGTCCGACAGAATTGAAGACTTGAGAGCTATCCCATGGGTCTTCTCTTGGTCCCAAGT

TAGAGTCATGTTGCCAGGTTGGTTCGGTTTCGGTCAAGCTTTGTACGACTTCGAAGACACTGA

ATTGTTGCAAGAAATGGCTTCTAGATGGCCATTCTTCAGAACCACTATTAGAAACATGGAACAA

GTTATGGCTAGATCCGACATGACCATCGCTAAGCACTACTTGGCTTTGGTCGAAGACCAAACT

AACGGTGAAGCTATTTACGACTCTATCGCTGACGGTTGGAACAAGGGTTGTGAAGGTTTGTTG

AAGGCTACCCAACAAAACTGGTTGTTGGAAAGATTCCCAGCTGTTGACAACTCCGTCCAAATG

AGAAGACCATACTTGGAACCATTGAACTACTTGCAAGTTGAATTGTTGAAGAAGTGGAGAGGT

GGTGACACTAACCCACACATTTTGGAATCTATCCAATTGACCATTAACGCTATCGCTACTGCTT

TGAGAAACTCCGGTTAATAACTCGAG

Example 4

Production of Pentose Sugar Utilizing Yeast Cells

The full length gene encoding the enzyme xylose isomerase from Ruminococcus flavefaciens strain 17 (also known as Ruminococcus flavefaciens strain Siijpesteijn 1948) with a substitution at position 513 (in which cytidine was replaced by guanidine) was synthesized by Integrated DNA Technologies, Inc. (“IDT”, Coralville, Iowa; www.idtdna.com). The sequence of this gene is set forth below as SEQ ID NO:22.

SEQ ID NO: 22

atggaatttttcagcaatatcggtaaaattcagtatcagggaccaaaaagtactgatcctctctcatttaagtactataaccctgaagaagtca

tcaacggaaagacaatgcgcgagcatctgaagttcgctctttcatggtggcacacaatgggcggcgacggaacagatatgttcggctgc

ggcacaacagacaagacctggggacagtccgatcccgctgcaagagcaaaggctaaggttgacgcagcattcgagatcatggataa

gctctccattgactactattgtttccacgatcgcgatctttctcccgagtatggcagcctcaaggctaccaacgatcagcttgacatagttacag

actatatcaaggagaagcagggcgacaagttcaagtgcctctggggtacagcaaagtgcttcgatcatccaagattcatgcacggtgca

ggtacatctccttctgctgatgtattcgctttctcagctgctcagatcaagaaggctctGgagtcaacagtaaagctcggcggtaacggttac

gttttctggggcggacgtgaaggctatgagacacttcttaatacaaatatgggactcgaactcgacaatatggctcgtcttatgaagatggct

gttgagtatggacgttcgatcggcttcaagggcgacttctatatcgagcccaagcccaaggagcccacaaagcatcagtacgatttcgata

cagctactgttctgggattcctcagaaagtacggtctcgataaggatttcaagatgaatatcgaagctaaccacgctacacttgctcagcata

cattccagcatgagctccgtgttgcaagagacaatggtgtgttcggttctatcgacgcaaaccagggcgacgttcttcttggatgggataca

gaccagttccccacaaatatctacgatacaacaatgtgtatgtatgaagttatcaaggcaggcggcttcacaaacggcggtctcaacttcg

acgctaaggcacgcagagggagcttcactcccgaggatatcttctacagctatatcgcaggtatggatgcatttgctctgggcttcagagct

gctctcaagcttatcgaagacggacgtatcgacaagttcgttgctgacagatacgcttcatggaataccggtatcggtgcagacataatcgc

aggtaaggcagatttcgcatctcttgaaaagtatgctcttgaaaagggcgaggttacagcttcactctcaagcggcagacaggaaatgctg

gagtctatcgtaaataacgttcttttcagtctgtaa

Separately, PCR was conducted to add a DNA sequence encoding 6 histidines (SEQ ID NO: 35) to the 3′ terminus of this gene.
Two variants designed to remove the translational pauses in the gene were prepared using the DNA self-assembly method of Larsen et al., supra. One variant contained DNA sequence encoding a 6-hisitidine tag (SEQ ID NO: 35) at the 5′ terminus, and the other version did not. The annealing temperature for the self assembly reactions was about 48 degrees Celsius. This gene variant is referred to as a “Hot Rod” or “HR” gene variant. The sequence of this HR gene is set forth below as SEQ ID NO: 23:

SEQ ID NO: 23

ATGGAGTTCTTTTCTAATATAGGTAAAATTCAGTATCAAGGTCCAAAATC

TACAGATCCATTGTCTTTTAAATATTATAATCCAGAAGAAGTTATAAATG

GTAAAACTATGAGAGAACATTTAAAATTTGCTTTGTCTTGGTGGCATACT

ATGGGTGGTGATGGTACTGATATGTTCGGTTGTGGTACTACTGATAAAAC

TTGGGGTCAATCTGATCCAGCTGCTAGAGCAAAAGCCAAAGTAGATGCAG

CCTTTGAAATTATGGATAAATTGTCTATTGATTATTATTGTTTTCATGAT

AGAGATTTGTCTCCTGAATATGGTTCTTTAAAAGCAACTAATGATCAATT

GGACATTGTTACGGATTATATTAAAGAAAAACAAGGTGATAAATTTAAAT

GTTTGTGGGGCACTGCGAAATGTTTTGATCATCCACGTTTTATGCATGGT

GCGGGGACGAGTCCTTCTGCTGATGTTTTTGCTTTTTCTGCCGCTCAAAT

TAAGAAGGCATTGGAATCAACTGTTAAATTAGGTGGGAACGGGTATGTAT

TCTGGGGAGGAAGGGAAGGTTATGAAACATTATTAAACACTAATATGGGT

TTGGAATTGGATAATATGGCTAGATTGATGAAAATGGCTGTAGAATACGG

AAGGTCTATTGGTTTTAAGGGTGACTTTTATATTGAACCAAAACCTAAAG

AGCCTACTAAACATCAATATGATTTTGATACTGCTACAGTTTTGGGATTC

TTGAGAAAATATGGTCTGGATAAAGATTTTAAAATGAATATAGAAGCTAA

TCATGCAACACTCGCACAACATACTTTTCAACATGAATTGAGAGTTGCCA

GAGATAACGGAGTTTTTGGATCTATCGATGCAAACCAGGGAGACGTTTTG

CTAGGATGGGATACTGATCAATTTCCAACTAACATTTATGATACTACTAT

GTGTATGTATGAAGTAATTAAGGCAGGAGGCTTTACTAATGGCGGATTAA

ACTTTGATGCGAAGGCTAGGCGTGGTAGTTTCACTCCAGAGGATATATTC

TATTCTTATATTGCTGGAATGGATGCTTTCGCGTTAGGTTTCAGGGCAGC

ACTAAAATTGATTGAAGATGGTAGAATTGATAAGTTTGTAGCTGATAGAT

ATGCTTCTTGGAATACTGGAATAGGAGCAGATATAATCGCTGGGAAAGCC

GACTTCGCCAGTCTGGAAAAATATGCGCTTGAAAAAGGAGAAGTTACTGC

CAGCTTAAGTTCCGGTCGTCAAGAAATGTTGGAATCTATTGTAAACAATG

TTTTATTTTCTCTG

For cloning purposes, PCR was used to engineer a unique SpeI restriction site into the 5′ end of each of the xylose isomerase genes, and to engineer a unique XhoI restriction site at the 3′ end. In addition, a version of each gene was created that contained a 6-HIS tag (SEQ ID NO: 35) at the 3′ end of each gene to enable detection of the proteins using Western analysis.
PCR amplifications were performed in about 50 μl reactions containing 1×PfuI I Ultra reaction buffer (Stratagene, San Diego, Calif.), 0.2 mM dNTPs, 0.2 μM specific 5′ and 3′ primers, and 1 U PfuUltra II polymerase (Stratagene, San Diego, Calif.). The reactions were cycled at 95° C. for 10 minutes, followed by 30 rounds of amplification (95° C. for 30 seconds, 62° C. for 30 seconds, 72° C. for 30 seconds) and a final extension incubation at 72° C. for 5 minutes. Amplified PCR products were cloned into pCR Blunt II TOPO (Life Sciences, Carlsbad, Calif.) and confirmed by sequencing (GeneWiz, La Jolla, Calif.). The PCR primers for these reactions were:

(SEQ ID NO: 26)

5′ACTTGACTACTAGTATGGAGTTCTTTTCTAATATAGGTAAAATT

3′ (without the His tag):

(SEQ ID NO: 27)

AGTCAAGTCTCGAGCAGAGAAAATAAAACATTGTTTACAATAGA

3′ (with the His tag):

(SEQ ID NO: 28)

AGTCAAGTCTCGAGCTAATGATGATGATGATGATGCAGAGAAAATAAAA

CATTGTTTAC

Separately, the xylose isomerase gene from Piromyces, strain E2 (Harhangi et al., Arch. Microbiol., 180(2): 134-141 (2003)) was synthesized by IDT. The sequence of this gene is set forth below as SEQ ID NO: 24.

1	atggctaagg aatatttccc acaaattcaa aagattaagt tcgaaggtaa ggattctaag

61	aatccattag ccttccacta ctacgatgct gaaaaggaag tcatgggtaa gaaaatgaag

121	gattggttac gtttcgccat ggcctggtgg cacactcttt gcgccgaagg tgctgaccaa

181	ttcggtggag gtacaaagtc tttcccatgg aacgaaggta ctgatgctat tgaaattgcc

241	aagcaaaagg ttgatgctgg tttcgaaatc atgcaaaagc ttggtattcc atactactgt

301	ttccacgatg ttgatcttgt ttccgaaggt aactctattg aagaatacga atccaacctt

361	aaggctgtcg ttgcttacct caaggaaaag caaaaggaaa ccggtattaa gcttctctgg

421	agtactgcta acgtcttcgg tcacaagcgt tacatgaacg gtgcctccac taacccagac

481	tttgatgttg tcgcccgtgc tattgttcaa attaagaacg ccatagacgc cggtattgaa

541	cttggtgctg aaaactacgt cttctggggt ggtcgtgaag gttacatgag tctccttaac

601	actgaccaaa agcgtgaaaa ggaacacatg gccactatgc ttaccatggc tcgtgactac

661	gctcgttcca agggattcaa gggtactttc ctcattgaac caaagccaat ggaaccaacc

721	aagcaccaat acgatgttga cactgaaacc gctattggtt tccttaaggc ccacaactta

781	gacaaggact tcaaggtcaa cattgaagtt aaccacgcta ctcttgctgg tcacactttc

841	gaacacgaac ttgcctgtgc tgttgatgct ggtatgctcg gttccattga tgctaaccgt

901	ggtgactacc aaaacggttg ggatactgat caattcccaa ttgatcaata cgaactcgtc

961	caagcttgga tggaaatcat ccgtggtggt ggtttcgtta ctggtggtac caacttcgat

1021	gccaagactc gtcgtaactc tactgacctc gaagacatca tcattgccca cgtttctggt

1081	atggatgcta tggctcgtgc tcttgaaaac gctgccaagc tcctccaaga atctccatac

1141	accaagatga agaaggaacg ttacgcttcc ttcgacagtg gtattggtaa ggactttgaa

1201	gatggtaagc tcaccctcga acaagtttac gaatacggta agaagaacgg tgaaccaaag

1261	caaacttctg gtaagcaaga actctacgaa gctattgttg ccatgtacca ataa

Two hot rod (“HR”) versions of the Piromyces xylose isomerase gene were prepared using the method of Larsen et al., supra. One version contained DNA sequence encoding a 6-histidine tag (SEQ ID NO: 35) at the 5′ terminus and the other did not. The annealing temperature for the self-assembling oligonucleotides was about 48 degrees Celsius. The sequence of this gene is set forth below as

SEQ ID NO: 25

ATGGCTAAAGAATATTTTCCACAAATTCAGAAAATTAAATTTGAAGGTAAAGATTCTAAAAATCCATTGGCTTTCCATTA

TTATGATGCTGAAAAAGAAGTTATGGGTAAAAAGATGAAAGATTGGTTGAGATTCGCTATGGCTTGGTGGCATACTCTAT

GTGCTGAAGGAGCTGATCAATTTGGAGGAGGTACTAAATCTTTTCCTTGGAATGAAGGTACTGACGCTATTGAAATTGCT

AAGCAGAAAGTAGACGCGGGTTTTGAAATTATGCAAAAATTGGGAATACCATATTATTGTTTTCATGATGTTGATTTGGT

ATCTGAGGGTAATTCTATTGAAGAATATGAATCTAATTTAAAAGCTGTTGTTGCTTACTTAAAAGAAAAACAAAAAGAAA

CTGGAATTAAATTGTTGTGGTCTACAGCTAATGTTTTCGGTCATAAAAGATATATGAATGGTGCTTCTACAAATCCAGAT

TTTGATGTTGTAGCTAGAGCTATTGTTCAAATTAAAAATGCTATAGATGCAGGAATTGAATTAGGTGCCGAAAATTATGT

TTTCTGGGGAGGTAGAGAAGGTTATATGTCTTTGTTAAATACTGATCAAAAACGTGAAAAGGAACACATGGCAACTATGT

TGACAATGGCTAGGGATTATGCTAGATCTAAAGGTTTTAAAGGTACTTTCTTGATTGAGCCAAAACCTATGGAACCAACT

AAACATCAATATGACGTTGACACTGAAACTGCTATTGGTTTCTTAAAAGCTCATAATTTGGATAAAGATTTTAAGGTTAA

TATAGAAGTTAATCATGCTACACTAGCTGGTCATACTTTTGAACATGAATTAGCTTGTGCAGTTGATGCCGGTATGTTAG

GTTCTATCGACGCAAATAGAGGTGATTATCAAAATGGTTGGGACACAGATCAATTTCCAATAGATCAATATGAATTGGTT

CAAGCATGGATGGAAATTATTAGGGGTGGAGGCTTCGTTACAGGTGGAACTAATTTTGATGCTAAAACTAGGAGAAATTC

TACAGATCTTGAAGATATAATTATTGCTCATGTATCTGGTATGGATGCGATGGCCCGTGCTTTGGAAAATGCAGCTAAAT

TACTTCAAGAATCTCCTTATACTAAAATGAAAAAGGAAAGATATGCTTCTTTTGATTCTGGAATAGGTAAGGATTTTGAA

GATGGTAAATTGACATTGGAACAAGTTTATGAATATGGTAAGAAGAATGGAGAACCAAAACAAACTTCTGGTAAACAAGA

ATTATATGAGGCTATAGTAGCTATGTATCAAtaa.

For cloning purposes, a unique SpeI restriction site was engineered at the 5′ end of each of the XI genes, and a unique XhoI restriction site was engineered at the 3′ end. When needed, a 6-HIS tag (SEQ ID NO: 35) was engineered at the 3′ end of each gene sequence to enable detection of the proteins using Western analysis. The primers are listed in Table X. PCR amplifications were performed in 50 μl reactions containing 1×PfuI I Ultra reaction buffer (Stratagene, San Diego, Calif.), 0.2 mM dNTPs, 0.2 μM specific 5′ and 3′ primers, and 1 U PfuUltra II polymerase (Stratagene, San Diego, Calif.). The reactions were cycled at 95° C. for 10 minutes, followed by 30 rounds of amplification (95° C. for 30 seconds, 62° C. for 30 seconds, 72° C. for 30 seconds) and a final extension incubation at 72° C. for 5 minutes. Amplified PCR products were cloned into pCR Blunt II TOPO (Life Sciences, Carlsbad, Calif.) and confirmed by sequencing (GeneWiz).
The primers used for PCR were:

5′ (native gene)

(SEQ ID NO: 46)

ACTAGTATGGCTAAGGAATATTTCCCACAAATTCAAAAG

3′ (native gene)

(SEQ ID NO: 47)

CTCGAGCTACTATTGGTACATGGCAACAATAGC

3′ (native gene plus His tag)

(SEQ ID NO: 48)

CTCGAGCTACTAATGATGATGATGATGATGTTGGTACATGGCAACAATA

GCTTCG

5′ (hot rod gene)

(SEQ ID NO: 49)

ACTAGTATGGCTAAAGAATATTTTCCACAAATTCAG

3′ (hot rod gene)

(SEQ ID NO: 50)

CTCGAGTTATTGATACATAGCTACTATAGCCTC

3′ (hot rod gene plus His tag)

(SEQ ID NO: 51)

CTCGAGTTAATGATGATGATGATGATGTTGATACATAGCTACTATAGC

CTCATTGTTTAC

The genes encoding the native and HR versions of xylose isomerase were separately inserted into the vector p426GDP (ATCC catalog number 87361).
Saccharomyces cerevisiae strain BY4742 cells (ATCC catalog number 201389) were cultured in YPD media (10 g Yeast Extract, 20 g Bacto-Peptone, 20 g Glucose, 1 L total) at about 30° C. Separate aliquots of the cells were transformed with the plasmid constructs containing the various xylose isomerase constructs or with the vector alone. Transformation was accomplished using the Zymo kit (Catalog number T2001; Zymo Research Corp., Orange, Calif. 92867) using about 1 μg plasmid DNA and cultured on SC media (set forth below) containing glucose but no uracil (20 g glucose; 2.21 g SC dry mix, 6.7 g Yeast Nitrogen Base, 1 L total) for 2-3 days at about 30° C.
Synthetic Complete Medium mix (minus uracil) contained:


0.4 g	Adenine hemisulfate
3.5 g	Arginine
1 g	Glutamic Acid
0.433 g	Histidine
0.4 g	Myo-Inositol
5.2 g	Isoleucine
2.63 g	Leucine
0.9 g	Lysine
1.5 g	Methionine
0.8 g	Phenylalanine
1.1 g	Serine
1.2 g	Threonine
0.8 g	Tryptophan
0.2 g	Tyrosine
1.2 g	Valine

For expression and activity analysis, transformed cells containing the various xylose isomerase constructs were selected from the cultures and grown in about 100 ml of SC-Dextrose (minus uracil) to an OD₆₀₀of about 4.0. The S. cerevisiae cultures that were transformed with the various xylose isomerase-histidine constructs were then lysed using YPER-Plus reagent (Thermo Scientific, catalog number 78999) according to the manufacturer's directions. Protein quantitation of the lysates was performed using the Coomassie-Plus kit (Thermo Scientific, catalog number 23236) as directed by the manufacturer. Denaturing and native Western blot analyses were then conducted. To detect his-tagged xylose isomerase polypeptides Western analysis was employed. Gels were transferred onto a nitrocellulose membrane (0.45 micron, Thermo Scientific, San Diego, Calif.) using Western blotting filter paper (Thermo Scientific) using a Bio-Rad Mini Trans-Blot Cell (BioRad, Hercules, Calif.) system for approximately 90 minutes at 40V. Following transfer, the membrane was washed in 1×PBS (EMD, San Diego, Calif.), 0.05% Tween-20 (Fisher Scientific, Fairlawn, N.J.) for 2-5 minutes with gentle shaking. The membrane was blocked in 3% BSA dissolved in 1×PBS and 0.05% Tween-20 at room temperature for about 2 hours with gentle shaking. The membrane was washed once in 1×PBS and 0.05% Tween-20 for about 5 minutes with gentle shaking. The membrane was then incubated at room temperature with the 1:5000 dilution of primary antibody (Ms mAB to 6×His Tag (SEQ ID NO: 35), AbCam, Cambridge, Mass.) in 0.3% BSA (Fraction V, EMD, San Diego, Calif.) dissolved in 1×PBS and 0.05% Tween-20 with gentle shaking. Incubation was allowed to proceed for about 1 hour with gentle shaking. The membrane was then washed three times for 5 minutes each with 1×PBS and 0.05% Tween-20 with gentle shaking. The secondary antibody [Dnk pAb to Ms IgG (HRP), AbCam, Cambridge, Mass.] was used at 1:15000 dilution in 0.3% BSA and allowed to incubate for about 90 minutes at room temperature with gentle shaking. The membrane was washed three times for about 5 minutes using 1×PBS and 0.05% Tween-20 with gentle shaking. The membrane was then incubated with 5 ml of Supersignal West Pico Chemiluminescent substrate (Thermo Scientific, San Diego, Calif.) for 1 minute and then was exposed to a phosphorimager (Bio-Rad Universal Hood II, Bio-Rad, Hercules, Calif.) for about 10-100 seconds. The results are shown in FIG. 7. As can be seen, both Piromyces (“P” in FIG. 7) and Ruminococcus (“R” in FIG. 7) xylose isomerases are expressed in both the soluble and insoluble fractions of the yeast cells.
To measure activity of the various xylose isomerase constructs, assays were performed according to Kuyper et al. (FEMS Yeast Res., 4:69 [2003]). About 20 μg of soluble whole cell extract was incubated in the presence of 100 mM Tris, pH 7.5, 10 mM MgCl₂, 0.15 mM NADH (Sigma, St. Louis, Mo.), and about 2 U sorbitol dehydrogenase (Roche) at about 30° C. To start the reaction, about 100 μl of xylose was added at various final concentrations of 40-500 mM. A Beckman DU-800 was utilized with an Enzyme Mechanism software package (Beckman Coulter, Inc.), and the change in the A₃₄₀was monitored for 2-3 minutes.

Example 5

Preparation of Selective Growth Yeast

The yeast gene cdc21 encodes thymidylate synthase, which is required for de novo synthesis of pyrimidine deoxyribonucleotides. A cdc 21 mutant, strain 17206, (ATCC accession number 208583) has a point mutation G139S relative to the initiating methionine. The restrictive temperature of this temperature sensitive mutant is 37° C., which arrests cell division at S phase, so that little or no cell growth and division occurs at or above this temperature.
Saccharomyces cerevisiae strain YGR420CBY4742ΔPFK2 was used as the starting cell line to create the cdc21 growth sensitive mutant. A construct for homologous recombination was prepared to replace the wild type thymidylate synthase YGR420CBY4742ΔPFK2 for the cdc21 mutant. This construct was made in various steps. First, the cdc21 mutant region from Saccharomyces cerevisiae strain 17206 was PCR amplified using the following primers:

CDC21_fwd:

(SEQ ID NO: 52)

5′-aatcgatcaaagcttctaaatacaagacgtgcgatgacgactatac

tggac-3′

CDC21_rev:

(SEQ ID NO: 53)

5′-taccgtactacccgggtatatagtctttttgccctggtgttcctt

aataatttc-3′

For this PCR amplification reaction Saccharomyces cerevisiae 17206 genomic DNA was used. The genomic DNA was extracted using Zymo research YeaStar Genomic DNA kit according to instructions. In the PCR amplification reaction 100 ng of 17206 genomic DNA, 1 μM of the oligonucleotide primer set listed above, 2.5 U of PfuUltra High-Fidelity DNA polymerase (Stratagene), 300 μM dNTPs (Roche), and 1×PfuUltra reaction buffer was mixed in a final reaction volume of 500. Using a BIORAD DNA Engine Tetrad 2 Peltier thermal cycler the following cycle conditions were used: 5 min denaturation step at 95° C., followed by 30 cycles of 20 sec at 95° C., 20 sec at 50° C., and 1 min at 72° C., and a final step of 5 min at 72° C. This PCR product was digested with HindIII and XmaI restriction endonucleases and cloned in the HindIII and XmaI sites of PUC19 (NEB) according to standard cloning procedures described by Maniatis in Molecular Cloning.
The genomic DNA of BR214-4a (ATTC accession number 208600) was extracted using Zymo research YeaStar Genomic DNA kit according to instructions. The lys2 gene with promoter and terminator regions was PCR amplified from BR214-4a genomic DNA using the following primers:

Lys2Fwd:

(SEQ ID NO: 54)

5′-tgctaatgacccgggaattccacttgcaattacataaaaaattcc

ggcgg-3′

Lys2Rev:

(SEQ ID NO: 55)

5′-atgatcattgagctcagcttcgcaagtattcattttagacccat

ggtgg-3′.

The PCR cycle was identical to that just described above but with genomic DNA of BR214-4a instead. XmaI and SacI restriction sites were designed to flank this DNA construct to clone it into the XmaI and SacI sites of the PUC19-cdc21 vector according to standard cloning procedures described by Maniatis in Molecular Cloning. The new construct with the cdc21 mutation with a lys2 directly downstream of that will be referred to as PUC19-cdc2′-lys2.
The final step involved the cloning of the downstream region of thymidylate synthase into the PUC19-cdc2′-lys2 vector immediately downstream of the lys2 gene. The downstream region of the thymidylate synthase was amplified from BY4742 genomic DNA (ATCC accession number 201389D-5 using the following primers:

ThymidylateSynthase_DownFwd:

(SEQ ID NO: 56)

5′-tgctaatgagagctctcattttttggtgcgatatgtttttggtt

gatg-3′

and

ThymidylateSynthatse_DownRev:

(SEQ ID NO: 57)

5′-aatgatcatgagctcgtcaacaagaactaaaaaattgttcaaaa

atgc-3′.

This final construct is referred as PUC19-cdc2′-lys2-ThymidylateSynthase_down. The sequence is set forth in the tables. A final PCR amplification reaction of this construct was performed using the following PCR primers:

ThymidylateSynthase::cdc21 fwd:

(SEQ ID NO: 58)

5′-ctaaatacaagacgtgcgatgacgactatactgg-3′

and

ThymidylateSynthase::cdc21 rev:

(SEQ ID NO: 59)

5′-gtcaacaagaactaaaaaattgttcaaaaatgcaattgtc-3′.

The PCR reaction was identical to that described above but using 100 ng of the PUC19-cdc2′-lys2-ThymidylateSynthase_down construct as a template.
The final PCR product was separated by agarose gel electrophoresis, excised, and purified using MP Biomedicals Geneclean II kit as recommended. Homologous recombination of YGR420CBY4742ΔPFK2 to replace the wt thymidylate synthase for the cdc21 mutant was accomplished using 10 μg of the purified PCR product to transform YGR420CBY4742ΔPFK2 strain using same transformation protocol described above. Transformants were selected by culturing the cells on selective media containing SC-Ethanol (0.67% yeast nitrogen base-2% ethanol) containing complete amino acids minus lysine.
The genome of this final engineered strain contains the mutated cdc21 gene, and has both the PFK1 and PFK2 genes deleted. This final engineered strain will be transformed with the best combination of edd-p426 GPD and eda-p425 GPD variant constructs. Ethanol and glucose measurements will be monitored during aerobic and anaerobic growth conditions using Roche ethanol and glucose kits according to instructions.

Example 6

Examples of Polynucleotide Regulators

Provided in the tables hereafter are non-limiting examples of regulator polynucleotides that can be utilized in embodiments herein. Such polynucleotides may be utilized in native form or may be modified for use herein. Examples of regulatory polynucleotides include those that are regulated by oxygen levels in a system (e.g., up-regulated or down-regulated by relatively high oxygen levels or relatively low oxygen levels)

Regulated Yeast Promoters - Up-regulated by oxygen

		Relative	Relative
	Gene	mRNA level	mRNA level
ORF name	name	(Aerobic)	(Anaerobic)	Ratio

YPL275W		4389	30	219.5
YPL276W		2368	30	118.4
YDR256C	CTA1	2076	30	103.8
YHR096C	HXT5	1846	30	72.4
YDL218W		1189	30	59.4
YCR010C		1489	30	48.8
YOR161C		599	30	29.9
YPL200W		589	30	29.5
YGR110W		1497	30	27
YNL237W	YTP1	505	30	25.2
YBR116C		458	30	22.9
YOR348C	PUT4	451	30	22.6
YBR117C	TKL2	418	30	20.9
YLL052C		635	30	20
YNL195C		1578	30	19.4
YPR193C		697	30	15.7
YDL222C		301	30	15
YNL335W		294	30	14.6
YPL036W	PMA2	487	30	12.8
YML122C		206	30	10.3
YGR067C		236	30	10.2
YPR192W		204	30	10.2
YNL014W		828	30	9.8
YFL061W		256	30	9.1
YNR056C		163	30	8.1
YOR186W		153	30	7.6
YDR222W		196	30	6.5
YOR338W		240	30	6.3
YPR200C		113	30	5.7
YMR018W		778	30	5.2
YOR364W		123	30	5.1
YNL234W		93	30	4.7
YNR064C		85	30	4.2
YGR213C	RTA1	104	30	4
YCL064C	CHA1	80	30	4
YOL154W		302	30	3.9
YPR150W		79	30	3.9
YPR196W	MAL63	30	30	3.6
YDR420W	HKR1	221	30	3.5
YJL216C		115	30	3.5
YNL270C	ALP1	67	30	3.3
YHL016C	DUR3	224	30	3.2
YOL131W		230	30	3
YOR077W	RTS2	210	30	3
YDR536W	STL1	55	30	2.7
YNL150W		78	30	2.6
YHR212C		149	30	2.4
YJL108C		106	30	2.4
YGR069W		49	30	2.4
YDR106W		60	30	2.3
YNR034W	SOL1	197	30	2.2
YEL073C		104	30	2.1
YOL141W		81	30	1.8

Regulated Yeast Promoters - Down-regulated by oxygen

YJR047C

ANB1

30	4901	231.1
YMR319C	FET4		30	1159	58
YPR194C		30	982	49.1
YIR019C	STA1		30	981	22.8
YHL042W		30	608	12
YHR210C		30	552	27.6
YHR079B	SAE3		30	401	2.7
YGL162W	STO1		30	371	9.6
YHL044W		30	334	16.7
YOL015W		30	320	6.1
YCLX07W		30	292	4.2
YIL013C	PDR11		30	266	10.6
YDR046C		30	263	13.2
YBR040W	FIG1		30	257	12.8
YLR040C		30	234	2.9
YOR255W		30	231	11.6
YOL014W		30	229	11.4
YAR028W		30	212	7.5
YER089C		30	201	6.2
YFL012W		30	193	9.7
YDR539W		30	187	3.4
YHL043W		30	179	8.9
YJR162C		30	173	6
YMR165C	SMP2		30	147	3.5
YER106W		30	145	7.3
YDR541C		30	140	7
YCRX07W		30	138	3.3
YHR048W		30	137	6.9
YCL021W		30	136	6.8
YOL160W		30	136	6.8
YCRX08W		30	132	6.6
YMR057C		30	109	5.5
YDR540C		30	83	4.2
YOR378W		30	78	3.9
YBR085W	AAC3	45	1281	28.3
YER188W		47	746	15.8
YLL065W	GIN11		50	175	3.5
YDL241W		58	645	11.1
YBR238C		59	274	4.6
YCR048W	ARE1		60	527	8.7
YOL165C		60	306	5.1
YNR075W		60	251	4.2
YJL213W		60	250	4.2
YPL265W	DIP5	61	772	12.7
YDL093W	PMT5		62	353	5.7
YKR034W	DAL80		63	345	5.4
YKR053C		66	1268	19.3
YJR147W		68	281	4.1


Known and putative DNA binding motifs

Regulator	Known Consensus Motif	SEQ ID NO:

Abf1	TCRNNNNNNACG	60

Cbf1	RTCACRTG

Gal4	CGGNNNNNNNNNNNCCG	61

Gcn4	TGACTCA

Gcr1	CTTCC

Hap2	CCAATNA

Hap3	CCAATNA

Hap4	CCAATNA

Hsf1	GAANNTTCNNGAA	62

Ino2	ATGTGAAA

Mata(A1)	TGATGTANNT	93

Mcm1	CCNNNWWRGG	94

Mig1	WWWWSYGGGG	95

Pho4	CACGTG

Rap1	RMACCCANNCAYY	96

Reb1	CGGGTRR

Ste12	TGAAACA

Swi4	CACGAAA

Swi6	CACGAAA

Yap1	TTACTAA

Putative DNA Binding Motifs

	Best Motif (scored by E-	SEQ	Best Motif (scored by	SEQ
Regulator	value)	ID NO:	Hypergeometric)	ID NO:

Abf1	TYCGT--R-ARTGAYA	97	TYCGT--R-ARTGAYA	210

Ace2	RRRAARARAA-A-RARAA	98	GTGTGTGTGTGTGTG	211

Adr1	A-AG-GAGAGAG-GGCAG	99	YTSTYSTT-TTGYTWTT	212

Arg80	T--CCW-TTTKTTTC	100	GCATGACCATCCACG	213

Arg81	AAAAARARAAAARMA	101	GSGAYARMGGAMAAAAA	214

Aro80	YKYTYTTYTT----KY	102	TRCCGAGRYW-SSSGCGS	215

Ash1	CGTCCGGCGC	103	CGTCCGGCGC	216

Azf1	GAAAAAGMAAAAAAA	104	AARWTSGARG-A--CSAA	217

Bas1	TTTTYYTTYTTKY-TY-T	105	CS-CCAATGK--CS	218

Cad1	CATKYTTTTTTKYTY	106	GCT-ACTAAT	219

Cbf1	CACGTGACYA	107	CACGTGACYA	220

Cha4	CA---ACACASA-A	108	CAYAMRTGY-C	221

Cin5	none		none

Crz1	GG-A-A--AR-ARGGC-	109	TSGYGRGASA	222

Cup9	TTTKYTKTTY-YTTTKTY	110	K-C-C---SCGCTACKGC	223

Dal81	WTTKTTTTTYTTTTT-T	111	SR-GGCMCGGC-SSG	224

Dal82	TTKTTTTYTTC	112	TACYACA-CACAWGA	225

Dig1	AAA--RAA-GARRAA-AR	132	CCYTG-AYTTCW-CTTC	226

Dot6	GTGMAK-MGRA-G-G	133	GTGMAK-MGRA-G-G	227

Fhl1	-TTWACAYCCRTACAY-Y	134	-TTWACAYCCRTACAY-Y	228

Fkh1	TTT-CTTTKYTT-YTTTT	135	AAW-RTAAAYARG	229

Fkh2	AAARA-RAAA-AAAR-AA	136	GG-AAWA-GTAAACAA	230

Fzf1	CACACACACACACACAC	137	SASTKCWCTCKTCGT	231

Gal4	TTGCTTGAACGSATGCCA	138	TTGCTTGAACGSATGCCA	232

Gal4 (Gal)	YCTTTTTTTTYTTYYKG	139	CGGM---CW-Y--CCCG	233

Gat1	none		none

Gat3	RRSCCGMCGMGRCGCGCS	140	RGARGTSACGCAKRTTCT	234

Gcn4	AAA-ARAR-RAAAARRAR	141	TGAGTCAY

Gcr1	GGAAGCTGAAACGYMWRR	142	GGAAGCTGAAACGYMWRR	235

Gcr2	GGAGAGGCATGATGGGGG	143	AGGTGATGGAGTGCTCAG	236

Gln3	CT-CCTTTCT	144	GKCTRR-RGGAGA-GM	237

Grf10	GAAARRAAAAAAMRMARA	145	-GGGSG-T-SYGT-CGA	238

Gts1	G-GCCRS--TM	146	AG-AWGTTTTTGWCAAMA	239

Haa1	none		none

Hal9	TTTTTTYTTTTY-KTTTT	147	KCKSGCAGGCWTTKYTCT	240

Hap2	YTTCTTTTYT-Y-C-KT-	148	G-CCSART-GC	241

Hap3	T-SYKCTTTTCYTTY	149	SGCGMGGG--CC-GACCG	242

Hap4	STT-YTTTY-TTYTYYYY	150	YCT-ATTSG-C-GS	243

Hap5	YK-TTTWYYTC	151	T-TTSMTT-YTTTCCK-C	244

Hir1	AAAA-A-AARAR-AG	152	CCACKTKSGSCCT-S	245

Hir2	WAAAAAAGAAAA-AAAAR	153	CRSGCYWGKGC	246

Hms1	AAA-GG-ARAM	154	-AARAAGC-GGGCAC-C	247

Hsf1	TYTTCYAGAA--TTCY	155	TYTTCYAGAA--TTCY	248

Ime4	CACACACACACACACACA	156	CACACACACACACACACA	249

Ino2	TTTYCACATGC	157	SCKKCGCKSTSSTTYAA	250

Ino4	G--GCATGTGAAAA	158	G--GCATGTGAAAA	251

Ixr1	GAAAA-AAAAAAAARA-A	159	CTTTTTTTYYTSGCC	252

Leu3	GAAAAARAARAA-AA	160	GCCGGTMMCGSYC--	253

Mac1	YTTKT--TTTTTYTYTTT	161	A--TTTTTYTTKYGC	254

Mal13	GCAG-GCAGG	162	AAAC-TTTATA-ATACA	255

Mal33	none		none

Mata1	GCCC-C		CAAT-TCT-CK	256

Mbp1	TTTYTYKTTT-YYTTTTT	163	G-RR-A-ACGCGT-R	257

Mcm1	TTTCC-AAW-RGGAAA	164	TTTCC-AAW-RGGAAA	258

Met31	YTTYYTTYTTTTYTYTTC	165

Met4	MTTTTTYTYTYTTC	166

Mig1	TATACA-AGMKRTATATG	167

Mot3	TMTTT-TY-CTT-TTTWK	168

Msn1	KT--TTWTTATTCC-C	169

Msn2	ACCACC

Msn4	R--AAAA-RA-AARAAAT	170

Mss11	TTTTTTTTCWCTTTKYC	171

Ndd1	TTTY-YTKTTTY-YTTYT	172

Nrg1	TTY--TTYTT-YTTTYYY	173

Pdr1	T-YGTGKRYGT-YG	174

Phd1	TTYYYTTTTTYTTTTYTT	175

Pho4	GAMAAAAAARAAAAR	176

Put3	CYCGGGAAGCSAMM-CCG	177

Rap1	GRTGYAYGGRTGY	178

Rcs1	KMAARAAAAARAAR	179

Reb1	RTTACCCGS

Rfx1	AYGRAAAARARAAAARAA	180

Rgm1	GGAKSCC-TTTY-GMRTA	181

Rgt1	CCCTCC

Rim101	GCGCCGC

Rlm1	TTTTC-KTTTYTTTTTC	182

Rme1	ARAAGMAGAAARRAA	183

Rox1	YTTTTCTTTTY-TTTTT	184

Rph1	ARRARAAAGG-	185

Rtg1	YST-YK-TYTT-CTCCCM	186

Rtg3	GARA-AAAAR-RAARAAA	187

Sfl1	CY--GGSSA-C	188

Sfp1	CACACACACACACAYA	189

Sip4	CTTYTWTTKTTKTSA	190

Skn7	YTTYYYTYTTTYTYYTTT	191

Sko1	none

Smp1	AMAAAAARAARWARA-AA	192

Sok2	ARAAAARRAAAAAG-RAA	193

Stb1	RAARAAAAARCMRSRAAA	194

Ste12	TTYTKTYTY-TYYKTTTY	195

Stp1	GAAAAMAA-AAAAA-AAA	196

Stp2	YAA-ARAARAAAAA-AAM	197

Sum1	TY-TTTTTTYTTTTT-TK	198

Swi4	RAARAARAAA-AA-R-AA	199

Swi5	CACACACACACACACACA	200

Swi6	RAARRRAAAAA-AAAMAA	201

Thi2	GCCAGACCTAC	202

Uga3	GG-GGCT

Yap1	TTYTTYTTYTTTY-YTYT	203

Yap3	none

Yap5	YKSGCGCGYCKCGKCGGS	204

Yap6	TTTTYYTTTTYYYYKTT	205

Yap7	none

Yfl044c	TTCTTKTYYTTTT	206

Yjl206c	TTYTTTTYTYYTTTYTTT	207

Zap1	TTGCTTGAACGGATGCCA	208

Zms1	MG-MCAAAAATAAAAS	209

Transcriptional repressors

Associated Gene(s)	Description(s)

WHI5	Repressor of G1 transcription that binds to SCB binding factor (SBF)
	at SCB target promoters in early G1; phosphorylation of Whi5p by
	the CDK, Cln3p/Cdc28p relieves repression and promoter binding by
	Whi5; periodically expressed in G1
TUP1	General repressor of transcription, forms complex with Cyc8p,
	involved in the establishment of repressive chromatin structure
	through interactions with histones H3 and H4, appears to enhance
	expression of some genes
ROX1	Heme-dependent repressor of hypoxic genes; contains an HMG
	domain that is responsible for DNA bending activity
SFL1	Transcriptional repressor and activator; involved in repression of
	flocculation-related genes, and activation of stress responsive
	genes; negatively regulated by cAMP-dependent protein kinase A
	subunit Tpk2p
RIM101	Transcriptional repressor involved in response to pH and in cell wall
	construction; required for alkaline pH-stimulated haploid invasive
	growth and sporulation; activated by proteolytic processing; similar
	to A. nidulans PacC
RDR1	Transcriptional repressor involved in the control of multidrug
	resistance; negatively regulates expression of the PDR5 gene;
	member of the Gal4p family of zinc cluster proteins
SUM1	Transcriptional repressor required for mitotic repression of middle
	sporulation-specific genes; also acts as general replication initiation
	factor; involved in telomere maintenance, chromatin silencing;
	regulated by pachytene checkpoint
XBP1	Transcriptional repressor that binds to promoter sequences of the
	cyclin genes, CYS3, and SMF2; expression is induced by stress or
	starvation during mitosis, and late in meiosis; member of the
	Swi4p/Mbp1p family; potential Cdc28p substrate
NRG2	Transcriptional repressor that mediates glucose repression and
	negatively regulates filamentous growth; has similarity to Nrg1p
NRG1	Transcriptional repressor that recruits the Cyc8p-Tup1p complex to
	promoters; mediates glucose repression and negatively regulates a
	variety of processes including filamentous growth and alkaline pH
	response
CUP9	Homeodomain-containing transcriptional repressor of PTR2, which
	encodes a major peptide transporter; imported peptides activate
	ubiquitin-dependent proteolysis, resulting in degradation of Cup9p
	and de-repression of PTR2 transcription
YOX1	Homeodomain-containing transcriptional repressor, binds to Mcm1p
	and to early cell cycle boxes (ECBs) in the promoters of cell cycle-
	regulated genes expressed in M/G1 phase; expression is cell cycle-
	regulated; potential Cdc28p substrate
RFX1	Major transcriptional repressor of DNA-damage-regulated genes,
	recruits repressors Tup1p and Cyc8p to their promoters; involved in
	DNA damage and replication checkpoint pathway; similar to a family
	of mammalian DNA binding RFX1-4 proteins
MIG3	Probable transcriptional repressor involved in response to toxic
	agents such as hydroxyurea that inhibit ribonucleotide reductase;
	phosphorylation by Snf1p or the Mec1p pathway inactivates Mig3p,
	allowing induction of damage response genes
RGM1	Putative transcriptional repressor with proline-rich zinc fingers;
	overproduction impairs cell growth
YHP1	One of two homeobox transcriptional repressors (see also Yox1p),
	that bind to Mcm1p and to early cell cycle box (ECB) elements of
	cell cycle regulated genes, thereby restricting ECB-mediated
	transcription to the M/G1 interval
HOS4	Subunit of the Set3 complex, which is a meiotic-specific repressor of
	sporulation specific genes that contains deacetylase activity;
	potential Cdc28p substrate
CAF20	Phosphoprotein of the mRNA cap-binding complex involved in
	translational control, repressor of cap-dependent translation
	initiation, competes with eIF4G for binding to eIF4E
SAP1	Putative ATPase of the AAA family, interacts with the Sin1p
	transcriptional repressor in the two-hybrid system
SET3	Defining member of the SET3 histone deacetylase complex which is
	a meiosis-specific repressor of sporulation genes; necessary for
	efficient transcription by RNAPII; one of two yeast proteins that
	contains both SET and PHD domains
RPH1	JmjC domain-containing histone demethylase which can specifically
	demethylate H3K36 tri- and dimethyl modification states;
	transcriptional repressor of PHR1; Rph1p phosphorylation during
	DNA damage is under control of the MEC1-RAD53 pathway
YMR181C	Protein of unknown function; mRNA transcribed as part of a
	bicistronic transcript with a predicted transcriptional repressor
	RGM1/YMR182C; mRNA is destroyed by nonsense-mediated decay
	(NMD); YMR181C is not an essential gene
YLR345W	Similar to 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase
	enzymes responsible for the metabolism of fructoso-2,6-
	bisphosphate; mRNA expression is repressed by the Rfx1p-Tup1p-
	Ssn6p repressor complex; YLR345W is not an essential gene
MCM1	Transcription factor involved in cell-type-specific transcription and
	pheromone response; plays a central role in the formation of both
	repressor and activator complexes
PHR1	DNA photolyase involved in photoreactivation, repairs pyrimidine
	dimers in the presence of visible light; induced by DNA damage;
	regulated by transcriptional repressor Rph1p
HOS2	Histone deacetylase required for gene activation via specific
	deacetylation of lysines in H3 and H4 histone tails; subunit of the
	Set3 complex, a meiotic-specific repressor of sporulation specific
	genes that contains deacetylase activity
RGT1	Glucose-responsive transcription factor that regulates expression of
	several glucose transporter (HXT) genes in response to glucose;
	binds to promoters and acts both as a transcriptional activator and
	repressor
SRB7	Subunit of the RNA polymerase II mediator complex; associates with
	core polymerase subunits to form the RNA polymerase II
	holoenzyme; essential for transcriptional regulation; target of the
	global repressor Tup1p
GAL11	Subunit of the RNA polymerase II mediator complex; associates with
	core polymerase subunits to form the RNA polymerase II
	holoenzyme; affects transcription by acting as target of activators
	and repressors

Transcriptional activators

Associated
Gene(s)	Description(s)

SKT5	Activator of Chs3p (chitin synthase III), recruits Chs3p to the bud neck
	via interaction with Bni4p; has similarity to Shc1p, which activates
	Chs3p during sporulation
MSA1	Activator of G1-specific transcription factors, MBF and SBF, that
	regulates both the timing of G1-specific gene transcription, and cell
	cycle initiation; potential Cdc28p substrate
AMA1	Activator of meiotic anaphase promoting complex (APC/C); Cdc20p
	family member; required for initiation of spore wall assembly; required
	for Clb1p degradation during meiosis
STB5	Activator of multidrug resistance genes, forms a heterodimer with
	Pdr1p; contains a Zn(II)2Cys6 zinc finger domain that interacts with a
	PDRE (pleotropic drug resistance element) in vitro; binds Sin3p in a
	two-hybrid assay
RRD2	Activator of the phosphotyrosyl phosphatase activity of PP2A, peptidyl-
	prolyl cis/trans-isomerase; regulates G1 phase progression, the
	osmoresponse, microtubule dynamics; subunit of the Tap42p-Pph21p-
	Rrd2p complex
BLM10	Proteasome activator subunit; found in association with core particles,
	with and without the 19S regulatory particle; required for resistance to
	bleomycin, may be involved in protecting against oxidative damage;
	similar to mammalian PA200
SHC1	Sporulation-specific activator of Chs3p (chitin synthase III), required for
	the synthesis of the chitosan layer of ascospores; has similarity to
	Skt5p, which activates Chs3p during vegetative growth;
	transcriptionally induced at alkaline pH
NDD1	Transcriptional activator essential for nuclear division; localized to the
	nucleus; essential component of the mechanism that activates the
	expression of a set of late-S-phase-specific genes
IMP2′	Transcriptional activator involved in maintenance of ion homeostasis
	and protection against DNA damage caused by bleomycin and other
	oxidants, contains a C-terminal leucine-rich repeat
LYS14	Transcriptional activator involved in regulation of genes of the lysine
	biosynthesis pathway; requires 2-aminoadipate semialdehyde as co-
	inducer
MSN1	Transcriptional activator involved in regulation of invertase and
	glucoamylase expression, invasive growth and pseudohyphal
	differentiation, iron uptake, chromium accumulation, and response to
	osmotic stress; localizes to the nucleus
HAA1	Transcriptional activator involved in the transcription of TPO2, YRO2,
	and other genes putatively encoding membrane stress proteins;
	involved in adaptation to weak acid stress
UGA3	Transcriptional activator necessary for gamma-aminobutyrate (GABA)-
	dependent induction of GABA genes (such as UGA1, UGA2, UGA4);
	zinc-finger transcription factor of the Zn(2)-Cys(6) binuclear cluster
	domain type; localized to the nucleus
GCR1	Transcriptional activator of genes involved in glycolysis; DNA-binding
	protein that interacts and functions with the transcriptional activator
	Gcr2p
GCR2	Transcriptional activator of genes involved in glycolysis; interacts and
	functions with the DNA-binding protein Gcr1p
GAT1	Transcriptional activator of genes involved in nitrogen catabolite
	repression; contains a GATA-1-type zinc finger DNA-binding motif;
	activity and localization regulated by nitrogen limitation and Ure2p
GLN3	Transcriptional activator of genes regulated by nitrogen catabolite
	repression (NCR), localization and activity regulated by quality of
	nitrogen source
PUT3	Transcriptional activator of proline utilization genes, constitutively binds
	PUT1 and PUT2 promoter sequences and undergoes a conformational
	change to form the active state; has a Zn(2)-Cys(6) binuclear cluster
	domain
ARR1	Transcriptional activator of the basic leucine zipper (bZIP) family,
	required for transcription of genes involved in resistance to arsenic
	compounds
PDR3	Transcriptional activator of the pleiotropic drug resistance network,
	regulates expression of ATP-binding cassette (ABC) transporters
	through binding to cis-acting sites known as PDREs (PDR responsive
	elements)
MSN4	Transcriptional activator related to Msn2p; activated in stress
	conditions, which results in translocation from the cytoplasm to the
	nucleus; binds DNA at stress response elements of responsive genes,
	inducing gene expression
MSN2	Transcriptional activator related to Msn4p; activated in stress
	conditions, which results in translocation from the cytoplasm to the
	nucleus; binds DNA at stress response elements of responsive genes,
	inducing gene expression
PHD1	Transcriptional activator that enhances pseudohyphal growth;
	regulates expression of FLO11, an adhesin required for pseudohyphal
	filament formation; similar to StuA, an A. nidulans developmental
	regulator; potential Cdc28p substrate
FHL1	Transcriptional activator with similarity to DNA-binding domain of
	Drosophila forkhead but unable to bind DNA in vitro; required for rRNA
	processing; isolated as a suppressor of splicing factor prp4
VHR1	Transcriptional activator, required for the vitamin H-responsive element
	(VHRE) mediated induction of VHT1 (Vitamin H transporter) and BIO5
	(biotin biosynthesis intermediate transporter) in response to low biotin
	concentrations
CDC20	Cell-cycle regulated activator of anaphase-promoting
	complex/cyclosome (APC/C), which is required for
	metaphase/anaphase transition; directs ubiquitination of mitotic cyclins,
	Pds1p, and other anaphase inhibitors; potential Cdc28p substrate
CDH1	Cell-cycle regulated activator of the anaphase-promoting
	complex/cyclosome (APC/C), which directs ubiquitination of cyclins
	resulting in mitotic exit; targets the APC/C to specific substrates
	including Cdc20p, Ase1p, Cin8p and Fin1p
AFT2	Iron-regulated transcriptional activator; activates genes involved in
	intracellular iron use and required for iron homeostasis and resistance
	to oxidative stress; similar to Aft1p
MET4	Leucine-zipper transcriptional activator, responsible for the regulation
	of the sulfur amino acid pathway, requires different combinations of the
	auxiliary factors Cbf1p, Met28p, Met31p and Met32p
CBS2	Mitochondrial translational activator of the COB mRNA; interacts with
	translating ribosomes, acts on the COB mRNA 5′-untranslated leader
CBS1	Mitochondrial translational activator of the COB mRNA; membrane
	protein that interacts with translating ribosomes, acts on the COB
	mRNA 5′-untranslated leader
CBP6	Mitochondrial translational activator of the COB mRNA;
	phosphorylated
PET111	Mitochondrial translational activator specific for the COX2 mRNA;
	located in the mitochondrial inner membrane
PET494	Mitochondrial translational activator specific for the COX3 mRNA, acts
	together with Pet54p and Pet122p; located in the mitochondrial inner
	membrane
PET122	Mitochondrial translational activator specific for the COX3 mRNA, acts
	together with Pet54p and Pet494p; located in the mitochondrial inner
	membrane
RRD1	Peptidyl-prolyl cis/trans-isomerase, activator of the phosphotyrosyl
	phosphatase activity of PP2A; involved in G1 phase progression,
	microtubule dynamics, bud morphogenesis and DNA repair; subunit of
	the Tap42p-Sit4p-Rrd1p complex
YPR196W	Putative maltose activator
POG1	Putative transcriptional activator that promotes recovery from
	pheromone induced arrest; inhibits both alpha-factor induced G1 arrest
	and repression of CLN1 and CLN2 via SCB/MCB promoter elements;
	potential Cdc28p substrate; SBF regulated
MSA2	Putative transcriptional activator, that interacts with G1-specific
	transcription factor, MBF and G1-specific promoters; ortholog of
	Msa2p, an MBF and SBF activator that regulates G1-specific
	transcription and cell cycle initiation
PET309	Specific translational activator for the COX1 mRNA, also influences
	stability of intron-containing COX1 primary transcripts; localizes to the
	mitochondrial inner membrane; contains seven pentatricopeptide
	repeats (PPRs)
TEA1	Ty1 enhancer activator required for full levels of Ty enhancer-mediated
	transcription; C6 zinc cluster DNA-binding protein
PIP2	Autoregulatory oleate-specific transcriptional activator of peroxisome
	proliferation, contains Zn(2)-Cys(6) cluster domain, forms heterodimer
	with Oaf1p, binds oleate response elements (OREs), activates beta-
	oxidation genes
CHA4	DNA binding transcriptional activator, mediates serine/threonine
	activation of the catabolic L-serine (L-threonine) deaminase (CHA1);
	Zinc-finger protein with Zn[2]-Cys[6] fungal-type binuclear cluster
	domain
SFL1	Transcriptional repressor and activator; involved in repression of
	flocculation-related genes, and activation of stress responsive genes;
	negatively regulated by cAMP-dependent protein kinase A subunit
	Tpk2p
RDS2	Zinc cluster transcriptional activator involved in conferring resistance to
	ketoconazole
CAT8	Zinc cluster transcriptional activator necessary for derepression of a
	variety of genes under non-fermentative growth conditions, active after
	diauxic shift, binds carbon source responsive elements
ARO80	Zinc finger transcriptional activator of the Zn2Cys6 family; activates
	transcription of aromatic amino acid catabolic genes in the presence of
	aromatic amino acids
SIP4	C6 zinc cluster transcriptional activator that binds to the carbon source-
	responsive element (CSRE) of gluconeogenic genes; involved in the
	positive regulation of gluconeogenesis; regulated by Snf1p protein
	kinase; localized to the nucleus
SPT10	Putative histone acetylase, sequence-specific activator of histone
	genes, binds specifically and highly cooperatively to pairs of UAS
	elements in core histone promoters, functions at or near the TATA box
MET28	Basic leucine zipper (bZIP) transcriptional activator in the Cbf1p-
	Met4p-Met28p complex, participates in the regulation of sulfur
	metabolism
GCN4	Basic leucine zipper (bZIP) transcriptional activator of amino acid
	biosynthetic genes in response to amino acid starvation; expression is
	tightly regulated at both the transcriptional and translational levels
CAD1	AP-1-like basic leucine zipper (bZIP) transcriptional activator involved
	in stress responses, iron metabolism, and pleiotropic drug resistance;
	controls a set of genes involved in stabilizing proteins; binds
	consensus sequence TTACTAA
INO2	Component of the heteromeric Ino2p/Ino4p basic helix-loop-helix
	transcription activator that binds inositol/choline-responsive elements
	(ICREs), required for derepression of phospholipid biosynthetic genes
	in response to inositol depletion
THI2	Zinc finger protein of the Zn(II)2Cys6 type, probable transcriptional
	activator of thiamine biosynthetic genes
SWI4	DNA binding component of the SBF complex (Swi4p-Swi6p), a
	transcriptional activator that in concert with MBF (Mbp1-Swi6p)
	regulates late G1-specific transcription of targets including cyclins and
	genes required for DNA synthesis and repair
HAP5	Subunit of the heme-activated, glucose-repressed Hap2/3/4/5 CCAAT-
	binding complex, a transcriptional activator and global regulator of
	respiratory gene expression; required for assembly and DNA binding
	activity of the complex
HAP3	Subunit of the heme-activated, glucose-repressed Hap2p/3p/4p/5p
	CCAAT-binding complex, a transcriptional activator and global
	regulator of respiratory gene expression; contains sequences
	contributing to both complex assembly and DNA binding
HAP2	Subunit of the heme-activated, glucose-repressed Hap2p/3p/4p/5p
	CCAAT-binding complex, a transcriptional activator and global
	regulator of respiratory gene expression; contains sequences sufficient
	for both complex assembly and DNA binding
HAP4	Subunit of the heme-activated, glucose-repressed Hap2p/3p/4p/5p
	CCAAT-binding complex, a transcriptional activator and global
	regulator of respiratory gene expression; provides the principal
	activation function of the complex
YML037C	Putative protein of unknown function with some characteristics of a
	transcriptional activator; may be a target of Dbf2p-Mob1p kinase; GFP-
	fusion protein co-localizes with clathrin-coated vesicles; YML037C is
	not an essential gene
TRA1	Subunit of SAGA and NuA4 histone acetyltransferase complexes;
	interacts with acidic activators (e.g., Gal4p) which leads to transcription
	activation; similar to human TRRAP, which is a cofactor for c-Myc
	mediated oncogenic transformation
YLL054C	Putative protein of unknown function with similarity to Pip2p, an oleate-
	specific transcriptional activator of peroxisome proliferation; YLL054C
	is not an essential gene
RTG2	Sensor of mitochondrial dysfunction; regulates the subcellular location
	of Rtg1p and Rtg3p, transcriptional activators of the retrograde (RTG)
	and TOR pathways; Rtg2p is inhibited by the phosphorylated form of
	Mks1p
YBR012C	Dubious open reading frame, unlikely to encode a functional protein;
	expression induced by iron-regulated transcriptional activator Aft2p
JEN1	Lactate transporter, required for uptake of lactate and pyruvate;
	phosphorylated; expression is derepressed by transcriptional activator
	Cat8p during respiratory growth, and repressed in the presence of
	glucose, fructose, and mannose
MRP1	Mitochondrial ribosomal protein of the small subunit; MRP1 exhibits
	genetic interactions with PET122, encoding a COX3-specific
	translational activator, and with PET123, encoding a small subunit
	mitochondrial ribosomal protein
MRP17	Mitochondrial ribosomal protein of the small subunit; MRP17 exhibits
	genetic interactions with PET122, encoding a COX3-specific
	translational activator
TPI1	Triose phosphate isomerase, abundant glycolytic enzyme; mRNA half-
	life is regulated by iron availability; transcription is controlled by
	activators Reb1p, Gcr1p, and Rap1p through binding sites in the 5′
	non-coding region
PKH3	Protein kinase with similarity to mammalian phosphoinositide-
	dependent kinase 1 (PDK1) and yeast Pkh1p and Pkh2p, two
	redundant upstream activators of Pkc1p; identified as a multicopy
	suppressor of a pkh1 pkh2 double mutant
YGL079W	Putative protein of unknown function; green fluorescent protein (GFP)-
	fusion protein localizes to the endosome; identified as a transcriptional
	activator in a high-throughput yeast one-hybrid assay
TFB1	Subunit of TFIIH and nucleotide excision repair factor 3 complexes,
	required for nucleotide excision repair, target for transcriptional
	activators
PET123	Mitochondrial ribosomal protein of the small subunit; PET123 exhibits
	genetic interactions with PET122, which encodes a COX3 mRNA-
	specific translational activator
MHR1	Protein involved in homologous recombination in mitochondria and in
	transcription regulation in nucleus; binds to activation domains of acidic
	activators; required for recombination-dependent mtDNA partitioning
MCM1	Transcription factor involved in cell-type-specific transcription and
	pheromone response; plays a central role in the formation of both
	repressor and activator complexes
EGD1	Subunit beta1 of the nascent polypeptide-associated complex (NAC)
	involved in protein targeting, associated with cytoplasmic ribosomes;
	enhances DNA binding of the Gal4p activator; homolog of human
	BTF3b
STE5	Pheromone-response scaffold protein; binds Ste11p, Ste7p, and
	Fus3p kinases, forming a MAPK cascade complex that interacts with
	the plasma membrane and Ste4p-Ste18p; allosteric activator of Fus3p
	that facilitates Ste7p-mediated activation
RGT1	Glucose-responsive transcription factor that regulates expression of
	several glucose transporter (HXT) genes in response to glucose; binds
	to promoters and acts both as a transcriptional activator and repressor
TYE7	Serine-rich protein that contains a basic-helix-loop-helix (bHLH) DNA
	binding motif; binds E-boxes of glycolytic genes and contributes to their
	activation; may function as a transcriptional activator in Ty1-mediated
	gene expression
VMA13	Subunit H of the eight-subunit V1 peripheral membrane domain of the
	vacuolar H+-ATPase (V-ATPase), an electrogenic proton pump found
	throughout the endomembrane system; serves as an activator or a
	structural stabilizer of the V-ATPase
GAL11	Subunit of the RNA polymerase II mediator complex; associates with
	core polymerase subunits to form the RNA polymerase II holoenzyme;
	affects transcription by acting as target of activators and repressors
VAC14	Protein involved in regulated synthesis of PtdIns(3,5)P(2), in control of
	trafficking of some proteins to the vacuole lumen via the MVB, and in
	maintenance of vacuole size and acidity; interacts with Fig4p; activator
	of Fab1p

Example 7

Heterologous Xylose Isomerase Expression in Yeast

Provided hereafter are non-limiting examples of certain organisms from which nucleic acids that encode a polypeptide having xylose isomerase activity can be obtained. Certain nucleic acid encoded polypeptides having active xylose isomerase activity can be expressed in an engineered yeast (S. cerevisiae).


		Xylose isomerase
	Active?	type
Donor Organism	(yes/no)	(Type 1/Type 2)

Piromyces	Yes	Type 2
Orpinomyces	Yes
Bacteroides thetaiotaomicron	Yes
Clostridium phytofermentans	Yes
Thermus thermophilus	Yes	Type 1
Ruminococcus flavefaciens	Yes
Escherichia coli	No
Bacillus subtilis	No
Lactobacillus pentoses	No
Leifsoria xyli subsp. Cynodontis	No
Clostridium thermosulfurogenes	No
Bacillus licheniformis	No
Burkholderia xenovorans	No
Psudomonas savastanoi	No
Robiginitalea biformata	No
Saccharophagus degradans	No
Staphylococcus xylosus	No
Streptomyces diastaticus subsp diastaticus	No
Xanthomonas campestris	No
Salmonella enterica serovar Typhimurium	No
Agrobacterium tumefaciens	No
Arabidopsis thaliana	No
Pseudomonas syringae	No
Actinoplanes missouriensis	No
Streptomyces rubiginosus	No
Epilopiscium	No

Example 8

Examples of Nucleic Acid and Amino Acid Sequences

Provided hereafter and non-limiting examples of certain nucleic acid sequences.


		Nucleic acid
	Organism/	Accession No. or
Gene Name	ATCC identifier	other identifier	Nucleotide Sequence

Xylose	Ruminococcus	AJ132472	atggaatttt tcagcaatat cggtaaaatt cagtatcagg gaccaaaaag tactgatcct
Isomerase	flavefaciens		ctctcattta agtactataa ccctgaagaa gtcatcaacg gaaagacaat gcgcgagcat
(XI-RF	strain 17		ctgaagttcg ctctttcatg gtggcacaca atgggcggcg acggaacaga tatgttcggc
Native)			tgcggcacaa cagacaagac ctggggacag tccgatcccg ctgcaagagc aaaggctaag
			gttgacgcag cattcgagat catggataag ctctccattg actactattg tttccacgat
			cgcgatcttt ctcccgagta tggcagcctc aaggctacca acgatcagct tgacatagtt
			acagactata tcaaggagaa gcagggcgac aagttcaagt gcctctgggg tacagcaaag
			tgcttcgatc atccaagatt catgcacggt gcaggtacat ctccttctgc tgatgtattc
			gctttctcag ctgctcagat caagaaggct ctcgagtcaa cagtaaagct cggcggtaac
			ggttacgttt tctggggcgg acgtgaaggc tatgagacac ttcttaatac aaatatggga
			ctcgaactcg acaatatggc tcgtcttatg aagatggctg ttgagtatgg acgttcgatc
			ggcttcaagg gcgacttcta tatcgagccc aagcccaagg agcccacaaa gcatcagtac
			gatttcgata cagctactgt tctgggattc ctcagaaagt acggtctcga taaggatttc
			aagatgaata tcgaagctaa ccacgctaca cttgctcagc atacattcca gcatgagctc
			cgtgttgcaa gagacaatgg tgtgttcggt tctatcgacg caaaccaggg cgacgttctt
			cttggatggg atacagacca gttccccaca aatatctacg atacaacaat gtgtatgtat
			gaagttatca aggcaggcgg cttcacaaac ggcggtctca acttcgacgc taaggcacgc
			agagggagct tcactcccga ggatatcttc tacagctata tcgcaggtat ggatgcattt
			gctctgggct tcagagctgc tctcaagctt atcgaagacg gacgtatcga caagttcgtt
			gctgacagat acgcttcatg gaataccggt atcggtgcag acataatcgc aggtaaggca
			gatttcgcat ctcttgaaaa gtatgctctt gaaaagggcg aggttacagc ttcactctca
			agcggcagac aggaaatgct ggagtctatc gtaaataacg ttcttttcag tctgtaa (SEQ ID NO: 259)

Xylose	Based on	Based on AJ132472	atggaatttttcagcaatatcggtaaaattcagtatcagggaccaaaaagtactgatcctctctcatttaagtactataacc
isomerase	Ruminococcus		ctgaagaagtcatcaacggaaagacaatgcgcgagcatctgaagttcgctctttcatggtggcacacaatgggcggc
(point	flavefaciens		gacggaacagatatgttcggctgcggcacaacagacaagacctggggacagtccgatcccgctgcaagagcaaa
mutation)	strain 17		ggctaaggttgacgcagcattcgagatcatggataagctctccattgactactattgtttccacgatcgcgatctttctccc
			gagtatggcagcctcaaggctaccaacgatcagcttgacatagttacagactatatcaaggagaagcagggcgaca
			agttcaagtgcctctggggtacagcaaagtgcttcgatcatccaagattcatgcacggtgcaggtacatctccttctgctg
			atgtattcgctttctcagctgctcagatcaagaaggctct G gagtcaacagtaaagctcggcggtaacggttacgttttct
			ggggcggacgtgaaggctatgagacacttcttaatacaaatatgggactcgaactcgacaatatggctcgtcttatga
			agatggctgttgagtatggacgttcgatcggcttcaagggcgacttctatatcgagcccaagcccaaggagcccaca
			aagcatcagtacgatttcgatacagctactgttctgggattcctcagaaagtacggtctcgataaggatttcaagatgaa
			tatcgaagctaaccacgctacacttgctcagcatacattccagcatgagctccgtgttgcaagagacaatggtgtgttcg
			gttctatcgacgcaaaccagggcgacgttcttcttggatgggatacagaccagttccccacaaatatctacgatacaac
			aatgtgtatgtatgaagttatcaaggcaggcggcttcacaaacggcggtctcaacttcgacgctaaggcacgcagag
			ggagcttcactcccgaggatatcttctacagctatatcgcaggtatggatgcatttgctctgggcttcagagctgctctcaa
			gcttatcgaagacggacgtatcgacaagttcgttgctgacagatacgcttcatggaataccggtatcggtgcagacata
			atcgcaggtaaggcagatttcgcatctcttgaaaagtatgctcttgaaaagggcgaggttacagcttcactctcaagcg
			gcagacaggaaatgctggagtctatcgtaaataacgttcttttcagtctgtaa (SEQ ID NO: 260)

Xylose			atggagttcttttctaatataggtaaaattcagtatcaaggtccaaaatc
isomerase			tacagatccattgtcttttaaatattataatccagaagaagttataaatg
(XI-RF_HR)			gtaaaactatgagagaacatttaaaatttgctttgtcttggtggcatact
			atgggtggtgatggtactgatatgttcggttgtggtactactgataaaac
			ttggggtcaatctgatccagctgctagagcaaaagccaaagtagatgcag
			cctttgaaattatggataaattgtctattgattattattgttttcatgat
			agagatttgtctcctgaatatggttctttaaaagcaactaatgatcaatt
			ggacattgttacggattatattaaagaaaaacaaggtgataaatttaaat
			gtttgtggggcactgcgaaatgttttgatcatccacgttttatgcatggt
			gcggggacgagtccttctgctgatgtttttgctttttctgccgctcaaat
			taagaaggcattggaatcaactgttaaattaggtgggaacgggtatgtat
			tctggggaggaagggaaggttatgaaacattattaaacactaatatgggt
			ttggaattggataatatggctagattgatgaaaatggctgtagaatacgg
			aaggtctattggttttaagggtgacttttatattgaaccaaaacctaaag
			agcctactaaacatcaatatgattttgatactgctacagttttgggattc
			ttgagaaaatatggtctggataaagattttaaaatgaatatagaagctaa
			tcatgcaacactcgcacaacatacttttcaacatgaattgagagttgcca
			gagataacggagtttttggatctatcgatgcaaaccagggagacgttttg
			ctaggatgggatactgatcaatttccaactaacatttatgatactactat
			gtgtatgtatgaagtaattaaggcaggaggctttactaatggcggattaa
			actttgatgcgaaggctaggcgtggtagtttcactccagaggatatattc
			tattcttatattgctggaatggatgctttcgcgttaggtttcagggcagc
			actaaaattgattgaagatggtagaattgataagtttgtagctgatagat
			atgcttcttggaatactggaataggagcagatataatcgctgggaaagcc
			gacttcgccagtctggaaaaatatgcgcttgaaaaaggagaagttactgc
			cagcttaagttccggtcgtcaagaaatgttggaatctattgtaaacaatg
			ttttattttctctg (SEQ ID NO: 261)

Xylose	Piromyces sp. E2	AJ249909	atggctaagg aatatttccc acaaattcaa aagattaagt tcgaaggtaa ggattctaag
isomerase			aatccattag ccttccacta ctacgatgct gaaaaggaag tcatgggtaa gaaaatgaag
(XI-P Native)			gattggttac gtttcgccat ggcctggtgg cacactcttt gcgccgaagg tgctgaccaa
			ttcggtggag gtacaaagtc tttcccatgg aacgaaggta ctgatgctat tgaaattgcc
			aagcaaaagg ttgatgctgg tttcgaaatc atgcaaaagc ttggtattcc atactactgt
			ttccacgatg ttgatcttgt ttccgaaggt aactctattg aagaatacga atccaacctt
			aaggctgtcg ttgcttacct caaggaaaag caaaaggaaa ccggtattaa gcttctctgg
			agtactgcta acgtcttcgg tcacaagcgt tacatgaacg gtgcctccac taacccagac
			tttgatgttg tcgcccgtgc tattgttcaa attaagaacg ccatagacgc cggtattgaa
			cttggtgctg aaaactacgt cttctggggt ggtcgtgaag gttacatgag tctccttaac
			actgaccaaa agcgtgaaaa ggaacacatg gccactatgc ttaccatggc tcgtgactac
			gctcgttcca agggattcaa gggtactttc ctcattgaac caaagccaat ggaaccaacc
			aagcaccaat acgatgttga cactgaaacc gctattggtt tccttaaggc ccacaactta
			gacaaggact tcaaggtcaa cattgaagtt aaccacgcta ctcttgctgg tcacactttc
			gaacacgaac ttgcctgtgc tgttgatgct ggtatgctcg gttccattga tgctaaccgt
			ggtgactacc aaaacggttg ggatactgat caattcccaa ttgatcaata cgaactcgtc
			caagcttgga tggaaatcat ccgtggtggt ggtttcgtta ctggtggtac caacttcgat
			gccaagactc gtcgtaactc tactgacctc gaagacatca tcattgccca cgtttctggt
			atggatgcta tggctcgtgc tcttgaaaac gctgccaagc tcctccaaga atctccatac
			accaagatga agaaggaacg ttacgcttcc ttcgacagtg gtattggtaa ggactttgaa
			gatggtaagc tcaccctcga acaagtttac gaatacggta agaagaacgg tgaaccaaag
			caaacttctg gtaagcaaga actctacgaa gctattgttg ccatgtacca ataa (SEQ ID NO: 262)

Xylose	Based on		ATGGCTAAAGAATATTTTCCACAAATTCAGAAAATTAAATTTGAAGGTAAAGATTC
Isomerase	Piromyces sp. E2		TAAAAATCCATTGGCTTTCCATTATTATGATGCTGAAAAAGAAGTTATGGGTAAAA
(XI-P-HR1)			AGATGAAAGATTGGTTGAGATTCGCTATGGCTTGGTGGCATACTCTATGTGCTG
			AAGGAGCTGATCAATTTGGAGGAGGTACTAAATCTTTTCCTTGGAATGAAGGTA
			CTGACGCTATTGAAATTGCTAAGCAGAAAGTAGACGCGGGTTTTGAAATTATGC
			AAAAATTGGGAATACCATATTATTGTTTTCATGATGTTGATTTGGTATCTGAGGGT
			AATTCTATTGAAGAATATGAATCTAATTTAAAAGCTGTTGTTGCTTACTTAAAAGA
			AAAACAAAAAGAAACTGGAATTAAATTGTTGTGGTCTACAGCTAATGTTTTCGGT
			CATAAAAGATATATGAATGGTGCTTCTACAAATCCAGATTTTGATGTTGTAGCTA
			GAGCTATTGTTCAAATTAAAAATGCTATAGATGCAGGAATTGAATTAGGTGCCGA
			AAATTATGTTTTCTGGGGAGGTAGAGAAGGTTATATGTCTTTGTTAAATACTGAT
			CAAAAACGTGAAAAGGAACACATGGCAACTATGTTGACAATGGCTAGGGATTAT
			GCTAGATCTAAAGGTTTTAAAGGTACTTTCTTGATTGAGCCAAAACCTATGGAAC
			CAACTAAACATCAATATGACGTTGACACTGAAACTGCTATTGGTTTCTTAAAAGC
			TCATAATTTGGATAAAGATTTTAAGGTTAATATAGAAGTTAATCATGCTACACTAG
			CTGGTCATACTTTTGAACATGAATTAGCTTGTGCAGTTGATGCCGGTATGTTAGG
			TTCTATCGACGCAAATAGAGGTGATTATCAAAATGGTTGGGACACAGATCAATTT
			CCAATAGATCAATATGAATTGGTTCAAGCATGGATGGAAATTATTAGGGGTGGA
			GGCTTCGTTACAGGTGGAACTAATTTTGATGCTAAAACTAGGAGAAATTCTACAG
			ATCTTGAAGATATAATTATTGCTCATGTATCTGGTATGGATGCGATGGCCCGTGC
			TTTGGAAAATGCAGCTAAATTACTTCAAGAATCTCCTTATACTAAAATGAAAAAGG
			AAAGATATGCTTCTTTTGATTCTGGAATAGGTAAGGATTTTGAAGATGGTAAATT
			GACATTGGAACAAGTTTATGAATATGGTAAGAAGAATGGAGAACCAAAACAAACT
			TCTGGTAAACAAGAATTATATGAGGCTATAGTAGCTATGTATCAAtaa (SEQ ID
			NO: 263)

PEP	Zymomonas	ATCC 31821	ACTAGTAAAAAAATGACCAAGCCGCGCACAATTAATCAGAACCCAGACCTTCGC
Carboxylase	mobilis		TATTTTGGTAACCTGCTCGGTCAGGTTATTAAGGAACAAGGCGGAGAGTCTTTAT
(PEPC-			TCAACCAGATCGAGCAAATTCGCTCTGCCGCGATTAGACGCCATCGGGGTATTG
Native)			TTGACAGCACCGAGCTAAGTTCTCGCTTAGCCGATCTCGACCTTAATGACATGT
			TCTCTTTTGCACATGCCTTTTTGCTGTTTTCAATGCTGGCCAATTTGGCTGATGA
			TCGTCAGGGAGATGCCCTTGATCCTGATGCCAATATGGCAAGTGCCCTTAAGGA
			CATAAAAGCCAAAGGCGTCAGTCAGCAGGCGATCATTGATATGATCGACAAAGC
			CTGCATTGTGCCTGTTCTGACAGCACATCCGACCGAAGTCCGTCGGAAAAGTAT
			GCTTGACCATTATAATCGCATTGCAGGTTTAATGCGGTTAAAAGATGCTGGACAA
			ACGGTGACCGAAGATGGTCTTCCGATCGAAGATGCGTTAATCCAGCAAATCACG
			ATATTATGGCAGACTCGTCCGCTCATGCTGCAAAAGCTGACCGTGGCTGATGAA
			ATCGAAACTGCCCTGTCTTTCTTAAGAGAAACTTTTCTGCCTGTTCTGCCCCAGA
			TTTATGCAGAATGGGAAAAATTGCTTGGTAGTTCTATTCCAAGCTTTATCAGACC
			TGGTAATTGGATTGGTGGTGACCGTGACGGTAACCCCAATGTCAATGCCGATAC
			GATCATGCTGTCTTTGAAGCGCAGCTCGGAAACGGTATTGACGGATTATCTCAA
			CCGTCTTGATAAACTGCTTTCCAACCTTTCGGTCTCAACCGATATGGTTTCGGTA
			TCCGATGATATTCTACGTCTAGCCGATAAAAGTGGTGACGATGCTGCGATCCGT
			GCGGATGAACCTTATCGTCGTGCCTTAAATGGTATTTATGACCGTTTAGCCGCTA
			CCTATCGTCAGATCGCCGGTCGCAACCCTTCGCGCCCAGCCTTGCGTTCTGCA
			GAAGCCTATAAACGGCCTCAAGAATTGCTGGCTGATTTGAAGACCTTGGCCGAA
			GGCTTGGGTAAATTGGCAGAAGGTAGTTTTAAGGCATTGATCCGTTCGGTTGAA
			ACCTTTGGTTTCCATTTGGCCACCCTCGATCTGCGTCAGAATTCGCAGGTTCAT
			GAAAGAGTTGTCAATGAACTGCTACGGACAGCCACCGTTGAAGCCGATTATTTA
			TCTCTATCGGAAGAAGATCGCGTTAAGCTGTTAAGACGGGAATTGTCGCAGCCG
			CGGACTCTATTCGTTCCGCGCGCCGATTATTCCGAAGAAACGCGTTCTGAACTT
			GATATTATTCAGGCAGCAGCCCGCGCCCATGAAATTTTTGGCCCTGAATCCATT
			ACGACTTATTTGATTTCGAATGGCGAAAGCATTTCCGATATTCTGGAAGTCTATT
			TGCTTTTGAAAGAAGCAGGGCTGTATCAAGGGGGTGCTAAGCCAAAAGCGGCG
			ATTGAAGCTGCGCCTTTATTCGAGACGGTGGCCGATCTTGAAAATGCGCCAAAG
			GTCATGGAGGAATGGTTCAAGCTGCCTGAAGCGCAAGCCATTGCAAAGGCACA
			TGGCGTTCAGGAAGTGATGGTTGGCTATTCTGACTCCAATAAGGACGGCGGATA
			TCTGACCTCGGTTTGGGGTCTTTATAAGGCTTGCCTCGCTTTGGTGCCGATTTTT
			GAGAAAGCCGGTGTACCGATCCAGTTTTTCCATGGACGGGGTGGTTCCGTTGG
			TCGCGGTGGTGGTTCCAACTTTAATGCCATTCTGTCGCAGCCAGCCGGAGCCG
			TCAAAGGGCGTATCCGTTATACAGAACAGGGTGAAGTCGTGGCGGCCAAATAT
			GGCACCCATGAAAGCGCTATTGCCCATCTGGATGAGGCCGTAGCGGCGACTTT
			GATTACGTCTTTGGAAGCACCGACCATTGTCGAGCCAGAGTTTAGTCGTTACCG
			TAAGGCCTTGGATCAGATCTCAGATTCAGCTTTCCAGGCCTATCGCCAATTGGT
			CTATGGAACGAAGGGCTTCCGTAAATTCTTTAGTGAATTTACGCCTTTGCCGGAA
			ATTGCCCTGTTAAAGATCGGGTCACGCCCACCTAGCCGCAAAAAATCCGACCG
			GATTGAAGATCTACGCGCTATTCCTTGGGTGTTTAGCTGGTCTCAAGTTCGAGT
			CATGTTACCCGGTTGGTTCGGTTTCGGTCAGGCTTTATATGACTTTGAAGATACC
			GAGCTGTTACAGGAAATGGCAAGCCGTTGGCCGTTTTTCCGCACGACTATTCGG
			AATATGGAACAGGTGATGGCACGTTCCGATATGACGATCGCCAAGCATTATCTG
			GCCTTGGTTGAGGATCAGACAAATGGTGAGGCTATCTATGATTCTATCGCGGAT
			GGCTGGAATAAAGGTTGTGAAGGTCTGTTAAAGGCAACCCAGCAGAATTGGCTG
			TTGGAACGCTTTCCGGCGGTTGATAATTCGGTGCAGATGCGTCGGCCTTATCTG
			GAACCGCTTAATTACTTACAGGTCGAATTGCTGAAGAAATGGCGGGGAGGTGAT
			ACCAACCCGCATATCCTCGAATCTATTCAGCTGACAATCAATGCCATTGCGACG
			GCACTTCGCAACAGCGGTTAATAACTCGAG (SEQ ID NO: 264)

PEP	Based on		ACTAGTAAAAAAATGACCAAGCCAAGAACTATTAACCAAAACCCAGACTTGAGAT
Carboxylase	Zymomonas		ACTTCGGTAACTTGTTGGGTCAAGTTATCAAGGAACAAGGTGGTGAATCTTTGTT
(PEPC-HR)	mobilis		CAACCAAATTGAACAAATCAGATCCGCTGCTATTAGAAGACACAGAGGTATCGT
			CGACTCTACCGAATTGTCCTCTAGATTGGCTGACTTGGACTTGAACGACATGTT
			CTCCTTCGCTCACGCTTTCTTGTTGTTCTCTATGTTGGCTAACTTGGCTGACGAC
			AGACAAGGTGACGCTTTGGACCCAGACGCTAACATGGCTTCCGCTTTGAAGGA
			CATTAAGGCTAAGGGTGTTTCTCAACAAGCTATCATTGACATGATCGACAAGGCT
			TGTATTGTCCCAGTTTTGACTGCTCACCCAACCGAAGTCAGAAGAAAGTCCATG
			TTGGACCACTACAACAGAATCGCTGGTTTGATGAGATTGAAGGACGCTGGTCAA
			ACTGTTACCGAAGACGGTTTGCCAATTGAAGACGCTTTGATCCAACAAATTACTA
			TCTTGTGGCAAACCAGACCATTGATGTTGCAAAAGTTGACTGTCGCTGACGAAA
			TTGAAACCGCTTTGTCTTTCTTGAGAGAAACTTTCTTGCCAGTTTTGCCACAAAT
			CTACGCTGAATGGGAAAAGTTGTTGGGTTCCTCTATTCCATCCTTCATCAGACCA
			GGTAACTGGATTGGTGGTGACAGAGACGGTAACCCAAACGTCAACGCTGACAC
			CATCATGTTGTCTTTGAAGAGATCCTCTGAAACTGTTTTGACCGACTACTTGAAC
			AGATTGGACAAGTTGTTGTCCAACTTGTCTGTCTCCACTGACATGGTTTCTGTCT
			CCGACGACATTTTGAGATTGGCTGACAAGTCTGGTGACGACGCTGCTATCAGAG
			CTGACGAACCATACAGAAGAGCTTTGAACGGTATTTACGACAGATTGGCTGCTA
			CCTACAGACAAATCGCTGGTAGAAACCCATCCAGACCAGCTTTGAGATCTGCTG
			AAGCTTACAAGAGACCACAAGAATTGTTGGCTGACTTGAAGACTTTGGCTGAAG
			GTTTGGGTAAGTTGGCTGAAGGTTCCTTCAAGGCTTTGATTAGATCTGTTGAAAC
			CTTCGGTTTCCACTTGGCTACTTTGGACTTGAGACAAAACTCCCAAGTCCACGA
			AAGAGTTGTCAACGAATTGTTGAGAACCGCTACTGTTGAAGCTGACTACTTGTCT
			TTGTCCGAAGAAGACAGAGTCAAGTTGTTGAGAAGAGAATTGTCTCAACCAAGA
			ACCTTGTTCGTTCCAAGAGCTGACTACTCCGAAGAAACTAGATCTGAATTGGAC
			ATCATTCAAGCTGCTGCTAGAGCTCACGAAATCTTCGGTCCAGAATCCATTACCA
			CTTACTTGATCTCTAACGGTGAATCCATTTCTGACATCTTGGAAGTCTACTTGTT
			GTTGAAGGAAGCTGGTTTGTACCAAGGTGGTGCTAAGCCAAAGGCTGCTATTGA
			AGCTGCTCCATTGTTCGAAACCGTTGCTGACTTGGAAAACGCTCCAAAGGTCAT
			GGAAGAATGGTTCAAGTTGCCAGAAGCTCAAGCTATCGCTAAGGCTCACGGTGT
			TCAAGAAGTCATGGTTGGTTACTCCGACTCTAACAAGGACGGTGGTTACTTGAC
			TTCCGTCTGGGGTTTGTACAAGGCTTGTTTGGCTTTGGTTCCAATTTTCGAAAAG
			GCTGGTGTCCCAATCCAATTCTTCCACGGTAGAGGTGGTTCTGTTGGTAGAGGT
			GGTGGTTCCAACTTCAACGCTATTTTGTCTCAACCAGCTGGTGCTGTCAAGGGT
			AGAATCAGATACACCGAACAAGGTGAAGTTGTCGCTGCTAAGTACGGTACTCAC
			GAATCCGCTATTGCTCACTTGGACGAAGCTGTTGCTGCTACCTTGATCACTTCTT
			TGGAAGCTCCAACCATTGTCGAACCAGAATTCTCCAGATACAGAAAGGCTTTGG
			ACCAAATCTCTGACTCCGCTTTCCAAGCTTACAGACAATTGGTTTACGGTACTAA
			GGGTTTCAGAAAGTTCTTCTCTGAATTCACCCCATTGCCAGAAATTGCTTTGTTG
			AAGATCGGTTCCAGACCACCATCTAGAAAGAAGTCCGACAGAATTGAAGACTTG
			AGAGCTATCCCATGGGTCTTCTCTTGGTCCCAAGTTAGAGTCATGTTGCCAGGT
			TGGTTCGGTTTCGGTCAAGCTTTGTACGACTTCGAAGACACTGAATTGTTGCAA
			GAAATGGCTTCTAGATGGCCATTCTTCAGAACCACTATTAGAAACATGGAACAAG
			TTATGGCTAGATCCGACATGACCATCGCTAAGCACTACTTGGCTTTGGTCGAAG
			ACCAAACTAACGGTGAAGCTATTTACGACTCTATCGCTGACGGTTGGAACAAGG
			GTTGTGAAGGTTTGTTGAAGGCTACCCAACAAAACTGGTTGTTGGAAAGATTCC
			CAGCTGTTGACAACTCCGTCCAAATGAGAAGACCATACTTGGAACCATTGAACT
			ACTTGCAAGTTGAATTGTTGAAGAAGTGGAGAGGTGGTGACACTAACCCACACA
			TTTTGGAATCTATCCAATTGACCATTAACGCTATCGCTACTGCTTTGAGAAACTC
			CGGTTAATAACTCGAG (SEQ ID NO: 265)

EDA	Zymomonas	31821D-5	5′-aactgactagtaaaaaaatgcgtgatatcgattcc-3′ (SEQ ID No: 1)
Primers	mobilis (ZM4)		5′-agtaactcgagctactaggcaacagcagcgcgcttg-3′ (SEQ ID No: 2)

EDD	Zymomonas	31821D-5	5′-aactgactagtaaaaaaatgactgatctgcattcaacg-3′ (SEQ ID NO: 3)
Primers	mobilis (ZM4)		5′-agtaactcgagctactagataccggcacctgcatatattgc-3′ (SEQ ID NO: 4)

EDA	Escherichia coli		5′-aactgactagtaaaaaaatgaaaaactggaaaacaagtgcagaatc-3′ (SEQ ID NO: 5)
Primers			5′-agtaactcgagctactacagcttagcgccttctacagcttcacg-3′ (SEQ ID NO: 6)

EDD	Escherichia coli		5′-aactgactagtaaaaaaatgaatccacaattgttacgcgtaacaaatcg-3′(SEQ ID NO: 7)
Primers			5′agtaactcgagctactaaaaagtgatacaggttgcgccctgttcggcac-3′ (SEQ ID NO: 8)

PFK primers	Saccharomyces	4015893	5′-tgcatattccgttcaatcttataaagctgccatagatttttacaccaagtcgttttaagagcttggtgagcgcta-3′
	cerevisiae		(SEQ ID NO: 9)
	YGR240CBY4742		5′-cttgccagtgaatgacctttggcattctcatggaaacttcagtttcatagtcgagttcaagagaaaaaaaaagaa-
			3′ (SEQ ID NO: 10)
			5′-atgactgttactactccttttgtgaatggtacttcttattgtaccgtcactgcatattccgttcaatcttataaa-3′ (SEQ ID
			NO: 11)
			5′-ttaatcaactctctttcttccaaccaaatggtcagcaatgagtctggtagcttgccagtgaatgacctttggcat-
			3′(SEQ ID NO: 12)

Thymidilate	Saccharomyces	208583	CDC21_fwd: 5′-aatcgatcaaagcttctaaatacaagacgtgcgatgacgactatactggac-3′ (SEQ ID
synthase	cerevisiae strain		NO: 52)

Primers	17206		CDC21_rev: 5′-taccgtactacccgggtatatagtctttttgccctggtgttccttaataatttc-3′ (SEQ ID NO:
(cdc21)			53)
			ThymidylateSynthase::cdc21 fwd: 5′-ctaaatacaagacgtgcgatgacgactatactgg-3′ (SEQ
			ID NO: 58)
			ThymidylateSynthase::cdc21 rev: 5′-gtcaacaagaactaaaaaattgttcaaaaatgcaattgtc-3′.
			(SEQ ID NO: 59)

LYS2	BR214-4a	208600	Lys2Fwd: 5′-tgctaatgacccgggaattccacttgcaattacataaaaaattccggcgg-3′ (SEQ ID NO:
			54)
			Lys2Rev: 5′-atgatcattgagctcagcttcgcaagtattcattttagacccatggtgg-3′. (SEQ ID NO: 55)

PEPC	Zymomonas			5′ forward (5′-
Primers	mobilis		GACTAACTGAACTAGTAAAAAAATGACCAAGCCGCGCACAATTAATCAG-3′)
			(SEQ ID NO: 13)
			3′ reverse (5′-
			AAGTGAGTAACTCGAGTTATTAACCGCTGTTGCGAAGTGCCGTCGC-3′). (SEQ ID
			NO: 14)

Provided hereafter are non-limiting examples of certain amino acid sequences.


		Amino acid
	Organism/ATCC	Accession No. or
Gene Name	identifier	other identifier	Amino Acid Sequence

Xylose	Ruminococcus	CAB51938.1	MEFFSNIGKIQYQGPKSTDPLSFKYYNPEEVINGKTMREHLKFALSWWHTMGGDGTDM
Isomerase	flavefaciens		FGCGTTDKTWGQSDPAARAKAKVDAAFEIMDKLSIDYYCFHDRDLSPEYGSLKATNDQL
(XI-RF	strain 17		DIVTDYIKEKQGDKFKCLWGTAKCFDHPRFMHGAGTSPSADVFAFSAAQIKKALESTVKL
Native)			GGNGYVFWGGREGYETLLNTNMGLELDNMARLMKMAVEYGRSIGFKGDFYIEPKPKEP
			TKHQYDFDTATVLGFLRKYGLDKDFKMNIEANHATLAQHTFQHELRVARDNGVFGSIDA
			NQGDVLLGWDTDQFPTNIYDTTMCMYEVIKAGGFTNGGLNFDAKARRGSFTPEDIFYSY
			IAGMDAFALGFRAALKLIEDGRIDKFVADRYASWNTGIGADIIAGKADFASLEKYALEKG
			EVTASLSSGRQEMLESIVNNVLFSL (SEQ ID NO: 274)

Xylose	Piromyces	CAB76571.1	MAKEYFPQIQKIKFEGKDSKNPLAFHYYDAEKEVMGKKMKDWLR
isomerase	sp. E2		FAMAWWHTLCAEGADQFGGGTKSFPWNEGTDAIEIAKQKVDAGFEIMQKLGIPYYCFH
(XI-P Native)			DVDLVSEGNSIEEYESNLKAVVAYLKEKQKETGIKLLWSTANVFGHKRYMNGASTNPD
			FDVVARAIVQIKNAIDAGIELGAENYVFWGGREGYMSLLNTDQKREKEHMATMLTMAR
			DYARSKGFKGTFLIEPKPMEPTKHQYDVDTETAIGFLKAHNLDKDFKVNIEVNHATLA
			GHTFEHELACAVDAGMLGSIDANRGDYQNGWDTDQFPIDQYELVQAWMEIIRGGGFVT
			GGTNFDAKTRRNSTDLEDIIIAHVSGMDAMARALENAAKLLQESPYTKMKKERYASFDSG
			IGKDFEDGKLTLEQVYEYGKKNGEPKQTSGKQELYEAIVAMYQ (SEQ ID NO: 275)

Example 9

Activation of the Entner-Doudoroff Pathway in Yeast Cells Using EDD and EDA Genes from Pseudomonas aeruginosa Strain PAO1

Pseudomonas aeruginosa strain PAO1 DNA was prepared using Qiagen DNeasy Blood and Tissue kit (Qiagen, Valencia, Calif.) according to the manufacture's instructions. The P. aeruginosa edd and eda constructs were isolated from P. aeruginosa genomic DNA using the following oligonucleotides:

The P. aeruginosa edd gene:

(SEQ ID NO: 63)

5′-aactgaactgactagtaaaaaaatgcaccctcgtgtgctcgaagt-

3′

(SEQ ID NO: 64)

5′-agtaaagtaaaagcttctactagcgccagccgttgaggctct-3′

The P. aeruginosa edd gene with 6-HIS c-terminal

tag (SEQ ID NO: 35):

(SEQ ID NO 63)

5′-aactgaactgactagtaaaaaaatgcaccctcgtgtgctcgaagt-

3′

(SEQ ID NO: 65)

5′-agtaaagtaaaagcttctactaatgatgatgatgatgatggcgccag

ccgttgaggctc-3′

The P. aeruginosa eda gene:

(SEQ ID NO: 66)

5′-aactgaactgactagtaaaaaaatgcacaaccttgaacagaagacc-

3′

(SEQ ID NO: 67)

5′-agtaaagtaactcgagctattagtgtctgcggtgctcggcgaa-3′

The P. aeruginosa eda gene with 6-HIS c-terminal

tag (SEQ ID NO: 35):

(SEQ ID NO: 66)

5′-aactgaactgactagtaaaaaaatgcacaaccttgaacagaagacc-

3′

(SEQ ID NO: 68)

5′-taaagtaactcgagctactaatgatgatgatgatgatggtgtctgcg

gtgctcggcgaa-3′

All oligonucleotides set forth above were purchased from Integrated technologies (“IDT”, Coralville, Iowa). These oligonucleotides were designed to incorporate a SpeI restriction endonuclease cleavage site upstream of a HindIII restriction endonuclease cleavage site or downstream of an XhoI restriction endonuclease cleavage site, with respect to the edd and eda gene constructs. These restriction endonuclease sites could be used to clone the edd and eda genes into yeast expression vectors p426GPD (ATCC accession number 87361) and p425GPD (ATCC accession number 87359). In addition to incorporating restriction endonuclease cleavage sites, the forward oligonucleotides also incorporate six consecutive A nucleotides (e.g., AAAAAA) immediately upstream of the ATG initiation codon. The six consecutive A nucleotides ensured that there was a conserved ribosome binding sequence for efficient translation initiation in yeast.
PCR amplification of the genes were performed as follows: about 100 ng of the genomic P. aeruginosa PAO1 DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers (SEQ. ID. NOS: 63-68, and combinations as indicated), and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. This was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 50° C. (eda amplifications) or 53° C. (edd amplifications) for 30 seconds, and 72° C. for 15 seconds (eda amplifications) or 30 seconds (edd amplifications). A final 5 minute extension reaction at 72° C. also was included. The about 670 bp (eda) or 1830 bp product (edd) was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations.
The nucleotide and amino acid sequences of the P. aeruginosa edd and eda genes are given below as SEQ ID NOS. 69-72.

P. aeruginosa edd nucleotide sequence:

SEQ ID NO: 69

ATGCACCCTCGTGTGCTCGAAGTCACCCGCCGCATCCAGGCCCGTAGCGCGGCCACTCGCC

AGCGCTACCTCGAGATGGTCCGGGCTGCGGCCAGCAAGGGGCCGCACCGCGGCACCCTGC

CGTGCGGCAACCTCGCCCACGGGGTCGCGGCCTGTGGCGAAAGCGACAAGCAGACCCTGC

GGCTGATGAACCAGGCCAACGTGGCCATCGTTTCCGCCTACAACGACATGCTCTCGGCGCAC

CAGCCGTTCGAGCGCTTTCCGGGGCTGATCAAGCAGGCGCTGCACGAGATCGGTTCGGTCG

GCCAGTTCGCCGGCGGCGTGCCGGCCATGTGCGACGGGGTGACCCAGGGCGAGCCGGGCA

TGGAACTGTCGCTGGCCAGCCGCGACGTGATCGCCATGTCCACCGCCATCGCGCTGTCTCA

CAACATGTTCGATGCAGCGCTGTGCCTGGGTGTTTGCGACAAGATCGTGCCGGGCCTGCTGA

TCGGCTCGCTGCGCTTCGGCCACCTGCCCACCGTGTTCGTCCCGGCCGGGCCGATGCCGAC

CGGCATCTCCAACAAGGAAAAGGCCGCGGTGCGCCAACTGTTCGCCGAAGGCAAGGCCACT

CGCGAAGAGCTGCTGGCCTCGGAAATGGCCTCCTACCATGCACCCGGCACCTGCACCTTCTA

TGGCACCGCCAATACCAACCAGTTGCTGGTGGAGGTGATGGGCCTGCACTTGCCCGGTGCC

TCCTTCGTCAACCCGAACACCCCCCTGCGCGACGAACTCACCCGCGAAGCGGCACGCCAGG

CCAGCCGGCTGACCCCCGAGAACGGCAACTACGTGCCGATGGCGGAGATCGTCGACGAGAA

GGCCATCGTCAACTCGGTGGTGGCGCTGCTCGCCACCGGCGGCTCGACCAACCACACCCTG

CACCTGCTGGCGATCGCCCAGGCGGCGGGCATCCAGTTGACCTGGCAGGACATGTCCGAGC

TGTCCCATGTGGTGCCGACCCTGGCGCGCATCTATCCGAACGGCCAGGCCGACATCAACCA

CTTCCAGGCGGCCGGCGGCATGTCCTTCCTGATCCGCCAACTGCTCGACGGCGGGCTGCTT

CACGAGGACGTACAGACCGTCGCCGGCCCCGGCCTGCGCCGCTACACCCGCGAGCCGTTC

CTCGAGGATGGCCGGCTGGTCTGGCGCGAAGGGCCGGAACGGAGTCTCGACGAAGCCATC

CTGCGTCCGCTGGACAAGCCGTTCTCCGCCGAAGGCGGCTTGCGCCTGATGGAGGGCAACC

TCGGTCGCGGCGTGATGAAGGTCTCGGCGGTGGCGCCGGAACACCAGGTGGTCGAGGCGC

CGGTACGGATCTTCCACGACCAGGCCAGCCTGGCCGCGGCCTTCAAGGCCGGCGAGCTGGA

GCGCGACCTGGTCGCCGTGGTGCGTTTCCAGGGCCCGCGGGCGAACGGCATGCCGGAGCT

GCACAAGCTCACGCCGTTCCTCGGGGTCCTGCAGGATCGTGGCTTCAAGGTGGCGCTGGTC

ACCGACGGGCGCATGTCCGGGGCGTCGGGCAAGGTGCCCGCGGCCATCCATGTGAGTCCG

GAAGCCATCGCCGGCGGTCCGCTGGCGCGCCTGCGCGACGGCGACCGGGTGCGGGTGGAT

GGGGTGAACGGCGAGTTGCGGGTGCTGGTCGACGACGCCGAATGGCAGGCGCGCAGCCTG

GAGCCGGCGCCGCAGGACGGCAATCTCGGTTGCGGCCGCGAGCTGTTCGCCTTCATGCGCA

ACGCCATGAGCAGCGCGGAAGAGGGCGCCTGCAGCTTTACCGAGAGCCTCAACGGCTGGCG

CTAGTAG

P. aeruginosa edd amino sequence:

SEQ ID NO: 70

MHPRVLEVTRRIQARSAATRQRYLEMVRAAASKGPHRGTLPCGNLAHGVAACGESDKQTLRLMN

QANVAIVSAYNDMLSAHQPFERFPGLIKQALHEIGSVGQFAGGVPAMCDGVTQGEPGMELSLASR

DVIAMSTAIALSHNMFDAALCLGVCDKIVPGLLIGSLRFGHLPTVFVPAGPMPTGISNKEKAAVRQL

FAEGKATREELLASEMASYHAPGTCTFYGTANTNQLLVEVMGLHLPGASFVNPNTPLRDELTREA

ARQASRLTPENGNYVPMAEIVDEKAIVNSVVALLATGGSTNHTLHLLAIAQAAGIQLTWQDMSELS

HVVPTLARIYPNGQADINHFQAAGGMSFLIRQLLDGGLLHEDVQTVAGPGLRRYTREPFLEDGRLV

WREGPERSLDEAILRPLDKPFSAEGGLRLMEGNLGRGVMKVSAVAPEHQVVEAPVRIFHDQASLA

AAFKAGELERDLVAVVRFQGPRANGMPELHKLTPFLGVLQDRGFKVALVTDGRMSGASGKVPAAI

HVSPEAIAGGPLARLRDGDRVRVDGVNGELRVLVDDAEWQARSLEPAPQDGNLGCGRELFAFM

RNAMSSAEEGACSFTESLNGWR

P. aeruginosa eda nucleotide sequence:

SEQ ID NO: 71

ATGCACAACCTTGAACAGAAGACCGCCCGCATCGACACGCTGTGCCGGGAGGCGCGCATCC

TCCCGGTGATCACCATCGACCGCGAGGCGGACATCCTGCCGATGGCCGATGCCCTCGCCGC

CGGCGGCCTGACCGCCCTGGAGATCACCCTGCGCACGGCGCACGGGCTGACCGCCATCCG

GCGCCTCAGCGAGGAGCGCCCGCACCTGCGCATCGGCGCCGGCACCGTGCTCGACCCGCG

GACCTTCGCCGCCGCGGAAAAGGCCGGGGCGAGCTTCGTGGTCACCCCGGGTTGCACCGA

CGAGTTGCTGCGCTTCGCCCTGGACAGCGAAGTCCCGCTGTTGCCCGGCGTGGCCAGCGCT

TCCGAGATCATGCTCGCCTACCGCCATGGCTACCGCCGCTTCAAGCTGTTTCCCGCCGAAGT

CAGCGGCGGCCCGGCGGCGCTGAAGGCGTTCTCGGGACCATTCCCCGATATCCGCTTCTGC

CCCACCGGAGGCGTCAGCCTGAACAATCTCGCCGACTACCTGGCGGTACCCAACGTGATGT

GCGTCGGCGGCACCTGGATGCTGCCCAAGGCCGTGGTCGACCGCGGCGACTGGGCCCAGG

TCGAGCGCCTCAGCCGCGAAGCCCTGGAGCGCTTCGCCGAGCACCGCAGACACTAATAG

P. aeruginosa eda amino sequence:

SEQ ID NO: 72

MHNLEQKTARIDTLCREARILPVITIDREADILPMADALAAGGLTALEITLRTAHGLTAIRRLSEERPH

LRIGAGTVLDPRTFAAAEKAGASFVVTPGCTDELLRFALDSEVPLLPGVASASEIMLAYRHGYRRF

KLFPAEVSGGPAALKAFSGPFPDIRFCPTGGVSLNNLADYLAVPNVMCVGGTWMLPKAVVDRGD

WAQVERLSREALERFAEHRRH

Cloning of PAO1 Edd and Eda Genes into Yeast Expression Vectors
Following sequence confirmation (GeneWiz), the about 670 bp SpeI-XhoI eda and about 1830 bp SpeI-HindIII edd fragments were cloned into the corresponding restriction sites in plasmids p425GPD and p426GPD vectors (Mumberg et al., 1995, Gene 156: 119-122; obtained from ATCC #87361; PubMed: 7737504), respectively. Briefly, about 50 ng of SpeI-XhoI-digested p425GPD vector was ligated to about 50 ng of SpeI/XhoI-restricted eda fragment in a 10 μl reaction with 1× T4 DNA ligase buffer and 1 U T4 DNA ligase (Fermentas) overnight at 16° C. About 3 μl of this reaction was used to transform DH5α competent cells (Zymo Research) and plated onto LB agar media containing 100 μg/ml ampicillin. Similarly, about 50 ng of SpeI-HindIII-digested p426GPD vector was ligated to about 42 ng of SpeI/HindIII-restricted edd fragment in a 10 μl reaction with 1× T4 DNA ligase buffer and 1 U T4 DNA ligase (Fermentas) overnight at 16° C. About 3 μl of this reaction was used to transform DH5α competent cells (Zymo Research) and plated onto LB agar media containing 100 μg/ml ampicillin.
A haploid Saccharomyces cerevisiae strain (BY4742; ATCC catalog number 201389) was cultured in YPD media (10 g Yeast Extract, 20 g Bacto-Peptone, 20 g Glucose, 1 L total) at about 30° C. Separate aliquots of these cultured cells were transformed with a plasmid construct(s) containing the eda gene alone, the eda and edd genes, or with vector alone. Transformation was accomplished using the Zymo frozen yeast transformation kit (Catalog number T2001; Zymo Research Corp., Orange, Calif.). To 50 μl of cells was added approximately 0.5-1 μg plasmid DNA and the cells were cultured on SC drop out media with glucose minus leucine (eda), minus uracil and minus leucine (eda and edd) (about 20 g glucose; about 2.21 g SC drop-out mix [described below], about 6.7 g yeast nitrogen base, all in about 1 L of water); this mixture was cultured for 2-3 days at about 30° C. SC drop-out mix contained the following ingredients (Sigma); all indicated weights are approximate:


0.4 g	Adenine hemisulfate
3.5 g	Arginine
1 g	Glutamic Acid
0.433 g	Histidine
0.4 g	Myo-Inositol
5.2 g	Isoleucine
2.63 g	Leucine
0.9 g	Lysine
1.5 g	Methionine
0.8 g	Phenylalanine
1.1 g	Serine
1.2 g	Threonine
0.8 g	Tryptophan
0.2 g	Tyrosine
0.2 g	Uracil
1.2 g	Valine

Activity and Western Analyses
Cell lysates of the various EDD and EDA expressing strains were prepared as follows. About 50 to 100 ml of SCD-ura-leu media containing 10 mM MnCl₂was used to culture strains containing the desired plasmid constructs. When cultured aerobically, strains were grown in a 250 ml baffled shaker flask. When grown anaerobically, 400 μl/L Tween-80 (British Drug Houses, Ltd., West Chester, Pa.) plus 0.01 g/L Ergosterol (Alef Aesar, Ward Hill, Mass.) were added and the culture was grown in a 250 ml serum bottle outfitted with a butyl rubber stopper with an aluminum crimp cap. Each strain was inoculated at an initial OD₆₀₀of about 0.2 and grown to an OD₆₀₀of about 3-4. Cells were grown at 30° C. at 200 rpm.
Yeast cells were harvested by centrifugation at 1046×g (e.g., approximately 3000 rpm) for 5 minutes at 4° C. The supernatant was discarded and the cells were resuspended in 25 mL cold sterile water. This wash step was repeated once. Washed cell pellets were resuspended in 1 mL sterile water, transferred to 1.5 mL screw cap tube, and centrifuged at 16,100×g (e.g., approximately 13,200 rpm) for 3 minutes at 4° C.
Cell pellets were resuspended in about 800-1000 μl of freshly prepared lysis buffer (50 mM Tris-Cl pH 7.0, 10 mM MgCl2, 1× protease inhibitor cocktail EDTA-free (Thermo Scientific, Waltham, Mass.) and the tube filled with zirconia beads to avoid any headspace in the tube. The tubes were placed in a Mini BeadBeater (Bio Spec Products, Inc., Bartlesville, Okla.) and vortexed twice for 30 seconds at room temperature. The supernatant was transferred to a new 1.5 mL microcentrifuge tube and centrifuged twice to remove cell debris at 16,100×g (e.g., approximately 13,200 rpm) for 10 minutes, at 4° C. Quantification of the lysates was performed using the Coomassie-Plus kit (Thermo Scientific, San Diego, Calif.) as directed by the manufacturer ('6-HIS' below disclosed as SEQ ID NO: 35).


Strain	EDD	EDA

BF428	p426GPD (vector control)	p425GPD (vector control)
BF604	E. coli native	E. coli native
BF460	E. coli native with 6-HIS	E. coli native with 6-HIS
BF591	PAO1 native	PAO1 native
BF568	PAO1 native with 6-HIS	PAO1 native with 6-HIS
BF592	PAO1 native	E. coli native
BF603	E. coli native	PAO1 native

About 5-10 μg of total cell extract was used for SDS-gel [NuPage 4-12% Bis-Tris gels (Life Technologies, Carlsbad, Calif.)] electrophoresis and Western blot analyses.
SDS-PAGE gels were performed according to the manufacturer's recommendation using NuPage MES-SDS Running Buffer at 1× concentration with the addition of NuPage antioxidant into the cathode chamber at a 1× concentration. Novex Sharp Protein Standards (Life Technologies, Carlsbad, Calif.) were used as standards. For Western analysis, gels were transferred onto a nitrocellulose membrane (0.45 micron, Thermo Scientific, San Diego, Calif.) using Western blotting filter paper (Thermo Scientific) using a Bio-Rad Mini Trans-Blot Cell (BioRad, Hercules, Calif.) system for approximately 90 minutes at 40V. Following transfer, the membrane was washed in 1× PBS (EMD, San Diego, Calif.), 0.05% Tween-20 (Fisher Scientific, Fairlawn, N.J.) for 2-5 minutes with gentle shaking. The membrane was blocked in 3% BSA dissolved in 1×PBS and 0.05% Tween-20 at room temperature for about 2 hours with gentle shaking. The membrane was washed once in 1×PBS and 0.05% Tween-20 for about 5 minutes with gentle shaking. The membrane was then incubated at room temperature with the 1:5000 dilution of primary antibody (Ms mAB to 6×His Tag (SEQ ID NO: 35), AbCam, Cambridge, Mass.) in 0.3% BSA (Fraction V, EMD, San Diego, Calif.) dissolved in 1×PBS and 0.05% Tween-20 with gentle shaking.
Incubation was allowed to proceed for about 1 hour with gentle shaking. The membrane was then washed three times for 5 minutes each with 1×PBS and 0.05% Tween-20 with gentle shaking. The secondary antibody [Dnk pAb to Ms IgG (HRP), AbCam, Cambridge, Mass.] was used at 1:15000 dilution in 0.3% BSA and allowed to incubate for about 90 minutes at room temperature with gentle shaking. The membrane was washed three times for about 5 minutes using 1×PBS and 0.05% Tween-20 with gentle shaking. The membrane incubated with 5 ml of Supersignal West Pico Chemiluminescent substrate (Thermo Scientific, San Diego, Calif.) for 1 minute and then was exposed to a phosphorimager (Bio-Rad Universal Hood II, Bio-Rad, Hercules, Calif.) for about 10-100 seconds.
The results of the Western blots, shown in FIGS. 8A and 8B. Included in the expression data are engineered and/or optimized versions of certain eda and edd genes. The genes were modified to include a C-terminal HIS tag to facilitate purification. The two letters refer to the EDD and EDA source, respectively. P is from P. aeruginosa, PAO1, E is from E. coli, Z is from Zymomonas mobilis ZM4, hot rod is the optimized version of Zymomonas mobilis, Harmonized is the codon harmonized version of Zymomonas mobilis, V refers to the vector(s). Both total crude extract and the solubilized extract are shown. The results presented in FIGS. 8A and 8B indicate that the PAO1 EDD protein is expressed and soluble in S. cerevisiae. The results also demonstrate that the E. coli EDA protein is expressed and soluble. It was not clear from these experiments if the PAO1 EDA was soluble in yeast.

Example 10

EDD and EDA Activity Assays

Cell lysates of the various EDD and EDA expressing strains were prepared as follows. About 50 to 100 ml of SCD-ura-leu media containing 10 mM MnCl₂was used. When cultured aerobically, strains were grown in a 250 ml baffled shake flask. When grown anaerobically, 4000/L Tween-80 (British Drug Houses, Ltd., West Chester, Pa.) plus 0.01 g/L Ergosterol (Alef Aesar, Ward Hill, Mass.) were added and the culture was grown in a 250 ml serum bottle outfitted with a butyl rubber stopper with an aluminum crimp cap. Each strain was inoculated at an initial OD₆₀₀of about 0.2 and grown to an OD₆₀₀of about 3-4. Cells were grown at 30° C. at 200 rpm.
Yeast cells were harvested by centrifugation at 1046×g (3000 rpm) for 5 minutes at 4° C. The supernatant was discarded and the cells were resuspended in 25 mL cold sterile water. This wash step was repeated once. Washed cell pellets were resuspended in 1 mL sterile water, transferred to 1.5 mL screw cap tube, and centrifuged at 16,100×g (13,200 rpm) for 3 minutes at 4° C. Cell pellets were resuspended in about 800-1000 μl of freshly prepared lysis buffer (50 mM Tris-Cl pH 7.0, 10 mM MgCl₂, 1× protease inhibitor cocktail EDTA-free (Thermo Scientific, Waltham, Mass.) and the tube filled with zirconia beads to avoid any headspace in the tube. The tubes were placed in a Mini BeadBeater (Bio Spec Products, Inc., Bartlesville, Okla.) and vortexed twice for 30 seconds at room temperature. The supernatant was transferred to a new 1.5 mL microcentrifuge tube and centrifuged twice to remove cell debris at 16,100×g (13,200 rpm) for 10 minutes, at 4° C. Quantification of the lysates was performed using the Coomassie-Plus kit (Thermo Scientific, San Diego, Calif.) as directed by the manufacturer.
About 750 μg of crude extract was assayed using 1× assay buffer (50 mM Tris-Cl pH 7.0, 10 mM MgCl2), 3 U lactate dehydrogenase (5 μg/μL in 50 mM Tris-Cl pH 7.0), and 10 μl 1 mM 6-phosphogluconate dissolved in 50 mM Tris-Cl pH 7.0 were mixed in a reaction of about 400 μl. This reaction mix was transferred to a 1 ml Quartz cuvette and allowed to incubate about 5 minutes at 30° C. To this reaction, 100 μl of 1.5 mM NADH (prepared in 50 mM Tris-Cl pH 7.0) was added, and the change in Abs_340nmover the course of 5 minutes at 30° C. was monitored in a Beckman DU-800 spectrophotometer using the Enzyme Mechanism software package (Beckman Coulter, Inc, Brea, Calif.).
The table below presents the relative specific activities for BY4742 strains expressing EDD and EDA from either P. aeruginosa (PAO1) or E. coli sources. The results presented in the table below indicate that each of the listed combinations of EDD and EDA genes, when expressed in S. cerevisiae strain BY4742, confers activity.


Gene	Km	Vmax	Specific Activity
Combination	(M⁻¹)	(mmol min⁻¹)	(mmol min⁻¹mg⁻¹)

EDD-P/EDA-P	1.04 × 10⁻³	0.21930	0.3451
EDD-P/EDA-E	2.06 × 10⁻³	0.27280	0.3637
EDD-E/EDA-P	1.43 × 10⁻³	0.09264	0.1235
EDD-E/EDA-E	0.839 × 10⁻³	0.16270	0.2169

The data presented above is also presented graphically in FIG. 9. FIG. 9 graphically displays the relative activities of the various EDD/EDA combinations presented in the table above, as measured in assays using 750 micrograms of crude extract. From the height of the PE bar in FIG. 9, and the data presented in the table above, it is evident that the combinations conferring the highest level of activity were the EDD-P/EDA-E (e.g., PE) and EDD-P/EDA-P (e.g., PP) combinations.

Example 11

Improved Ethanol Yield from Yeast Strains Expressing EDD and EDA Constructs

Strains BF428 (vector control), BF591 (EDD-PAO1/EDA-PAO1), BF592 (EDD-PAO1/EDA-E. coli), BF603 (EDD-E. coli/EDA-PAO1) and BF604 (EDD-E. coli/EDA-E. coli) were inoculated into 15 ml SCD-ura-leu media containing 400 μl/L Tween-80 (British Drug Houses, Ltd., West Chester, Pa.) plus 0.01 g/L Ergosterol (EMD, San Diego, Calif.) in 20 ml Hungate tubes outfitted with a butyl rubber stopper and sealed with an aluminum crimped cap to prevent oxygen from entering the culture at an initial OD₆₀₀of 0.5 and grown for about 20 hours. Glucose and ethanol in the culture media were assayed using YSI 2700 BioAnalyzer instruments (world wide web uniform resource locator ysi.com), according to the manufacturer's recommendations at 0 and 20 hours post inoculation. The results of the fermentation of glucose to ethanol are showing graphically in FIG. 10. The results presented in FIG. 9 indicate that the presence of the EDD/EDA combinations in S. cerevisiae increase the yield of ethanol produced, when compared to a vector-only control. The EDD/EDA combinations that showed the greatest fermentation efficiency in yeast were EDD-P/EDA-E (e.g., PE) and EDD-E/EDA-P (e.g., EP).

Example 12

Improved Ethanol Yield from Yeast Strains Expressing EDD and EDA from PAO1 in Fermentors

A fermentation test of the strain BF591 [BY4742 with plasmids pBF290 (p426GPD-EDD_PAO1) and pBF292 (p425GPD-EDA_PAO1)] was conducted against BF428 (BY4742 p426GPD/p425GPD) control strain in 700 ml w.v. Multifors multiplexed fermentors. The fermentation medium was SC-Ura-Leu with about 2% glucose. Vessels were inoculated with about a 6.25% inoculum from overnight cultures grown in about 50 ml SC-Ura-Leu with about 2% glucose.
The cultures were grown aerobically at about 30° C. with about 250 rpm agitation, 1 vvm sparge of process air, (21% O2). The pH was controlled at around 5.0 with 0.25 N NaOH. Once glucose concentrations dropped below 0.5 g/L the fermentation was switched to anaerobic conditions. Before changing to anaerobic conditions, samples were taken to measure glucose concentrations and biomass by OD₆₀₀as reported in Table B. Ethanol and glucose concentrations in the fermentation broth were monitored using YSI 2700 BioAnalyzer instruments.
The table below presents the elapsed fermentation time (EFT), the biomass and glucose at the start of anaerobic fermentation in a 400 ml fermentor. The edd and eda combinations carried by the strains are described above.


			Glucose
Strain	EFT (hrs)	OD_{600 nm}	(g/L)

BF591	32	4.50	.047
BF428	27	4.81	.062

At the beginning of the anaerobic portion of the fermentation, a bolus of 20 g/L glucose plus 3.35 g/L of yeast nitrogen base without amino acids was added to the fermentors. In addition, 4 ml/L of 2.5 g/L ergosterol in ethanol, 0.4 ml/L Tween 80, and 0.01% AF-204 were added to each fermentor. Oxygen was purged with 100% N2 sparged at about 1 vvm until pO2 was below 1%.
Samples were taken every 2 to 7 hours and measured for ethanol and glucose concentrations and OD₆₀₀. The fermentation was harvested when the glucose concentration was below 0.05 g/L, at 50 hours elapsed fermentation time (EFT). Ethanol and glucose concentrations and OD₆₀₀of the final sample are reported in the table below.


		Ethanol	Glucose
Strain	OD_{600 nm}	(g/L)	(g/L)

BF591	5.6	17.1	.04
BF428	5.6	15.8	0

The data presented in the table above also is presented graphically in FIGS. 11A and 11B. FIG. 11A presents the fermentation data from strain BF428 (BY4742 with vector controls) and FIG. 11B presents the fermentation data from strain BF591 (BY4742 with EDD-PAO1/EDA-PAO1). Fermentation profiles for strains BF 428 and BF 591, grown on 2% dextrose, were calculated and are presented in the table below.


Strain	Yx/s	Yp/s	Yp/x	Qp	qp

BF428	0.24	0.40	7.19	0.02	0.05
BF591	0.23	0.43	7.44	0.02	0.07

Yx/s = OD/g glucose
Yp/s = q ethanol/g glucose
Yp/x = g ethanol/OD
Qp = g ethanol/Lh⁻¹
qp = g ethanol/ODh⁻¹

The results from the fermentation show that the BF591 has a higher ethanol yield (triangles, compare FIG. 11A and FIG. 11B) than the control BF428 strain. The calculated yield of ethanol was also determined to be higher in the engineered BF591 strain (0.43 g ethanol/g glucose) than that of the BF428 control strain (0.40 g ethanol/g glucose).

Example 13

Improved Ethanol Yield in a Tall Strain of S. cerevisiae Expressing EDD and EDA from PAO1

To generate BY4741 and BY4742 tal1 mutant strains, the following procedure was used:

Oligonucleotides

(SEQ ID NO: 276)

#350 - 5′-TAAAACGACGGCCAGTGAAT-3′

(SEQ ID NO: 277)

#351 - 5′-TGCAGGTCGACTCTAGAGGAT-3′

(SEQ ID NO: 278)

#352 - 5′-GTGTGCGTGTATGTGTACACCTGTATTTAATTTCCTTACT

CGCGGGTTTTTCTAAAACGACGGCCAGTGAAT-3′

(SEQ ID NO: 279)

#353 - 5′-TGTACCAGTCTAGAATTCTACCAACAAATGGGGAAATCAA

AGTAACTTGGGCTGCAGGTCGACTCTAGAGGA-3′

All oligonucleotides set forth above were purchased from Integrated Technologies (“IDT”, Coralville, Iowa). PCR amplification of the genes were performed as follows: about 50 ng of the pBFU-719 DNA (e.g., plasmid with unique 200-mer sequence) was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers (#350/#351 in the first round), and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction mixture was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 60° C. for 30 seconds, and 72° C. for 45 seconds. A final 5 minute extension reaction at 72° C. was also included. A second round of PCR amplification was done using 50 ng of the first round PCR amplification with 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers (#352/#353 in the second round), and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The second reaction mixture was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 60° C. for 30 seconds, and 72° C. for 45 seconds. A final 5 minute extension reaction at 72° C. was also included. The final PCR product was purified using the Zymo Research DNA Clean & Concentrator-25 kit (Zymo Research, Orange, Calif.).
Transformation was accomplished by a high-efficiency competency method. A 5 ml culture of the BY4742 or BY4741 strain was grown overnight at about 30° C. with shaking at about 200 rpm. A suitable amount of this overnight culture was added to 60 ml of YPD media to obtain an initial OD600 of about 0.2 (approximately 2×10⁶cells/ml). The cells were allowed to grow at 30° C. with agitation (about 200 rpm) until the OD₆₀₀was about 1. The cells were then centrifuged at 3000 rpm for 5 min, washed with 10 ml sterile water and re-centrifuged. The cell pellet was resuspended in 1 ml sterile water, transferred to a 1.5 ml sterile microcentrifuge tube and spun down at 4000×g for about 5 minutes. This cell pellet was resuspended in 1 ml sterile 1×TE/LiOAC solution (10 mM Tris-HCl, 1 mM EDTA, 100 mM LiOAc, pH7.5) and re-centrifuged at about 4000×g for about 5 minutes. The cell pellet was resuspended in 0.25 ml 1×TE/LiOAc solution. For the transformation, 50 μl of these cells were aliquoted to a 1.5 ml microcentrifuge tube and about 1 μg purified PCR product and 5 μl of salmon sperm DNA that had been previously boiled for about 5 minutes and placed on ice. 300 μl of a sterile PEG solution was then added (40% PEG 3500, 10 mM Tris-HCl, 1 mM EDTA, 100 mM LiOAc, pH7.5). This mixture was allowed to incubate at 30° C. for about one hour with gentle mixing every 15 minutes. About 40 μl DMSO (Sigma, St. Louis, Mo.) was added to the incubating mixture, and the mixture heat shocked at about 42° C. for about 15 minutes. The cells were pelleted in a microcentrifuge at 13000 rpm for about 30 seconds and the supernatant removed. The cells were resuspended in 1 ml 1×TE (10 mM Tris-HCl, 1 mM EDTA, pH 7.5), centrifuged at 13000 rpm for about 30 seconds and resuspended in 1 ml 1×TE. About 100-200 μl of cells were plated onto SCD-URA media, as described above, and allowed to grow at about 30° C. for about 3 days. After 3 days, transformed colonies were streaked for single colonies on SCD-URA plates and allowed to grow at about 30° C. for about 3 days. From these plates, single colonies were streaked onto SCD agar plates (20 g/L agar in SCD media) containing 1 g/L 5-FOA (Research Products International Corp, Mt. Prospect, Ill.), and also inoculated into YPD liquid broth. The plates were allowed to grow at about 30° C. for about 4 days and the liquid culture was grown overnight at about 30° C. with agitation of about 200 rpm.
To confirm that integration of the construct was correct, genomic DNA was prepared from the YPD overnight cultures. Briefly, the yeast cells were pelleted by centrifugation at room temperature for 5 minutes at approximately 3000 rpm. The cell pellet was resuspended in 200 μl of breaking buffer (2% Triton X-100, 1% SDS, 100 mM NaCl, 10 mM Tris pH8, 1 mM EDTA) and placed into a 1.5 ml microcentrifuge tube containing about 200 μl glass beads and about 200 μl of phenol:chloroform:isoamyl alcohol (Ambion, Austin, Tex.). The mixture was vortexed for about 2 to 5 minutes at room temperature. About 200 μl of sterile water was then added and the mixture vortexed again. The mixture was centrifuged for about 10 minutes at about 13000 rpm and the aqueous layer transferred to a new microcentrifuge tube. About 1/10th of the aqueous layers volume of 3M NaOAc ((British Drug Houses, Ltd., West Chester, Pa.) was added to the aqueous layer and 2.5× the total volume of the mixture of ethanol was added and mixed well. The genomic DNA was then precipitated by placing the tubes at −80° C. for at least one hour (or in a dry ice/ethanol bath for about 30 minutes). The tubes were then centrifuged at about 13000 rpm for 5 minutes at about 4° C. to pellet the DNA. The DNA pellet was then washed two times or more times with about 200 μl of 70% ethanol and re-centrifuged. The DNA pellet was dried using vacuum assisted air drying and resuspended in about 50 to 200 μl 1×TE.
The genomic DNA isolated as described above was used in a PCR amplification reaction consisting of about 50 ng of the genomic DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers (#276/#277), and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction mix was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 60° C. for 30 seconds, and 72° C. for 45 seconds. A final 5 minute extension reaction at 72° C. was also included. A second round of PCR amplification was done using 50 ng of the first round PCR amplification with 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers (#352/#353 in the second round), and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The second mixture was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for about 30 seconds. A final 5 minute extension reaction at 72° C. was also included.
Positive colonies from the screen in YPD that had a PCR product of about 1600 bp indicating the insertion of the integration construct in the TAL1 locus, and that grew on the plates containing 5-FOA were grown overnight in YPD at about 30° C. with agitation of about 200 rpm. Genomic DNA was prepared as above and checked by PCR amplification using primers #276 and #277 (described below). Positive clones were identified which had a PCR product of 359 bp indicating the deletion of the tal1 locus and the remaining portion of the 200-mer tag. The strain carrying the correct traits was labeled as BF716. The BY4741 version was labeled as BF717.
Oligonucleotides

(SEQ ID NO: 280)

#276 - 5′-GTCGACTGGAAATCTGGAAGGTTGGT-3′

(SEQ ID NO: 281)

#277 - 5′-GTCGACGCTTTGCTGCAAGGATTCAT-3′
The BY4742 tal1 strain was then made competent using the high efficiency competent method as described above. About 500 ng of plasmids pBF290 and pBF292 or with plasmids p426GPD and p425GPD were used to transform the BY4742 tal1 strain. The final transformation mixture was plated onto SCD-ura-leu plates and grown at about 30° C. for about 3 days. Strain BF716 (BY4742 tal1) with p426GPD/p425GPD was labeled as BF738. Strain BF716 with pBF290/pBF292 was labeled as BF741.
A fermentation test of the BF738 was conducted against BF741 in a 400 ml multiplexed fermentor. The fermentation medium utilized was SC-Ura-Leu with 2% glucose. Cultures were grown overnight in 50 ml SC-Ura-Leu 2% glucose and used to inoculate the fermentors at 4 to 5% inoculum. OD₆₀₀readings of the inoculum are shown in the table below.


	Strain	OD_{600 nm}

	BF741 (tal1 PP)	3.70
	BF738 (tal1 VV)	3.80

The cultures were grown aerobically at about 30° C. with about 250 rpm agitation, 0.5 vvm sparge of process air, 21% O₂. pH was controlled at 5.0 with 1N NaOH. Glucose concentrations in the fermentation broth were monitored by YSI 2700 BioAnalyzers during aerobic fermentation. Once glucose was depleted the fermentation was switched to anaerobic conditions. Before changing to anaerobic conditions samples were taken to measure glucose usage. Biomass was measured by monitoring the optical density of the growth medium at 600 nanometers (e.g., OD₆₀₀). EFT at glucose depletion, glucose concentrations and OD₆₀₀are shown in the table below. The table below reports the amount of biomass in the fermentor and the amount of ethanol produced in grams per liter, after the specified amount of time (EFT), by the respective strains.


Strain	EFT (hrs)	OD_{600 nm}	Glucose (g/L)

BF741 (tal1 PP)	43.5	2.50	0.045
BF738 (tal1 VV)	31	2.95	0.192

At the beginning of anaerobic fermentation, about 19 g/L glucose, 3.7 g/L YNB, 4 ml/L of 2.5 g/L ergosterol (in ethanol), 0.4 ml/L Tween 80, and 0.01% AF-204 were added to each fermentor. Oxygen was purged with 100% N₂sparged at 0.25 vvm for the remainder of the fermentation. Samples were taken every 4 to 12 hours and analyzed for ethanol production and glucose utilization using the YSI Bioanalyzers, and amount of biomass by OD₆₀₀. The fermentations were harvested when the glucose bolus was depleted. Anaerobic ethanol produced, anaerobic glucose consumption and OD₆₀₀of the final sample are shown in the table below.


		Ethanol	Glucose
Strain	OD_{600 nm}	Produced (g/L)	Consumed (g/L)

BF741 (tal1 PP)	3.75	8.1	18.99
BF738 (tal1 VV)	3.6	6.5	18.168

The results are also presented graphically in FIGS. 12A and 12B. FIG. 12A illustrates the fermentation data for strain BF738 (BY4742 tal1 with vector controls p426GPD and p425GPD) and FIG. 12B illustrates the fermentation data for strain BF741 (BY4742 tal1 with plasmids pBF290 (EDD-PAO1) and pBF292 (EDA-PAO1). The results presented above and in FIGS. 12A and 12B indicate that strain BF741, which expresses the activities encoded by the eda and edd genes, yields more ethanol than control strain BF738. Strain BF741 produced about 0.43 g ethanol per gram of glucose consumed whereas strain BF738 produced only 0.36 g ethanol per gram of glucose consumed. Fermentation profiles were calculated for strains BF738 and BF741 and are presented below.


Strain	Yx/s	Yp/s	Yp/x	Qp	qp

BF738	0.198	0.358	3.76	0.371	0.103
BF741	0.203	0.439	2.16	0.439	0.131

Yx/s = OD/g glucose,
Yp/s = q ethanol/g glucose,
Yp/x = g ethanol/OD
Qp = g ethanol/Lh⁻¹,
qp = g ethanol/ODh⁻¹

Example 14

Complementation and Improved Ethanol Yield in a pfk1 Strain of S. cerevisiae expressing the EDA and EDD Genes from P. aeruginosa

Strain BF205 (YGR240C/BY4742, ATCC Cat. No. 4015893; PubMed: 10436161) was transformed with plasmids p426GPD and p425GPD or with plasmids pBF290 (p426GPD/EDD-PAO1) and pBF292 (p426GPD/EDA-PAO1), generating strains BF740 (vector controls) and BF743, respectively. Transformation was accomplished by a high-efficiency competency method using 500 ng of plasmids p426GPD and p425GPD or plasmids pBF290 and pBF292. Transformants were plated onto SCD-ura-leu agar plates and grown at about 30° C. for about 3 days. The final strains were named BF740 (BY4742 pfk1 with plasmids p426GPD and p425GPD) and BF743 (BY4742-pfk1, pBF290/pBF292).
A fermentation test of the control strain BF740 (BY4742 pfk1 with plasmids p426GPD and p425GPD) was conducted against BF743 (BY4742-pfk1, pBF290/pBF292) in 400 ml w.v. Multifors multiplexed fermentors. The fermentation medium was SC-Ura-Leu with 2% glucose. Vessels were inoculated with about a 10% inoculum from overnight cultures grown in about 50 ml SC-Ura-Leu with about 2% glucose and normalized to 0.5 OD₆₀₀. The actual inoculated ODs for the fermentations are shown in the table below.


	Strain	OD_{600 nm}

	BF740 (pfk1 VV)	0.571
	BF743 (pfk1 PP)	0.535

The cultures were grown aerobically at about 30° C. with about 250 rpm agitation, 1 vvm sparge of process air, (21% O₂). The pH was controlled at around 5.0 with 0.25 N NaOH. Once glucose concentrations dropped below 0.5 g/L the fermentation was switched to anaerobic conditions. Before changing to anaerobic conditions, samples were taken to measure glucose concentrations and biomass by OD₆₀₀as shown in the table below. The table below shows the beginning cell biomass and glucose concentration (in grams per liter of nutrient broth). Ethanol and glucose concentrations in the fermentation broth were monitored using a YSI 2700 BioAnalyzer.


		Ethanol	Glucose
Strain	OD_{600 nm}	(g/L)	(g/L)

BF740	5.94	5.67	0.033
BF743	5.82	5.82	0.034

At the beginning of the anaerobic portion of the fermentation, a bolus of about 18 g/L glucose plus about 4 ml/L of 2.5 g/L ergosterol in Ethanol, 0.4 ml/L Tween 80, and 0.01% AF-204 were added to each fermentor. Oxygen was purged with 100% N₂sparged at about 1 vvm until pO₂was below 1%. Samples were taken every 4 to 8 hours and measured for ethanol and glucose concentrations and biomass (OD₆₀₀). The fermentation was harvested when the glucose concentration was below 0.05 g/L, at about 42 hours elapsed fermentation time (EFT). Ethanol and glucose concentrations and OD₆₀₀of the final sample are shown in the table below.


		Ethanol	Glucose
Strain	OD_{600 nm}	(g/L)	(g/L)

BF740	6.4	5.07	14.6
BF743	5.09	13.37	0.042

The results also are present graphically in FIGS. 13A and 13B. The results presented in FIG. 13A illustrate the fermentation data for strain BF740 grown on 2% dextrose and the results presented in FIG. 13B illustrate the fermentation data for strain BF743 grown on 2% dextrose. The results indicate that the BY4742 pfk1 mutant strain, BF740 cannot utilize glucose nor produce ethanol under anaerobic conditions. However, the engineered strain BF743 is capable of both utilizing glucose and producing ethanol under anaerobic conditions. Strain BF743 has a yield of about 0.39 g ethanol per gram of glucose consumed versus no yield in the control strain BF740. The fermentation profile for strains BF740 and BF743 are presented in the table below.


Strain	Yx/s	Yp/s	Yp/x	Qp	qp

BF740	2.133	−0.700	−0.328	−0.022	−0.003
BF743	0.264	0.390	1.483	0.178	0.035

Yx/s = OD/g glucose,
Yp/s = q ethanol/g glucose,
Yp/x = g ethanol/OD
Qp = g ethanol/Lh⁻¹,
qp = g ethanol/ODh⁻¹

Example 15

EDD and EDA Activities from Other Sources

The EDD and EDA genes also have been isolated from additional sources and tested for the ability to direct fermentation in yeast. The additional EDD and EDA genes have been isolated from Shewanella oneidensis, Gluconobacter oxydans, and Ruminococcus flavefaciens. Genomic DNA was purchased from ATCC for both S. oneidensis (Cat. No. 700550D) and G. oxydans (621 HD-5). R. flavefaciens, strain C94 (NCDO 2213) was also purchased from ATCC (Cat. No. 19208). To prepare genomic DNA, R. flavefaciens was grown in cooked meat media (Becton Dickinson, Franklin Lakes, N.J. USA) overnight at 37° C. and genomic DNA was isolated using a Qiagen DNeasy Blood and Tissue kit according to the manufacture's protocol. The eda and edd genes were PCR amplified from the corresponding genomic DNA using the following sets of PCR oligonucleotides. The nucleotide and amino acid sequences of eda and edd genes PCR amplified using the following sets of PCR oligonucleotide primers, also is given below.

The S. oneidensis edd gene:

(SEQ. ID. NO: 73)

5′-GTTCACTGCactagtaaaaaaATGCACTCAGTCGTTCAATCTG-3′

(SEQ. ID. NO: 74)

5′-CTTCGAGATCTCGAGTTAGTAAAGTTCATCGATGGC-3′

The S. oneidensis eda gene:

(SEQ. ID. NO: 75)

5′-GTTCACTGCactagtaaaaaaATGCTTGAGAATAACTGGTC-3′

(SEQ. ID. NO: 76)

5′-CTTCGAGATCTCGAGTTAAAGTCCGCCAATCGCCTC-3′

The G. oxydans edd gene:

(SEQ. ID. NO: 77)

5′-GTTCACTGCactagtaaaaaaATGTCTCTGAATCCCGTCGTC-3′

(SEQ. ID. NO: 78)

5′-CTTCGAGATCTCGAGTTAGTGAATGTCGTCGCCAAC-3′

The G. oxydans eda gene:

(SEQ. ID. NO: 79)

5′-GTTCACTGCactagtaaaaaaATGATCGATACTGCCAAACTC-3′

(SEQ. ID. NO: 80)

5′-CTTCGAGATCTCGAGTCAGACCGTGAAGAGTGCCGC-3′

The R. flavefaciens edd gene:

(SEQ. ID. NO: 81)

5′-GTTCACTGCactagtaaaaaaATGAGCGATAATTTTTTCTGCG-3′

(SEQ. ID. NO: 82)

5′-CTTCGAGATCTCGAGCTATTTCCTGTTGATGATAGC-3′

S. oneidensis 6-phosphogluconate dehydratase (edd)

(SEQ. ID. NO: 83)

ATGCACTCAGTCGTTCAATCTGTTACTGACAGAATTATTGCCCGTAGCAAAGCATCTCGTGAA

GCATACCTTGCTGCGTTAAACGATGCCCGTAACCATGGTGTACACCGAAGTTCCTTAAGTTGC

GGTAACTTAGCCCACGGTTTTGCGGCTTGTAATCCCGATGACAAAAATGCATTGCGTCAATTG

ACGAAGGCCAATATTGGGATTATCACCGCATTCAACGATATGTTATCTGCACACCAACCCTAT

GAAACCTATCCTGATTTGCTGAAAAAAGCCTGTCAGGAAGTCGGTAGTGTTGCGCAGGTGGC

TGGCGGTGTTCCCGCCATGTGTGACGGCGTGACTCAAGGTCAGCCCGGTATGGAATTGAGCT

TACTGAGCCGTGAAGTGATTGCGATGGCAACCGCGGTTGGCTTATCACACAATATGTTTGATG

GAGCCTTACTCCTCGGTATTTGCGATAAAATTGTACCGGGTTTACTGATTGGTGCCTTAAGTTT

TGGCCATTTACCTATGTTGTTTGTGCCCGCAGGCCCAATGAAATCGGGTATTCCTAATAAGGA

AAAAGCTCGCATTCGTCAGCAATTTGCTCAAGGTAAGGTCGATAGAGCACAACTGCTCGAAGC

GGAAGCCCAGTCTTACCACAGTGCGGGTACTTGTACCTTCTATGGTACCGCTAACTCGAACCA

ACTGATGCTCGAAGTGATGGGGCTGCAATTGCCGGGTTCATCTTTTGTGAATCCAGACGATCC

ACTGCGCGAAGCCTTAAACAAAATGGCGGCCAAGCAGGTTTGTCGTTTAACTGAACTAGGCA

CTCAATACAGTCCGATTGGTGAAGTCGTTAACGAAAAATCGATAGTGAATGGTATTGTTGCATT

GCTCGCGACGGGTGGTTCAACAAACTTAACCATGCACATTGTGGCGGCGGCCCGTGCTGCA

GGTATTATCGTCAACTGGGATGACTTTTCGGAATTATCCGATGCGGTGCCTTTGCTGGCACGT

GTTTATCCAAACGGTCATGCGGATATTAACCATTTCCACGCTGCGGGTGGTATGGCTTTCCTT

ATCAAAGAATTACTCGATGCAGGTTTGCTGCATGAGGATGTCAATACTGTCGCGGGTTATGGT

CTGCGCCGTTACACCCAAGAGCCTAAACTGCTTGATGGCGAGCTGCGCTGGGTCGATGGCC

CAACAGTGAGTTTAGATACCGAAGTATTAACCTCTGTGGCAACACCATTCCAAAACAACGGTG

GTTTAAAGCTGCTGAAGGGTAACTTAGGCCGCGCTGTGATTAAAGTGTCTGCCGTTCAGCCAC

AGCACCGTGTGGTGGAAGCGCCCGCAGTGGTGATTGACGATCAAAACAAACTCGATGCGTTA

TTTAAATCCGGCGCATTAGACAGGGATTGTGTGGTGGTGGTGAAAGGCCAAGGGCCGAAAGC

CAACGGTATGCCAGAGCTGCATAAACTAACGCCGCTGTTAGGTTCATTGCAGGACAAAGGCTT

TAAAGTGGCACTGATGACTGATGGTCGTATGTCGGGCGCATCGGGCAAAGTACCTGCGGCGA

TTCATTTAACCCCTGAAGCGATTGATGGCGGGTTAATTGCAAAGGTACAAGACGGCGATTTAA

TCCGAGTTGATGCACTGACCGGCGAGCTGAGTTTATTAGTCTCTGACACCGAGCTTGCCACC

AGAACTGCCACTGAAATTGATTTACGCCATTCTCGTTATGGCATGGGGCGTGAGTTATTTGGA

GTACTGCGTTCAAACTTAAGCAGTCCTGAAACCGGTGCGCGTAGTACTAGCGCCATCGATGA

ACTTTACTAA

S. oneidensis 6-phosphogluconate dehydratase (edd)-Amino Acid sequence

(SEQ. ID. NO: 84)

MHSVVQSVTDRIIARSKASREAYLAALNDARNHGVHRSSLSCGNLAHGFAACNPDDKNALRQLTK

ANIGIITAFNDMLSAHQPYETYPDLLKKACQEVGSVAQVAGGVPAMCDGVTQGQPGMELSLLSRE

VIAMATAVGLSHNMFDGALLLGICDKIVPGLLIGALSFGHLPMLFVPAGPMKSGIPNKEKARIRQQF

AQGKVDRAQLLEAEAQSYHSAGTCTFYGTANSNQLMLEVMGLQLPGSSFVNPDDPLREALNKMA

AKQVCRLTELGTQYSPIGEVVNEKSIVNGIVALLATGGSTNLTMHIVAAARAAGIIVNWDDFSELSD

AVPLLARVYPNGHADINHFHAAGGMAFLIKELLDAGLLHEDVNTVAGYGLRRYTQEPKLLDGELR

WVDGPTVSLDTEVLTSVATPFQNNGGLKLLKGNLGRAVIKVSAVQPQHRVVEAPAVVIDDQNKLD

ALFKSGALDRDCVVVVKGQGPKANGMPELHKLTPLLGSLQDKGFKVALMTDGRMSGASGKVPAA

IHLTPEAIDGGLIAKVQDGDLIRVDALTGELSLLVSDTELATRTATEIDLRHSRYGMGRELFGVLRSN

LSSPETGARSTSAIDELY

G. oxydans 6-phosphogluconate dehydratase (edd)

(SEQ. ID. NO: 85)

ATGTCTCTGAATCCCGTCGTCGAGAGCGTGACTGCCCGTATCATCGAGCGTTCGAAAGTCTC

CCGTCGCCGGTATCTCGCCCTGATGGAGCGCAACCGCGCCAAGGGTGTGCTCCGGCCCAAG

CTGGCCTGCGGTAATCTGGCGCATGCCATCGCAGCGTCCAGCCCCGACAAGCCGGATCTGA

TGCGTCCCACCGGGACCAATATCGGCGTGATCACGACCTATAACGACATGCTCTCGGCGCAT

CAGCCGTATGGCCGCTATCCCGAGCAGATCAAGCTGTTCGCCCGTGAAGTCGGTGCGACGG

CCCAGGTTGCAGGCGGCGCACCAGCAATGTGTGATGGTGTGACGCAGGGGCAGGAGGGCAT

GGAACTCTCCCTGTTCTCCCGTGACGTGATCGCCATGTCCACGGCGGTCGGGCTGAGCCAC

GGCATGTTTGAGGGCGTGGCGCTGCTGGGCATCTGTGACAAGATTGTGCCGGGCCTTCTGAT

GGGCGCGCTGCGCTTCGGTCATCTCCCGGCCATGCTGATCCCGGCAGGGCCAATGCCGTCC

GGTCTTCCAAACAAGGAAAAGCAGCGCATCCGCCAGCTCTATGTGCAGGGCAAGGTCGGGC

AGGACGAGCTGATGGAAGCGGAAAACGCCTCCTATCACAGCCCGGGCACCTGCACGTTCTAT

GGCACGGCCAATACGAACCAGATGATGGTCGAAATCATGGGTCTGATGATGCCGGACTCGGC

TTTCATCAATCCCAACACGAAGCTGCGTCAGGCAATGACCCGCTCGGGTATTCACCGTCTGG

CCGAAATCGGCCTGAACGGCGAGGATGTGCGCCCGCTCGCTCATTGCGTAGACGAAAAGGC

CATCGTGAATGCGGCGGTCGGGTTGCTGGCGACGGGTGGTTCGACCAACCATTCGATCCATC

TTCCTGCTATCGCCCGTGCCGCTGGTATCCTGATCGACTGGGAAGACATCAGCCGCCTGTCG

TCCGCGGTTCCGCTGATCACCCGTGTTTATCCGAGCGGTTCCGAGGACGTGAACGCGTTCAA

CCGCGTGGGTGGTATGCCGACCGTGATCGCCGAACTGACGCGCGCCGGGATGCTGCACAAG

GACATTCTGACGGTCTCTCGTGGCGGTTTCTCCGATTATGCCCGTCGCGCATCGCTGGAAGG

CGATGAGATCGTCTACACCCACGCGAAGCCGTCCACGGACACCGATATCCTGCGCGATGTGG

CTACGCCTTTCCGGCCCGATGGCGGTATGCGCCTGATGACTGGTAATCTGGGCCGCGCGAT

CTACAAGAGCAGCGCTATTGCGCCCGAGCACCTGACCGTTGAAGCGCCGGCACGGGTCTTC

CAGGACCAGCATGACGTCCTCACGGCCTATCAGAATGGTGAGCTTGAGCGTGATGTTGTCGT

GGTCGTCCGGTTCCAGGGACCGGAAGCCAACGGCATGCCGGAGCTTCACAAGCTGACCCCG

ACTCTGGGCGTGCTTCAGGATCGCGGCTTCAAGGTGGCCCTGCTGACGGATGGACGCATGT

CCGGTGCGAGCGGCAAGGTGCCGGCCGCCATTCATGTCGGTCCCGAAGCGCAGGTTGGCG

GTCCGATCGCCCGCGTGCGGGACGGCGACATGATCCGTGTCTGCGCGGTGACGGGACAGAT

CGAGGCTCTGGTGGATGCCGCCGAGTGGGAGAGCCGCAAGCCGGTCCCGCCGCCGCTCCC

GGCATTGGGAACGGGCCGCGAACTGTTCGCGCTGATGCGTTCGGTGCATGATCCGGCCGAG

GCTGGCGGATCCGCGATGCTGGCCCAGATGGATCGCGTGATCGAAGCCGTTGGCGACGACA

TTCACTAA

G. oxydans 6-phosphogluconate dehydratase (edd)-Amino Acid sequence

(SEQ. ID. NO: 86)

MSLNPVVESVTARIIERSKVSRRRYLALMERNRAKGVLRPKLACGNLAHAIAASSPDKPDLMRPTG

TNIGVITTYNDMLSAHQPYGRYPEQIKLFAREVGATAQVAGGAPAMCDGVTQGQEGMELSLFSRD

VIAMSTAVGLSHGMFEGVALLGICDKIVPGLLMGALRFGHLPAMLIPAGPMPSGLPNKEKQRIRQL

YVQGKVGQDELMEAENASYHSPGTCTFYGTANTNQMMVEIMGLMMPDSAFINPNTKLRQAMTR

SGIHRLAEIGLNGEDVRPLAHCVDEKAIVNAAVGLLATGGSTNHSIHLPAIARAAGILIDWEDISRLSS

AVPLITRVYPSGSEDVNAFNRVGGMPTVIAELTRAGMLHKDILTVSRGGFSDYARRASLEGDEIVY

THAKPSTDTDILRDVATPFRPDGGMRLMTGNLGRAIYKSSAIAPEHLTVEAPARVFQDQHDVLTAY

QNGELERDVVVVVRFQGPEANGMPELHKLTPTLGVLQDRGFKVALLTDGRMSGASGKVPAAIHV

GPEAQVGGPIARVRDGDMIRVCAVTGQIEALVDAAEWESRKPVPPPLPALGTGRELFALMRSVHD

PAEAGGSAMLAQMDRVIEAVGDDIH

R. flavefaciens phosphogluconate dehydratase/DHAD

(SEQ. ID. NO: 87)

ATGAGCGATAATTTTTTCTGCGAGGGTGCGGATAAAGCCCCTCAGCGTTCACTTTTCAATGCA

CTGGGCATGACTAAAGAGGAAATGAAGCGTCCCCTCGTTGGTATCGTTTCTTCCTACAATGAG

ATCGTTCCCGGCCATATGAACATCGACAAGCTGGTCGAAGCCGTTAAGCTGGGTGTAGCTAT

GGGCGGCGGCACTCCTGTTGTTTTCCCTGCTATCGCTGTATGCGACGGTATCGCTATGGGTC

ACACAGGCATGAAGTACAGCCTTGTTACCCGTGACCTTATTGCCGATTCTACAGAGTGTATGG

CTCTTGCTCATCACTTCGACGCACTGGTAATGATACCTAACTGCGACAAGAACGTTCCCGGCC

TGCTTATGGCGGCTGCACGTATCAATGTTCCTACTGTATTCGTAAGCGGCGGCCCTATGCTTG

CAGGCCATGTAAAGGGTAAGAAGACCTCTCTTTCATCCATGTTCGAGGCTGTAGGCGCTTACA

CAGCAGGCAAGATAGACGAGGCTGAACTTGACGAATTCGAGAACAAGACCTGCCCTACCTGC

GGTTCATGTTCGGGTATGTATACCGCTAACTCCATGAACTGCCTCACTGAGGTACTGGGTATG

GGTCTCAGAGGCAACGGCACTATCCCTGCTGTTTACTCCGAGCGTATCAAGCTTGCAAAGCA

GGCAGGTATGCAGGTTATGGAACTCTACAGAAAGAATATCCGCCCTCTCGATATCATGACAGA

GAAGGCTTTCCAGAACGCTCTCACAGCTGATATGGCTCTTGGATGTTCCACAAACAGTATGCT

CCATCTCCCTGCTATCGCCAACGAATGCGGCATAAATATCAACCTTGACATGGCTAACGAGAT

AAGCGCCAAGACTCCTAACCTCTGCCATCTTGCACCGGCAGGCCACACCTACATGGAAGACC

TCAACGAAGCAGGCGGAGTTTATGCAGTTCTCAACGAGCTGAGCAAAAAGGGACTTATCAACA

CCGACTGCATGACTGTTACAGGCAAGACCGTAGGCGAGAATATCAAGGGCTGCATCAACCGT

GACCCTGAGACTATCCGTCCTATCGACAACCCATACAGTGAAACAGGCGGAATCGCCGTACT

CAAGGGCAATCTTGCTCCCGACAGATGTGTTGTGAAGAGAAGCGCAGTTGCTCCCGAAATGC

TGGTACACAAAGGCCCTGCAAGAGTATTCGACAGCGAGGAAGAAGCTATCAAGGTCATCTAT

GAGGGCGGTATCAAGGCAGGCGACGTTGTTGTTATCCGTTACGAAGGCCCTGCAGGCGGCC

CCGGCATGAGAGAAATGCTCTCTCCTACATCAGCTATACAGGGTGCAGGTCTCGGCTCAACT

GTTGCTCTAATCACTGACGGACGTTTCAGCGGCGCTACCCGTGGTGCGGCTATCGGACACGT

ATCCCCCGAAGCTGTAAACGGCGGTACTATCGCATATGTCAAGGACGGCGATATTATCTCCAT

CGACATACCGAATTACTCCATCACTCTTGAAGTATCCGACGAGGAGCTTGCAGAGCGCAAAAA

GGCAATGCCTATCAAGCGCAAGGAGAACATCACAGGCTATCTGAAGCGCTATGCACAGCAGG

TATCATCCGCAGACAAGGGCGCTATCATCAACAGGAAATAG

R. flavefaciens phosphogluconate dehydratase/DHAD-Amino Acid sequence

(SEQ. ID. NO: 88)

MSDNFFCEGADKAPQRSLFNALGMTKEEMKRPLVGIVSSYNEIVPGHMNIDKLVEAVKLGVAMGG

GTPVVFPAIAVCDGIAMGHTGMKYSLVTRDLIADSTECMALAHHFDALVMIPNCDKNVPGLLMAAA

RINVPTVFVSGGPMLAGHVKGKKTSLSSMFEAVGAYTAGKIDEAELDEFENKTCPTCGSCSGMYT

ANSMNCLTEVLGMGLRGNGTIPAVYSERIKLAKQAGMQVMELYRKNIRPLDIMTEKAFQNALTAD

MALGCSTNSMLHLPAIANECGININLDMANEISAKTPNLCHLAPAGHTYMEDLNEAGGVYAVLNEL

SKKGLINTDCMTVTGKTVGENIKGCINRDPETIRPIDNPYSETGGIAVLKGNLAPDRCVVKRSAVAP

EMLVHKGPARVFDSEEEAIKVIYEGGIKAGDVVVIRYEGPAGGPGMREMLSPTSAIQGAGLGSTVA

LITDGRFSGATRGAAIGHVSPEAVNGGTIAYVKDGDIISIDIPNYSITLEVSDEELAERKKAMPIKRKE

NITGYLKRYAQQVSSADKGAIINRK

Pair wise homology comparisons for various edd proteins are presented in the table below. The comparisons were made using ClustalW software (ClustalW and ClustalX version 2; Larkin M. A., Blackshields G., Brown N. P., Chema R., McGettigan P. A., McWilliam H., Valentin F., Wallace I. M., Wilm A., Lopez R., Thompson J. D., Gibson T. J. and Higgins D. G., Bioinformatics 2007 23(21): 2947-2948). ClustalW is a free alignment tool available at the European Bioinformatics Institute website (e.g., world wide web uniform resource locator ebi.ac.uk, specific ClustalW location is ebi.ac.uk/Tools/clustalw2/index.html). PAO1=Pseudomonas aeruginosa PAO1, E.C.=Eschericia coli, S.O.=S. oneidensis, G.O.=G. oxydans, R.F.=Ruminococcus flavefaciens.


PAO1	E.C.	S.O.	G.O.	R.F.

PAO1	100	62	62	55	29
E.C.	62	100	66	56	30
S.O.	62	66	100	56	28
G.O.	55	56	56	100	28
R.F.	29	30	28	28	100

S. oneidensis keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase (eda)

(SEQ. ID. NO: 89)

ATGCTTGAGAATAACTGGTCATTACAACCACAAGATATTTTTAAACGCAGCCCTATTGTTCCTG

TTATGGTGATTAACAAGATTGAACATGCGGTGCCCTTAGCTAAAGCGCTGGTTGCCGGAGGG

ATAAGCGTGTTGGAAGTGACATTACGCACGCCATGCGCCCTTGAAGCTATCACCAAAATCGCC

AAGGAAGTGCCTGAGGCGCTGGTTGGCGCGGGGACTATTTTAAATGAAGCCCAGCTTGGACA

GGCTATCGCCGCTGGTGCGCAATTTATTATCACTCCAGGTGCGACAGTTGAGCTGCTCAAAG

CGGGCATGCAAGGACCGGTGCCGTTAATTCCGGGCGTTGCCAGTATTTCCGAGGTGATGACG

GGCATGGCGCTGGGCTACACTCACTTTAAATTCTTCCCTGCTGAAGCGTCAGGTGGCGTTGA

TGCGCTTAAGGCTTTCTCTGGGCCGTTAGCAGATATCCGCTTCTGCCCAACAGGTGGAATTAC

CCCGAGCAGCTATAAAGATTACTTAGCGCTGAAGAATGTCGATTGTATTGGTGGCAGCTGGAT

TGCTCCTACCGATGCGATGGAGCAGGGCGATTGGGATCGTATCACTCAGCTGTGTAAAGAGG

CGATTGGCGGACTTTAA

S. oneidensis keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase
(eda)-Amino Acid sequence

(SEQ. ID. NO: 90)

MLENNWSLQPQDIFKRSPIVPVMVINKIEHAVPLAKALVAGGISVLEVTLRTPCALEAITKIAKEVPEA

LVGAGTILNEAQLGQAIAAGAQFIITPGATVELLKAGMQGPVPLIPGVASISEVMTGMALGYTHFKF

FPAEASGGVDALKAFSGPLADIRFCPTGGITPSSYKDYLALKNVDCIGGSWIAPTDAMEQGDWDRI

TQLCKEAIGGL

G. oxydans keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase (eda)

(SEQ. ID. NO: 91)

ATGATCGATACTGCCAAACTCGACGCCGTCATGAGCCGTTGTCCGGTCATGCCGGTGCTGGT

GGTCAATGATGTGGCTCTGGCCCGCCCGATGGCCGAGGCTCTGGTGGCGGGTGGACTGTCC

ACGCTGGAAGTCACGCTGCGCACGCCCTGCGCCCTTGAAGCTATTGAGGAAATGTCGAAAGT

ACCAGGCGCGCTGGTCGGTGCCGGTACGGTGCTGAATCCGTCCGACATGGACCGTGCCGTG

AAGGCGGGTGCGCGCTTCATCGTCAGCCCCGGCCTGACCGAGGCGCTGGCAAAGGCGTCG

GTTGAGCATGACGTCCCCTTCCTGCCAGGCGTTGCCAATGCGGGTGACATCATGCGGGGTCT

GGATCTGGGTCTGTCACGCTTCAAGTTCTTCCCGGCTGTGACGAATGGCGGCATTCCCGCGC

TCAAGAGCTTGGCCAGTGTTTTTGGCAGCAATGTCCGTTTCTGCCCCACGGGCGGCATTACG

GAAGAGAGCGCACCGGACTGGCTGGCGCTTCCCTCCGTGGCCTGCGTCGGCGGATCCTGG

GTGACGGCCGGCACGTTCGATGCGGACAAGGTCCGTCAGCGCGCCACGGCTGCGGCACTCT

TCACGGTCTGA

G. oxydans keto-hydroxyglutarate-aldolase/keto-deoxy-phosphogluconate aldolase
(eda)-Amino Acid

(SEQ. ID. NO: 92)

MIDTAKLDAVMSRCPVMPVLVVNDVALARPMAEALVAGGLSTLEVTLRTPCALEAIEEMSKVPGAL

VGAGTVLNPSDMDRAVKAGARFIVSPGLTEALAKASVEHDVPFLPGVANAGDIMRGLDLGLSRFK

FFPAVTNGGIPALKSLASVFGSNVRFCPTGGITEESAPDWLALPSVACVGGSWVTAGTFDADKVR

QRATAAALFTV

Pair wise homology comparisons for various eda proteins are presented in the table below. The comparisons were made using ClustalW software (ClustalW and ClustalX version 2; Larkin M. A., Blackshields G., Brown N. P., Chema R., McGettigan P. A., McWilliam H., Valentin F., Wallace I. M., Wilm A., Lopez R., Thompson J. D., Gibson T. J. and Higgins D. G., Bioinformatics 2007 23(21): 2947-2948). PAO1=Pseudomonas aeruginosa PAO1, E.C.=Eschericia coli, S.O.=S. oneidensis, G.O.=G. oxydans, R.F.=Ruminococcus flavefaciens.


PAO1	E.C.	S.O.	G.O.

PAO1	100	41	44	40
E.C.	41	100	60	46
S.O.	44	60	100	45
G.O.	40	46	45	100

All oligonucleotides set forth above were purchased from Integrated technologies (“IDT”, Coralville, Iowa). These oligonucleotides were designed to incorporate a SpeI restriction endonuclease cleavage site upstream and an XhoI restriction endonuclease cleavage site downstream of the edd and eda gene constructs, such that the sites could be used to clone the genes into yeast expression vectors p426GPD (ATCC accession number 87361) and p425GPD (ATCC accession number 87359). In addition to incorporating restriction endonuclease cleavage sites, the forward oligonucleotides were designed to incorporate six consecutive A nucleotides immediately upstream of the ATG initiation codon.
PCR amplification of the genes were performed as follows: about 100 ng of the genomic DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction mixture was cycled as follows: 95° C. 10 minutes followed by 30 rounds of 95° C. for 20 seconds, 50° C. (eda amplifications) or 53° C. (edd amplifications) for 30 seconds, and 72° C. for 15 seconds (eda amplifications) or 30 seconds (edd amplifications). A final 5 minute extension reaction at 72° C. was also included. Each amplified product was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations and the sequences verified (GeneWiz, La Jolla, Calif.).
Cloning of New Edd and Eda Genes into Yeast Expression Vectors
Each of the sequence-verified eda and edd fragments were subcloned into the corresponding restriction sites in plasmids p425GPD and p426GPD vectors (ATCC #87361; PubMed: 7737504). Briefly, about 50 ng of SpeI-XhoI-digested p425GPD vector was ligated to about 50 ng of SpeI/XhoI-restricted eda or edd fragment in a 10 μl reaction with 1× T4 DNA ligase buffer and 1 U T4 DNA ligase (Fermentas) overnight at 16° C. About 3 μl of this reaction was used to transform DH5α competent cells (Zymo Research) and plated onto LB agar media containing 100 μg/ml ampicillin. Final constructs were confirmed by restriction endonuclease digests and sequence verification (GeneWiz, La Jolla, Calif.).
In Vivo Assay to Determine Optimal EDD/EDA Combination
To determine the optimal EDD/EDA gene combinations, a yeast strain was developed to enable in vivo gene combination evaluation. Growth on glucose was impaired in this strain by disrupting both copies of phosphofructokinase (PFK), however, the strain could grow normally on galactose due to the presence of a single plasmid copy of the PFK2 gene under the control of a GAL1 promoter. The strain can only grow on glucose if a functional EDD/EDA is present in the cell. The strain was generated using strain BF205 (YGR240C/BY4742, ATCC Cat. No. 4015893; Winzeler E A, et al. Science 285: 901-906, 1999, PubMed: 10436161) as the starting strain.
PFK2 Expressing Plasmid
The plasmid expressing the PFK2 gene under the control of the GAL1 promoter, for use in the in vivo edd/eda gene combination evaluations, was constructed by first isolating the PFK2 gene. Primers JML/89 and JML/95 were used to amplify the PFK2 gene from BY4742 in a PCR reaction containing about 100 ng of the genomic DNA, 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reactions were cycled as follows: 95° C. for 10 minutes followed by 10 rounds of 95° C. for 20 seconds, 55° C. for 20 seconds, and 72° C. for 90 seconds and 25 rounds of 95° C. for 20 seconds, 62° C. for 20 seconds, and 72° C. for 90 seconds. A final 5 minute extension reaction at 72° C. was also included. Each amplified product was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations and sequence verified (GeneWiz, San Diego, Calif.). The sequences of JML/89 and JML/95 are given below.

JML/89

(SEQ ID NO: 282)

	ACTAGTATGACTGTTACTACTCCTTTTGTGAATGGTAC

	JML/95

(SEQ ID NO: 283)

CTCGAGTTAATCAACTCTCTTTCTTCCAACCAAATGGTC

The primers used were designed to include a unique SpeI restriction site at the 5′ end of the gene and a unique XhoI restriction site at the 3′ end of the gene. This SpeI-XhoI fragment (approximately 2900 bp) was cloned into the SpeI-XhoI sites of the yeast vector p416GAL (ATCC Cat. No. 87332; Mumberg D, et al., Nucleic Acids Res. 22: 5767-5768, 1994. PubMed: 7838736) in a 10 μl ligation reaction containing about 50 ng of the p416GAL plasmid and about 100 ng of the PFK2 fragment with 1× ligation buffer and 1 U T4 DNA ligase (Fermentas). This ligation reaction was allowed to incubate at room temperature for about one hour and was transformed into competent DH5α (Zymo Research, Orange, Calif.) and plated onto LB plates containing 100 μg/ml ampicillin. The final plasmid was verified by restriction digests and sequence confirmed (GeneWiz, San Diego, Calif.) and was called pBF744. Plasmid pBF744 was transformed in yeast strain BF205 (BY4742 pfk1) using the procedure outlined below. This resulting strain was called BF1477.

- 1. Inoculate 5 mLs YPD with a single yeast colony. Grow 0/N at 30° C.
- 2. Next day: add 50 μl culture to 450 μl fresh YPD, check A660. Add suitable amount of cells to 60 mLs fresh YPD to give an A660=0.2 (2×10⁶cells/mL). Grow to A660=1.0 (2×10⁷cells/mL), approximately 5 hours.
- 3. Boil a solution of 10 mg/ml salmon sperm DNA for 5 min, then quick chill on ice.
- 4. Spin down 50 mL cells at 3000 rpm for 5 min, wash in 10 mL sterile water, recentrifuge.
- 5. Resuspend in 1 mL sterile water. Transfer to 1.5 mL sterile microfuge tube, spin down.
- 6. Resuspend in 1 mL sterile TE/LiOAC solution. Spin down, resuspend in 0.25 mLs TE/LiOAc (4×10⁹cells).
- 7. In a 1.5 mL microfuge tube, mix 50 μl yeast cells with 1-5 μg transforming DNA and 5 μl single stranded carrier DNA (boiled salmon sperm DNA).
- 8. Add 300 μl sterile PEG solution. Mix thoroughly. Incubate at 30° C. for 60 min with gentle mixing every 15 min.
- 9. Add 40 μl DMSO, mix thoroughly. Heat shock at 42° C. for 15 min.
- 10. Microfuge cells at 13000 rpm for 30 seconds, remove supernatant. Resuspend in 1 mL 1×TE, microfuge 30 sec. Resuspend in 1 mL 1×TE. Plate 100-200 μl on selective media (SCD-ura).

pfk2 Knockout Cassette
A knockout cassette for the PFK2 gene was constructed by first PCR amplifying about 300 bp of the 5′ and 3′ flanking regions of the PFK2 gene from S. cerevisiae, strain BY4742 using primers JML/85 and JML/87 and primers JML/86 and JML/88, respectively. These flanking regions were designed such that the 5′ flanking region had a HindIII site at its 5′ edge and a BamHI site at its 3′ end. The 3′ flanking region had a BamHI site at its 5′ edge and a EcoRI site at its 3′ edge. The nucleotide sequence of the PFK2 gene and the primers used for amplification of the PFK2 gene are given below.

S. cerevisiae PFK2 (from genomic sequence)

SEQ. ID. NO: 121

ATGACTGTTACTACTCCTTTTGTGAATGGTACTTCTTATTGTACCGTCACTGCATATTCCGTTCA

ATCTTATAAAGCTGCCATAGATTTTTACACCAAGTTTTTGTCATTAGAAAACCGCTCTTCTCCAG

ATGAAAACTCCACTTTATTGTCTAACGATTCCATCTCTTTGAAGATCCTTCTACGTCCTGATGAA

AAAATCAATAAAAATGTTGAGGCTCATTTGAAGGAATTGAACAGTATTACCAAGACTCAAGACT

GGAGATCACATGCCACCCAATCCTTGGTATTTAACACTTCCGACATCTTGGCAGTCAAGGACA

CTCTAAATGCTATGAACGCTCCTCTTCAAGGCTACCCAACAGAACTATTTCCAATGCAGTTGTA

CACTTTGGACCCATTAGGTAACGTTGTTGGTGTTACTTCTACTAAGAACGCAGTTTCAACCAAG

CCAACTCCACCACCAGCACCAGAAGCTTCTGCTGAGTCTGGTCTTTCCTCTAAAGTTCACTCT

TACACTGATTTGGCTTACCGTATGAAAACCACCGACACCTATCCATCTCTGCCAAAGCCATTG

AACAGGCCTCAAAAGGCAATTGCCGTCATGACTTCCGGTGGTGATGCTCCAGGTATGAACTCT

AACGTTAGAGCCATCGTGCGTTCCGCTATCTTCAAAGGTTGTCGTGCCTTTGTTGTCATGGAA

GGTTATGAAGGTTTGGTTCGTGGTGGTCCAGAATACATCAAGGAATTCCACTGGGAAGACGTC

CGTGGTTGGTCTGCTGAAGGTGGTACCAACATTGGTACTGCCCGTTGTATGGAATTCAAGAAG

CGCGAAGGTAGATTATTGGGTGCCCAACATTTGATTGAGGCCGGTGTCGATGCTTTGATCGTT

TGTGGTGGTGACGGTTCTTTGACTGGTGCTGATCTGTTTAGATCAGAATGGCCTTCTTTGATC

GAGGAATTGTTGAAAACAAACAGAATTTCCAACGAACAATACGAAAGAATGAAGCATTTGAATA

TTTGCGGTACTGTCGGTTCTATTGATAACGATATGTCCACCACGGATGCTACTATTGGTGCTTA

CTCTGCCTTGGACAGAATCTGTAAGGCCATCGATTACGTTGAAGCCACTGCCAACTCTCACTC

AAGAGCTTTCGTTGTTGAAGTTATGGGTAGAAACTGTGGTTGGTTAGCTTTATTAGCTGGTATC

GCCACTTCCGCTGACTATATCTTTATTCCAGAGAAGCCAGCCACTTCCAGCGAATGGCAAGAT

CAAATGTGTGACATTGTCTCCAAGCACAGATCAAGGGGTAAGAGAACCACCATTGTTGTTGTT

GCAGAAGGTGCTATCGCTGCTGACTTGACCCCAATTTCTCCAAGCGACGTCCACAAAGTTCTA

GTTGACAGATTAGGTTTGGATACAAGAATTACTACCTTAGGTCACGTTCAAAGAGGTGGTACT

GCTGTTGCTTACGACCGTATCTTGGCTACTTTACAAGGTCTTGAGGCCGTTAATGCCGTTTTG

GAATCCACTCCAGACACCCCATCACCATTGATTGCTGTTAACGAAAACAAAATTGTTCGTAAAC

CATTAATGGAATCCGTCAAGTTGACCAAAGCAGTTGCAGAAGCCATTCAAGCTAAGGATTTCA

AGAGAGCTATGTCTTTAAGAGACACTGAGTTCATTGAACATTTAAACAATTTCATGGCTATCAA

CTCTGCTGACCACAACGAACCAAAGCTACCAAAGGACAAGAGACTGAAGATTGCCATTGTTAA

TGTCGGTGCTCCAGCTGGTGGTATCAACTCTGCCGTCTACTCGATGGCTACTTACTGTATGTC

CCAAGGTCACAGACCATACGCTATCTACAATGGTTGGTCTGGTTTGGCAAGACATGAAAGTGT

TCGTTCTTTGAACTGGAAGGATATGTTGGGTTGGCAATCCCGTGGTGGTTCTGAAATCGGTAC

TAACAGAGTCACTCCAGAAGAAGCAGATCTAGGTATGATTGCTTACTATTTCCAAAAGTACGAA

TTTGATGGTTTGATCATCGTTGGTGGTTTCGAAGCTTTTGAATCTTTACATCAATTAGAGAGAG

CAAGAGAAAGTTATCCAGCTTTCAGAATCCCAATGGTCTTGATACCAGCTACTTTGTCTAACAA

TGTTCCAGGTACTGAATACTCTTTGGGTTCTGATACCGCTTTGAATGCTCTAATGGAATACTGT

GATGTTGTTAAACAATCCGCTTCTTCAACCAGAGGTAGAGCCTTCGTTGTCGATTGTCAAGGT

GGTAACTCAGGCTATTTGGCCACTTACGCTTCTTTGGCTGTTGGTGCTCAAGTCTCTTATGTC

CCAGAAGAAGGTATTTCTTTGGAGCAATTGTCCGAGGATATTGAATACTTAGCTCAATCTTTTG

AAAAGGCAGAAGGTAGAGGTAGATTTGGTAAATTGATTTTGAAGAGTACAAACGCTTCTAAGG

CTTTATCAGCCACTAAATTGGCTGAAGTTATTACTGCTGAAGCCGATGGCAGATTTGACGCTA

AGCCAGCTTATCCAGGTCATGTACAACAAGGTGGTTTGCCATCTCCAATTGATAGAACAAGAG

CCACTAGAATGGCCATTAAAGCTGTCGGCTTCATCAAAGACAACCAAGCTGCCATTGCTGAAG

CTCGTGCTGCCGAAGAAAACTTCAACGCTGATGACAAGACCATTTCTGACACTGCTGCTGTCG

TTGGTGTTAAGGGTTCACATGTCGTTTACAACTCCATTAGACAATTGTATGACTATGAAACTGA

AGTTTCCATGAGAATGCCAAAGGTCATTCACTGGCAAGCTACCAGACTCATTGCTGACCATTT

GGTTGGAAGAAAGAGAGTTGATTAA

JML/85

(SEQ ID NO: 284)

AAGCTTTTAATTAATATAACGCTATGACGGTAGTTGAATGTTAAAAAC

JML/86

(SEQ ID NO: 285)

GAATTCTTAATTAAAGAGAACAAAGTATTTAACGCACATGTATAAATATTG

JML/87

(SEQ ID NO: 286)

GGATCCGCATGCGGCCGGCCAGCTTTTAATCAAGGAAGTAATAAATAAAGGAC

JML/88

(SEQ ID NO: 287)

GGATCCGAGCTCGCGGCCGCAGCTTTTGAACAATGAATTTTTTGTTCCTTTC

The nucleic acid fragments were amplified using the following conditions; about 100 ng of the BY4742 genomic DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 58° C. for 30 seconds, and 72° C. for 20 seconds. A final 5 minute extension reaction at 72° C. was also included. Each amplified product was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations and the sequence of the construct was verified (GeneWiz, San Diego, Calif.). The resulting plasmids were named pBF648 (5′ flanking region) and pBF649 (3′ flanking region). A three fragment ligation was performed using about 100 ng of the 5′ flanking region HindIII-BamHI fragment, about 100 ng of the 3′ flanking region BamHI-EcoRI fragment and about 50 ng of pUC19 digested with HindIII and EcoRI in a 5 μl ligation reaction containing 1× ligation buffer and 1 U T4 DNA ligase (Fermentas). This reaction was incubated at room temperature for about one hour. About 2 μl of this reaction mix was used to transform competent DH5α cells (Zymo Research, Orange, Calif.) and plated onto LB agar media containing 100 μg/ml ampicillin. The final construct was confirmed by restriction endonuclease digests and sequence verification (GeneWiz, San Diego, Calif.), resulting in plasmid pBF653.
Lys 2 Gene Cloning
The Lys2 gene was isolated by PCR amplification from pRS317 (ATCC Cat. No. 77157; Sikorski R S, Boeke J D. Methods Enzymol. 194: 302-318, 1991. PubMed: 2005795) using primers JML/93 and JML/94. PCR amplification was performed as follows: about 25 ng of the pRS317 plasmid DNA was added to 1× Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reactions were cycled at: 95° C. 10 minutes followed by 10 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 2 minutes, followed by 25 more rounds of 95° C. for 20 seconds, 62° C. for 30 seconds, and 72° C. for 2 minutes. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector as described herein, resulting in plasmid pBF656. The nucleotide sequence of Lys2 gene and the primers used for amplification of the Lys2 gene are given below.

JML/93

(SEQ ID NO: 288)

GCGGCCGCAGCTTCGCAAGTATTCATTTTAGACCCATG

JML/94

(SEQ ID NO: 289)

GGCCGGCCGGTACCAATTCCACTTGCAATTACATAAAAAATTCC

Lys 2 (from genomic sequence database),

SEQ. ID. NO: 122

ATGACTAACGAAAAGGTCTGGATAGAGAAGTTGGATAATCCAACTCTTTCAGTGTTACCACAT

GACTTTTTACGCCCACAACAAGAACCTTATACGAAACAAGCTACATATTCGTTACAGCTACCTC

AGCTCGATGTGCCTCATGATAGTTTTTCTAACAAATACGCTGTCGCTTTGAGTGTATGGGCTG

CATTGATATATAGAGTAACCGGTGACGATGATATTGTTCTTTATATTGCGAATAACAAAATCTTA

AGATTCAATATTCAACCAACGTGGTCATTTAATGAGCTGTATTCTACAATTAACAATGAGTTGAA

CAAGCTCAATTCTATTGAGGCCAATTTTTCCTTTGACGAGCTAGCTGAAAAAATTCAAAGTTGC

CAAGATCTGGAAAGGACCCCTCAGTTGTTCCGTTTGGCCTTTTTGGAAAACCAAGATTTCAAAT

TAGACGAGTTCAAGCATCATTTAGTGGACTTTGCTTTGAATTTGGATACCAGTAATAATGCGCA

TGTTTTGAACTTAATTTATAACAGCTTACTGTATTCGAATGAAAGAGTAACCATTGTTGCGGAC

CAATTTACTCAATATTTGACTGCTGCGCTAAGCGATCCATCCAATTGCATAACTAAAATCTCTC

TGATCACCGCATCATCCAAGGATAGTTTACCTGATCCAACTAAGAACTTGGGCTGGTGCGATT

TCGTGGGGTGTATTCACGACATTTTCCAGGACAATGCTGAAGCCTTCCCAGAGAGAACCTGTG

TTGTGGAGACTCCAACACTAAATTCCGACAAGTCCCGTTCTTTCACTTATCGCGACATCAACC

GCACTTCTAACATAGTTGCCCATTATTTGATTAAAACAGGTATCAAAAGAGGTGATGTAGTGAT

GATCTATTCTTCTAGGGGTGTGGATTTGATGGTATGTGTGATGGGTGTCTTGAAAGCCGGCGC

AACCTTTTCAGTTATCGACCCTGCATATCCCCCAGCCAGACAAACCATTTACTTAGGTGTTGCT

AAACCACGTGGGTTGATTGTTATTAGAGCTGCTGGACAATTGGATCAACTAGTAGAAGATTAC

ATCAATGATGAATTGGAGATTGTTTCAAGAATCAATTCCATCGCTATTCAAGAAAATGGTACCA

TTGAAGGTGGCAAATTGGACAATGGCGAGGATGTTTTGGCTCCATATGATCACTACAAAGACA

CCAGAACAGGTGTTGTAGTTGGACCAGATTCCAACCCAACCCTATCTTTCACATCTGGTTCCG

AAGGTATTCCTAAGGGTGTTCTTGGTAGACATTTTTCCTTGGCTTATTATTTCAATTGGATGTC

CAAAAGGTTCAACTTAACAGAAAATGATAAATTCACAATGCTGAGCGGTATTGCACATGATCCA

ATTCAAAGAGATATGTTTACACCATTATTTTTAGGTGCCCAATTGTATGTCCCTACTCAAGATGA

TATTGGTACACCGGGCCGTTTAGCGGAATGGATGAGTAAGTATGGTTGCACAGTTACCCATTT

AACACCTGCCATGGGTCAATTACTTACTGCCCAAGCTACTACACCATTCCCTAAGTTACATCAT

GCGTTCTTTGTGGGTGACATTTTAACAAAACGTGATTGTCTGAGGTTACAAACCTTGGCAGAA

AATTGCCGTATTGTTAATATGTACGGTACCACTGAAACACAGCGTGCAGTTTCTTATTTCGAAG

TTAAATCAAAAAATGACGATCCAAACTTTTTGAAAAAATTGAAAGATGTCATGCCTGCTGGTAA

AGGTATGTTGAACGTTCAGCTACTAGTTGTTAACAGGAACGATCGTACTCAAATATGTGGTATT

GGCGAAATAGGTGAGATTTATGTTCGTGCAGGTGGTTTGGCCGAAGGTTATAGAGGATTACCA

GAATTGAATAAAGAAAAATTTGTGAACAACTGGTTTGTTGAAAAAGATCACTGGAATTATTTGG

ATAAGGATAATGGTGAACCTTGGAGACAATTCTGGTTAGGTCCAAGAGATAGATTGTACAGAA

CGGGTGATTTAGGTCGTTATCTACCAAACGGTGACTGTGAATGTTGCGGTAGGGCTGATGATC

AAGTTAAAATTCGTGGGTTCAGAATCGAATTAGGAGAAATAGATACGCACATTTCCCAACATCC

ATTGGTAAGAGAAAACATTACTTTAGTTCGCAAAAATGCCGACAATGAGCCAACATTGATCACA

TTTATGGTCCCAAGATTTGACAAGCCAGATGACTTGTCTAAGTTCCAAAGTGATGTTCCAAAGG

AGGTTGAAACTGACCCTATAGTTAAGGGCTTAATCGGTTACCATCTTTTATCCAAGGACATCAG

GACTTTCTTAAAGAAAAGATTGGCTAGCTATGCTATGCCTTCCTTGATTGTGGTTATGGATAAA

CTACCATTGAATCCAAATGGTAAAGTTGATAAGCCTAAACTTCAATTCCCAACTCCCAAGCAAT

TAAATTTGGTAGCTGAAAATACAGTTTCTGAAACTGACGACTCTCAGTTTACCAATGTTGAGCG

CGAGGTTAGAGACTTATGGTTAAGTATATTACCTACCAAGCCAGCATCTGTATCACCAGATGAT

TCGTTTTTCGATTTAGGTGGTCATTCTATCTTGGCTACCAAAATGATTTTTACCTTAAAGAAAAA

GCTGCAAGTTGATTTACCATTGGGCACAATTTTCAAGTATCCAACGATAAAGGCCTTTGCCGC

GGAAATTGACAGAATTAAATCATCGGGTGGATCATCTCAAGGTGAGGTCGTCGAAAATGTCAC

TGCAAATTATGCGGAAGACGCCAAGAAATTGGTTGAGACGCTACCAAGTTCGTACCCCTCTCG

AGAATATTTTGTTGAACCTAATAGTGCCGAAGGAAAAACAACAATTAATGTGTTTGTTACCGGT

GTCACAGGATTTCTGGGCTCCTACATCCTTGCAGATTTGTTAGGACGTTCTCCAAAGAACTAC

AGTTTCAAAGTGTTTGCCCACGTCAGGGCCAAGGATGAAGAAGCTGCATTTGCAAGATTACAA

AAGGCAGGTATCACCTATGGTACTTGGAACGAAAAATTTGCCTCAAATATTAAAGTTGTATTAG

GCGATTTATCTAAAAGCCAATTTGGTCTTTCAGATGAGAAGTGGATGGATTTGGCAAACACAG

TTGATATAATTATCCATAATGGTGCGTTAGTTCACTGGGTTTATCCATATGCCAAATTGAGGGA

TCCAAATGTTATTTCAACTATCAATGTTATGAGCTTAGCCGCCGTCGGCAAGCCAAAGTTCTTT

GACTTTGTTTCCTCCACTTCTACTCTTGACACTGAATACTACTTTAATTTGTCAGATAAACTTGT

TAGCGAAGGGAAGCCAGGCATTTTAGAATCAGACGATTTAATGAACTCTGCAAGCGGGCTCA

CTGGTGGATATGGTCAGTCCAAATGGGCTGCTGAGTACATCATTAGACGTGCAGGTGAAAGG

GGCCTACGTGGGTGTATTGTCAGACCAGGTTACGTAACAGGTGCCTCTGCCAATGGTTCTTCA

AACACAGATGATTTCTTATTGAGATTTTTGAAAGGTTCAGTCCAATTAGGTAAGATTCCAGATAT

CGAAAATTCCGTGAATATGGTTCCAGTAGATCATGTTGCTCGTGTTGTTGTTGCTACGTCTTTG

AATCCTCCCAAAGAAAATGAATTGGCCGTTGCTCAAGTAACGGGTCACCCAAGAATATTATTC

AAAGACTACTTGTATACTTTACACGATTATGGTTACGATGTCGAAATCGAAAGCTATTCTAAAT

GGAAGAAATCATTGGAGGCGTCTGTTATTGACAGGAATGAAGAAAATGCGTTGTATCCTTTGC

TACACATGGTCTTAGACAACTTACCTGAAAGTACCAAAGCTCCGGAACTAGACGATAGGAACG

CCGTGGCATCTTTAAAGAAAGACACCGCATGGACAGGTGTTGATTGGTCTAATGGAATAGGTG

TTACTCCAGAAGAGGTTGGTATATATATTGCATTTTTAAACAAGGTTGGATTTTTACCTCCACCA

ACTCATAATGACAAACTTCCACTGCCAAGTATAGAACTAACTCAAGCGCAAATAAGTCTAGTTG

CTTCAGGTGCTGGTGCTCGTGGAAGCTCCGCAGCAGCTTAA

The knockout cassette was fully assembled by cloning the NotI-FseI LYS2 fragment from plasmid pBF656 into the NotI-FseI sites located between the 5′ and 3′ flanking PFK2 regions in plasmid pBF653. About 50 ng of plasmid pBF653 digested with NotI and FseI was ligated to about 100 ng of the NotI-FseI LYS2 fragment from plasmid pBF656 in a 5 μl reaction containing 1× ligation buffer and 1 U T4 DNA ligase (Fermentas) for about 1 hour at room temperature. About 2 μl of this reaction was used to transform competent DH5α (Zymo Research, Orange, Calif.) and plated on 100 μg/ml ampicillin. The structure of the final plasmid, pBF745, was confirmed by restriction enzyme digests. The approximately 5 kbp PacI fragment containing the LYS2 cassette and PFK2 flanking regions was gel extracted using the Zymoclean Gel DNA Recovery Kit (Zymo Research, Orange, Calif.) according to the manufacturer's conditions.
Strain BF1477 was transformed with the about 5 kbp PacI fragment using the method described above (LiOAc/PEG method) generating strain BF1411. Strain BF1411 has the ability to grow on galactose as a carbon source, but cannot grow on glucose. Various combinations of the EDD and EDA constructs can be expressed in this strain and monitored for growth on glucose. Strains which show growth on glucose (or the highest growth rate on glucose) can be further characterized to determine which combination of EDD and EDA genes is present. Using the strain and method described herein, libraries of EDD and EDA genes can be screened for improved activities and activity combinations in a host organism.

Example 16

Single Plasmid System for Industrial Yeast

A single plasmid system expressing EDD and EDA for industrial yeast was constructed as follows: The approximately 2800 bp fragment containing the GPD1 promoter, EDD-PAO1 gene and CYC1 terminator from plasmid pBF291 (p426GPD with EDD-PAO1) was PCR amplified using primers KAS/5′-BamHI-Pgpd and KAS/3′-NdeI-CYCt, described below. About 25 ng of the plasmid DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 45 seconds. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector, as described herein, and the final plasmid was sequence verified and designated, pBF475.

KAS/5′-BamHI-Pgpd

(SEQ ID NO: 290)

	GGATCCgtttatcattatcaatactcgccatttcaaag

	KAS/3′-Ndel-CYCt

(SEQ ID NO: 291)

CATATGttgggtaccggccgcaaattaaagccttcgagcg

An approximately 1500 bp KANMX4 cassette was PCR amplified from plasmid pBF413 HO-poly-KanMX4-HO (ATCC Cat. No. 87804) using primers KAS/5′-Bam_NdeI-KANMX4 and KAS/3′-Sal_NheI-KANMX4, described below.

KAS/5′-Bam_Ndel-KANMX4

(SEQ ID NO: 292)

GGATTCagtcagatCATATGggtacccccgggttaattaaggcgcgccag

atctg

KAS/3′-Sal_Nhel-KANMX4

(SEQ ID NO: 293)

GTCGACaggcctactgtacgGCTAGCgaattcgagctcgttttcgacact

ggatggcggc

About 25 ng of plasmid pBF413 HO-poly-KanMX4-HO DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 30 seconds. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector, as described herein. The resulting plasmid was sequence verified and designated, pBF465.
An approximately 225 bp ADH1 terminator was PCR amplified from the genome of BY4742 using primers KAS/5′-Xba-XhoI-ADHt and KAS/3′-StuI-ADHS. The sequence of primers KAS/5′-Xba-XhoI-ADHt and KAS/3′-StuI-ADHS is given below.

KAS/5′-Xba-Xhol-ADHt

(SEQ ID NO: 294)

	tctagaCTCGAGtaataagcgaatttcttatgatttatg

	KAS/3′-Stul-ADH5

(SEQ ID NO: 295)

aagcttAGGCCTggagcgatttgcaggcatttgc

About 100 ng of genomic DNA from BY4742 was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 15 seconds. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector according to the manufacturer's recommendations and sequence verified. The resulting plasmid was designated pBF437.
The TEF2 promoter was PCR amplified from the genome of BY4742 using primers KAS/5′-Xba-XhoI-ADHt and KAS/3′-StuI-ADHS, described below.

KAS/5′-Bam-Nhel-Ptef

(SEQ ID NO: 296)

	GGATCCgctagcACCGCGAATCCTTACATCACACCC

	KAS/3′-Xbal-Spel-Ptef

(SEQ ID NO: 297)

tctagaCTCGAGtaataagcgaatttcttatgatttatg

About 100 ng of genomic DNA from BY4742 was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. This was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 15 seconds. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations and sequence verified (GeneWiz, San Diego, Calif.). The resulting plasmid was called pBF440.
The EDA gene cassettes were constructed as follows: First the TEF2 promoter from the plasmid pBF440 was digested with BamHI and XbaI and was cloned into the BamHI and XbaI sites of pUC19 creating plasmid pBF480. Plasmid pBF480 was then digested with XbaI and HindIII and was ligated to the XbaI-HindIII fragment from plasmid pBF437 containing the ADH1 terminator, creating plasmid pBF521. Plasmid pBF521 was then digested with SpeI and XhoI and then ligated to either SpeI-XhoI fragment containing either the PAO1 eda gene from plasmid pBF292 or the E. coli eda gene from plasmid pBF268. The 2 plasmids generated, depending on the eda gene chosen, were designated pBF523 (e.g., containing the PAO1-eda) and pBF568 (e.g., containing the E. coli-eda), respectively. The approximately 1386 bp TEF-EDA-ADHt cassette from either plasmid pBF 523 or pBF568 was then gel extracted using the NheI-StuI sites.
The final vector was generated by first altering the Nde1 site in pUC19 using the mutagenesis primers described below.

KAS/SDM-Ndel-pUC18-5

(SEQ ID NO: 298)

	gattgtactgagagtgcacaatatgcggtgtgaaatacc

	KAS/SDM-Ndel-pUC18-3

(SEQ ID NO: 299)

ggtatttcacaccgcatattgtgcactctcagtacaatc

About 50 ng of pUC19 plasmid DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol SDM-specific primers and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 15 rounds of 95° C. for 15 seconds, 55° C. for 40 seconds, and 72° C. for 3 minutes. A final 10 minute extension reaction at 72° C. was also included. The PCR reaction mixture was then digested with 30 U of DpnI for about 2 hours and 5 μl of the digested PCR reaction mixture was used to transform competent DH5α (Zymo Research, Orange, Calif.) and plated onto LB plates containing 100 μg/ml ampicillin. The structure of the final plasmid, pBF421, was confirmed by restriction digests.
An approximately 1359 bp EcoRI fragment containing the 2μ yeast origin cassette was cloned into the EcoRI site of plasmid pBF421 in a 10 μl ligation reaction mixture containing 1× ligation buffer, 50 ng of EcoRI-digested pBF421 80 ng of EcoRI-digested 2μ cassette, and 1 U T4 DNA ligase (Fermentas). The reaction was incubated at room temperature for about 2 hours and 3 μl of this was used to transform competent DH5α (Zymo Research, Orange, Calif.). The structure of the resultant plasmid, pBF429, was confirmed by restriction enzyme digests.
Plasmid pBF429 was then digested with BamHI and SalI and ligated to the BamHI-SalI KANMX4 cassette described above. The resultant plasmid, designated pBF515, was digested with BamHI and NdeI and ligated to the BamHI-NdeI fragment containing the 2802 bp GPD-EDD-CYCt fragment from pBF475. The resulting plasmid, designated pBF522, was digested with NheI-StuI and was ligated to the 1386 bp NheI-StuI TEF-EDA-ADHt fragment from plasmids pBF523 or pBF568, creating final plasmids pBF524 and pBF612.
Expression levels of each of the single plasmid eda/edd expression system vectors was assayed and compared against the original eda/edd two plasmid expression system vectors. The results, presented in FIG. 14, graphically illustrate edd/eda coupled assay kinetics for the single and two plasmid systems. The kinetics graphs for both expression systems show substantially similar enzyme kinetics over the major of the time course.

Example 17

Nucleotide and Amino Acid Sequences of Over Expressed Activities Useful for Increasing Sugar Transport and/or Sugar Metabolism

As noted herein, increased or over expression of certain activities can result in increased ethanol production due to an increase in the utilization of the fermentation substrate, sometimes due to an increase in transport and/or metabolism of a desired sugar. Non-limiting examples of activities that can be over expressed to increase ethanol production by increasing sugar transport and/or metabolism include activities encoded by the genes gxf1, gxs1, hxt7, zwf1, gal2, sol3, sol4, the like, homologs thereof (e.g., Candida albicans Sol1p, Schizosaccharomyces pombe Sol1p, human PGLS and human H6PD), that can be expressed in a desired host organism, and combinations thereof. Nucleotide and amino acid sequences for some of these additional activities are given below. In some embodiments, 1, 2, 3, 4, 5, 6 or more of the non-limiting additional activities can be increased in expression or over expressed in an engineered host, thereby increasing transport and/or metabolism of a desired carbon source, wherein increased transport and/or metabolism of a desired carbon source results in increased ethanol production.

Nucleotide Sequences
Debaryomyces hansenii gxf1

(SEQ ID NO: 113)

ATGTCTCAAGAAGAATATAGTTCTGGGGTACAAACCCCAGTTTCTAACCATTCTGGTTTAGAGA

AAGAAGAGCAACACAAGTTAGACGGTTTAGATGAGGATGAAATTGTCGATCAATTACCTTCTTT

ACCAGAAAAATCAGCTAAGGATTATTTATTAATTTCTTTCTTCTGTGTATTAGTTGCATTTGGTG

GTTTTGTTTTCGGTTTCGATACTGGTACTATCTCAGGTTTCGTTAACATGAGTGATTACTTGGA

AAGATTCGGTGAGCTTAATGCAGATGGTGAATATTTCTTATCTAATGTTAGAACTGGTTTGATT

GTTGCTATTTTTAATGTTGGTTGTGCTGTCGGTGGTATTTTCTTATCTAAGATTGCTGATGTTTA

TGGTAGAAGAATTGGTCTTATGTTTTCCATGATTATTTATGTGATTGGTATAATTGTTCAAATCT

CAGCTTCTGACAAGTGGTATCAAATCGTTGTTGGTAGAGCTATTGCAGGTTTAGCTGTTGGTA

CCGTTTCTGTCTTATCCCCATTATTCATTGGTGAATCAGCACCTAAAACCTTAAGAGGTACTTT

AGTGTGTTGTTTCCAATTATGTATTACCTTAGGTATCTTCTTAGGTTACTGTACTACATATGGTA

CTAAAACCTACACCGACTCTAGACAATGGAGAATTCCATTAGGTTTATGTTTTGTTTGGGCTAT

CATGTTGGTTATTGGTATGGTTTGCATGCCAGAATCACCAAGATACTTAGTTGTCAAGAACAAG

ATTGAAGAAGCTAAGAAATCGATTGGTAGATCCAACAAGGTTTCACCAGAAGATCCTGCTGTT

TACACCGAAGTCCAATTGATTCAAGCAGGTATTGAAAGAGAAAGTTTAGCTGGTTCTGCCTCTT

GGACCGAATTGGTTACTGGTAAGCCAAGAATCTTTCGTAGAGTCATTATGGGTATTATGTTACA

ATCTTTACAACAATTGACTGGTGACAACTATTTCTTCTACTATGGTACTACTATTTTCCAAGCTG

TCGGTATGACTGATTCCTTCCAAACATCTATTGTTTTAGGTGTTGTTAACTTTGCATCTACATTT

CTCGGTATCTACACAATTGAAAGATTCGGTAGAAGATTATGTTTGTTAACTGGTTCTGTCTGTA

TGTTCGTTTGTTTCATCATTTACTCCATTTTGGGTGTTACAAACTTATATATTGATGGCTACGAT

GGTCCAACTTCGGTTCCAACCGGTGATGCGATGATTTTCATTACTACCTTATACATTTTCTTCT

TCGCATCCACCTGGGCTGGTGGTGTCTACTGTATCGTTTCCGAAACATACCCATTGAGAATTA

GATCTAAGGCCATGTCCGTTGCCACCGCTGCTAACTGGATTTGGGGTTTCTTGATCTCTTTCT

TCACTCCATTCATCACCTCGGCTATCCACTTCTACTACGGTTTCGTTTTCACAGGATGTTTGTT

ATTCTCGTTCTTTTACGTTTACTTCTTTGTTGTTGAAACTAAGGGATTAACTTTAGAAGAAGTTG

ATGAATTGTATGCCCAAGGTGTTGCCCCATGGAAGTCATCGAAATGGGTTCCACCAACCAAGG

AAGAAATGGCCCATTCTTCAGGATATGCTGCTGAAGCCAAACCTCACGATCAACAAGTATAA

Saccharomyces cerevisiae gal2

(SEQ ID NO: 114)

ATGGCAGTTGAGGAGAACAATATGCCTGTTGTTTCACAGCAACCCCAAGCTGGTGAAGAC

GTGATCTCTTCACTCAGTAAAGATTCCCATTTAAGCGCACAATCTCAAAAGTATTCTAAT

GATGAATTGAAAGCCGGTGAGTCAGGGTCTGAAGGCTCCCAAAGTGTTCCTATAGAGATA

CCCAAGAAGCCCATGTCTGAATATGTTACCGTTTCCTTGCTTTGTTTGTGTGTTGCCTTC

GGCGGCTTCATGTTTGGCTGGGATACCGGTACTATTTCTGGGTTTGTTGTCCAAACAGAC

TTTTTGAGAAGGTTTGGTATGAAACATAAGGATGGTACCCACTATTTGTCAAACGTCAGA

ACAGGTTTAATCGTCGCCATTTTCAATATTGGCTGTGCCTTTGGTGGTATTATACTTTCC

AAAGGTGGAGATATGTATGGCCGTAAAAAGGGTCTTTCGATTGTCGTCTCGGTTTATATA

GTTGGTATTATCATTCAAATTGCCTCTATCAACAAGTGGTACCAATATTTCATTGGTAGA

ATCATATCTGGTTTGGGTGTCGGCGGCATCGCCGTCTTATGTCCTATGTTGATCTCTGAA

ATTGCTCCAAAGCACTTGAGAGGCACACTAGTTTCTTGTTATCAGCTGATGATTACTGCA

GGTATCTTTTTGGGCTACTGTACTAATTACGGTACAAAGAGCTATTCGAACTCAGTTCAA

TGGAGAGTTCCATTAGGGCTATGTTTCGCTTGGTCATTATTTATGATTGGCGCTTTGACG

TTAGTTCCTGAATCCCCACGTTATTTATGTGAGGTGAATAAGGTAGAAGACGCCAAGCGT

TCCATTGCTAAGTCTAACAAGGTGTCACCAGAGGATCCTGCCGTCCAGGCAGAGTTAGAT

CTGATCATGGCCGGTATAGAAGCTGAAAAACTGGCTGGCAATGCGTCCTGGGGGGAATTA

TTTTCCACCAAGACCAAAGTATTTCAACGTTTGTTGATGGGTGTGTTTGTTCAAATGTTC

CAACAATTAACCGGTAACAATTATTTTTTCTACTACGGTACCGTTATTTTCAAGTCAGTT

GGCCTGGATGATTCCTTTGAAACATCCATTGTCATTGGTGTAGTCAACTTTGCCTCCACT

TTCTTTAGTTTGTGGACTGTCGAAAACTTGGGACATCGTAAATGTTTACTTTTGGGCGCT

GCCACTATGATGGCTTGTATGGTCATCTACGCCTCTGTTGGTGTTACTAGATTATATCCT

CACGGTAAAAGCCAGCCATCTTCTAAAGGTGCCGGTAACTGTATGATTGTCTTTACCTGT

TTTTATATTTTCTGTTATGCCACAACCTGGGCGCCAGTTGCCTGGGTCATCACAGCAGAA

TCATTCCCACTGAGAGTCAAGTCGAAATGTATGGCGTTGGCCTCTGCTTCCAATTGGGTA

TGGGGGTTCTTGATTGCATTTTTCACCCCATTCATCACATCTGCCATTAACTTCTACTAC

GGTTATGTCTTCATGGGCTGTTTGGTTGCCATGTTTTTTTATGTCTTTTTCTTTGTTCCA

GAAACTAAAGGCCTATCGTTAGAAGAAATTCAAGAATTATGGGAAGAAGGTGTTTTACCT

TGGAAATCTGAAGGCTGGATTCCTTCATCCAGAAGAGGTAATAATTACGATTTAGAGGAT

TTACAACATGACGACAAACCGTGGTACAAGGCCATGCTAGAATAA

Saccharomyces cerevisiae sol3

(SEQ ID NO: 115)

ATGGTGACAGTCGGTGTGTTTTCTGAGAGGGCTAGTTTGACCCATCAATTGGGGGAATTC

ATCGTCAAGAAACAAGATGAGGCGCTGCAAAAGAAGTCAGACTTTAAAGTTTCCGTTAGC

GGTGGCTCTTTGATCGATGCTCTGTATGAAAGTTTAGTAGCGGACGAATCACTATCTTCT

CGAGTGCAATGGTCTAAATGGCAAATCTACTTCTCTGATGAAAGAATTGTGCCACTGACG

GACGCTGACAGCAATTATGGTGCCTTCAAGAGAGCTGTTCTAGATAAATTACCCTCGACT

AGTCAGCCAAACGTTTATCCCATGGACGAGTCCTTGATTGGCAGCGATGCTGAATCTAAC

AACAAAATTGCTGCAGAGTACGAGCGTATCGTACCTCAAGTGCTTGATTTGGTACTGTTG

GGCTGTGGTCCTGATGGACACACTTGTTCCTTATTCCCTGGAGAAACACATAGGTACTTG

CTGAACGAAACAACCAAAAGAGTTGCTTGGTGCCACGATTCTCCCAAGCCTCCAAGTGAC

AGAATCACCTTCACTCTGCCTGTGTTGAAAGACGCCAAAGCCCTGTGTTTTGTGGCTGAG

GGCAGTTCCAAACAAAATATAATGCATGAGATCTTTGACTTGAAAAACGATCAATTGCCA

ACCGCATTGGTTAACAAATTATTTGGTGAAAAAACATCCTGGTTCGTTAATGAGGAAGCT

TTTGGAAAAGTTCAAACGAAAACTTTTTAG

Saccharomyces cerevisiae zwf1

(SEQ ID NO: 116)

ATGAGTGAAGGCCCCGTCAAATTCGAAAAAAATACCGTCATATCTGTCTTTGGTGCGTCA

GGTGATCTGGCAAAGAAGAAGACTTTTCCCGCCTTATTTGGGCTTTTCAGAGAAGGTTAC

CTTGATCCATCTACCAAGATCTTCGGTTATGCCCGGTCCAAATTGTCCATGGAGGAGGAC

CTGAAGTCCCGTGTCCTACCCCACTTGAAAAAACCTCACGGTGAAGCCGATGACTCTAAG

GTCGAACAGTTCTTCAAGATGGTCAGCTACATTTCGGGAAATTACGACACAGATGAAGGC

TTCGACGAATTAAGAACGCAGATCGAGAAATTCGAGAAAAGTGCCAACGTCGATGTCCCA

CACCGTCTCTTCTATCTGGCCTTGCCGCCAAGCGTTTTTTTGACGGTGGCCAAGCAGATC

AAGAGTCGTGTGTACGCAGAGAATGGCATCACCCGTGTAATCGTAGAGAAACCTTTCGGC

CACGACCTGGCCTCTGCCAGGGAGCTGCAAAAAAACCTGGGGCCCCTCTTTAAAGAAGAA

GAGTTGTACAGAATTGACCATTACTTGGGTAAAGAGTTGGTCAAGAATCTTTTAGTCTTG

AGGTTCGGTAACCAGTTTTTGAATGCCTCGTGGAATAGAGACAACATTCAAAGCGTTCAG

ATTTCGTTTAAAGAGAGGTTCGGCACCGAAGGCCGTGGCGGCTATTTCGACTCTATAGGC

ATAATCAGAGACGTGATGCAGAACCATCTGTTACAAATCATGACTCTCTTGACTATGGAA

AGACCGGTGTCTTTTGACCCGGAATCTATTCGTGACGAAAAGGTTAAGGTTCTAAAGGCC

GTGGCCCCCATCGACACGGACGACGTCCTCTTGGGCCAGTACGGTAAATCTGAGGACGGG

TCTAAGCCCGCCTACGTGGATGATGACACTGTAGACAAGGACTCTAAATGTGTCACTTTT

GCAGCAATGACTTTCAACATCGAAAACGAGCGTTGGGAGGGCGTCCCCATCATGATGCGT

GCCGGTAAGGCTTTGAATGAGTCCAAGGTGGAGATCAGACTGCAGTACAAAGCGGTCGCA

TCGGGTGTCTTCAAAGACATTCCAAATAACGAACTGGTCATCAGAGTGCAGCCCGATGCC

GCTGTGTACCTAAAGTTTAATGCTAAGACCCCTGGTCTGTCAAATGCTACCCAAGTCACA

GATCTGAATCTAACTTACGCAAGCAGGTACCAAGACTTTTGGATTCCAGAGGCTTACGAG

GTGTTGATAAGAGACGCCCTACTGGGTGACCATTCCAACTTTGTCAGAGATGACGAATTG

GATATCAGTTGGGGCATATTCACCCCATTACTGAAGCACATAGAGCGTCCGGACGGTCCA

ACACCGGAAATTTACCCCTACGGATCAAGAGGTCCAAAGGGATTGAAGGAATATATGCAA

AAACACAAGTATGTTATGCCCGAAAAGCACCCTTACGCTTGGCCCGTGACTAAGCCAGAA

GATACGAAGGATAATTAG

Amino Acid Sequences
Debaryomyces hansenii gxf1

(SEQ ID NO: 117)

1	MSQEEYSSGV QTPVSNHSGL EKEEQHKLDG LDEDEIVDQL PSLPEKSAKD YLLISFFCVL

61	VAFGGFVFGF DTGTISGFVN MSDYLERFGE LNADGEYFLS NVRTGLIVAI FNVGCAVGGI

121	FLSKIADVYG RRIGLMFSMI IYVIGIIVQI SASDKWYQIV VGRAIAGLAV GTVSVLSPLF

181	IGESAPKTLR GTLVCCFQLC ITLGIFLGYC TTYGTKTYTD SRQWRIPLGL CFVWAIMLVI

241	GMVCMPESPR YLVVKNKIEE AKKSIGRSNK VSPEDPAVYT EVQLIQAGIE RESLAGSASW

301	TELVTGKPRI FRRVIMGIML QSLQQLTGDN YFFYYGTTIF QAVGMTDSFQ TSIVLGVVNF

361	ASTFLGIYTI ERFGRRLCLL TGSVCMFVCF IIYSILGVTN LYIDGYDGPT SVPTGDAMIF

421	ITTLYIFFFA STWAGGVYCI VSETYPLRIR SKAMSVATAA NWIWGFLISF FTPFITSAIH

481	FYYGFVFTGC LLFSFFYVYF FVVETKGLTL EEVDELYAQG VAPWKSSKWV PPTKEEMAHS

541	SGYAAEAKPH DQQV

Saccharomyces cerevisiae gal2

(SEQ ID NO: 118)

1	MAVEENNMPV VSQQPQAGED VISSLSKDSH LSAQSQKYSN DELKAGESGS

51	EGSQSVPIEI PKKPMSEYVT VSLLCLCVAF GGFMFGWDTG TISGFVVQTD

101	FLRRFGMKHK DGTHYLSNVR TGLIVAIFNI GCAFGGIILS KGGDMYGRKK

151	GLSIVVSVYI VGIIIQIASI NKWYQYFIGR IISGLGVGGI AVLCPMLISE

201	IAPKHLRGTL VSCYQLMITA GIFLGYCTNY GTKSYSNSVQ WRVPLGLCFA

251	WSLFMIGALT LVPESPRYLC EVNKVEDAKR SIAKSNKVSP EDPAVQAELD

301	LIMAGIEAEK LAGNASWGEL FSTKTKVFQR LLMGVFVQMF QQLTGNNYFF

351	YYGTVIFKSV GLDDSFETSI VIGVVNFAST FFSLWTVENL GHRKCLLLGA

401	ATMMACMVIY ASVGVTRLYP HGKSQPSSKG AGNCMIVFTC FYIFCYATTW

451	APVAWVITAE SFPLRVKSKC MALASASNWV WGFLIAFFTP FITSAINFYY

501	GYVFMGCLVA MFFYVFFFVP ETKGLSLEEI QELWEEGVLP WKSEGWIPSS

551	RRGNNYDLED LQHDDKPWYK AMLE

Saccharomyces cerevisiae zwf1

(SEQ ID NO: 119)

1	MSEGPVKFEK NTVISVFGAS GDLAKKKTFP ALFGLFREGY LDPSTKIFGY

51	ARSKLSMEED LKSRVLPHLK KPHGEADDSK VEQFFKMVSY ISGNYDTDEG

101	FDELRTQIEK FEKSANVDVP HRLFYLALPP SVFLTVAKQI KSRVYAENGI

151	TRVIVEKPFG HDLASARELQ KNLGPLFKEE ELYRIDHYLG KELVKNLLVL

201	RFGNQFLNAS WNRDNIQSVQ ISFKERFGTE GRGGYFDSIG IIRDVMQNHL

251	LQIMTLLTME RPVSFDPESI RDEKVKVLKA VAPIDTDDVL LGQYGKSEDG

301	SKPAYVDDDT VDKDSKCVTF AAMTFNIENE RWEGVPIMMR AGKALNESKV

351	EIRLQYKAVA SGVFKDIPNN ELVIRVQPDA AVYLKFNAKT PGLSNATQVT

401	DLNLTYASRY QDFWIPEAYE VLIRDALLGD HSNFVRDDEL DISWGIFTPL

451	LKHIERPDGP TPEIYPYGSR GPKGLKEYMQ KHKYVMPEKH PYAWPVTKPE

501	DTKDN

Saccharomyces cerevisiae sol3

(SEQ ID NO: 120)

1	MVTVGVFSER ASLTHQLGEF IVKKQDEALQ KKSDFKVSVS GGSLIDALYE

51	SLVADESLSS RVQWSKWQIY FSDERIVPLT DADSNYGAFK RAVLDKLPST

101	SQPNVYPMDE SLIGSDAESN NKIAAEYERI VPQVLDLVLL GCGPDGHTCS

151	LFPGETHRYL LNETTKRVAW CHDSPKPPSD RITFTLPVLK DAKALCFVAE

201	GSSKQNIMHE IFDLKNDQLP TALVNKLFGE KTSWFVNEEA FGKVQTKTF

Example 18

Cloning of Additional ZWF1 Candidate Genes

A variety of ZWF1 genes were cloned from S. cerevisiae, Zymomonas mobilis, Pseudomonas fluorescens (zwf1 and zwf2), and P. aeruginosa strain PAO1. The sequences of these additional ZWF1 genes are given below.

zwf1 from P. fluorescens
Amino Acid Sequence

(SEQ. ID. NO: 123)

MTTTRKKSKALPAPPTTLFLFGARGDLVKRLLMPALYNLSRDGLLDEGLRIVGVDHNAVSDAEFAT

LLEDFLRDEVLNKQGQGAAVDAAVWARLTRGINYVQGDFLDDSTYAELAARIAASGTGNAVFYLA

TAPRFFSEVVRRLGSAGLLEEGPQAFRRVVIEKPFGSDLQTAEALNGCLLKVMSEKQIYRIDHYLG

KETVQNILVSRFSNSLFEAFWNNHYIDHVQITAAETVGVETRGSFYEHTGALRDMVPNHLFQLLAM

VAMEPPAAFGADAVRGEKAKVVGAIRPWSVEEARANSVRGQYSAGEVAGKALAGYREEANVAP

DSSTETYVALKVMIDNWRWVGVPFYLRTGKRMSVRDTEIVICFKPAPYAQFRDTEVERLLPTYLRI

QIQPNEGMWFDLLAKKPGPSLDMANIELGFAYRDFFEMQPSTGYETLIYDCLIGDQTLFQRADNIE

NGWRAVQPFLDAWQQDASLQNYPAGVDGPAAGDELLARDGRVWRPLG

Nucleotide Sequence

(SEQ. ID. NO: 124)

ATGACCACCACGCGAAAGAAGTCCAAGGCGTTGCCGGCGCCGCCGACCACGCTGTTCCTGT

TCGGCGCCCGCGGTGATCTGGTCAAGCGCCTGCTGATGCCGGCGCTGTACAACCTCAGCCG

CGACGGTTTGCTGGATGAGGGGCTGCGGATTGTCGGCGTCGACCACAACGCGGTGAGCGAC

GCCGAGTTCGCCACGCTGCTGGAAGACTTCCTTCGCGATGAAGTGCTCAACAAGCAAGGCCA

GGGGGCGGCGGTGGATGCCGCCGTCTGGGCCCGCCTGACCCGGGGCATCAACTATGTCCA

GGGCGATTTTCTCGACGACTCCACCTATGCCGAACTGGCGGCGCGGATTGCCGCCAGCGGC

ACCGGCAACGCGGTGTTCTACCTGGCCACCGCACCGCGCTTCTTCAGTGAAGTGGTGCGCC

GCCTGGGCAGCGCCGGGTTGCTGGAGGAGGGGCCGCAGGCTTTTCGCCGGGTGGTGATCG

AAAAACCCTTCGGCTCCGACCTGCAGACCGCCGAAGCCCTCAACGGCTGCCTGCTCAAGGTC

ATGAGCGAGAAGCAGATCTATCGCATCGACCATTACCTGGGCAAGGAAACGGTCCAGAACAT

CCTGGTCAGCCGTTTTTCCAACAGCCTGTTCGAGGCATTCTGGAACAACCATTACATCGACCA

CGTGCAGATCACCGCGGCGGAAACCGTCGGCGTGGAAACCCGTGGCAGCTTTTATGAACAC

ACCGGTGCCCTGCGGGACATGGTGCCCAACCACCTGTTCCAGTTGCTGGCGATGGTGGCCA

TGGAGCCGCCCGCTGCCTTTGGCGCCGATGCGGTACGTGGCGAAAAGGCCAAGGTGGTGG

GGGCTATCCGCCCCTGGTCCGTGGAAGAGGCCCGGGCCAACTCGGTGCGCGGCCAGTACA

GCGCCGGTGAAGTGGCCGGCAAGGCCCTGGCGGGCTACCGCGAGGAAGCCAACGTGGCGC

CGGACAGCAGCACCGAAACCTACGTTGCGCTGAAGGTGATGATCGACAACTGGCGCTGGGT

CGGGGTGCCGTTCTACCTGCGCACCGGCAAGCGCATGAGTGTGCGCGACACCGAGATCGTC

ATCTGCTTCAAGCCGGCGCCCTATGCACAGTTCCGCGATACCGAGGTCGAGCGCCTGTTGCC

GACCTACCTGCGGATCCAGATCCAGCCCAACGAAGGCATGTGGTTCGACCTGCTGGCGAAAA

AGCCCGGGCCGAGCCTGGACATGGCCAACATCGAACTGGGTTTTGCCTACCGCGACTTTTTC

GAGATGCAGCCCTCCACCGGCTACGAAACCCTGATCTACGACTGCCTGATCGGCGACCAGAC

CCTGTTCCAGCGCGCCGACAACATCGAGAACGGCTGGCGCGCGGTGCAACCCTTCCTCGAT

GCCTGGCAACAGGACGCCAGCTTGCAGAACTACCCGGCGGGCGTGGATGGCCCGGCAGCC

GGGGATGAACTGCTGGCCCGGGATGGCCGCGTATGGCGACCCCTGGGGTGA

zwf2 from P. fluorescens
Amino Acid Sequence

(SEQ. ID. NO: 125)

MPSITVEPCTFALFGALGDLALRKLFPALYQLDAAGLLHDDTRILALAREPGSEQEHLANIETELHKY

VGDKDIDSQVLQRFLVRLSYLHVDFLKAEDYVALAERVGSEQRLIAYFATPAAVYGAICENLSRVGL

NQHTRVVLEKPIGSDLDSSRKVNDAVAQFFPETRIYRIDHYLGKETVQNLIALRFANSLFETQWNQ

NYISHVEITVAEKVGIEGRWGYFDKAGQLRDMIQNHLLQLLCLIAMDPPADLSADSIRDEKVKVLKA

LAPISPEGLTTQVVRGQYIAGHSEGQSVPGYLEEENSNTQSDTETFVALRADIRNWRWAGVPFYL

RTGKRMPQKLSQIVIHFKEPSHYIFAPEQRLQISNKLIIRLQPDEGISLRVMTKEQGLDKGMQLRSG

PLQLNFSDTYRSARIPDAYERLLLEVMRGNQNLFVRKDEIEAAWKWCDQLIAGWKKSGDAPKPYA

AGSWGPMSSIALITRDGRSWYGDI

Nucleotide Sequence

(SEQ. ID. NO: 126)

ATGCCTTCGATAACGGTTGAACCCTGCACCTTTGCCTTGTTTGGCGCGCTGGGCGATCTGGC

GCTGCGTAAGCTGTTTCCTGCCCTGTACCAACTCGATGCCGCCGGTTTGCTGCATGACGACA

CGCGCATCCTGGCCCTGGCCCGCGAGCCTGGCAGCGAGCAGGAACACCTGGCGAATATCGA

AACCGAGCTGCACAAGTATGTCGGCGACAAGGATATCGATAGCCAGGTCCTGCAGCGTTTTC

TCGTCCGCCTGAGCTACCTGCATGTGGACTTCCTCAAGGCCGAGGACTACGTCGCCCTGGCC

GAACGTGTCGGCAGCGAGCAGCGCCTGATTGCCTACTTCGCCACGCCGGCGGCGGTGTATG

GCGCGATCTGCGAAAACCTCTCCCGGGTCGGGCTCAACCAGCACACCCGTGTGGTCCTGGA

AAAACCCATCGGCTCGGACCTGGATTCATCACGCAAGGTCAACGACGCGGTGGCGCAGTTCT

TCCCGGAAACCCGCATCTACCGGATCGACCACTACCTGGGCAAGGAAACGGTGCAGAACCTG

ATTGCCCTGCGTTTCGCCAACAGCCTGTTCGAAACCCAGTGGAACCAGAACTACATCTCCCAC

GTGGAAATCACCGTGGCCGAGAAGGTCGGCATCGAAGGTCGCTGGGGCTATTTCGACAAGG

CCGGCCAACTGCGGGACATGATCCAGAACCACTTGCTGCAACTGCTCTGCCTGATCGCGATG

GACCCGCCGGCCGACCTTTCGGCCGACAGCATCCGCGACGAGAAGGTCAAGGTGCTCAAGG

CCCTGGCGCCCATCAGCCCGGAAGGCCTGACCACCCAGGTGGTGCGCGGCCAGTACATCGC

CGGCCACAGCGAAGGCCAGTCGGTGCCGGGCTACCTGGAGGAAGAAAACTCCAACACCCAG

AGCGACACCGAGACCTTCGTCGCCCTGCGCGCCGATATCCGCAACTGGCGCTGGGCCGGTG

TGCCTTTCTACCTGCGCACCGGCAAGCGCATGCCACAGAAGCTGTCGCAGATCGTCATCCAC

TTCAAGGAACCCTCGCACTACATCTTCGCCCCCGAGCAGCGCCTGCAGATCAGCAACAAGCT

GATCATCCGCCTGCAGCCGGACGAAGGTATCTCGTTGCGGGTGATGACCAAGGAGCAGGGC

CTGGACAAGGGCATGCAACTGCGCAGCGGTCCGTTGCAGCTGAATTTTTCCGATACCTATCG

CAGTGCACGGATCCCCGATGCCTACGAGCGGTTGTTGCTGGAAGTGATGCGCGGCAATCAG

AACCTGTTTGTGCGCAAAGATGAAATCGAAGCCGCGTGGAAGTGGTGTGACCAGTTGATTGC

CGGGTGGAAGAAATCCGGCGATGCGCCCAAGCCGTACGCGGCCGGGTCCTGGGGGCCGAT

GAGCTCCATTGCACTGATCACGCGGGATGGGAGGTCTTGGTATGGCGATATCTaA

zwf1 from P. aeruginosa, PAO1
Amino Acid Sequence

(SEQ. ID. NO: 127)

MPDVRVLPCTLALFGALGDLALRKLFPALYQLDRENLLHRDTRVLALARDEGAPAEHLATLEQRLR

LAVPAKEWDDVVWQRFRERLDYLSMDFLDPQAYVGLREAVDDELPLVAYFATPASVFGGICENLA

AAGLAERTRVVLEKPIGHDLESSREVNEAVARFFPESRIYRIDHYLGKETVQNLIALRFANSLFETQ

WNQNHISHVEITVAEKVGIEGRWGYFDQAGQLRDMVQNHLLQLLCLIAMDPPSDLSADSIRDEKV

KVLRALEPIPAEQLASRVVRGQYTAGFSDGKAVPGYLEEEHANRDSDAETFVALRVDIRNWRWS

GVPFYLRTGKRMPQKLSQIVIHFKEPPHYIFAPEQRSLISNRLIIRLQPDEGISLQVMTKDQGLGKG

MQLRTGPLQLSFSETYHAARIPDAYERLLLEVTQGNQYLFVRKDEVEFAWKWCDQLIAGWERLSE

APKPYPAGSWGPVASVALVARDGRSWYGDF

Nucleotide Sequence

(SEQ. ID. NO: 128)

ATGCCTGATGTCCGCGTTCTGCCTTGCACGTTAGCGCTGTTCGGTGCGCTGGGCGATCTCGC

CTTGCGCAAGCTGTTCCCGGCGCTCTACCAACTCGATCGTGAGAACCTGCTGCACCGCGATA

CCCGCGTCCTGGCCCTGGCCCGTGACGAAGGCGCTCCCGCCGAACACCTGGCGACGCTGG

AGCAGCGCCTGCGCCTGGCAGTGCCGGCGAAGGAGTGGGACGACGTGGTCTGGCAGCGTT

TCCGCGAACGCCTCGACTACCTGAGCATGGACTTCCTCGACCCGCAGGCCTATGTCGGCTTG

CGCGAGGCGGTGGATGACGAACTGCCGCTGGTCGCCTACTTCGCCACGCCGGCCTCGGTGT

TCGGCGGCATCTGCGAGAACCTCGCCGCCGCCGGTCTCGCCGAGCGCACCCGGGTGGTGC

TGGAGAAGCCCATCGGTCATGACCTGGAGTCGTCCCGCGAGGTCAACGAGGCAGTCGCCCG

GTTCTTCCCGGAAAGCCGCATCTACCGGATCGACCATTACCTGGGCAAGGAGACGGTGCAGA

ACCTGATCGCCCTGCGCTTCGCCAACAGCCTCTTCGAGACCCAGTGGAACCAGAACCACATC

TCCCACGTGGAGATCACCGTGGCCGAGAAGGTCGGCATCGAAGGCCGCTGGGGCTACTTCG

ACCAGGCCGGGCAACTGCGCGACATGGTGCAGAACCACCTGCTGCAACTGCTCTGCCTGAT

CGCCATGGATCCGCCCAGCGACCTTTCGGCGGACAGCATTCGCGACGAGAAGGTCAAGGTC

CTCCGCGCCCTCGAGCCGATTCCCGCAGAACAACTGGCTTCGCGCGTGGTGCGTGGGCAGT

ACACCGCCGGTTTCAGCGACGGCAAGGCAGTGCCGGGCTACCTGGAGGAGGAACATGCGAA

TCGCGACAGCGACGCGGAAACCTTCGTCGCCCTGCGCGTGGACATCCGCAACTGGCGCTGG

TCGGGCGTGCCGTTCTACCTGCGCACCGGCAAGCGCATGCCGCAGAAGCTGTCGCAGATCG

TCATCCACTTCAAGGAGCCGCCGCACTACATCTTCGCTCCCGAGCAGCGTTCGCTGATCAGC

AACCGGCTGATCATCCGCCTGCAGCCGGACGAAGGTATCTCCCTGCAAGTGATGACCAAGGA

CCAGGGCCTGGGCAAGGGCATGCAATTGCGTACCGGCCCGCTGCAACTGAGTTTTTCCGAG

ACCTACCACGCGGCGCGGATTCCCGATGCCTACGAGCGTCTGCTGCTGGAGGTCACCCAGG

GCAACCAGTACCTGTTCGTGCGCAAGGACGAGGTGGAGTTCGCCTGGAAGTGGTGCGACCA

GCTGATCGCTGGCTGGGAACGCCTGAGCGAAGCGCCCAAGCCGTATCCGGCGGGGAGTTG

GGGGCCGGTGGCCTCGGTGGCCCTGGTGGCCCGCGATGGGAGGAGTTGGTATGGCGATTT

CTGA

zwf1 from Z. mobilis
Amino Acid Sequence

(SEQ. ID. NO: 129)

MTNTVSTMILFGSTGDLSQRMLLPSLYGLDADGLLADDLRIVCTSRSEYDTDGFRDFAEKALDRFV

ASDRLNDDAKAKFLNKLFYATVDITDPTQFGKLADLCGPVEKGIAIYLSTAPSLFEGAIAGLKQAGLA

GPTSRLALEKPLGQDLASSDHINDAVLKVFSEKQVYRIDHYLGKETVQNLLTLRFGNALFEPLWNS

KGIDHVQISVAETVGLEGRIGYFDGSGSLRDMVQSHILQLVALVAMEPPAHMEANAVRDEKVKVF

RALRPINNDTVFTHTVTGQYGAGVSGGKEVAGYIDELGQPSDTETFVAIKAHVDNWRWQGVPFYI

RTGKRLPARRSEIVVQFKPVPHSIFSSSGGILQPNKLRIVLQPDETIQISMMVKEPGLDRNGAHMRE

VWLDLSLTDVFKDRKRRIAYERLMLDLIEGDATLFVRRDEVEAQWVWIDGIREGWKANSMKPKTY

VSGTWGPSTAIALAERDGVTWYD

Nucleotide Sequence

(SEQ. ID. NO: 130)

ATGACAAATACCGTTTCGACGATGATATTGTTTGGCTCGACTGGCGACCTTTCACAGCGTATG

CTGTTGCCGTCGCTTTATGGTCTTGATGCCGATGGTTTGCTTGCAGATGATCTGCGTATCGTC

TGCACCTCTCGTAGCGAATACGACACAGATGGTTTCCGTGATTTTGCAGAAAAAGCTTTAGAT

CGCTTTGTCGCTTCTGACCGGTTAAATGATGACGCTAAAGCTAAATTCCTTAACAAGCTTTTCT

ACGCGACGGTCGATATTACGGATCCGACCCAATTCGGAAAATTAGCTGACCTTTGTGGCCCG

GTCGAAAAAGGTATCGCCATTTATCTTTCGACTGCGCCTTCTTTGTTTGAAGGGGCAATCGCT

GGCCTGAAACAGGCTGGTCTGGCTGGTCCAACTTCTCGCCTGGCGCTTGAAAAACCTTTAGG

TCAAGATCTTGCTTCTTCCGATCATATTAATGATGCGGTTTTGAAAGTTTTCTCTGAAAAGCAA

GTTTATCGTATTGACCATTATCTGGGTAAAGAAACGGTTCAGAATCTTCTGACCCTGCGTTTTG

GTAATGCTTTGTTTGAACCGCTTTGGAATTCAAAAGGCATTGACCACGTTCAGATCAGCGTTG

CTGAAACGGTTGGTCTTGAAGGTCGTATCGGTTATTTCGACGGTTCTGGCAGCTTGCGCGATA

TGGTTCAAAGCCATATCCTTCAGTTGGTCGCTTTGGTTGCAATGGAACCACCGGCTCATATGG

AAGCCAACGCTGTTCGTGACGAAAAGGTAAAAGTTTTCCGCGCTCTGCGTCCGATCAATAACG

ACACCGTCTTTACGCATACCGTTACCGGTCAATATGGTGCCGGTGTTTCTGGTGGTAAAGAAG

TTGCCGGTTACATTGACGAACTGGGTCAGCCTTCCGATACCGAAACCTTTGTTGCTATCAAAG

CGCATGTTGATAACTGGCGTTGGCAGGGTGTTCCGTTCTATATCCGCACTGGTAAGCGTTTAC

CTGCACGTCGTTCTGAAATCGTGGTTCAGTTTAAACCTGTTCCGCATTCGATTTTCTCTTCTTC

AGGTGGTATCTTGCAGCCGAACAAGCTGCGTATTGTCTTACAGCCTGATGAAACCATCCAGAT

TTCTATGATGGTGAAAGAACCGGGTCTTGACCGTAACGGTGCGCATATGCGTGAAGTTTGGCT

GGATCTTTCCCTCACGGATGTGTTTAAAGACCGTAAACGTCGTATCGCTTATGAACGCCTGAT

GCTTGATCTTATCGAAGGCGATGCTACTTTATTTGTGCGTCGTGACGAAGTTGAGGCGCAGTG

GGTTTGGATTGACGGAATTCGTGAAGGCTGGAAAGCCAACAGTATGAAGCCAAAAACCTATGT

CTCTGGTACATGGGGGCCTTCAACTGCTATAGCTCTGGCCGAACGTGATGGAGTAACTTGGT

ATGACTGA

All the above genes were PCR amplified from their genomic DNA sources with and without c-terminal 6-HIS tags (SEQ ID NO: 35) and cloned into the yeast expression vector p426GPD for testing.
Assays of Candidate ZWF1 Genes
Strain BY4742 zwf1 (ATCC Cat. No. 4011971; Winzeler E A, et al. Science 285: 901-906, 1999. PubMed: 10436161) was used as the base strain for all ZWF1 assays. The assays were performed as follows: A 5 ml overnight of the strain expressing the ZWF1 gene was grown in SCD-ura. A 50 ml culture of the strain was then grown for about 18 hours from an initial (OD₆₀₀of about 0.2 until it had reached about OD₆₀₀of about 4. The cells were centrifuged at 1046×g washed twice with 25 ml cold sterile water, and resuspended in 2 ml/g Yper Plus (Thermo Scientific) plus 1× protease inhibitors (EDTA-free). The cells were allowed to lyse at room temperature for about 30 minutes with constant rotation of the tubes. The lysate was centrifuged at 16,100×g for 10 minutes at 4° C. and the supernatants were transferred to a new 1.5 ml microcentrifuge tube. Quantification of the lysates was performed using the Coomassie-Plus kit (Thermo Scientific, San Diego, Calif.) as directed by the manufacturer.
Each kinetic assay was done using approximately 50 to 60 μg of crude extract in a reaction mixture containing 50 mM Tris-HCl, pH 8.9, and 1 mM NADP+ or NAD+. The reaction was started with 20 mM glucose-6-phosphate and the reaction was monitored at A340. The specific activity was measured as the μmol substrate/min/mg protein. The results of the assays are presented in the table below.


		Vmax	Km	Specific Activity
Zwf1	Cofactors	(μmol min⁻¹)	(M⁻¹)	(μmol min⁻¹mg⁻¹)

S. cerevisiae	NAD+	NA	NA	NA
	NADP+	0.9523	0.4546	224.07
S. cerevisiae +	NAD+	NA	NA	NA
His	NADP+	0.7267	0.4109	164.79
ZM4	NAD+	NA	NA	NA
	NADP+	NA	NA	NA
ZM4 + His	NAD+	0.0213	0.0156	0.1267
	NADP+	0.0027	0.0140	0.0160
P. fluorescens	NAD+	0.0158	0.6201	0.3132
1	NADP+	0.0213	0.8171	0.4208
P. fluorescens	NAD+	0.0126	4.9630	0.2473
1 + His	NADP+	0.0139	0.9653	0.2739
P. fluorescens	NAD+	ND	ND	ND
2	NADP+	NA	NA	NA
P. fluorescens	NAD+	NA	NA	NA
2 + His	NADP+	ND	ND	ND
PAO1	NAD+	NA	NA	NA
	NADP+	0.0104	0.6466	0.1564
PAO1 + His	NAD+	0.0074	0.0071	0.1098
	NADP+	0.0123	3.9050	0.1823

NA = cannot be calculated (substrate not used by enzyme)
ND = was not determined (either not enough crude available or cells did not grow)

Altering Cofactor Preference of S. cerevisiae ZWF1
ZWF1 from S. cerevisiae is an NADP⁺-only utilizing enzyme. Site-directed mutagenesis was used to alter of ZWF1 so that the altered ZWF1 could also utilize NAD+, thereby improving the REDOX balance within the cell. Site directed mutagenesis reactions were performed in the same manner for all mutations, and for mutants which include more than one mutation, each mutation was performed sequentially. About 50 ng of plasmid DNA was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol site directed mutagenesis specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 15 rounds of 95° C. for 15 seconds, 55° C. for 40 seconds, and 72° C. for 3 minutes. A final 10 minute extension reaction at 72° C. was also included. The PCR reaction mixture was then digested with 30 U of DpnI for about 2 hours and 5 μl of the digested PCR reaction mixture was used to transform competent DH5α (Zymo Research, Orange, Calif.) and plated onto LB plates containing the appropriate antibiotics. The table below lists mutants generated in a first round of mutagenesis.


Mutant #	zwf1_sc	Codon changes

1	A24G	GCA -> GGT

2	A24G/T28G	GCA -> GGT, ACT -> GGT

3	A51N	GCC -> AAT

4	A51D	GCC -> GAT

5	T28F	ACT -> TTT

6	K46R	AAG -> AGA

7	Y40L	TAC -> TTG

8	F33Y	TTT -> TAC

9	T28L	ACT -> TTG

10	V16L	GTC -> TTG

11	V13T	GTC -> ACT

12	L66E	CTA -> GAA

13	A24G/A51D	GCA -> GGT, GCC -> GAT

14	A24G/T28G/A51D	GCA -> GGT, ACT -> GGT,
		GCC -> GAT

15	R52D	CGG -> GAT

16	A51D/R52A	GCC -> GAT, CGG -> GCT

17	A24G/A51D/R52A	GCA -> GGT, GCC -> GAT,
		CGG -> GCT

18	A24G/T28G/A51D/	GCA -> GGT, ACT -> GGT,
	R52A	GCC -> GAT, CGG -> GCT

19	A51D/R52H	GCC -> GAT, CGG -> CAT

20	R52H	CGG -> CAT

21	D22R	GAT -> AGA

The oligonucleotides, utilized to generate the mutants listed in the table above, are listed in the table below. All oligonucleotides were purchased from Integrated DNA Technologies (IDT).


	Base
Mutation	plasmid	Oligo Name	Nucleotide sequence	SEQ ID NO:

1	pBF300	ka/zwf1sc_A24Gfor	gtgcgtcaggtgatctgggtaagaagaagacttttccc	300

1	pBF300	ka/zwf1sc_A24Grev	gggaaaagtcttcttcttacccagatcacctgacgcac	301

2	pBF300	ka/zwf1sc_T28Gfor	gtgatctgggtaagaagaagggttttcccgccttatttgg	302

2	pBF300	ka/zwf1sc_T28Grev	CCAAATAAGGCGGGAAAACCCTTCTTCT	303
			TACCCAGATCAC

3	pBF300	ka/zwf1sc_A51Nfor	ccttgatccatctaccaagatcttcggttataatcggtccaaa	304
			ttgtccat

3	pBF300	ka/zwf1sc_A51Nrev	atggacaatttggaccgattataaccgaagatcttggtagat	305
			ggatcaagg

4	pBF300	ka/zwf1sc_A51Dfor	atctaccaagatcttcggttatgatcggtccaaattgtccatg	306

4	pBF300	ka/zwf1sc_A51Drev	catggacaatttggaccgatcataaccgaagatcttggtag	307
			at

5	pBF300	ka/zwf1sc_T28Ffor	ggtgatctggcaaagaagaagttttttcccgccttatttggg	308

5	pBF300	ka/zwf1sc_T28Frev	cccaaataaggcgggaaaaaacttcttctttgccagatcacc	309

6	pBF300	ka/zwf1sc_K46Rfor	taccttgatccatctaccagaatcttcggttatgcccggt	310

6	pBF300	ka/zwf1sc_K46Rrev	accgggcataaccgaagattctggtagatggatcaaggta	311


7	pBF300	ka/zwf1sc_Y39Lfor	gggcttttcagagaaggtttgcttgatccatctaccaaga	312

7	pBF300	ka/zwf1sc_Y39Lrev	tcttggtagatggatcaagcaaaccttctctgaaaagccc	313

8	pBF300	ka/zwf1sc_F33Yfor	gaagaagacttttcccgccttatacgggcttttcagagaag	314

8	pBF300	ka/zwf1sc_F33Yrev	cttctctgaaaagcccgtataaggcgggaaaagtcttcttc	315

9	pBF300	ka/zwf1sc_T28Lfor	gtcaggtgatctggcaaagaagaagttgtttcccgccttattt	316
			gg

9	pBF300	ka/zwf1sc_T28Lrev	ccaaataaggcgggaaacaacttcttctttgccagatcacc	317
			tgac

10	pBF300	ka/zwf1sc_V16Lfor	cgaaaaaaataccgtcatatctttgtttggtgcgtcaggtgat	318
			ctg

10	pBF300	ka/zwf1sc_V16rev	cagatcacctgacgcaccaaacaaagatatgacggtattt	319
			ttttcg

12	pBF300	ka/zwf1sc_L66Efor	gacctgaagtcccgtgtcgaaccccacttgaaaaaacc	320

12	pBF300	ka/zwf1sc_L66Erev	ggttttttcaagtggggttcgacacgggacttcaggtc	321

13	pBF374	ka/zwf1sc_A24Gfor	gtgcgtcaggtgatctgggtaagaagaagacttttccc	322

13	pBF374	ka/zwf1sc_A24Grev	gggaaaagtcttcttcttacccagatcacctgacgcac	323

14	pBF374	ka/zwf1sc_A24Gfor	gtgcgtcaggtgatctgggtaagaagaagacttttccc	324

14	pBF374	ka/zwf1sc_A24Grev	gggaaaagtcttcttcttacccagatcacctgacgcac	325

15	pBF300	KA/zwf1mut15for	accaagatcttcggttatgccgattccaaattgtccatggag	326
			gag

15	pBF300	KA/zwf1mut15rev	ctcctccatggacaatttggaatcggcataaccgaagatctt	327
			ggt

16	pBF374	KA/zwf1mut16for	tccatctaccaagatcttcggttatgatgcttccaaattgtcca	328
			tggaggaggac

16	pBF374	KA/zwf1mut16rev	gtcctcctccatggacaatttggaagcatcataaccgaaga	329
			tcttggtagatgga

17	pBF441	KA/zwf1mut16for	tccatctaccaagatcttcggttatgatgcttccaaattgtcca	330
			tggaggaggac

17	pBF441	KA/zwf1mut16rev	gtcctcctccatggacaatttggaagcatcataaccgaaga	331
			tcttggtagatgga

18	pBF442	KA/zwf1mut16for	tccatctaccaagatcttcggttatgatgcttccaaattgtcca	332
			tggaggaggac

18	pBF442	KA/zwf1mut16rev	gtcctcctccatggacaatttggaagcatcataaccgaaga	333
			tcttggtagatgga

19	pBF374	KA/zwf1sc_mut19for	aagatcttcggttatgatcattccaaattgtccatggagg	334

19	pBF374	KA/zwf1sc_mut19rev	cctccatggacaatttggaatgatcataaccgaagatctt	335

20	pBF300	KA/zwf1sc_mut20for	aagatcttcggttatgcccattccaaattgtccatggagg	336

20	pBF300	KA/zwf1sc_mut20rev	cctccatggacaatttggaatgggcataaccgaagatctt	337

Initial kinetic screening of the ZWF1 mutants generated as described above, identified the following altered ZWF1 genes and preliminary cofactor phenotype.


		NAD+	NADP+
Mutant #	zwf1_sc	usage	usage

1	A24G	No	Yes
2	A24G/T28G	No	No
3	A51N	No	Yes
4	A51D	Yes	No
5	T28F	No	Yes
6	K46R	No	Yes
7	Y40L	No	Yes
8	F33Y	No	Yes
9	T28L	No	Yes
10	V16L	No	Yes
11	V13T	ND	ND
12	L66E	No	Yes
13	A24G/A51D	Yes	No
14	A24G/T28G/A51D	No	No
15	R52D	No	No
16	A51D/R52A	No	No
17	A24G/A51D/R52A	No	No
18	A24G/T28G/A51D/R52A	ND	ND
19	A51D/R52H	ND	ND
20	R52H	ND	ND
21	D22R	ND	ND

ND = not determined

Mutants 4 (A51D) and 13 (A24G/A51D) were identified as mutants which enabled NAD+ utilization with concomitant loss of NADP+ utilization.
Cloning of SOL3
The SOL3 gene from S. cerevisiae was cloned as follows. The approximately 750 bp SOL3 gene was PCR amplified from the BY4742 genome using primers KAS/5-SOL3-NheI and KAS/3′-SOL3-SalI, shown below.

KAS/5-SOL3-NheI

(SEQ ID NO: 338)

	gctagcatggtgacagtcggtgtgttttctgag

	KAS/3′-SOL3-SalI

(SEQ ID NO: 339)

gtcgacctaaaaagttttcgtttgaacttttcc

About 100 ng of genomic DNA from S. cerevisiae strain BY4742 was added to 1×Pfu Ultra II buffer, 0.3 mM dNTPs, 0.3 μmol gene-specific primers, and 1 U Pfu Ultra II polymerase (Agilent, La Jolla, Calif.) in a 50 μl reaction mix. The reaction was cycled at 95° C. for 10 minutes, followed by 30 rounds of 95° C. for 20 seconds, 55° C. for 30 seconds, and 72° C. for 15 seconds. A final 5 minute extension reaction at 72° C. was also included. The amplified product was TOPO cloned into the pCR Blunt II TOPO vector (Life Technologies, Carlsbad, Calif.) according to the manufacturer's recommendations and sequence verified (GeneWiz, San Diego, Calif.). The resultant plasmid was designated pBF301. The sequence of the S. cerevisiae SOL3 gene is given below.

S. cerevisiae SOL3

(SEQ. ID. NO: 131)

ATGGTGACAGTCGGTGTGTTTTCTGAGAGGGCTAGTTTGACCCATCAAT

TGGGGGAATTCATCGTCAAGAAACAAGATGAGGCGCTGCAAAAGAAGTCA

GACTTTAAAGTTTCCGTTAGCGGTGGCTCTTTGATCGATGCTCTGTATG

AAAGTTTAGTAGCGGACGAATCACTATCTTCTCGAGTGCAATGGTCTAA

ATGGCAAATCTACTTCTCTGATGAAAGAATTGTGCCACTGACGGACGCT

GACAGCAATTATGGTGCCTTCAAGAGAGCTGTTCTAGATAAATTACCCT

CGACTAGTCAGCCAAACGTTTATCCCATGGACGAGTCCTTGATTGGCAG

CGATGCTGAATCTAACAACAAAATTGCTGCAGAGTACGAGCGTATCGTA

CCTCAAGTGCTTGATTTGGTACTGTTGGGCTGTGGTCCTGATGGACACA

CTTGTTCCTTATTCCCTGGAGAAACACATAGGTACTTGCTGAACGAAAC

AACCAAAAGAGTTGCTTGGTGCCACGATTCTCCCAAGCCTCCAAGTGAC

AGAATCACCTTCACTCTGCCTGTGTTGAAAGACGCCAAAGCCCTGTGTT

TTGTGGCTGAGGGCAGTTCCAAACAAAATATAATGCATGAGATCTTTGA

CTTGAAAAACGATCAATTGCCAACCGCATTGGTTAACAAATTATTTGGT

GAAAAAACATCCTGGTTCGTTAATGAGGAAGCTTTTGGAAAAGTTCAAA

CGAAAACTTTTTAG

The NheI-SalI SOL3 gene fragment from plasmid pBF301 will be cloned into the SpeI-XhoI site in plasmids p413GPD and p423GPD (HIS3 marker-based plasmids; ATCC 87354 and ATCC 87355).
Testing of ZWF1/SOL3 Combinations in BY4742
A URA blaster cassette was digested with NotI and ligated into the MET17 integration cassette plasmid pBF691 to generate the Met17 knockout plasmid pBF772. Plasmid pBF772 was digested with PacI and linear fragments were purified by Zymo PCR purification kit (Zymo Research, Orange, Calif.) and concentrated in 10 μl ddH2O. LiCl2 high efficiency transformation was performed as shown described. About 1 μg linear MET17 knockout fragment was transformed into 50 μl fresh made BY4742 competent cells and cells were plated onto SCD-Ura plates at 30° C. for about 2-3 days. A single URA+ colony was streaked out on a SCD-Ura plate and grown at 30° C. for about 2-3 days. A single colony was inoculated overnight in YPD medium at 30° C. 50 μl of the overnight culture was then plated onto SCD complete −5FOA plates and incubated at 30° C. for about 3 days.
A single colony which grew on SCD complete-5FOA plates was then picked and inoculated in YPD medium and grown at 30° C. overnight. Yeast genomic DNA was extracted by YeaStar genomic extraction kit (Zymo Research, Orange, Calif.) and confirmation of the strain was confirmed by PCR using primers JML/237 and JML/238, shown below.

JML/237:

(SEQ ID NO: 340)

	CCAACACTAAGAAATAATTTCGCCATTTCTTG

	JML/238:

(SEQ ID NO: 341)

GCCAACAATTAAATCCAAGTTCACCTATTCTG

The PCR amplification was performed as follows: 10 ng of yeast genomic DNA with 0.1 μmol gene specific primers, 1×Pfu Ultra II buffer, 0.2 mmol dNTPs, and 0.2 U Taq DNA polymerase. The PCR mixture was cycled at 95° C. for 2 minutes, followed by 30 cycles of 95° C. for 20 seconds, 55° C. for 30 seconds and 72° C. for 45 seconds. A final step of 72° C. for 5 minutes was also included. The resultant strain was designated BF1618.
Strain BF1618 is undergoing transformation with the following plasmid combinations. Additionally, the affect of the ZWF1 mutant constructs will also be evaluated with and without SOL3 constructs. The table below shows the plasmid combinations being transformed into strain BF1618.


Test Strain	EDD	EDA	ZWF1	SOL3

1	2μ	2μ	cen/ars	NONE
2	2μ	2μ	2μ	NONE
3	2μ	2μ	cen/ars	cen/ars
4	2μ	2μ	2μ	2μ
5	2μ	2μ	NONE	cen/ars
6	2μ	2μ	NONE	2μ

Strains with improved ethanol production may benefit from two or more copies of the ZWF1 gene due to increased flux of the carbon towards the alternative pathway. A strain embodiment currently under construction has the phenotype; pfk1, ZWF1, SOL3, tal1, EDD-PAO1*, EDA-E. coli*, where the “*” represents additional copies of the gene. It is believed that multiple copies of the EDD and EDA genes may provide additional increases in ethanol production.

Example 19

Construction of the KanMX-ATO1-L75Q Cassette

A unique disruption cassette suitable for use when auxotrophic markers are unavailable, such as in diploid industrial strains or haploids derived from such strains, was constructed to allow homologous recombination or integration of sequences in the absence of traditional auxotrophic marker selection. The primers used for amplification of nucleic acids utilized to generate the disruption cassette are described in the table below.

JML/	ACTAGTATGTCTGACAAGGAACAAACGAGC (SEQ ID NO:	5′ScAto1SpeI
51	342)

JML/	CTCGAGTTAAAAGATTACCCTTTCAGTAGATGGTAATG	3′ScAto1XhoI
52	(SEQ ID NO: 343)

JML/	caagcctttggtggtacccagaatccagggttagctcc	ScATO(L75Q)_For
55	(SEQ ID NO: 344)

JML/	ggagctaaccctggattctgggtaccaccaaaggcttg	ScATO(L75Q)_Rev
56	(SEQ ID NO: 345)

JML/	ggtacaacgcatatgcagatgttgctacaaagcagaa (SEQ	ScATO1G259D_For
57	ID NO: 346)

JML/	ttctgctttgtagcaacatctgcatatgcgttgtacc (SEQ	ScATO1G259D_Rev
58	ID NO: 347)

JML/	GACGACGTCTAGAAAAGAATACTGGAGAAATGAAAAGAAAAC	ReplacesJML/30
59	(SEQ ID NO: 348)

JML/	GCATGCTTAATTAATGCGAGGCATATTTATGGTGAAGG	F′of5′FlankingRegionof
63	(SEQ ID NO: 349)	ScURA3

JML/	GGCCGGCCAGATCTGCGGCCGCGGCCAGCAAAACTAAAAAAC	F′of3′FlankingRegionof
64	TGTATTATAAG (SEQ ID NO: 350)	ScURA3

JML/	GCGGCCGCAGATCTGGCCGGCCGATTTATCTTCGTTTCCTGC	R′of5′FlankingRegionof
65	AGGTTTTTG (SEQ ID NO: 351)	ScURA3

JML/	GAATTCTTAATTAACTTTTGTTCCACTACTTTTTGGAACTCT	R′of3FlankingRegionofSc
66	TG (SEQ ID NO: 352)	URA3

JML/	GCATGCGCGGCCGCACGTCGGCAGGCCCG (SEQ ID NO:	F′200mer-R
67	353)

JML/	CGAAGGACGCGCGACCAAGTTTATCATTATCAATACTCGCCA	F′200mer-R-pGPD-ATO1-
68	TTTC (SEQ ID NO: 354)	CYC

JML/	GAAATGGCGAGTATTGATAATGATAAACTTGGTCGCGCGTCC	R′pGPD-ATO1-CYC-
69	TTCG (SEQ ID NO: 355)	200mer-R

JML/	GTCGACCCGCAAATTAAAGCCTTCGAGC (SEQ ID NO:	R-pGPD-ATO1-CYC
70	356)

JML/	GTCGACGTACCCCCGGGTTAATTAAGGCG (SEQ ID NO:	F-KanMX
71	357)

JML/	GTCGAAAACGAGCTCGAATTCGACGTCGGCAGGCCCG	F-KanMX-200mer-R
72	(SEQ ID NO: 358)

JML/	CGGGCCTGCCGACGTCGAATTCGAGCTCGTTTTCGAC (SEQ	R-200mer-R-KanMX
73	ID NO: 359)

JML/	GGATCCGCGGCCGCTGGTCGCGCGTCCTTCG (SEQ ID	R-200mer-R
74	NO: 360)

ScATO1 was amplified from genomic DNA (gDNA) isolated from BY4742 with primers oJML51 and oJML52 and cloned into pCR Blunt II-TOPO (Invitrogen, Carlsbad, Calif.). Site Directed Mutagenesis (SDM) was performed on that plasmid with oJML55 and oJML56, as described herein. The mutagenized clone was re-amplified with primers oJML51 and oJML52 and cloned into pCR Blunt II-TOPO (Invitrogen, Carlsbad, Calif.), and designated ATO1-L75Q. ATO1-L75Q was subcloned into p416GPD using SpeI/XhoI restriction enzyme sites. The resulting plasmid was designated pJLV048.
The 5′ and 3′ flanking regions of URA3 were amplified via PCR of the 5′ regions with primers oJML63 and oJML65, the 3′ region with primers oJML64 and oJML66. The amplified nucleic acids were annealed and re-amplified with oligonucleotides oJML63 and oJML66. The template used was TURBO gDNA. The PCR product was Topo cloned into pCR-Blunt II. The desired sequence was moved as an EcoRI-SphI fragment into vector pUC19 and designated pJLV63.
The R-KanMX fragment was made as follows: The KANMX fragment was first amplified from pBF524 with primers oJML71 and oJML73. The R-200-mer from plasmid pBF32 was then amplified using primers oJML72 and oJML74. The two fragments were annealed together and PCR amplified using primers oJML67 and oJML70 and topo cloned using pCR-Blunt II. The final plasmid construct was designated pJLV062. The R-P_TDH3-ATO1-L75Q construct was generated by amplifying a mixture of PCR oJML67-oJM L69 (pBF32)+PCR oJML68-oJML70 (pJLV048). The resulting plasmid was designated pJLV065. The R-PT_DH3-ATO1 L75Q (SalI/SphI) fragment from pJLV065 was ligated in a 3 piece ligation to the SalI/BamHI (R-KanMX) fragment from pJLV063 into the BamHI/SphI site of pUC19. The entire R-KanMX-P_TDH3-ATO1-L75Q-R fragment was ligated as a NotI piece into the NotI site of pJLV63 and designated pJLV74. The letter “R” with reference to nucleic acid fragments, primers, plasmids and unique 200-mer sequence tags, refers to a unique 200-mer tag identification number. The unique sequence tags are described in Example 28. A table describing the intermediate and final plasmids is presented below.


pJLV0035	pBF493	pCR-Topo BluntII-ScATO1	PCR oJML51, oJML52 (SDM
		L75Q	oJML55, oJML56 (Clone of ScATO1 Not Kept)
pJLV0048	pBF506	pRS416-ProGPD-ScATO1	XhoI-SpeI (pRAS416-GPD) + XhoI-
		L75Q	SpeI(pJLV035)
pJLV0061	pBF604	pCR-Topo BluntII-5′ + 3′	PCR oJML63, oJML66 (PCR oJML63, oJML65
		ScURA3	gDNA ScTURBO + PCR oJML64, oJML66
			gDNA ScTURBO)
pJLV0062	pBF605	pCR-Topo BluntII-KanMX-	PCR oJML71-oJML74 (PCR oJML71, oJML73
		200m-448	pBF524 + PCR oJML72, oJML74 pBF32)
pJLV0063	pBF606	pUC19-5 + 3′ ScURA3	EcoR1-SphI(pJLV0061) + EcoR1-
			SphI(pUC19)
pJLV0065	pBF608	pCR-Topo BluntII-200m448-	PCR oJML67-oJML70 (PCR oJML67-oJML59
		ProGDP-ScATO1 L75Q	(pBF32) + PCR oJML68-oJML70 (pJLV048))
pJLV0070	pBF650	pUC19-200m448-ProGDP-	SalI/SphI (pJLV0065) + BamHI/SalI
		ScATO1 L75Q-KanMX-	(pJLV0062) + SphI/BamHI (pUC19)
		200m448
pJLV0074	pBF654	pUC19-5′ URA3-200m448-	NotI(pJLV070) + NotI(pJLV063)
		ProGDP-ScATO1 L75Q-
		KanMX-200m448-3′ URA3

Example 20

Construction of the Ura3 Disruptions in Each Haploid

Haploid yeast strains were transformed with 2 to 3 μg of a PvuII, SphI digested ura3::R-KanMX-ATO1-L75Q-R disruption cassette using the high-efficiency Li-PEG procedure with a heat shock time of 8 minutes. Transformants were plated on YPD plus G418 (200 μg/ml) plates. Colonies were re-streaked onto ScD FOA plates. Single colonies were replica plated on ScD-ura, ScD+FOA, YPD, and YPD G418 200 μg/ml plates. Ura-FOA^RG418^Rcolonies were grown overnight in YPD. Genomic DNA was extracted and the presence of the KanMX-ATO1-L75Q gene in the URA3 loci was verified by PCR. 50 μl of each overnight culture was plated on ScD Acetate (2 g/L), pH 4.0, plates. Colonies were restreaked on ScD Acetate plates and single colonies grown overnight in YPD. Disruptions of the URA3 loci were verified by PCR with primers complementary to a region outside of the flanking region used for the disruption. The presence of the unique 200-mer sequence was verified by PCR with primers complementary to the 200-mer in combination with primers complementary to a region outside of the flanking region used for the disruption. The absence of the URA3 loci was verified by PCR that amplifies a 500 bp region of the Actin gene open reading frame and a 300 bp region of the URA3 open reading frame. The primers utilized for amplification and verification are presented, respectively, in the tables below.
Primers used for amplification of URA and Actin

JML/211	GAGGGCACAGTTAAGCCGCTAAAGG(SEQ ID NO:	URA3
	361)

JML/212	GTCAACAGTACCCTTAGTATATTCTCCAGTAGCTAGG	URA3
	GAG(SEQ ID NO: 362)

JML/213	CGTTACCCAATTGAACACGGTATTGTCAC(SEQ ID	ACT1
	NO: 363)

JML/214	GAAGATTGAGCAGCGGTTTGCATTTC(SEQ ID NO:	ACT1
	364)

Primers used to verify the presence or absence of URA3

JML/67	GCATGCgcggccgcACGTC	F′200mer-R
	GGCAGGCCCG(SEQ ID
	NO: 365)

JML/74	GGATCCgcggccgcTGGTC	R-200mer-R
	GCGCGTCCTTCG(SEQ ID
	NO: 366)

JML/102	gagtcaaacgacgttgaaa	PCRtoverifydisruptiono
	ttgaggctactgc(SEQ	fURA3
	ID NO: 367)

JML/103	GATTACTGCTGCTGTTCCA	PCRtoverifydisruptiono
	GCCCATATCCAAC(SEQ	fURA3
	ID NO: 368)

Example 21

EDA Gene Integration Method and Constructs

Plasmid DNA was digested with PacI using manufacturers suggestions. The digestions were purified using the GeneJET™ Gel Extraction Kit I (Fermentas). Each column was eluted with 20 μl of Elution buffer and multiple digests were combined. S. cerevisiae was transformed using the high-efficiency Li-PEG procedure with 2 to 3 μg of DNA and transformants were selected on ScD-ura solid media. Correct integrations were confirmed by PCR analysis with primers outside the flanking regions used as the disruption cassette and primers complementary to either the open reading frame of EDA or the 200-mer repeat. Oligonucleotide primers utilized for verification are described in the tables below.
Primers—Outside

YBR110.5	5′ GGCAATCAAATTGGGAACGAACAA	JML/187
	TG (SEQ ID NO: 369)
	3′ CTCAAGGTATCCTCATGGCCAAGCAATAC	JML/188
	(SEQ ID NO: 370)

YDL075.5	5′ GGGTCTACAAACTGTTGTTGTCGAAGAAGA	JML/189
	TG (SEQ ID NO: 371)
	3′ CATTCAGTTCCAATGATTTATTGACAGTGC	JML/190
	AC (SEQ ID NO: 372)

Primers—Repeat and EDA Going Out

JML/276	CCTACCCGCCTCGGATCCCAGCTACC	R-repeat
	(SEQ ID NO: 373)

JML/277	GGTAGCTGGGATCCGAGGCGGGTAGG	R-repeat
	(SEQ ID NO: 374)

JML/278	CCTCCCGGCACAGCGTGTCGATGC	R at the 5′EDA
	(SEQ ID NO: 375)

PaEDA Going Out and Similar Primers for EcEDA

JML/	CGAAGCCCTGGAGCGCTTCGC	PCR for PaEDA
297	(SEQ ID NO: 376)	going out at the
		3′ of the ORF

JML/	GTGGTCAGGATTGATTCTGCACTTGTTTT	PCR for EcEDA
298	CCAG (SEQ ID NO: 377)	Reverse at
		the 5′ end

JML/	CGCGTGAAGCTGTAGAAGGCGCTAAG	PCR for EcEDA
299	(SEQ ID NO: 378)	Forward at the
		3′ end

The PCR reactions were performed in a final reaction volume of 25 μl using the following amplification profile; 1 cycle at 94 degrees C. for 2 minutes, followed by 35 cycles of 94 degrees C. for 30 seconds, 52 degrees C. for 30 second and 72 degrees C. for 2 minutes.
Construction of EDA Disruption Cassettes
P_TDH3-PaEDA was amplified from pBF292 using primers oJML225 and oJML226, shown in the table below and Topo cloned in pCR Blunt II to make pJLV95.

JML/225	GAGCTCGGCCGCAAATTAAAGCCTT	3′cyCTERMINATOR
	CGAG (SEQ ID NO: 379)

JML/226	GGCCGGCCGTTTATCATTATCAATAC	5′PROMOTERgpd
	TCGCCATTTCAAAGAATACG
	(SEQ ID NO: 380)

The desired fragment was moved as a FseI-SacI piece into pBF730 or pBF731 (the integration cassette of either YBR110.5 or YDL075.5, respectively) to make plasmids pJLV114 and pJLV115, respectively. YBR110.5 is located in between loci YBR110 and YBR111, and YDL075.5 is located in between loci YDL075 and YDL076. The R-URA3-R sequence was moved into these plasmids as a NotI fragment to make pJLV119 and pJLV120. The resultant plasmids are described in the table below.


pJLV0095	pBF777	pCR-Topo BluntII-PaEDA	PCR oJML225-
			oJML226 (pBF292)
pJLV0114	pBF862	pUC19-5′-YBR110.5-PGDP1-	FseI-
		PaEDA-TCYC-3′YBR110.5	SacI(pBF730) +
			FseI-SacI(pJLV95)
pJLV0115	pBF863	pUC19-5′-YDL075.5-PGDP1-	FseI-
		PaEDA-TCYC-3′YDL075.5	SacI(pBF731) +
			FseI-SacI(pJLV95)
pJLV0119	pBF867	pUC19-5′-YBR110.5-PGDP1-	NotI(pBF742) +
		PaEDA-TCYC-R-URA3-R-	NotI(pJLV114)
		3′YBR110.5
pJLV0120	pBF868	pUC19-5′-YDL075.5-PGDP1-	NotI(pBF742) +
		PaEDA-TCYC-R-URA3-R-	NotI(pJLV115)
		3′YDL075.5

Example 22

Isolation and Evaluation of Additional EDA Genes

EDA genes isolated from a variety of sources were expressed in yeast and evaluated independently of EDA activity, to identify EDA activities suitable of inclusion in an engineered yeast strain. The EDA activities were was independently assessed by adding saturating amounts of over expressed E. coli EDD extracts to S. cerevisiae EDA extracts lacking EDD (Chemyan et al., Protein Science 16:2368-2377, 2007). The relative activities of EDAs, expressed in S. cerevisiae, were compared and ranked in this way. The activity of integrated EDAs in Thermosacc-Gold haploids, were also evaluated in this manner. The table below describes oligonucleotide primers used to isolate the various EDA genes.


			SEQ ID
Name	Description	Sequence	NO:

KA/EDA-	Cloning primer for Shewanella	GTTCACTGCACTAGTAAAAAAATG	381
SoFor	oneidensis EDA	CTTGAGAATAACTGGTC

KA/EDA-	Cloning primer for Shewanella	CTTCGAGATCTCGAGTTAAAGTCC	382
SoRev	oneidensis EDA	GCCAATCGCCTC

KA/EDA-	Cloning primer for Gluconobacter	GTTCACTGCACTAGTAAAAAAATG	383
GoFor	oxydansEDA	ATCGATACTGCCAAACTC

KA/EDA-	Cloning primer for Gluconobacter	CTTCGAGATCTCGAGTCAGACCGT	384
GoRev	oxydans EDA	GAAGAGTGCCGC

KA/EDA-	Cloning primer for Bacilluis	GTTCACTGCACTAGTAAAAAAATG	385
BLFor	licheniformis EDA	GTATTGTCACACATCGAAG

KA/EDA-	Cloning primer for Bacilluis	CTTCGAGATCTCGAGTTACTGTTT	386
BLRev	licheniformis EDA	TGCTGCTTCAACAAATTG

KA/EDA-	Cloning primer for Bacillus subtilis	GTTCACTGCACTAGTAAAAAAATG	387
BsFor	EDA	GAGTCCAAAGTCGTTGAAAACC

KA/EDA-	Cloning primer for Bacillus subtilis	CTTCGAGATCTCGAGTTACACTTG	388
BsRev	EDA	GAAAACAGCCTGCAAATCC

KA/EDA-	Cloning primer for Pseudomonas	GTTCACTGCACTAGTAAAAAAATG	389
PfFor	fluorescens EDA	ACAAACCTCGCCCCGACC

KA/EDA-	Cloning primer for Pseudomonas	CTTCGAGATCTCGAGTCAGTCCAG	390
PfRev	fluorescens EDA	CAGGGCCAGG

KA/EDA-	Cloning primer for	GTTCACTGCACTAGTAAAAAAATG	391
PsFor	Pseudomonas syringae EDA	ACACAGAACGAAAATAATCAGCCGC

KA/EDA-	Cloning primer for	CTTCGAGATCTCGAGTCAGTCAAA	392
PsRev	Pseudomonas syringae EDA	CAGCGCCAGCGC

KA/EDA-	Cloning primer for	GTTCACTGCACTAGTAAAAAAATG	393
SdFor	Saccharaophagus degradans	GCTATTACAAAAGAATTTTTAGCT
	EDA	CCAG

KA/EDA-	Cloning primer for	CTTCGAGATCTCGAGTTAGCTAGA	394
SdRev	Saccharaophagus degradans	AATTTTAGCGGTAGTTGCC
	EDA

KA/EDA-	Cloning primer for	GTTCACTGCACTAGTAAAAAAATG	395
XaFor	Xanthamonas axonopodis EDA	ACGATTGCCCAGACCCAG

KA/EDA-	Cloning primer for	CTTCGAGATCTCGAGTCAGCCCGC	396
XaRev	Xanthamonas axonopodis EDA	CCGCACC

KA/NdeI	Cloning primer for E. coli	GTTCACTGCCATATGAATCCACAA	397
EDDfor	EDD	TTGTTACGCGTAACAAATCGAATC
		ATTG

KA/XhoI	Cloning primer for E. coli	CTTCGAGATCTCGAGTTAAAAAGT	398
EDDrev	EDD	GATACAGGTTGCGCCCTGTTCGGC

Listed below are the amino acid sequences, nucleotide sequences and accession numbers of the EDA genes evaluated as described in this Example.


Accession		Strain		Amino Acid
Number	Species	Number	Nucleotide Sequence	Sequence

YP_526856.1	Saccharophagus	2-40	ATGGCTATTACAAAAGAATTTTTAGCTCCAGTTGGCGTAATGCCTGT	MAITKEFLAPVGVMPVV
	degradans		TGTGGTTGTGGATCGTGTAGAAGATGCGGTGCCTATTACAAACGCAT	VVDRVEDAVPITNALKA
			TAAAAGCCGGCGGTATTAAAGCAGTTGAGATTACTTTACGTACTCCT	GGIKAVEITLRTPAALD
			GCGGCACTGGATGCTATTCGCGCTATTAAAGCTGAGTGTGAAGACAT	AIRAIKAECEDILVGVG
			CCTGGTGGGGGTAGGTACGGTTATTAACCATCAAAACCTTAAAGATA	TVINHQNLKDIAAIGVD
			TTGCTGCAATTGGTGTTGATTTCGCCGTATCTCCTGGTTACACCCCA	FAVSPGYTPTLLKQAQD
			ACATTGCTGAAGCAAGCGCAAGATTTGGGCGTAGAAATGTTGCCTGG	LGVEMLPGVTSPSEVML
			TGTAACTTCGCCTTCTGAAGTTATGCTTGGTATGGAGCTAGGTTTGT	GMELGLSCFKLFPAVAV
			CTTGCTTCAAGCTATTCCCTGCGGTTGCAGTAGGTGGTTTGCCATTA	GGLPLLKSIGGPLPQVS
			CTTAAGTCTATTGGTGGCCCATTACCACAGGTTTCCTTCTGTCCAAC	FCPTGGLTIDTFTDFLA
			AGGCGGTTTGACTATCGATACTTTCACCGACTTCTTGGCATTGCCTA	LPNVACVGGTWLVPADA
			ACGTTGCTTGTGTGGGTGGTACTTGGTTGGTGCCTGCAGATGCTGTT	VAAKNWQAITDIAAATT
			GCAGCTAAAAACTGGCAAGCTATTACTGATATTGCGGCGGCAACTAC	AKISS (SEQ ID NO:
			CGCTAAAATTTCTAGCTAA (SEQ ID NO: 399)	400)

	Xanthomonas	ATCC	ATGACGATTGCCCAGACCCAGAACACCGCCGAACAGTTGCTGCGCGA	MTIAQTQNTAEQLLRDA
	axonopodis pv.	13902	TGCCGGCATCTTGCCCGTGGTCACCGTGGACACGCTGGATCAGGCGC	GILPVVTVDTLDQARRV
	Vasculorum		GCCGCGTCGCCGATGCGTTGCTCGAAGGCGGCCTGCCCGCGATCGAG	ADALLEGGLPAIELTLR
			CTGACCCTTCGCACGCCAGTGGCGATCGACGCGCTGGCGATGCTCAA	TPVAIDALAMLKRELPN
			GCGCGAGCTTCCTAACATCTTGATCGGTGCCGGCACCGTGCTGAGCG	ILIGAGTVLSELQLRQS
			AATTGCAGCTGCGTCAGTCGGTGGATGCCGGTGCAGACTTCCTGGTG	VDAGADFLVTPGTPAPL
			ACCCCGGGCACGCCGGCGCCGCTGGCGCGCCTGCTGGCGGATGCGCC	ARLLADAPIPAVPGAAT
			GATCCCGGCCGTTCCCGGCGCGGCCACTCCGACCGAGCTGCTGACCT	PTELLTLMGLGFRVCKL
			TGATGGGTCTTGGCTTTCGCGTCTGCAAGCTGTTCCCGGCCACCGCC	FPATAVGGLQMLRGLAG
			GTGGGCGGTCTGCAGATGCTCAGGGGCCTGGCCGGCCCGCTGTCCGA	PLSELKLCPTGGISEAN
			GCTCAAGCTGTGCCCCACCGGCGGCATCAGCGAGGCCAACGCCGCCG	AAEFLSQPNVLCIGGSW
			AGTTCCTGTCGCAGCCGAACGTGCTGTGCATCGGCGGTTCGTGGATG	MVPKDWLAHGQWDKVKE
			GTCCCCAAGGATTGGCTGGCGCACGGCCAATGGGACAAGGTCAAGGA	SSAKAAAIVRQVRAG
			AAGCTCGGCCAAGGCGGCGGCGATCGTGCGGCAGGTGCGGGCGGGCT	(SEQ ID NO: 402)
			GA (SEQ ID NO: 401)

AA055695.1	Pseudomonas	Pv.	ATGACACAGAACGAAAATAATCAGCCGCTCACCAGCATGGCGAACAA	MTQNENNQPLTSMANKI
	syringiae	Tomato	GATTGCCCGGATCGACGAACTCTGCGCCAAGGCAAAGATTCTGCCGG	ARIDELCAKAKILPVIT
		str	TCATCACCATTGCCCGTGATCAGGACGTATTGCCACTGGCCGACGCG	IARDQDVLPLADALAAG
		DC3000	CTGGCCGCTGGTGGCATGACGGCTCTGGAAATCACCCTGCGCTCGGC	GMTALEITLRSAFGLSA
			GTTCGGACTGAGTGCGATCCGCATTTTGCGCGAGCAGCGCCCAGAGC	IRILREQRPELCTGAGT
			TGTGCACTGGCGCCGGGACCATTCTGGACCGCAAGATGCTGGCCGAC	ILDRKMLADAEAAGSQF
			GCCGAGGCGGCGGGCTCGCAATTCATTGTGACCCCCGGCAGCACGCA	IVTPGSTQELLQAALDS
			GGAACTGTTGCAGGCGGCGCTCGACAGCCCGTTGCCCCTGTTGCCAG	PLPLLPGVSSASEIMIG
			GCGTCAGCAGCGCGTCGGAAATCATGATCGGCTATGCCTTGGGTTAT	YALGYRRFKLFPAEISG
			CGCCGCTTCAAGCTGTTCCCGGCAGAAATCAGCGGCGGTGTGGCAGC	GVAAIKALGGPFNEVRF
			GATCAAGGCCTTGGGCGGGCCTTTCAACGAGGTGCGTTTCTGCCCGA	CPTGGVNEQNLKNYMAL
			CGGGCGGCGTCAACGAGCAGAACCTCAAGAACTACATGGCCTTGCCC	PNVMCVGGTWMIDNAWV
			AACGTCATGTGCGTCGGCGGGACATGGATGATTGATAACGCCTGGGT	KNGDWGRIQEATAQALA
			CAAGAATGGCGACTGGGGCCGCATTCAGGAAGCCACGGCACAGGCGC	LFD (SEQ ID NO:
			TGGCGCTGTTTGACTGA (SEQ ID NO: 403)	404)

NP_718073.1	Shewanella	MR-1	ATGCTTGAGAATAACTGGTCATTACAACCACAAGATATTTTTAAACG	MLENNWSLQPQDIFKRS
	oneidensis		CAGCCCTATTGTTCCTGTTATGGTGATTAACAAGATTGAACATGCGG	PIVPVMVINKIEHAVPL
			TGCCCTTAGCTAAAGCGCTGGTTGCCGGAGGGATAAGCGTGTTGGAA	AKALVAGGISVLEVTLR
			GTGACATTACGCACGCCATGCGCCCTTGAAGCTATCACCAAAATCGC	TPCALEAITKIAKEVPE
			CAAGGAAGTGCCTGAGGCGCTGGTTGGCGCGGGGACTATTTTAAATG	ALVGAGTILNEAQLGQA
			AAGCCCAGCTTGGACAGGCTATCGCCGCTGGTGCGCAATTTATTATC	IAAGAQFIITPGATVEL
			ACTCCAGGTGCGACAGTTGAGCTGCTCAAAGCGGGCATGCAAGGACC	LKAGMQGPVPLIPGVAS
			GGTGCCGTTAATTCCGGGCGTTGCCAGTATTTCCGAGGTGATGACGG	ISEVMTGMALGYTHFKF
			GCATGGCGCTGGGCTACACTCACTTTAAATTCTTCCCTGCTGAAGCG	FPAEASGGVDALKAFSG
			TCAGGTGGCGTTGATGCGCTTAAGGCTTTCTCTGGGCCGTTAGCAGA	PLADIRFCPTGGITPSS
			TATCCGCTTCTGCCCAACAGGTGGAATTACCCCGAGCAGCTATAAAG	YKDYLALKNVDCIGGSW
			ATTACTTAGCGCTGAAGAATGTCGATTGTATTGGTGGCAGCTGGATT	IAPTDAMEQGDWDRITQ
			GCTCCTACCGATGCGATGGAGCAGGGCGATTGGGATCGTATCACTCA	LCKEAIGGL (SEQ ID
			GCTGTGTAAAGAGGCGATTGGCGGACTTTAA (SEQ ID NO:	NO: 406)
			405)

YP_261692	Pseudomonas	Pf-5	ATGACAAACCTCGCCCCGACCGTTTCCATGGCGGACAAAGTTGCCCT	MTNLAPTVSMADKVALI
	fluorescens		GATCGACAGCCTCTGCGCCAAGGCGCGGATCCTGCCGGTGATCACCA	DSLCAKARILPVITIAR
			TTGCCCGCGAGCAGGATGTCCTGCCGCTGGCCGATGCCCTGGCGGCC	EQDVLPLADALAAGGLT
			GGCGGCCTGACCGCCCTGGAAGTGACCCTGCGTTCGCAGTTCGGCCT	ALEVTLRSQFGLKAIQI
			CAAGGCGATCCAGATCCTGCGCGAACAGCGCCCGGAGCTGGTGACCG	LREQRPELVTGAGTVLD
			GTGCCGGCACCGTGCTCGACCCGCAGATGCTGGTGGCGGCGGAAGCG	PQMLVAAEAAGSQFIVT
			GCAGGTTCGCAGTTCATCGTCACCCCGGGCATCACCCGCGACCTGCT	PGITRDLLQASVASPIP
			GCAAGCCAGCGTGGCCAGCCCGATTCCCCTGCTGCCGGGGATCAGCA	LLPGISNASGIMEGYAL
			ATGCCTCCGGGATCATGGAGGGTTATGCCCTGGGCTACCGCCGCTTC	GYRRFKLFPAEVSGGVA
			AAGCTGTTCCCGGCGGAAGTCAGTGGTGGCGTGGCGGCGATCAAGGC	AIKALGGPFGEVKFCPT
			CCTGGGCGGGCCGTTCGGCGAGGTCAAGTTCTGCCCTACCGGCGGCG	GGVGPANIKSYMALKNV
			TCGGCCCGGCCAATATCAAGAGCTACATGGCGCTCAAGAATGTGATG	MCVGGSWMLDPEWIKNG
			TGTGTCGGCGGTAGCTGGATGCTCGATCCCGAGTGGATCAAGAACGG	DWARIQECTAEALALLD
			CGACTGGGCACGGATCCAGGAGTGCACGGCCGAGGCCCTGGCCCTGC	(SEQ ID NO: 408)
			TGGACTGA (SEQ ID NO: 407)

ZP_03591973.1	Bacillus	subtilis	ATGGAGTCCAAAGTCGTTGAAAACCGTCTGAAAGAAGCAAAGCTGAT	MESKVVENRLKEAKLIA
	subtilis	str.	TGCAGTCATTCGTTCAAAGGATAAGCAGGAGGCCTGTCAGCAGATTG	VIRSKDKQEACQQIESL
		168	AGAGTTTATTAGATAAAGGGATTCGTGCAGTTGAAGTGACGTATACG	LDKGIRAVEVTYTTPGA
			ACCCCCGGGGCATCAGATATTATCGAATCCTTCCGTAATAGGGAAGA	SDIIESFRNREDILIGA
			TATTTTAATTGGCGCGGGTACGGTCATCAGCGCGCAGCAAGCTGGGG	GTVISAQQAGEAAKAGA
			AAGCTGCTAAGGCTGGCGCGCAGTTTATTGTCAGTCCGGGTTTTTCA	QFIVSPGFSADLAEHLS
			GCTGATCTTGCTGAACATCTATCTTTTGTAAAGACACATTATATCCC	FVKTHYIPGVLTPSEIM
			CGGCGTCTTGACTCCGAGCGAAATTATGGAAGCGCTGACATTCGGTT	EALTFGFTTLKLFPSGV
			TTACGACATTAAAGCTGTTCCCAAGCGGTGTGTTTGGCATTCCGTTT	FGIPFMKNLAGPFPQVT
			ATGAAAAATTTAGCGGGTCCTTTCCCGCAGGTGACCTTTATTCCGAC	FIPTGGIHPSEVPDWLR
			AGGCGGGATACATCCGTCTGAAGTGCCTGATTGGCTTAGAGCCGGAG	AGAGAVGVGSQLGSCSK
			CTGGCGCCGTCGGAGTCGGCAGCCAGTTGGGCAGCTGTTCAAAAGAG	EDLQAVFQV (SEQ ID
			GATTTGCAGGCTGTTTTCCAAGTGTAA (SEQ ID NO: 409)	NO: 410)

YP_081150.2	Bacillus	ATCC	ATGGTATTGTCACACATCGAAGAACAAAAACTGATTGCGATCATCCG	MVLSHIEEQKLIAIIRG
	licheniformis	14580	CGGATACAATCCGGAGGAGGCAGTGAGCATTGCCGGCGCCTTAAAAG	YNPEEAVSIAGALKAGG
			CGGGCGGCATCAGGCTTGTGGAGATTACGCTTAATTCCCCTCAAGCG	IRLVEITLNSPQAIKAI
			ATCAAAGCGATTGAAGCGGTTTCAGAGCATTTTGGGGACGAAATGCT	EAVSEHFGDEMLVGAGT
			TGTCGGAGCGGGAACCGTACTTGATCCCGAATCTGCGAGAGCGGCGC	VLDPESARAALLAGARF
			TTTTAGCCGGCGCGCGGTTTATCCTGTCTCCGACCGTCAATGAAGAG	ILSPTVNEETIKLTKRY
			ACGATCAAGCTGACAAAACGGTATGGAGCGGTCAGCATTCCAGGCGC	GAVSIPGAFTPTEILTA
			TTTTACCCCGACTGAAATATTGACGGCGTATGAAAGCGGGGGAGACA	YESGGDIIKVFPGTMGP
			TCATCAAGGTATTTCCCGGAACAATGGGGCCTGGCTATATCAAGGAT	GYIKDIHGPLPHIPLLP
			ATCCACGGACCGCTTCCGCATATTCCGCTGCTTCCGACTGGAGGAGT	TGGVGLENLHEFLQAGA
			CGGATTGGAAAACCTTCACGAGTTTCTGCAGGCCGGTGCGGTCGGAG	VGAGIGGSLVRANKDVN
			CGGGAATCGGCGGTTCGCTTGTTCGGGCTAATAAAGATGTTAATGAC	DAFLEELSKKAKQFVEA
			GCGTTTTTAGAAGAGCTGTCCAAAAAAGCAAAGCAATTTGTTGAAGC	AKQ (SEQ ID NO:
			AGCAAAACAGTAA (SEQ ID NO: 411)	412)

YP_190869.1	Gluconobacter	62IH	ATGATCGATACTGCCAAACTCGACGCCGTCATGAGCCGTTGTCCGGT	MIDTAKLDAVMSRCPVM
	oxydans		CATGCCGGTGCTGGTGGTCAATGATGTGGCTCTGGCCCGCCCGATGG	PVLVVNDVALARPMAEA
			CCGAGGCTCTGGTGGCGGGTGGACTGTCCACGCTGGAAGTCACGCTG	LVAGGLSTLEVTLRTPC
			CGCACGCCCTGCGCCCTTGAAGCTATTGAGGAAATGTCGAAAGTACC	ALEAIEEMSKVPGALVG
			AGGCGCGCTGGTCGGTGCCGGTACGGTGCTGAATCCGTCCGACATGG	AGTVLNPSDMDRAVKAG
			ACCGTGCCGTGAAGGCGGGTGCGCGCTTCATCGTCAGCCCCGGCCTG	ARFIVSPGLTEALAKAS
			ACCGAGGCGCTGGCAAAGGCGTCGGTTGAGCATGACGTCCCCTTCCT	VEHDVPFLPGVANAGDI
			GCCAGGCGTTGCCAATGCGGGTGACATCATGCGGGGTCTGGATCTGG	MRGLDLGLSRFKFFPAV
			GTCTGTCACGCTTCAAGTTCTTCCCGGCTGTGACGAATGGCGGCATT	TNGGIPALKSLASVFGS
			CCCGCGCTCAAGAGCTTGGCCAGTGTTTTTGGCAGCAATGTCCGTTT	NVRFCPTGGITEESAPD
			CTGCCCCACGGGCGGCATTACGGAAGAGAGCGCACCGGACTGGCTGG	WLALPSVACVGGSWVTA
			CGCTTCCCTCCGTGGCCTGCGTCGGCGGATCCTGGGTGACGGCCGGC	GTFDADKVRQRATAAAL
			ACGTTCGATGCGGACAAGGTCCGTCAGCGCGCCACGGCTGCGGCACT	FTV (SEQ ID NO:
			CTTCACGGTCTGA (SEQ ID NO: 413)	414)

NP_251871.1	P. aeruginosa	PAO1	ATGAAAAACTGGAAAACAAGTGCAGAATCAATCCTGACCACCGGCCC	MKNWKTSAESILTTGPV
		Codon	GGTTGTACCGGTTATCGTGGTAAAAAAACTGGAACACGCGGTGCCGA	VPVIVVKKLEHAVPMAK
		Optimized	TGGCAAAAGCGTTGGTTGCTGGTGGGGTGCGCGTTCTGGAAGTGACT	ALVAGGVRVLEVTLRTE
			CTGCGTACCGAGTGTGCAGTTGACGCTATCCGTGCTATCGCCAAAGA	CAVDAIRAIAKEVPEAI
			AGTGCCTGAAGCGATTGTGGGTGCCGGTACGGTGCTGAATCCACAGC	VGAGTVLNPQQLAEVTE
			AGCTGGCAGAAGTCACTGAAGCGGGTGCACAGTTCGCAATTAGCCCG	AGAQFAISPGLTEPLLK
			GGTCTGACCGAGCCGCTGCTGAAAGCTGCTACCGAAGGGACTATTCC	AATEGTIPLIPGISTVS
			TCTGATTCCGGGGATCAGCACTGTTTCCGAACTGATGCTGGGTATGG	ELMLGMDYGLKEFKFFP
			ACTACGGTTTGAAAGAGTTCAAATTCTTCCCGGCTGAAGCTAACGGC	AEANGGVKALQAIAGPF
			GGCGTGAAAGCCCTGCAGGCGATCGCGGGTCCGTTCTCCCAGGTCCG	SQVRFCPTGGISPANYR
			TTTCTGCCCGACGGGTGGTATTTCTCCGGCTAACTACCGTGACTACC	DYLALKSVLCIGGSWLV
			TGGCGCTGAAAAGCGTGCTGTGCATCGGTGGTTCCTGGCTGGTTCCG	PADALEAGDYDRITKLA
			GCAGATGCGCTGGAAGCGGGCGATTACGACCGCATTACTAAGCTGGC	REAVEGAKL (SEQ ID
			GCGTGAAGCTGTAGAAGGCGCTAAGCTGTAA (SEQ ID NO:	NO: 416)
			415)

	PAO1-Ec5		ATGAAAAACTGGAAACAGAAGACCGCCCGCATCGACACGCTGTGCCG	MKNWKQKTARIDTLCRE
			GGAGGCGCGCATCCTCCCGGTGATCACCATCGACCGCGAGGCGGACA	ARILPVITIDREADILP
			TCCTGCCGATGGCCGATGCCCTCGCCGCCGGCGGCCTGACCGCCCTG	MADALAAGGLTALEITL
			GAGATCACCCTGCGCACGGCGCACGGGCTGACCGCCATCCGGCGCCT	RTAHGLTAIRRLSEERP
			CAGCGAGGAGCGCCCGCACCTGCGCATCGGCGCCGGCACCGTGCTCG	HLRIGAGTVLDPRTFAA
			ACCCGCGGACCTTCGCCGCCGCGGAAAAGGCCGGGGCGAGCTTCGTG	AEKAGASFVVTPGCTDE
			GTCACCCCGGGTTGCACCGACGAGTTGCTGCGCTTCGCCCTGGACAG	LLRFALDSEVPLLPGVA
			CGAAGTCCCGCTGTTGCCCGGCGTGGCCAGCGCTTCCGAGATCATGC	SASEIMLAYRHGYRRFK
			TCGCCTACCGCCATGGCTACCGCCGCTTCAAGCTGTTTCCCGCCGAA	LFPAEVSGGPAALKAFS
			GTCAGCGGCGGCCCGGCGGCGCTGAAGGCGTTCTCGGGACCATTCCC	GPFPDIRFCPTGGVSLN
			CGATATCCGCTTCTGCCCCACCGGAGGCGTCAGCCTGAACAATCTCG	NLADYLAVPNVMCVGGT
			CCGACTACCTGGCGGTACCCAACGTGATGTGCGTCGGCGGCACCTGG	WMLPKAVVDRGDWAQVE
			ATGCTGCCCAAGGCCGTGGTCGACCGCGGCGACTGGGCCCAGGTCGA	RLSREALERFAEHRRH
			GCGCCTCAGCCGCGAAGCCCTGGAGCGCTTCGCCGAGCACCGCAGAC	(SEQ ID NO: 418)
			ACTAATAGCTCGAGTTACTTTACT (SEQ ID NO: 417)

	PAO1-Ec10		ATGAAAAACTGGAAAACAAGTGCAGAATCAATCGACACGCTGTGCCG	MKNWKTSAESIDTLCRE
			GGAGGCGCGCATCCTCCCGGTGATCACCATCGACCGCGAGGCGGACA	ARILPVITIDREADILP
			TCCTGCCGATGGCCGATGCCCTCGCCGCCGGCGGCCTGACCGCCCTG	MADALAAGGLTALEITL
			GAGATCACCCTGCGCACGGCGCACGGGCTGACCGCCATCCGGCGCCT	RTAHGLTAIRRLSEERP
			CAGCGAGGAGCGCCCGCACCTGCGCATCGGCGCCGGCACCGTGCTCG	HLRIGAGTVLDPRTFAA
			ACCCGCGGACCTTCGCCGCCGCGGAAAAGGCCGGGGCGAGCTTCGTG	AEKAGASFVVTPGCTDE
			GTCACCCCGGGTTGCACCGACGAGTTGCTGCGCTTCGCCCTGGACAG	LLRFALDSEVPLLPGVA
			CGAAGTCCCGCTGTTGCCCGGCGTGGCCAGCGCTTCCGAGATCATGC	SASEIMLAYRHGYRRFK
			TCGCCTACCGCCATGGCTACCGCCGCTTCAAGCTGTTTCCCGCCGAA	LFPAEVSGGPAALKAFS
			GTCAGCGGCGGCCCGGCGGCGCTGAAGGCGTTCTCGGGACCATTCCC	GPFPDIRFCPTGGVSLN
			CGATATCCGCTTCTGCCCCACCGGAGGCGTCAGCCTGAACAATCTCG	NLADYLAVPNVMCVGGT
			CCGACTACCTGGCGGTACCCAACGTGATGTGCGTCGGCGGCACCTGG	WMLPKAVVDRGDWAQVE
			ATGCTGCCCAAGGCCGTGGTCGACCGCGGCGACTGGGCCCAGGTCGA	RLSREALERFAEHRRH
			GCGCCTCAGCCGCGAAGCCCTGGAGCGCTTCGCCGAGCACCGCAGAC	(SEQ ID NO: 420)
			ACTAATAGCTCGAGTTACTTTACT (SEQ ID NO: 419)

	PAO1-Ec15		ATGAAAAACTGGAAAACAAGTGCAGAATCAATCCTGACCACCGGCCG	MKNWKTSAESILTTGRE
			GGAGGCGCGCATCCTCCCGGTGATCACCATCGACCGCGAGGCGGACA	ARILPVITIDREADILP
			TCCTGCCGATGGCCGATGCCCTCGCCGCCGGCGGCCTGACCGCCCTG	MADALAAGGLTALEITL
			GAGATCACCCTGCGCACGGCGCACGGGCTGACCGCCATCCGGCGCCT	RTAHGLTAIRRLSEERP
			CAGCGAGGAGCGCCCGCACCTGCGCATCGGCGCCGGCACCGTGCTCG	HLRIGAGTVLDPRTFAA
			ACCCGCGGACCTTCGCCGCCGCGGAAAAGGCCGGGGCGAGCTTCGTG	AEKAGASFVVTPGCTDE
			GTCACCCCGGGTTGCACCGACGAGTTGCTGCGCTTCGCCCTGGACAG	LLRFALDSEVPLLPGVA
			CGAAGTCCCGCTGTTGCCCGGCGTGGCCAGCGCTTCCGAGATCATGC	SASEIMLAYRHGYRRFK
			TCGCCTACCGCCATGGCTACCGCCGCTTCAAGCTGTTTCCCGCCGAA	LFPAEVSGGPAALKAFS
			GTCAGCGGCGGCCCGGCGGCGCTGAAGGCGTTCTCGGGACCATTCCC	GPFPDIRFCPTGGVSLN
			CGATATCCGCTTCTGCCCCACCGGAGGCGTCAGCCTGAACAATCTCG	NLADYLAVPNVMCVGGT
			CCGACTACCTGGCGGTACCCAACGTGATGTGCGTCGGCGGCACCTGG	WMLPKAVVDRGDWAQVE
			ATGCTGCCCAAGGCCGTGGTCGACCGCGGCGACTGGGCCCAGGTCGA	RLSREALERFAEHRRH
			GCGCCTCAGCCGCGAAGCCCTGGAGCGCTTCGCCGAGCACCGCAGAC	(SEQ ID NO: 422)
			ACTAATAGCTCGAGTTACTTTACT (SEQ ID NO: 421)

EDA extracts were prepared using the following protocol.

Day 1

Grow 5 ml LB-Kan preps of BF1055 (BL21/DE3 with pET26b empty vector) and BF1706 (BL21DE3 with pET26b+E. coli EDD).
Grow 5 ml preps of each EDA construct expressed in S. cerevisiae in appropriate selective media (e.g. ScD-leu).

Day 2

Grow 50 ml LB-Kan prep of BF1055, 2% (v/v) inoculate.
Grow 50 ml prep of BF1706 using Novagen's Overnight Express (46.45 ml LB-Kan, 1 ml solution 1, 2.5 ml solution 2, 50 μl solution 3, 5 μl of 1M MnCl₂, 50 μl of 0.5 M FeCl₂), 2% (v/v) inoculate.
Grow 50 ml prep of each EDA construct expressed in S. cerevisiae in appropriate selective media+10 mM MnCl₂. Inoculate to OD₆₀₀of 0.2.

Day 3

EDD extractions (adapted from Chemyan et al, Protein Science 16:2368-2377, 2007):

- 1) Pellet cells in 50 ml conical tubes, 4° C., 3,000 rpm, 10 mins, discard supernatant.
- 2) Resuspend in 2 ml degassed PDGH buffer (20 mM MES pH 6.5, 30 mM NaCl, 5 mM MnCl₂, 0.5 mM FeCl₂, 10 mM 2-mercaptoethanol, 10 mM cysteine, sparged with nitrogen gas). Move to hungate tube.
- 3) Add 0.1% Triton X-100, 10 ng/ml DNase, 10 μg/ml PMSF, 10 μg/ml TAME (Nα-(p-toluene sulfonyl)-L-arginine methyl ester), 100 μg/ml lysozyme.
- 4) Sparge hungate tube with nitrogen gas, cap and seal. Incubate 2 hours at 37° C., swirl occasionally.
- 5) Clarify by centrifugation in 2-ml tube, 4° C., 10 mins, 14,000 rpm. Keep supernatant.
- 6) Treat with 150 mM pyruvate and 10 mM sodium cyanoborohydride (work in hood) to inactivate aldolase activity. Incubate 30 mins at room temperature.
- 7) During incubation, pre-equilibrate PD-10 column from GE
  - a. Remove top cap, pour off storage buffer.
  - b. Cut off bottom tip, fit in 50 ml conical with adapter.
  - c. Pour 5 ml of 20 mM MES buffer, pH 6.5 (total of 5 times). Discard flow-through.
- 8) Run sample through column, then add MES buffer to a total of 2.5 ml volume added. Discard flow-through.
- 9) Run 3.5 ml 20 mM MES pH 6.5 buffer to elute protein. Discard column in appropriate waste receptacle.
- 10) Perform Bradford assay (1:10 or 1:20 dilution).

EDA Extractions:

- 1) Spin down in 50 ml conicals, 4° C., 3,400 rpm, 5 mins. Wash 2× with 25 ml water.
- 2) Resuspend in 1 ml lysis buffer (50 mM Tris-HCl, pH 7, 10 mM MgCl₂, 1× protease inhibitor.
- 3) Add 1 cap of zirconia beads, vortex 4-6 times, 15 sec bursts, ice in between.
- 4) Spin down cell debris, 4° C., 14,000 rpm, 10 mins. Save supernatant.
- 5) Perform Bradford assay (1:2 dilution).

Activity Assays:

Each reaction contains 50 mM Tris-HCl, pH 7, 10 mM MgCl₂, 0.15 mM NADH, 15 μg LDH, saturating amounts of EDD determined empirically (usually ˜100 μg), 1-50 μg EDA (depending on level of activity), and 1 mM 6-phosphogluconate. Reactions are started by the addition of 6-phosphogluconate and monitored for 5 mins at 30° C.
Results
The S. cerevisiae strains tested for EDA activity are described in the table below. yCH strains are Thermosacc-based (Lallemand). BF strains are based on BY4742.


Strain	Vector	Construct

BF542	pBF150	Zymomonas mobilis EDA
BF1689	pBF892	PAO1 + 5aa E. coli EDA
BF1691	pBF894	PAO1 + 10aa E. coli EDA
BF1693	pBF896	PAO1 + 15aa E. coli EDA
BF1721	pBF909	Bacilluis licheniformis EDA
BF1722	pBF910	Bacillus subtilis EDA
BF1723	pBF911	Pseudomonas fluorescens EDA
BF1724	pBF912	Pseudomonas syringae EDA
BF1725	pBF913	Saccharaophagus degradans EDA
BF1726	pBF914	Xanthamonas axonopodis EDA
BF1727	pBF766	Escherichia coli EDA
BF1728	pBF764	Pseudomonas aeruginosa EDA
BF1729	pBF729	Gluconobacter oxydans EDA
BF1730	pBF727	Shewanella oneidensis EDA
BF1775	pBF87	p425GPD (empty vector)
BF1776	pBF928	PAO1 EDA codon optimized for S. cerevisiae

E. coli expressed EDD was prepared and confirmed by western blot analysis as shown in FIG. 15. The expected size of EDD is approximately 66 kilodaltons (kDa). A band of approximately that size (e.g., as determined by the nearest sized protein standard of approximately 60 kDa) was identified by western blot. The E. coli expressed EDD was used with S. cerevisiae expressed EDA's to evaluate the EDA activities. The results of EDA kinetic assays are presented in the table below.


EDD/EDA	slope	% max

EC/EC	0.3467	100.00
EC/SO	0.1907	55.00
EC/BS	0.0897	25.87
EC/GO	0.0848	24.46
EC/PCO	0.084	24.23
EC/PA	0.0533	15.37
EC/PE5	0.0223	6.43
EC/PE10	0.0218	6.29
EC/SD	0.015	4.33
EC/PS	0.0135	3.89
EC/BL	0.0112	3.23
EC/ZM	0.0109	3.14
EC/PF	0.0082	2.37
EC/V	0.0074	2.13
EC/XA	0.0065	1.87
EC/PE15	0.005	1.44

In the results presented above, the slope of the E. coli (EC) EDA is outside the linear range for accurate detection, and is therefore underestimated. For the other EDA's, when compared to the E. coli EDA, the calculated percentage of maximum activity (e.g., % max) is overestimated, however the slopes are accurate. The results of this experiment indicate that the E. coli EDA has higher activity as compared to the other EDA activities evaluated herein, and is approximately 16-fold more active than the EDA from P. aeruginosa. EDA's from X. anoxopodis and a chimera between E. coli EDA and P. aeruginosa (e.g., PE15) show less activity than the vector control. Codon-optimized EDA from P. aeruginosa showed a slight improvement over the native sequence, however chimeric versions (e.g., PE5, PE10, PE15) showed less activity than native. The experiments were repeated using 100 μg of EDD and 25 μg of EDA cell lysates in each reaction (unless otherwise noted, such as 5 μg of E. coli EDA). The reactions in the repeated experiment all were in the linear range of detection and the results of these additional kinetic assays are shown graphically in FIG. 16, and in the table below. E. coli EDA was again found to be the most active of those EDA's tested.


EDA	slope	% max

EC	0.462	100.00
SO	0.128	27.71
GO	0.0544	11.77
PCO	0.0539	11.67
BS	0.0505	10.93
PA	0.0273	5.91
V	0.0006	0.13

Example 23

Nucleotide and Amino Acid Sequence of S. cerevisiae Phosphoglucose Isomerase

Phosphoglucose isomerase (PGI1) activity was decreased or disrupted, in some embodiments, to favor the conversion of glucose-6-phosphate to gluconolactone-6-phosphate by the activity of ZWF1 (e.g., glucose-6-phosphate dehydrogenase). The nucleotide sequence of the S. cerevisiae PGI1 gene altered to decrease or disrupt phosphoglucose isomerase activity is shown below.

PGI1 nucleotide sequence

(SEQ ID NO: 423)

ATGTCCAATAACTCATTCACTAACTTCAAACTGGCCACTGAATTGCCAG

CCTGGTCTAAGTTGCAAAAAATTTATGAATCTCAAGGTAAGACTTTGTC

TGTCAAGCAAGAATTCCAAAAAGATGCCAAGCGTTTTGAAAAATTGAAC

AAGACTTTCACCAACTATGATGGTTCCAAAATCTTGTTCGACTACTCAA

AGAACTTGGTCAACGATGAAATCATTGCTGCATTGATTGAACTGGCCAA

GGAGGCTAACGTCACCGGTTTGAGAGATGCTATGTTCAAAGGTGAACAC

ATCAACTCCACTGAAGATCGTGCTGTCTACCACGTCGCATTGAGAAACA

GAGCTAACAAGCCAATGTACGTTGATGGTGTCAACGTTGCTCCAGAAGT

CGACTCTGTCTTGAAGCACATGAAGGAGTTCTCTGAACAAGTTCGTTCT

GGTGAATGGAAGGGTTATACCGGTAAGAAGATCACCGATGTTGTTAACA

TCGGTATTGGTGGTTCCGATTTGGGTCCAGTCATGGTCACTGAGGCTTT

GAAGCACTACGCTGGTGTCTTGGATGTCCACTTCGTTTCCAACATTGAC

GGTACTCACATTGCTGAAACCTTGAAGGTTGTTGACCCAGAAACTACTT

TGTTTTTGATTGCTTCCAAGACTTTCACTACCGCTGAAACTATCACTAA

CGCTAACACTGCCAAGAACTGGTTCTTGTCGAAGACAGGTAATGATCCA

TCTCACATTGCTAAGCATTTCGCTGCTTTGTCCACTAACGAAACCGAAG

TTGCCAAGTTCGGTATTGACACCAAAAACATGTTTGGTTTCGAAAGTTG

GGTCGGTGGTCGTTACTCTGTCTGGTCGGCTATTGGTTTGTCTGTTGCC

TTGTACATTGGCTATGACAACTTTGAGGCTTTCTTGAAGGGTGCTGAAG

CCGTCGACAACCACTTCACCCAAACCCCATTGGAAGACAACATTCCATT

GTTGGGTGGTTTGTTGTCTGTCTGGTACAACAACTTCTTTGGTGCTCAA

ACCCATTTGGTTGCTCCATTCGACCAATACTTGCACAGATTCCCAGCCTA

CTTGCAACAATTGTCAATGGAATCTAACGGTAAGTCTGTTACCAGAGGT

AACGTGTTTACTGACTACTCTACTGGTTCTATCTTGTTTGGTGAACCAG

CTACCAACGCTCAACACTCTTTCTTCCAATTGGTTCACCAAGGTACCAA

GTTGATTCCATCTGATTTCATCTTAGCTGCTCAATCTCATAACCCAATT

GAGAACAAATTACATCAAAAGATGTTGGCTTCAAACTTCTTTGCTCAAG

CTGAAGCTTTAATGGTTGGTAAGGATGAAGAACAAGTTAAGGCTGAAGG

TGCCACTGGTGGTTTGGTCCCACACAAGGTCTTCTCAGGTAACAGACCA

ACTACCTCTATCTTGGCTCAAAAGATTACTCCAGCTACTTTGGGTGCTT

TGATTGCCTACTACGAACATGTTACTTTCACTGAAGGTGCCATTTGGAA

TATCAACTCTTTCGACCAATGGGGTGTTGAATTGGGTAAAGTCTTGGCT

AAAGTCATCGGCAAGGAATTGGACAACTCCTCCACCATTTCTACCCACG

ATGCTTCTACCAACGGTTTAATCAATCAATTCAAGGAATGGATGTGA

Example 24

Nucleotide and Amino Acid Sequence of S. cerevisiae 6-Phosphogluconate Dehydrogenase (Decarboxylating)

6-phosphogluconate dehydrogenase (decarboxylating) (GND1) activity was decreased or disrupted, in some embodiments, to minimize or eliminate the conversion of gluconate-6-phophate to ribulose-5-phosphate. The nucleotide sequence of the S. cerevisiae GND1 and GND2 genes altered to decrease or disrupt 6-phosphogluconate dehydrogenase (decarboxylating) activity is shown below.

GND1/YHR183W

(SEQ ID NO: 424)

ATGTCTGCTGATTTCGGTTTGATTGGTTTGGCCGTCATGGGTCAAAATT

TGATCTTGAACGCTGCTGACCACGGTTTCACTGTTTGTGCTTACAACAG

AACTCAATCCAAGGTCGACCATTTCTTGGCCAATGAAGCTAAGGGCAAA

TCTATCATCGGTGCTACTTCCATTGAAGATTTCATCTCCAAATTGAAGA

GACCTAGAAAGGTCATGCTTTTGGTTAAAGCTGGTGCTCCAGTTGACGC

TTTGATCAACCAAATCGTCCCACTTTTGGAAAAGGGTGATATTATCATC

GATGGTGGTAACTCTCACTTCCCAGATTCTAATAGACGTTACGAAGAAT

TGAAGAAGAAGGGTATTCTTTTCGTTGGTTCTGGTGTCTCCGGTGGTGA

GGAAGGTGCCCGTTACGGTCCATCTTTGATGCCAGGTGGTTCTGAAGAA

GCTTGGCCACATATTAAGAACATCTTCCAATCCATCTCTGCTAAATCCG

ACGGTGAACCATGTTGCGAATGGGTTGGCCCAGCCGGTGCTGGTCACTA

CGTCAAGATGGTTCACAACGGTATTGAATACGGTGATATGCAATTGATT

TGTGAAGCTTATGACATCATGAAGAGATTGGGTGGGTTTACCGATAAGG

AAATCAGTGACGTTTTTGCCAAATGGAACAATGGTGTCTTGGATTCCTT

CTTGGTCGAAATTACCAGAGATATTTTGAAATTCGACGACGTCGACGGT

AAGCCATTAGTTGAAAAAATCATGGATACTGCTGGTCAAAAGGGTACTG

GTAAGTGGACTGCCATCAACGCCTTGGATTTGGGTATGCCAGTTACTTT

GATTGGTGAAGCTGTCTTTGCCCGTTGTCTATCTGCTTTGAAGAACGAG

AGAATTAGAGCCTCCAAGGTCTTACCAGGCCCAGAAGTTCCAAAAGACG

CCGTCAAGGACAGAGAACAATTTGTCGATGATTTGGAACAAGCTTTGTA

TGCTTCCAAGATTATTTCTTACGCTCAAGGTTTCATGTTGATCCGTGAA

GCTGCTGCTACTTATGGCTGGAAACTAAACAACCCTGCCATCGCTTTGAT

GTGGAGAGGTGGTTGTATCATTAGATCTGTTTTCTTGGGTCAAATCACA

AAGGCCTACAGAGAAGAACCAGATTTGGAAAACTTGTTGTTCAACAAGT

TCTTCGCTGATGCCGTCACCAAGGCTCAATCTGGTTGGAGAAAGTCAAT

TGCGTTGGCTACCACCTACGGTATCCCAACACCAGCCTTTTCCACCGCT

TTGTCTTTCTACGATGGGTACAGATCTGAAAGATTGCCAGCCAACTTAC

TACAAGCTCAACGTGACTACTTTGGTGCTCACACTTTCAGAGTGTTGCC

AGAATGTGCTTCTGACAACTTGCCAGTAGACAAGGATATCCATATCAAC

TGGACTGGCCACGGTGGTAATGTTTCTTCCTCTACATACCAAGCTTAA

GND2/YGR256W

(SEQ ID NO: 425)

ATGTCAAAGGCAGTAGGTGATTTAGGCTTAGTTGGTTTAGCCGTGATGG

GTCAAAATTTGATCTTAAACGCAGCGGATCACGGATTTACCGTGGTTGC

TTATAATAGGACGCAATCAAAGGTAGATAGGTTTCTAGCTAATGAGGCA

AAAGGAAAATCAATAATTGGTGCAACTTCAATTGAGGACTTGGTTGCGA

AACTAAAGAAACCTAGAAAGATTATGCTTTTAATCAAAGCCGGTGCTCC

GGTCGACACTTTAATAAAGGAACTTGTACCACATCTTGATAAAGGCGAC

ATTATTATCGACGGTGGTAACTCACATTTCCCGGACACTAACAGACGCT

ACGAAGAGCTAACAAAGCAAGGAATTCTTTTTGTGGGCTCTGGTGTCTC

AGGCGGTGAAGATGGTGCACGTTTTGGTCCATCTTTAATGCCTGGTGGG

TCAGCAGAAGCATGGCCGCACATCAAGAACATCTTTCAATCTATTGCCG

CCAAATCAAACGGTGAGCCATGCTGCGAATGGGTGGGGCCTGCCGGTTC

TGGTCACTATGTGAAGATGGTACACAACGGTATCGAGTACGGTGATATG

CAGTTGATTTGCGAGGCTTACGATATCATGAAACGAATTGGCCGGTTTA

CGGATAAAGAGATCAGTGAAGTATTTGACAAGTGGAACACTGGAGTTTT

GGATTCTTTCTTGATTGAAATCACGAGGGACATTTTAAAATTCGATGAC

GTCGACGGTAAGCCATTGGTGGAAAAAATTATGGATACTGCCGGTCAAA

AGGGTACTGGTAAATGGACTGCAATCAACGCCTTGGATTTAGGAATGCC

AGTCACTTTAATTGGGGAGGCTGTTTTCGCTCGTTGTTTGTCAGCCATA

AAGGACGAACGTAAAAGAGCTTCGAAACTTCTGGCAGGACCAACAGTAC

CAAAGGATGCAATACATGATAGAGAACAATTTGTGTATGATTTGGAACA

AGCATTATACGCTTCAAAGATTATTTCATATGCTCAAGGTTTCATGCTG

ATCCGCGAAGCTGCCAGATCATACGGCTGGAAATTAAACAACCCAGCTA

TTGCTCTAATGTGGAGAGGTGGCTGTATAATCAGATCTGTGTTCTTAGC

TGAGATTACGAAGGCTTATAGGGACGATCCAGATTTGGAAAATTTATTA

TTCAACGAGTTCTTCGCTTCTGCAGTTACTAAGGCCCAATCCGGTTGGA

GAAGAACTATTGCCCTTGCTGCTACTTACGGTATTCCAACTCCAGCTTT

CTCTACTGCTTTAGCGTTTTACGACGGCTATAGATCTGAGAGGCTACCA

GCAAACTTGTTACAAGCGCAACGTGATTATTTTGGCGCTCATACATTTA

GAATTTTACCTGAATGTGCTTCTGCCCATTTGCCAGTAGACAAGGATAT

TCATATCAATTGGACTGGGCACGGAGGTAATATATCTTCCTCAACCTAC

CAAGCTTAA

Example 25

Nucleotide and Amino Acid Sequence of S. cerevisiae Transaldolase

Transaldolase (TAL1) activity was increased in some embodiments, and in certain embodiments transaldolase activity was decreased or disrupted. Transaldolase converts sedoheptulose 7-phosphate and glyceraldehyde 3-phosphate to erythrose 4-phosphate and fructose 6-phosphate. The rationale for increasing or decreasing transaldolase activity is described herein with respect to various embodiments. The nucleotide sequence of the S. cerevisiae TAL1 gene altered to increase or decrease transaldolase activity, and the encoded amino acid sequence are shown below.

TAL1 nucleotide sequence

(SEQ ID NO: 426)

ATGTCTGAACCAGCTCAAAAGAAACAAAAGGTTGCTAACAACTCTCTAG

AACAATTGAAAGCCTCCGGCACTGTCGTTGTTGCCGACACTGGTGATTT

CGGCTCTATTGCCAAGTTTCAACCTCAAGACTCCACAACTAACCCATCA

TTGATCTTGGCTGCTGCCAAGCAACCAACTTACGCCAAGTTGATCGATG

TTGCCGTGGAATACGGTAAGAAGCATGGTAAGACCACCGAAGAACAAGT

CGAAAATGCTGTGGACAGATTGTTAGTCGAATTCGGTAAGGAGATCTTA

AAGATTGTTCCAGGCAGAGTCTCCACCGAAGTTGATGCTAGATTGTCTT

TTGACACTCAAGCTACCATTGAAAAGGCTAGACATATCATTAAATTGTT

TGAACAAGAAGGTGTCTCCAAGGAAAGAGTCCTTATTAAAATTGCTTCC

ACTTGGGAAGGTATTCAAGCTGCCAAAGAATTGGAAGAAAAGGACGGTA

TCCACTGTAATTTGACTCTATTATTCTCCTTCGTTCAAGCAGTTGCCTG

TGCCGAGGCCCAAGTTACTTTGATTTCCCCATTTGTTGGTAGAATTCTA

GACTGGTACAAATCCAGCACTGGTAAAGATTACAAGGGTGAAGCCGACC

CAGGTGTTATTTCCGTCAAGAAAATCTACAACTACTACAAGAAGTACGG

TTACAAGACTATTGTTATGGGTGCTTCTTTCAGAAGCACTGACGAAATC

AAAAACTTGGCTGGTGTTGACTATCTAACAATTTCTCCAGCTTTATTGG

ACAAGTTGATGAACAGTACTGAACCTTTCCCAAGAGTTTTGGACCCTGT

CTCCGCTAAGAAGGAAGCCGGCGACAAGATTTCTTACATCAGCGACGAA

TCTAAATTCAGATTCGACTTGAATGAAGACGCTATGGCCACTGAAAAAT

TGTCCGAAGGTATCAGAAAATTCTCTGCCGATATTGTTACTCTATTCGA

CTTGATTGAAAAGAAAGTTACCGCTTAA

TAL1 amino acid sequence

(SEQ ID NO: 427)

MSEPAQKKQKVANNSLEQLKASGTVVVADTGDFGSIAKFQPQDSTTNPS

LILAAAKQPTYAKLIDVAVEYGKKHGKTTEEQVENAVDRLLVEFGKEIL

KIVPGRVSTEVDARLSFDTQATIEKARHIIKLFEQEGVSKERVLIKIAS

TWEGIQAAKELEEKDGIHCNLTLLFSFVQAVACAEAQVTLISPFVGRIL

DWYKSSTGKDYKGEADPGVISVKKIYNYYKKYGYKTIVMGASFRSTDEI

KNLAGVDYLTISPALLDKLMNSTEPFPRVLDPVSAKKEAGDKISYISDE

SKFRFDLNEDAMATEKLSEGIRKFSADIVTLFDLIEKKVTA

Example 26

Nucleotide and Amino Acid Sequence of S. cerevisiae Transketolase

Transketolase (TKL1 and TKL2) activity was increased in some embodiments, and in certain embodiments transaldolase activity was decreased or disrupted. Transketolase converts xylulose-5-phosphate and ribose-5-phosphate to sedoheptulose-7-phosphate and glyceraldehyde-3-phosphate. The rationale for increasing or decreasing transketolase activity is described herein with respect to various embodiments. The nucleotide sequence of the S. cerevisiae TKL1 gene altered to increase or decrease transketolase activity, and the encoded amino acid sequence are shown below.

TKL1 nucleotide sequence

(SEQ ID NO: 428)

ATGACTCAATTCACTGACATTGATAAGCTAGCCGTCTCCACCATAAGAA

TTTTGGCTGTGGACACCGTATCCAAGGCCAACTCAGGTCACCCAGGTGC

TCCATTGGGTATGGCACCAGCTGCACACGTTCTATGGAGTCAAATGCGC

ATGAACCCAACCAACCCAGACTGGATCAACAGAGATAGATTTGTCTTGT

CTAACGGTCACGCGGTCGCTTTGTTGTATTCTATGCTACATTTGACTGG

TTACGATCTGTCTATTGAAGACTTGAAACAGTTCAGACAGTTGGGTTCC

AGAACACCAGGTCATCCTGAATTTGAGTTGCCAGGTGTTGAAGTTACTA

CCGGTCCATTAGGTCAAGGTATCTCCAACGCTGTTGGTATGGCCATGGC

TCAAGCTAACCTGGCTGCCACTTACAACAAGCCGGGCTTTACCTTGTCT

GACAACTACACCTATGTTTTCTTGGGTGACGGTTGTTTGCAAGAAGGTA

TTTCTTCAGAAGCTTCCTCCTTGGCTGGTCATTTGAAATTGGGTAACTT

GATTGCCATCTACGATGACAACAAGATCACTATCGATGGTGCTACCAGT

ATCTCATTCGATGAAGATGTTGCTAAGAGATACGAAGCCTACGGTTGGG

AAGTTTTGTACGTAGAAAATGGTAACGAAGATCTAGCCGGTATTGCCAA

GGCTATTGCTCAAGCTAAGTTATCCAAGGACAAACCAACTTTGATCAAA

ATGACCACAACCATTGGTTACGGTTCCTTGCATGCCGGCTCTCACTCTG

TGCACGGTGCCCCATTGAAAGCAGATGATGTTAAACAACTAAAGAGCAA

ATTCGGTTTCAACCCAGACAAGTCCTTTGTTGTTCCACAAGAAGTTTAC

GACCACTACCAAAAGACAATTTTAAAGCCAGGTGTCGAAGCCAACAACA

AGTGGAACAAGTTGTTCAGCGAATACCAAAAGAAATTCCCAGAATTAGG

TGCTGAATTGGCTAGAAGATTGAGCGGCCAACTACCCGCAAATTGGGAA

TCTAAGTTGCCAACTTACACCGCCAAGGACTCTGCCGTGGCCACTAGAA

AATTATCAGAAACTGTTCTTGAGGATGTTTACAATCAATTGCCAGAGTT

GATTGGTGGTTCTGCCGATTTAACACCTTCTAACTTGACCAGATGGAAG

GAAGCCCTTGACTTCCAACCTCCTTCTTCCGGTTCAGGTAACTACTCTG

GTAGATACATTAGGTACGGTATTAGAGAACACGCTATGGGTGCCATAAT

GAACGGTATTTCAGCTTTCGGTGCCAACTACAAACCATACGGTGGTACT

TTCTTGAACTTCGTTTCTTATGCTGCTGGTGCCGTTAGATTGTCCGCTT

TGTCTGGCCACCCAGTTATTTGGGTTGCTACACATGACTCTATCGGTGTA

CGGTGAAGATGGTCCAACCATCAACCTATTGAAACTTTAGCACACTTCA

GATCCCTACCAAACATTCAAGTTTGGAGACCAGCTGATGGTAACGAAGT

TTCTGCCGCCTACAAGAACTCTTTAGAATCCAAGCATACTCCAAGTATC

ATTGCTTTGTCCAGACAAAACTTGCCACAATTGGAAGGTAGCTCTATTG

AAAGCGCTTCTAAGGGTGGTTACGTACTACAAGATGTTGCTAACCCAGA

TATTATTTTAGTGGCTACTGGTTCCGAAGTGTCTTTGAGTGTTGAAGCT

GCTAAGACTTTGGCCGCAAAGAACATCAAGGCTCGTGTTGTTTCTCTAC

CAGATTTCTTCACTTTTGACAAACAACCCCTAGAATACAGACTATCAGT

CTTACCAGACAACGTTCCAATCATGTCTGTTGAAGTTTTGGCTACCACA

TGTTGGGGCAAATACGCTCATCAATCCTTCGGTATTGACAGATTTGGTG

CCTCCGGTAAGGCACCAGAAGTCTTCAAGTTCTTCGGTTTCACCCCAGA

AGGTGTTGCTGAAAGAGCTCAAAAGACCATTGCATTCTATAAGGGTGAC

AAGCTAATTTCTCCTTTGAAAAAAGCTTTCTAA

TKL1 amino acid sequence

(SEQ ID NO: 429)

MTQFTDIDKLAVSTIRILAVDTVSKANSGHPGAPLGMAPAAHVLWSQMR

MNPTNPDWINRDRFVLSNGHAVALLYSMLHLTGYDLSIEDLKQFRQLGS

RTPGHPEFELPGVEVTTGPLGQGISNAVGMAMAQANLAATYNKPGFTLS

DNYTYVFLGDGCLQEGISSEASSLAGHLKLGNLIAIYDDNKITIDGATS

ISFDEDVAKRYEAYGWEVLYVENGNEDLAGIAKAIAQAKLSKDKPTLIK

MTTTIGYGSLHAGSHSVHGAPLKADDVKQLKSKFGFNPDKSFVVPQEVY

DHYQKTILKPGVEANNKWNKLFSEYQKKFPELGAELARRLSGQLPANWE

SKLPTYTAKDSAVATRKLSETVLEDVYNQLPELIGGSADLTPSNLTRWK

EALDFQPPSSGSGNYSGRYIRYGIREHAMGAIMNGISAFGANYKPYGGT

FLNFVSYAAGAVRLSALSGHPVIWVATHDSIGVGEDGPTHQPIETLAHF

RSLPNIQVWRPADGNEVSAAYKNSLESKHTPSIIALSRQNLPQLEGSSI

ESASKGGYVLQDVANPDIILVATGSEVSLSVEAAKTLAAKNIKARVVSL

PDFFTFDKQPLEYRLSVLPDNVPIMSVEVLATTCWGKYAHQSFGIDRFG

ASGKAPEVFKFFGFTPEGVAERAQKTIAFYKGDKLISPLKKAF

Example 27

Nucleotide and Amino Acid Sequences of Additional EDD Genes Evaluated for Activity


Accession		Strain		Amino Acid
Number	Species	Number	NUCLEOTIDE SEQUENCE	Sequence

YP_526855.1	Saccharophagus	2-40	ATGAATAGCGTAATCGAAGCTGTAACTCAGCGAATTATTGAGCGCAGT	MNSVIEAVTQRIIERSR
	degradans		CGACATTCTCGTCAGGCGTATTTGAATTTAATGCGCAACACCATGGAG	HSRQAYLNLMRNTME
			CAGCATCCTCCTAAAAAGCGTCTATCTTGCGGCAATTTGGCTCATGCCT	QHPPKKRLSCGNLAHA
			ATGCAGCATGTGGTCAATCCGATAAGCAAACAATTCGTTTAATGCAAA	YAACGQSDKQTIRLMQ
			GTGCAAACATAAGTATTACTACGGCATTTAACGATATGCTTTCGGCGC	SANISITTAFNDMLSAH
			ATCAGCCTTTAGAAACATACCCTCAAATAATCAAAGAAACTGCGCGTG	QPLETYPQIIKETARAM
			CAATGGGTTCAACTGCTCAAGTTGCAGGCGGCGTGCCGGCAATGTGTG	GSTAQVAGGVPAMCD
			ATGGTGTAACTCAAGGCCAGCCCGGTATGGAGCTGAGTTTGTTTAGCC	GVTQGQPGMELSLFSR
			GCGAAGTTGTAGCAATGGCTACAGCAGTAGGCCTTTCGCACAATATGT	EVVAMATAVGLSHNM
			TTGATGGCAATATGTTTTTGGGTGTATGCGATAAAATTGTTCCTGGCAT	FDGNMFLGVCDKIVPG
			GCTAATTGGCGCGTTGCAGTTTGGTCATATTCCTGGGGTGTTTGTGCCT	MLIGALQFGHIPGVFVP
			GCCGGACCAATGCCTTCTGGTATTCCCAACAAAGAAAAAGCAAAAGTT	AGPMPSGIPNKEKAKV
			CGTCAGCAATATGCGGCGGGCATTGTGGGGGAAGATAAGCTTTTAGAA	RQQYAAGIVGEDKLLE
			ACCGAGTCGGCTTCCTATCACAGTGCAGGCACGTGTACTTTTTACGGTA	TESASYHSAGTCTFYGT
			CAGCGAATACAAACCAAATGATGGTTGAAATGTTGGGTGTTCAGTTGC	ANTNQMMVEMLGVQL
			CTGGCTCGTCGTTTGTTTACCCCGGTACTGAGTTGCGTGATGCCTTAAC	PGSSFVYPGTELRDALT
			GAGAGCTGCTGTTGAAAAGTTGGTAAAAATCACAGATTCAGCCGGTAA	RAAVEKLVKITDSAGN
			CTACCGTCCGCTCTACGAAGTCATTACGGAAAAATCCATCGTCAATTC	YRPLYEVITEKSIVNSII
			AATAATTGGTTTGTTGGCTACCGGCGGTTCTACTAACCACACGCTACAC	GLLATGGSTNHTLHIVA
			ATTGTTGCTGTGGCTCGCGCTGCGGGTATAGAGGTTACGTGGGCAGAT	VARAAGIEVTWADMD
			ATGGACGAGCTTTCGCGTGCTGTGCCATTACTTGCACGTGTTTACCCTA	ELSRAVPLLARVYPNGE
			ACGGCGAAGCTGATGTTAACCAATTCCAGCAGGCTGGCGGCATGGCTT	ADVNQFQQAGGMAYL
			ATTTAGTAAGAGAGCTGCGCAGCGGCGGTTTGCTAAATGAAGATGTGG	VRELRSGGLLNEDVVTI
			TTACTATTATGGGTGAGGGCCTCGAGGCCTACGAAAAAGAGCCCATGC	MGEGLEAYEKEPMLND
			TTAACGATAAGGGGCAGGCTGAATGGGTAAATGATGTACCTGTTAGCC	KGQAEWVNDVPVSRD
			GCGACGATACCGTTGTGCGTCCAGTTACCTCGCCTTTCGATAAAGAGG	DTVVRPVTSPFDKEGGL
			GTGGGTTGCGTCTACTCAAGGGTAACTTAGGGCAGGGCGTAATCAAAA	RLLKGNLGQGVIKISAV
			TTTCTGCGGTAGCGCCAGAAAATCGCGTTGTTGAGGCCCCATGTATTGT	APENRVVEAPCIVFEAQ
			ATTCGAGGCCCAAGAAGAGCTAATAGCTGCGTTTAAGCGTGGTGAGCT	EELIAAFKRGELEKDFV
			CGAAAAAGACTTTGTTGCGGTAGTGCGCTTCCAAGGGCCTTCTGCCAA	AVVRFQGPSANGMPEL
			TGGCATGCCAGAACTTCATAAAATGACCCCGCCTTTAGGTGTGCTTCA	HKMTPPLGVLQDKGFK
			AGATAAGGGTTTCAAGGTAGCGTTAGTTACCGATGGCAGAATGTCTGG	VALVTDGRMSGASGKV
			TGCATCTGGTAAAGTGCCGGCCGGTATACACTTGTCGCCAGAAGCGAG	PAGIHLSPEASKGGLLN
			TAAGGGTGGCCTGTTGAATAAGCTGCGCACGGGTGATGTGATTCGCTT	KLRTGDVIRFDAEAGVI
			CGATGCCGAAGCGGGCGTTATTCAAGCGCTTGTTAGTGATGAAGAGTT	QALVSDEELAAREPAV
			AGCTGCGCGTGAGCCAGCTGTGCAACCGGTCGTGGAGCAGAACCTCGG	QPVVEQNLGRSLFGGL
			ACGCTCTCTGTTTGGTGGTTTGCGCGATTTGGCTGGTGTATCGCTACAA	RDLAGVSLQGGTVFDF
			GGCGGAACAGTTTTCGATTTTGAAAGAGAGTTTGGCGAAAAATAG	EREFGEK (SEQ
			(SEQ ID NO: 430)	ID NO: 431)

NP_642389.1	Xanthomonas	Pv.	ATGAGCCTGCATCCGAATATCCAAGCCGTCACCGACCGTATCCGCAAG	MSLHPNIQAVTDRIRKR
	axonopodis	citri	CGCAGTGCTCCCTCGCGCGCGGCGTATCTGGCCGGCCTCGATGCCGCC	SAPSRAAYLAGIDAALR
		str. 306	CTGCGTGAGGGCCCGTTCCGTAGCCGGTTGAGCTGCGGCAATCTCGCG	EGPFRSRLSCGNLAHGF
			CATGGCTTCGCTGCGTCCGAGCCGGGCGACAAATCGCGCCTGCGCGGT	AASEPTDKSRLRGAATP
			GCGGCCACGCCGAACCTGGGCATCATCACTGCCTATAACGACATGTTG	NLGIITAYNDMLSAHQP
			TCGGCACATCAGCCGTTCGAGCACTACCCGCAGCTGATCCGCGAAACC	FEHYPQLIRETARSLGA
			GCGCGCTCACTTGGCGCCACTGCGCAGGTGGCCGGCGGCGTGCCGGCG	TAQVAGGVPAMCDGV
			ATGTGTGACGGCGTGACCCAGGGCCGCGCCGGCATGGAGCTGTCGCTG	TQGRAGMELSLFSRDNI
			TTCTCGCGCGACAACATCGCTCAGGCTGCGGCCATTGGCCTGAGCCAT	AQAAAIGLSHDMFDSV
			GACATGTTCGACAGCGTGGTGTACCTGGGGGTGTGCGACAAGATCGTG	VYLGVCDKIVPGLLIGA
			CCGGGTCTGCTGATCGGTGCGCTGGCGTTTGGCCATTTGCCGGCGATCT	LAFGHLPAIFMPAGPMT
			TCATGCCGGCTGGTCCGATGACCCCGGGCATCCCGAACAAGCAGAAAG	PGIPNKQKAEVRERYA
			CCGAAGTCCGCGAACGCTACGCCGCTGGCGAAGCCACCCGCGCCGAAT	AGEATRAELLEAESSSY
			TGCTGGAGGCCGAATCCTCGTCTTATCACTCGCCCGGCACCTGCACCTT	HSPGTCTFYGTANSNQ
			TTACGGCACGGCGAACTCCAACCAGGTGTTGCTCGAAGCGATGGGCGT	VLLEAMGVQLPGASFV
			GCAGTTGCCCGGCGCCTCGTTCGTCAATCCGGAGCTGCCGCTGCGCGA	NPELPLRDALTREGTAR
			TGCACTGACCCGCGAAGGCACCGCACGCGCATTGGCGATCTCCGCGCT	ALAISALGDDFRPFGRLI
			GGGCGATGACTTCCGCCCGTTCGGTCGTTTGATCGACGAACGGGCCAT	DERAIVNAVVALMATG
			CGTCAATGCCGTGGTCGCGCTGATGGCGACCGGCGGTTCGACCAACCA	GSTNHTIHWIAVARAA
			CACCATCCACTGGATCGCAGTGGCGCGTGCGGCCGGCATCGTGTTGAC	GIVLTWDDMDLISQTVP
			CTGGGACGACATGGATCTGATCTCGCAGACCGTGCCGCTGTTGACACG	LLTRIYPNGEADVNRFQ
			CATCTACCCGAACGGCGAAGCCGACGTGAACCGCTTCCAGGCCGCAGG	AAGGTAFVFRELMDAG
			CGGCACGGCGTTCGTGTTCCGCGAATTGATGGACGCCGGCTACATGCA	YMHDDLPTIVEGGMRA
			CGACGACCTGCCGACCATCGTCGAAGGCGGCATGCGCGCGTACGTCAA	YVNEPRLQDGKVTYVP
			CGAACCGCGCCTGCAGGACGGCAAGGTGACCTACGTGCCCGGCACCG	GTATTADDSVARPVSD
			CGACCACTGCCGACGACAGCGTCGCGCGTCCGGTCAGCGATGCATTCG	AFESQGGLRLLRGNLG
			AATCACAAGGCGGCCTGCGCCTGCTGCGCGGCAACCTCGGCCGCTCGT	RSLIKLSAVKPQHRSIQ
			TGATCAAGCTGTCGGCGGTCAAGCCGCAGCACCGCAGCATCCAAGCGC	APAVVIDTPQVLNKLH
			CAGCGGTGGTGATCGACACCCCGCAAGTGCTCAACAAACTGCATGCGG	AAGVLPHDFVVVLRYQ
			CGGGCGTACTGCCGCACGATTTCGTGGTGGTACTGCGCTATCAGGGCC	GPRANGMPELHSMAPL
			CACGCGCAAACGGCATGCCGGAGCTGCATTCGATGGCGCCGCTACTGG	LGLLQNQGRRVALVTD
			GCCTGCTGCAGAACCAGGGCCGGCGCGTGGCGTTGGTCACCGACGGCC	GRLSGASGKFPAAIHMT
			GTCTGTCCGGCGCCTCGGGCAAGTTCCCGGCGGCGATCCACATGACCC	PEAARGGPIGRVREGDI
			CGGAAGCCGCACGCGGCGGCCCGATCGGGCGCGTACGCGAAGGCGAC	VRLDGEAGTLEVLVSA
			ATCGTGCGACTGGACGGCGAAGCCGGCACCTTGGAAGTGCTGGTTTCG	EEWASREVAPNTALAG
			GCCGAAGAATGGGCATCGCGCGAGGTCGCACCGAACACTGCGTTGGC	NDLGRNLFAINRQVVG
			CGGCAACGACCTGGGCCGCAACCTGTTCGCCATCAACCGCCAGGTGGT	PADQGAISISCGPTHPD
			TGGCCCGGCCGACCAGGGCGCGATTTCCATTTCCTGCGGCCCGACCCA	GALWSYDAEYELGAD
			TCCGGACGGTGCGCTGTGGAGCTACGACGCCGAGTACGAACTCGGTGC	AAAAAAPHESKDA
			CGATGCAGCTGCAGCCGCCGCGCCGCACGAGTCCAAGGACGCCTGA	(SEQ ID NO: 433)
			(SEQ ID NO: 432)

NP_791117.1	Pseudomonas	Pv.	ATGCATCCCCGCGTCCTTGAAGTAACCGAGCGGCTCATTGCTCGCAGT	MHPRVLEVTERLIARSR
	syringae	tomato	CGCGATACCCGTCAGCGCTACCTTCAATTGATTCGAGGCGCAGCGAGC	DTRQRYLQLIRGAASD
		str.	GATGGCCCGATGCGCGGCAAGCTTCAATGTGCCAACTTTGCTCACGGC	GPMRGKLQCANFAHG
		DC3000	GTCGCCGCCTGCGGACCGGAGGACAAGCAAAGCCTGCGTTTGATGAAC	VAACGPEDKQSLRLMN
			GCCGCCAACGTGGCAATCGTCTCTTCCTACAATGAAATGCTCTCGGCG	AANVAIVSSYNEMLSA
			CATCAGCCCTACGAGCACTTTCCTGCACAGATCAAACAGGCGTTACGT	HQPYEHFPAQIKQALRD
			GACATTGGTTCGGTCGGTCAGTTTGCCGGCGGCGTGCCTGCCATGTGC	IGSVGQFAGGVPAMCD
			GATGGCGTGACTCAGGGTGAGCCGGGCATGGAACTGGCCATTGCCAGC	GVTQGEPGMELAIASRE
			CGCGAAGTGATTGCCATGTCCACGGCAATTGCCTTGTCACACAATATG	VIAMSTAIALSHNMFDA
			TTCGACGCCGCCATGATGCTGGGTATCTGCGACAAGATCGTCCCCGGC	AMMLGICDKIVPGLMM
			CTGATGATGGGGGCGTTGCGTTTCGGTCATCTGCCGACCATCTTCGTGC	GALRFGHLPTIFVPGGP
			CGGGCGGGCCGATGGTGTCAGGTATCTCCAACAAGGAAAAAGCCGAC	MVSGISNKEKADVRQR
			GTACGGCAGCGTTACGCTGAAGGCAAGGCCAGCCGTGAAGAGCTGCT	YAEGKASREELLDSEM
			GGACTCGGAAATGAAGTCCTATCACGGCCCGGGAACCTGCACGTTCTA	KSYHGPGTCTFYGTAN
			CGGCACCGCCAACACCAATCAGTTGGTGATGGAAGTCATGGGCATGCA	TNQLVMEVMGMHLPG
			CCTTCCCGGTGCCTCGTTCGTCAATCCCTACACACCACTGCGTGATGCG	ASFVNPYTPLRDALTAE
			CTGACAGCTGAAGCGGCTCGTCAGGTCACGCGTCTGACCATGCAAAGC	AARQVTRLTMQSGSFM
			GGCAGTTTCATGCCGATTGGTGAAATCGTCGACGAGCGCTCGCTGGTC	PIGEIVDERSLVNSIVAL
			AATTCCATCGTTGCGCTGCACGCCACCGGCGGCTCGACCAACCACACG	HATGGSTNHTLHMPAI
			CTGCACATGCCGGCGATTGCTCAGGCTGCGGGTATTCAGCTGACCTGG	AQAAGIQLTWQDMAD
			CAGGACATGGCCGACCTCTCCGAAGTGGTGCCGACCCTCAGTCACGTC	LSEVVPTLSHVYPNGK
			TACCCCAACGGCAAGGCCGACATCAACCATTTCCAGGCCGCAGGCGGC	ADINHFQAAGGMSFLIR
			ATGTCGTTCCTGATTCGCGAGCTGCTGGCAGCCGGTCTGCTGCACGAA	ELLAAGLLHENVNTVA
			AACGTTAACACCGTGGCCGGTTATGGCCTGAGCCGCTACACCAAAGAG	GYGLSRYTKEPFLEDG
			CCATTCCTGGAGGATGGCAAACTGGTCTGGCGTGAAGGCCCGCTGGAC	KLVWREGPLDSLDENIL
			AGCCTGGATGAAAACATCCTGCGCCCGGTGGCGCGTCCGTTCTCCCCT	RPVARPFSPEGGLRVME
			GAAGGCGGTTTGCGGGTCATGGAAGGCAACCTGGGTCGCGGTGTCATG	GNLGRGVMKVSAVAL
			AAAGTATCGGCCGTTGCGCTGGAGCATCAGATTGTCGAAGCGCCAGCC	EHQIVEAPARVFQDQK
			CGAGTGTTTCAGGATCAGAAGGAGCTGGCCGATGCGTTCAAGGCCGGC	ELADAFKAGELECDFV
			GAGCTGGAATGTGATTTCGTCGCCGTCATGCGTTTTCAGGGCCCGCGCT	AVMRFQGPRCNGMPEL
			GCAACGGCATGCCCGAACTGCACAAGATGACCCCGTTTCTGGGCGTGC	HKMTPFLGVLQDRGFK
			TGCAGGATCGTGGTTTCAAAGTGGCGCTGGTCACCGATGGACGGATGT	VALVTDGRMSGASGKI
			CGGGCGCCTCAGGCAAGATTCCGGCGGCGATTCACGTCTGCCCGGAAG	PAAIHVCPEAFDGGPLA
			CGTTCGATGGTGGCCCGTTGGCACTGGTACGCGACGGCGATGTGATCC	LVRDGDVIRVDGVKGT
			GCGTGGATGGCGTAAAAGGCACGTTACAAGTGCTGGTCGAAGCGTCA	LQVLVEASELAAREPAI
			GAATTGGCCGCCCGAGAACCGGCCATCAACCAGATCGACAACAGTGTC	NQIDNSVGCGRELFGF
			GGCTGCGGTCGCGAGCTTTTTGGATTCATGCGCATGGCCTTCAGCTCCG	MRMAFSSAEQGASAFT
			CAGAGCAAGGCGCCAGCGCCTTTACCTCTAGTCTGGAGACGCTCAAGT	SSLETLK (SEQ
			GA (SEQ ID NO: 434)	ID NO: 435)

YP_261706.1	Pseudomonas	Pf-5	ATGCATCCCCGCGTTCTTGAGGTCACCGAACGGCTTATCGCCCGTAGTC	MHPRVLEVTERLIARSR
	fluorescens		GCGCCACTCGCCAGGCCTATCTCGCGCTGATCCGCGATGCCGCCAGCG	ATRQAYLALIRDAASD
			ACGGCCCGCAGCGGGGCAAGCTGCAATGTGCGAACTTCGCCCACGGC	GPQRGKLQCANFAHGV
			GTGGCCGGTTGCGGCACCGACGACAAGCACAACCTGCGGATGATGAA	AGCGTDDKHNLRMMN
			TGCGGCCAACGTGGCAATTGTTTCGTCATATAACGACATGTTGTCGGC	AANVAIVSSYNDMLSA
			GCACCAGCCTTACGAGGTGTTCCCCGAGCAGATCAAGCGCGCCCTGCG	HQPYEVFPEQIKRALRE
			CGAGATCGGCTCGGTGGGCCAGTTCGCCGGCGGCACCCCGGCCATGTG	IGSVGQFAGGTPAMCD
			CGATGGCGTGACCCAGGGCGAGGCCGGTATGGAACTGAGCCTGCCGA	GVTQGEAGMELSLPSR
			GCCGTGAAGTGATCGCCCTGTCTACGGCGGTGGCCCTCTCTCACAACA	EVIALSTAVALSHNMFD
			TGTTCGATGCCGCGCTGATGCTGGGGATCTGCGACAAGATTGTCCCGG	AALMLGICDKIVPGLM
			GGTTGATGATGGGCGCTCTGCGCTTCGGTCACCTGCCGACCATCTTCGT	MGALRFGHLPTIFVPGG
			TCCGGGCGGGCCCATGGTCTCGGGCATTTCCAACAAGCAGAAAGCCGA	PMVSGISNKQKADVRQ
			CGTGCGCCAGCGTTACGCCGAAGGCAAGGCCAGCCGCGAGGAACTGC	RYAEGKASREELLESE
			TGGAGTCGGAAATGAAGTCCTACCACAGCCCCGGCACCTGCACTTTCT	MKSYHSPGTCTFYGTA
			ACGGCACCGCCAACACCAACCAGTTGCTGATGGAAGTGATGGGCCTGC	NTNQLLMEVMGLHLPG
			ACCTGCCGGGCGCCTCTTTCGTCAACCCCAATACGCCGCTGCGCGACG	ASFVNPNTPLRDALTHE
			CCCTGACCCATGAGGCGGCGCAGCAGGTCACGCGCCTGACCAAGCAG	AAQQVTRLTKQSGAFM
			AGCGGGGCCTTCATGCCGATTGGCGAGATCGTCGACGAGCGCGTGCTG	PIGEIVDERVLVNSIVAL
			GTCAACTCCATCGTTGCCCTGCACGCCACGGGCGGCTCCACCAACCAC	HATGGSTNHTLHMPAI
			ACCCTGCACATGCCGGCCATCGCCCAGGCGGCGGGCATCCAGCTGACC	AQAAGIQLTWQDMAD
			TGGCAGGACATGGCCGACCTCTCCGAGGTGGTGCCGACCCTGTCCCAC	LSEVVPTLSHVYPNGK
			GTCTATCCAAACGGCAAGGCCGATATCAACCACTTCCAGGCGGCGGGC	ADINHFQAAGGMSFLIR
			GGCATGTCTTTCCTGATCCGCGAGCTGCTGGAAGCCGGCCTGCTCCAC	ELLEAGLLHEDVNTVA
			GAAGACGTCAATACCGTGGCCGGCCGCGGCCTGAGCCGCTATACCCAG	GRGLSRYTQEPFLDNG
			GAACCCTTCCTGGACAACGGCAAGCTGGTGTGGCGCGACGGCCCGATT	KLVWRDGPIESLDENIL
			GAAAGCCTGGACGAAAACATCCTGCGCCCGGTGGCCCGGGCGTTCTCT	RPVARAFSAEGGLRVM
			GCGGAGGGCGGCTTGCGGGTCATGGAAGGCAACCTCGGTCGCGGCGT	EGNLGRGVMKVSAVAP
			GATGAAGGTTTCCGCCGTGGCCCCGGAGCACCAGATCGTCGAGGCCCC	EHQIVEAPAVVFQDQQ
			GGCCGTGGTGTTCCAGGACCAGCAGGACCTGGCCGATGCCTTCAAGGC	DLADAFKAGLLEKDFV
			CGGCCTGCTGGAGAAGGACTTCGTCGCGGTGATGCGCTTCCAGGGCCC	AVMRFQGPRSNGMPEL
			GCGCTCCAACGGCATGCCCGAGCTGCACAAGATGACCCCCTTCCTCGG	HKMTPFLGVLQDRGFK
			GGTGCTGCAGGACCGCGGCTTCAAGGTGGCGCTGGTCACCGACGGGCG	VALVTDGRMSGASGKI
			CATGTCCGGCGCTTCGGGCAAGATTCCGGCAGCGATCCATGTCAGCCC	PAAIHVSPEAQVGGAL
			CGAAGCCCAGGTGGGTGGCGCGCTGGCCCGGGTGCTGGACGGCGATA	ARVLDGDIIRVDGVKG
			TCATCCGAGTGGATGGCGTCAAGGGCACCCTGGAGCTTAAGGTAGACG	TLELKVDAAEFAAREP
			CCGCAGAATTCGCCGCCCGGGAGCCGGCCAAGGGCCTGCTGGGCAAC	AKGLLGNNVGTGRELF
			AACGTTGGCACCGGCCGCGAACTCTTCGCCTTCATGCGCATGGCCTTC	AFMRMAFSSAEQGASA
			AGCTCGGCAGAGCAGGGCGCCAGCGCCTTTACCTCTGCCCTGGAGACG	FTSALETLK (SEQ ID
			CTCAAGTGA (SEQ ID NO: 436)	NO: 437)

ZP_0359148.1	Bacillus	subtilis	ATGGCAGAATTACGCAGTAATATGATCACACAAGGAATCGATAGAGCT	MAELRSNMITQGIDRAP
	subtilis	str. 168	CCGCACCGCAGTTTGCTTCGTGCAGCAGGGGTAAAAGAAGAGGATTTC	HRSLLRAAGVKEEDFG
			GGCAAGCCGTTTATTGCGGTGTGTAATTCATACATTGATATCGTTCCCG	KPFIAVCNSYIDIVPGHV
			GTCATGTTCACTTGCAGGAGTTTGGGAAAATCGTAAAAGAAGCAATCA	HLQEFGKIVKEAIREAG
			GAGAAGCAGGGGGCGTTCCGTTTGAATTTAATACCATTGGGGTAGATG	GVPFEFNTIGVDDGIAM
			ATGGCATCGCAATGGGGCATATCGGTATGAGATATTCGCTGCCAAGCC	GHIGMRYSLPSREIIADS
			GTGAAATTATCGCAGACTCTGTGGAAACGGTTGTATCCGCACACTGGT	VETVVSAHWFDGMVCI
			TTGACGGAATGGTCTGTATTCCGAACTGCGACAAAATCACACCGGGAA	PNCDKITPGMLMAAMR
			TGCTTATGGCGGCAATGCGCATCAACATTCCGACGATTTTTGTCAGCG	INIPTIFVSGGPMAAGRT
			GCGGACCGATGGCGGCAGGAAGAACAAGTTACGGGCGAAAAATCTCC	SYGRKISLSSVFEGVGA
			CTTTCCTCAGTATTCGAAGGGGTAGGCGCCTACCAAGCAGGGAAAATC	YQAGKINENELQELEQF
			AACGAAAACGAGCTTCAAGAACTAGAGCAGTTCGGATGCCCAACGTG	GCPTCGSCSGMFTANS
			CGGGTCTTGCTCAGGCATGTTTACGGCGAACTCAATGAACTGTCTGTC	MNCLSEALGLALPGNG
			AGAAGCACTTGGTCTTGCTTTGCCGGGTAATGGAACCATTCTGGCAAC	TILATSPERKEFVRKSA
			ATCTCCGGAACGCAAAGAGTTTGTGAGAAAATCGGCTGCGCAATTAAT	AQLMETIRKDIKPRDIV
			GGAAACGATTCGCAAAGATATCAAACCGCGTGATATTGTTACAGTAAA	TVKAIDNAFALDMALG
			AGCGATTGATAACGCGTTTGCACTCGATATGGCGCTCGGAGGTTCTAC	GSTNTVLHTLALANEA
			AAATACCGTTCTTCATACCCTTGCCCTTGCAAACGAAGCCGGCGTTGA	GVEYSLERINEVAERVP
			ATACTCTTTAGAACGCATTAACGAAGTCGCTGAGCGCGTGCCGCACTT	HLAKLAPASDVFIEDLH
			GGCTAAGCTGGCGCCTGCATCGGATGTGTTTATTGAAGATCTTCACGA	EAGGVSAALNELSKKE
			AGCGGGCGGCGTTTCAGCGGCTCTGAATGAGCTTTCGAAGAAAGAAG	GALHLDALTVTGKTLG
			GAGCGCTTCATTTAGATGCGCTGACTGTTACAGGAAAAACTCTTGGAG	ETIAGHEVKDYDVIHPL
			AAACCATTGCCGGACATGAAGTAAAGGATTATGACGTCATTCACCCGC	DQPFTEKGGLAVLFGN
			TGGATCAACCATTCACTGAAAAGGGAGGCCTTGCTGTTTTATTCGGTA	LAPDGAIIKTGGVQNGI
			ATCTAGCTCCGGACGGCGCTATCATTAAAACAGGCGGCGTACAGAATG	TRHEGPAVVFDSQDEA
			GGATTACAAGACACGAAGGGCCGGCTGTCGTATTCGATTCTCAGGACG	LDGIINRKVKEGDVVIIR
			AGGCGCTTGACGGCATTATCAACCGAAAAGTAAAAGAAGGCGACGTT	YEGPKGGPGMPEMLAP
			GTCATCATCAGATACGAAGGGCCAAAAGGCGGACCTGGCATGCCGGA	TSQIVGMGLGPKVALIT
			AATGCTGGCGCCAACATCCCAAATCGTTGGAATGGGACTCGGGCCAAA	DGRFSGASRGLSIGHVS
			AGTGGCATTGATTACGGACGGACGTTTTTCCGGAGCCTCCCGTGGCCT	PEAAEGGPLAFVENGD
			CTCAATCGGCCACGTATCACCTGAGGCCGCTGAGGGCGGGCCGCTTGC	HIIVDIEKRILDVQVPEE
			CTTTGTTGAAAACGGAGACCATATTATCGTTGATATTGAAAAACGCAT	EWEKRKANWKGFEPK
			CTTGGATGTACAAGTGCCAGAAGAAGAGTGGGAAAAACGAAAAGCGA	VKTGYLARYSKLVTSA
			ACTGGAAAGGTTTTGAACCGAAAGTGAAAACCGGCTACCTGGCACGTT	NTGGIMKI
			ATTCTAAACTTGTGACAAGTGCCAACACCGGCGGTATTATGAAAATCT	(SEQ ID NO: 439)
			AG (SEQ ID NO: 438)

YP_091897.1	Bacillus	ATCC	ATGACAGGTTTACGCAGTGACATGATTACAAAAGGGATCGACAGAGC	MTGLRSDMITKGIDRAP
	licheniformis	14580	GCCGCACCGCAGTTTGCTGCGCGCGGCTGGGGTAAAAGAAGAGGACTT	HRSLLRAAGVKEEDFG
			CGGCAAACCGTTTATTGCCGTTTGCAACTCATACATCGATATCGTACCG	KPFIAVCNSYIDIVPGHV
			GGTCATGTCCATTTGCAGGAGTTTGGAAAAATCGTCAAAGAGGCGATC	HLQEFGKIVKEAIREAG
			AGAGAGGCCGGCGGTGTTCCGTTTGAATTTAATACAATCGGGGTCGAC	GVPFEFNTIGVDDGIAM
			GACGGAATTGCGATGGGGCACATCGGAATGAGGTATTCTCTCCCGAGC	GHIGMRYSLPSREIIADS
			CGCGAAATCATCGCAGATTCAGTGGAAACGGTTGTATCGGCGCACTGG	VETVVSAHWFDGMVCI
			TTTGACGGAATGGTATGTATTCCAAACTGTGATAAAATCACACCGGGC	PNCDKITPGMIMAAMRI
			ATGATCATGGCGGCAATGCGGATCAACATTCCGACCGTGTTTGTCAGC	NIPTVFVSGGPMEAGRT
			GGGGGGCCGATGGAAGCGGGAAGAACGAGCGACGGACGAAAAATCTC	SDGRKISLSSVFEGVGA
			GCTTTCCTCTGTATTTGAAGGCGTTGGCGCTTATCAATCAGGCAAAATC	YQSGKIDEKGLEELEQF
			GATGAGAAAGGACTCGAGGAGCTTGAACAGTTCGGCTGTCCGACTTGC	GCPTCGSCSGMFTANS
			GGATCATGCTCGGGCATGTTTACGGCGAACTCGATGAACTGTCTTTCTG	MNCLSEALGIAMPGNG
			AAGCTCTTGGCATCGCCATGCCGGGCAACGGCACCATTTTGGCGACAT	TILATSPDRREFAKQSA
			CGCCCGACCGCAGGGAATTTGCCAAACAGTCGGCCCGCCAGCTGATGG	RQLMELIKSDIKPRDIVT
			AGCTGATCAAGTCGGATATCAAACCGCGCGACATCGTGACCGAAAAA	EKAIDNAFALDMALGG
			GCGATCGACAACGCGTTCGCTTTAGACATGGCGCTCGGCGGATCAACG	STNTILHTLAIANEAGV
			AATACGATCCTTCATACGCTTGCGATCGCCAATGAAGCGGGTGTAGAC	DYSLERINEVAARVPHL
			TATTCGCTTGAACGGATCAATGAGGTAGCGGCAAGGGTTCCGCATTTA	SKLAPASDVFIEDLHEA
			TCGAAGCTTGCACCGGCTTCCGATGTGTTTATTGAAGATTTGCATGAAG	GGVSAVLNELSKKEGA
			CAGGAGGCGTATCGGCAGTCTTAAACGAGCTGTCGAAAAAAGAAGGC	LHLDTLTVTGKTLGENI
			GCGCTTCACTTGGATACGCTGACTGTAACGGGGAAAACGCTTGGCGAA	AGREVKDYEVIHPIDQP
			AATATTGCCGGACGCGAAGTGAAAGATTACGAGGTCATTCATCCGATC	FSEQGGLAVLFGNLAP
			GATCAGCCGTTTTCAGAGCAAGGCGGACTCGCCGTCCTGTTCGGCAAC	DGAIIKTGGVQDGITRH
			CTGGCTCCTGACGGTGCGATCATTAAAACGGGCGGCGTCCAAGACGGG	EGPAVVFDSQEEALDGI
			ATTACCCGCCATGAAGGACCTGCGGTTGTCTTTGATTCACAGGAAGAA	INRKVKAGDVVIIRYEG
			GCGCTTGACGGCATCATCAACCGTAAAGTAAAAGCGGGAGATGTCGTC	PKGGPGMPEMLAPTSQI
			ATCATCCGCTATGAAGGCCCTAAAGGCGGACCGGGAATGCCTGAAATG	VGMGLGPKVALITDGR
			CTTGCGCCGACTTCACAGATCGTCGGAATGGGCCTCGGCCCGAAAGTC	FSGASRGLSIGHVSPEA
			GCCTTGATTACCGACGGCCGCTTTTCAGGAGCCTCCCGCGGTCTTTCGA	AEGGPLAFVENGDHIV
			TCGGCCACGTTTCACCGGAAGCAGCCGAAGGCGGCCCGCTTGCTTTCG	VDIEKRILNIEISDEEWE
			TAGAAAACGGCGACCATATCGTTGTCGATATCGAAAAGCGGATTTTAA	KRKANWPGFEPKVKTG
			ACATCGAAATCTCCGATGAGGAATGGGAAAAAAGAAAAGCAAACTGG	YLARYSKLVTSANTGGI
			CCCGGCTTTGAACCGAAAGTGAAAACGGGCTATCTCGCCAGGTATTCA	MKI
			AAGCTTGTGACATCTGCCAATACCGGCGGCATTATGAAAATCTAG	(SEQ ID NO: 441)
			(SEQ ID NO: 440)

NP_0718074.1	Sewanella	MR-1	ATGCACTCAGTCGTTCAATCTGTTACTGACAGAATTATTGCCCGTAGCA	MHSVVQSVTDRIIARSK
	oneidensis		AAGCATCTCGTGAAGCATACCTTGCTGCGTTAAACGATGCCCGTAACC	ASREAYLAALNDARNH
			ATGGTGTACACCGAAGTTCCTTAAGTTGCGGTAACTTAGCCCACGGTTT	GVHRSSLSCGNLAHGF
			TGCGGCTTGTAATCCCGATGACAAAAATGCATTGCGTCAATTGACGAA	AACNPDDKNALRQLTK
			GGCCAATATTGGGATTATCACCGCATTCAACGATATGTTATCTGCACA	ANIGIITAFNDMLSAHQ
			CCAACCCTATGAAACCTATCCTGATTTGCTGAAAAAAGCCTGTCAGGA	PYETYPDLLKKACQEV
			AGTCGGTAGTGTTGCGCAGGTGGCTGGCGGTGTTCCCGCCATGTGTGA	GSVAQVAGGVPAMCD
			CGGCGTGACTCAAGGTCAGCCCGGTATGGAATTGAGCTTACTGAGCCG	GVTQGQPGMELSLLSR
			TGAAGTGATTGCGATGGCAACCGCGGTTGGCTTATCACACAATATGTT	EVIAMATAVGLSHNMF
			TGATGGAGCCTTACTCCTCGGTATTTGCGATAAAATTGTACCGGGTTTA	DGALLLGICDKIVPGLLI
			CTGATTGGTGCCTTAAGTTTTGGCCATTTACCTATGTTGTTTGTGCCCG	GALSFGHLPMLFVPAGP
			CAGGCCCAATGAAATCGGGTATTCCTAATAAGGAAAAAGCTCGCATTC	MKSGIPNKEKARIRQQF
			GTCAGCAATTTGCTCAAGGTAAGGTCGATAGAGCACAACTGCTCGAAG	AQGKVDRAQLLEAEAQ
			CGGAAGCCCAGTCTTACCACAGTGCGGGTACTTGTACCTTCTATGGTA	SYHSAGTCTFYGTANS
			CCGCTAACTCGAACCAACTGATGCTCGAAGTGATGGGGCTGCAATTGC	NQLMLEVMGLQLPGSS
			CGGGTTCATCTTTTGTGAATCCAGACGATCCACTGCGCGAAGCCTTAA	FVNPDDPLREALNKMA
			ACAAAATGGCGGCCAAGCAGGTTTGTCGTTTAACTGAACTAGGCACTC	AKQVCRLTELGTQYSPI
			AATACAGTCCGATTGGTGAAGTCGTTAACGAAAAATCGATAGTGAATG	GEVVNEKSIVNGIVALL
			GTATTGTTGCATTGCTCGCGACGGGTGGTTCAACAAACTTAACCATGC	ATGGSTNLTMHIVAAA
			ACATTGTGGCGGCGGCCCGTGCTGCAGGTATTATCGTCAACTGGGATG	RAAGIIVNWDDFSELSD
			ACTTTTCGGAATTATCCGATGCGGTGCCTTTGCTGGCACGTGTTTATCC	AVPLLARVYPNGHADI
			AAACGGTCATGCGGATATTAACCATTTCCACGCTGCGGGTGGTATGGC	NHFHAAGGMAFLIKEL
			TTTCCTTATCAAAGAATTACTCGATGCAGGTTTGCTGCATGAGGATGTC	LDAGLLHEDVNTVAGY
			AATACTGTCGCGGGTTATGGTCTGCGCCGTTACACCCAAGAGCCTAAA	GLRRYTQEPKLLDGEL
			CTGCTTGATGGCGAGCTGCGCTGGGTCGATGGCCCAACAGTGAGTTTA	RWVDGPTVSLDTEVLT
			GATACCGAAGTATTAACCTCTGTGGCAACACCATTCCAAAACAACGGT	SVATPFQNNGGLKLLK
			GGTTTAAAGCTGCTGAAGGGTAACTTAGGCCGCGCTGTGATTAAAGTG	GNLGRAVIKVSAVQPQ
			TCTGCCGTTCAGCCACAGCACCGTGTGGTGGAAGCGCCCGCAGTGGTG	HRVVEAPAVVIDDQNK
			ATTGACGATCAAAACAAACTCGATGCGTTATTTAAATCCGGCGCATTA	LDALFKSGALDRDCVV
			GACAGGGATTGTGTGGTGGTGGTGAAAGGCCAAGGGCCGAAAGCCAA	VVKGQGPKANGMPEL
			CGGTATGCCAGAGCTGCATAAACTAACGCCGCTGTTAGGTTCATTGCA	HKLTPLLGSLQDKGFK
			GGACAAAGGCTTTAAAGTGGCACTGATGACTGATGGTCGTATGTCGGG	VALMTDGRMSGASGK
			CGCATCGGGCAAAGTACCTGCGGCGATTCATTTAACCCCTGAAGCGAT	VPAAIHLTPEAIDGGLIA
			TGATGGCGGGTTAATTGCAAAGGTACAAGACGGCGATTTAATCCGAGT	KVQDGDLIRVDALTGE
			TGATGCACTGACCGGCGAGCTGAGTTTATTAGTCTCTGACACCGAGCT	LSLLVSDTELATRTATEI
			TGCCACCAGAACTGCCACTGAAATTGATTTACGCCATTCTCGTTATGGC	DLRHSRYGMGRELFGV
			ATGGGGCGTGAGTTATTTGGAGTACTGCGTTCAAACTTAAGCAGTCCT	LRSNLSSPETGARSTSAI
			GAAACCGGTGCGCGTAGTACTAGCGCCATCGATGAACTTTACTAA	DELY
			(SEQ ID NO: 442)	(SEQ ID NO: 443)

YP_190870.1	Gluconobacter	621H	ATGTCTCTGAATCCCGTCGTCGAGAGCGTGACTGCCCGTATCATCGAG	MSLNPVVESVTARIIER
	oxydans		CGTTCGAAAGTCTCCCGTCGCCGGTATCTCGCCCTGATGGAGCGCAAC	SKVSRRRYLALMERNR
			CGCGCCAAGGGTGTGCTCCGGCCCAAGCTGGCCTGCGGTAATCTGGCG	AKGVLRPKLACGNLAH
			CATGCCATCGCAGCGTCCAGCCCCGACAAGCCGGATCTGATGCGTCCC	AIAASSPDKPDLMRPTG
			ACCGGGACCAATATCGGCGTGATCACGACCTATAACGACATGCTCTCG	TNIGVITTYNDMLSAHQ
			GCGCATCAGCCGTATGGCCGCTATCCCGAGCAGATCAAGCTGTTCGCC	PYGRYPEQIKLFAREVG
			CGTGAAGTCGGTGCGACGGCCCAGGTTGCAGGCGGCGCACCAGCAAT	ATAQVAGGAPAMCDG
			GTGTGATGGTGTGACGCAGGGGCAGGAGGGCATGGAACTCTCCCTGTT	VTQGQEGMELSLFSRD
			CTCCCGTGACGTGATCGCCATGTCCACGGCGGTCGGGCTGAGCCACGG	VIAMSTAVGLSHGMFE
			CATGTTTGAGGGCGTGGCGCTGCTGGGCATCTGTGACAAGATTGTGCC	GVALLGICDKIVPGLLM
			GGGCCTTCTGATGGGCGCGCTGCGCTTCGGTCATCTCCCGGCCATGCTG	GALRFGHLPAMLIPAGP
			ATCCCGGCAGGGCCAATGCCGTCCGGTCTTCCAAACAAGGAAAAGCA	MPSGLPNKEKQRIRQLY
			GCGCATCCGCCAGCTCTATGTGCAGGGCAAGGTCGGGCAGGACGAGCT	VQGKVGQDELMEAEN
			GATGGAAGCGGAAAACGCCTCCTATCACAGCCCGGGCACCTGCACGTT	ASYHSPGTCTFYGTANT
			CTATGGCACGGCCAATACGAACCAGATGATGGTCGAAATCATGGGTCT	NQMMVEIMGLMMPDS
			GATGATGCCGGACTCGGCTTTCATCAATCCCAACACGAAGCTGCGTCA	AFINPNTKLRQAMTRSG
			GGCAATGACCCGCTCGGGTATTCACCGTCTGGCCGAAATCGGCCTGAA	IHRLAEIGLNGEDVRPL
			CGGCGAGGATGTGCGCCCGCTCGCTCATTGCGTAGACGAAAAGGCCAT	AHCVDEKAIVNAAVGL
			CGTGAATGCGGCGGTCGGGTTGCTGGCGACGGGTGGTTCGACCAACCA	LATGGSTNHSIHLPAIA
			TTCGATCCATCTTCCTGCTATCGCCCGTGCCGCTGGTATCCTGATCGAC	RAAGILIDWEDISRLSSA
			TGGGAAGACATCAGCCGCCTGTCGTCCGCGGTTCCGCTGATCACCCGT	VPLITRVYPSGSEDVNA
			GTTTATCCGAGCGGTTCCGAGGACGTGAACGCGTTCAACCGCGTGGGT	FNRVGGMPTVIAELTR
			GGTATGCCGACCGTGATCGCCGAACTGACGCGCGCCGGGATGCTGCAC	AGMLHKDILTVSRGGF
			AAGGACATTCTGACGGTCTCTCGTGGCGGTTTCTCCGATTATGCCCGTC	SDYARRASLEGDEIVYT
			GCGCATCGCTGGAAGGCGATGAGATCGTCTACACCCACGCGAAGCCGT	HAKPSTDTDILRDVATP
			CCACGGACACCGATATCCTGCGCGATGTGGCTACGCCTTTCCGGCCCG	FRPDGGMRLMTGNLGR
			ATGGCGGTATGCGCCTGATGACTGGTAATCTGGGCCGCGCGATCTACA	AIYKSSAIAPEHLTVEAP
			AGAGCAGCGCTATTGCGCCCGAGCACCTGACCGTTGAAGCGCCGGCAC	ARVFQDQHDVLTAYQN
			GGGTCTTCCAGGACCAGCATGACGTCCTCACGGCCTATCAGAATGGTG	GELERDVVVVVRFQGP
			AGCTTGAGCGTGATGTTGTCGTGGTCGTCCGGTTCCAGGGACCGGAAG	EANGMPELHKLTPTLG
			CCAACGGCATGCCGGAGCTTCACAAGCTGACCCCGACTCTGGGCGTGC	VLQDRGFKVALLTDGR
			TTCAGGATCGCGGCTTCAAGGTGGCCCTGCTGACGGATGGACGCATGT	MSGASGKVPAAIHVGP
			CCGGTGCGAGCGGCAAGGTGCCGGCCGCCATTCATGTCGGTCCCGAAG	EAQVGGPIARVRDGDM
			CGCAGGTTGGCGGTCCGATCGCCCGCGTGCGGGACGGCGACATGATCC	IRVCAVTGQIEALVDAA
			GTGTCTGCGCGGTGACGGGACAGATCGAGGCTCTGGTGGATGCCGCCG	EWESRKPVPPPLPALGT
			AGTGGGAGAGCCGCAAGCCGGTCCCGCCGCCGCTCCCGGCATTGGGA	GRELFALMRSVHDPAE
			ACGGGCCGCGAACTGTTCGCGCTGATGCGTTCGGTGCATGATCCGGCC	AGGSAMLAQMDRVIEA
			GAGGCTGGCGGATCCGCGATGCTGGCCCAGATGGATCGCGTGATCGAA	VGDDIH (SEQ ID NO:
			GCCGTTGGCGACGACATTCACTAA (SEQ ID NO: 444)	445)

ZP_06145432.1	Ruminococcus	FD-1	ATGAGCGATAATTTTTTCTGCGAGGGTGCGGATAAAGCCCCTCAGCGT	MSDNFFCEGADKAPQR
	flavefaciens		TCACTTTTCAATGCACTGGGCATGACTAAAGAGGAAATGAAGCGTCCC	SLFNALGMTKEEMKRP
			CTCGTTGGTATCGTTTCTTCCTACAATGAGATCGTTCCCGGCCATATGA	LVGIVSSYNEIVPGHMN
			ACATCGACAAGCTGGTCGAAGCCGTTAAGCTGGGTGTAGCTATGGGCG	IDKLVEAVKLGVAMGG
			GCGGCACTCCTGTTGTTTTCCCTGCTATCGCTGTATGCGACGGTATCGC	GTPVVFPAIAVCDGIAM
			TATGGGTCACACAGGCATGAAGTACAGCCTTGTTACCCGTGACCTTAT	GHTGMKYSLVTRDLIA
			TGCCGATTCTACAGAGTGTATGGCTCTTGCTCATCACTTCGACGCACTG	DSTECMALAHHFDALV
			GTAATGATACCTAACTGCGACAAGAACGTTCCCGGCCTGCTTATGGCG	MIPNCDKNVPGLLMAA
			GCTGCACGTATCAATGTTCCTACTGTATTCGTAAGCGGCGGCCCTATGC	ARINVPTVFVSGGPMLA
			TTGCAGGCCATGTAAAGGGTAAGAAGACCTCTCTTTCATCCATGTTCG	GHVKGKKTSLSSMFEA
			AGGCTGTAGGCGCTTACACAGCAGGCAAGATAGACGAGGCTGAACTT	VGAYTAGKIDEAELDE
			GACGAATTCGAGAACAAGACCTGCCCTACCTGCGGTTCATGTTCGGGT	FENKTCPTCGSCSGMY
			ATGTATACCGCTAACTCCATGAACTGCCTCACTGAGGTACTGGGTATG	TANSMNCLTEVLGMGL
			GGTCTCAGAGGCAACGGCACTATCCCTGCTGTTTACTCCGAGCGTATC	RGNGTIPAVYSERIKLA
			AAGCTTGCAAAGCAGGCAGGTATGCAGGTTATGGAACTCTACAGAAA	KQAGMQVMELYRKNI
			GAATATCCGCCCTCTCGATATCATGACAGAGAAGGCTTTCCAGAACGC	RPLDIMTEKAFQNALTA
			TCTCACAGCTGATATGGCTCTTGGATGTTCCACAAACAGTATGCTCCAT	DMALGCSTNSMLHLPA
			CTCCCTGCTATCGCCAACGAATGCGGCATAAATATCAACCTTGACATG	IANECGININLDMANEIS
			GCTAACGAGATAAGCGCCAAGACTCCTAACCTCTGCCATCTTGCACCG	AKTPNLCHLAPAGHTY
			GCAGGCCACACCTACATGGAAGACCTCAACGAAGCAGGCGGAGTTTA	MEDLNEAGGVYAVLN
			TGCAGTTCTCAACGAGCTGAGCAAAAAGGGACTTATCAACACCGACTG	ELSKKGLINTDCMTVT
			CATGACTGTTACAGGCAAGACCGTAGGCGAGAATATCAAGGGCTGCAT	GKTVGENIKGCINRDPE
			CAACCGTGACCCTGAGACTATCCGTCCTATCGACAACCCATACAGTGA	TIRPIDNPYSETGGIAVL
			AACAGGCGGAATCGCCGTACTCAAGGGCAATCTTGCTCCCGACAGATG	KGNLAPDRCVVKRSAV
			TGTTGTGAAGAGAAGCGCAGTTGCTCCCGAAATGCTGGTACACAAAGG	APEMLVHKGPARVFDS
			CCCTGCAAGAGTATTCGACAGCGAGGAAGAAGCTATCAAGGTCATCTA	EEEAIKVIYEGGIKAGD
			TGAGGGCGGTATCAAGGCAGGCGACGTTGTTGTTATCCGTTACGAAGG	VVVIRYEGPAGGPGMR
			CCCTGCAGGCGGCCCCGGCATGAGAGAAATGCTCTCTCCTACATCAGC	EMLSPTSAIQGAGLGST
			TATACAGGGTGCAGGTCTCGGCTCAACTGTTGCTCTAATCACTGACGG	VALITDGRFSGATRGAA
			ACGTTTCAGCGGCGCTACCCGTGGTGCGGCTATCGGACACGTATCCCC	IGHVSPEAVNGGTIAYV
			CGAAGCTGTAAACGGCGGTACTATCGCATATGTCAAGGACGGCGATAT	KDGDIISIDIPNYSITLE
			TATCTCCATCGACATACCGAATTACTCCATCACTCTTGAAGTATCCGAC	VSDEELAERKKAMPIKR
			GAGGAGCTTGCAGAGCGCAAAAAGGCAATGCCTATCAAGCGCAAGGA	KENITGYLKRYAQQVS
			GAACATCACAGGCTATCTGAAGCGCTATGCACAGCAGGTATCATCCGC	SADKGAIINRK (SEQ
			AGACAAGGGCGCTATCATCAACAGGAAATAG (SEQ ID NO: 446)	ID NO: 447)

Example 28

Unique 200-Mer Nucleotide Sequences Used for Integration Constructs


200-mer
number	Sequence

11	GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCCC
	GCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCGGG
	GTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGGCG
	ACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCTGGT
	CA (SEQ ID NO: 448)

17	AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG
	CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTTAT
	ACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCTCTA
	GAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGGGCG
	CA (SEQ ID NO: 449)

21	CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGCA
	GGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACCCC
	TACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGACCC
	CGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCGTGCG
	A (SEQ ID NO: 450)

24	GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGGC
	GTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCCGT
	CTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAGGC
	GCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCGTGC
	GA (SEQ ID NO: 451)

25	AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCGG
	GCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGCC
	TCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTAG
	GCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAGTT
	GGA (SEQ ID NO: 452)

448	ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAGG
	CCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAGTA
	TCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGCG
	TGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGCG
	ACCA (SEQ ID NO: 453)

Example 29

Examples of Embodiments

Provided hereafter are certain non-limiting embodiments of the technology.
A1. A composition comprising a nucleic acid that includes heterologous polynucleotides that encode a phosphogluconate dehydratase enzyme, a 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme and a nucleotide sequence identification tag selected from the group of six (6) nucleotide sequences consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

A2. The composition of embodiment A1, wherein the yeast is a Saccharomyces spp. yeast.
A3. The composition of embodiment A2, wherein the yeast is a Saccharomyces cerevisiae yeast strain.
A3.1. The composition of any one of embodiments A1 to A3, wherein the polynucleotides encoding the phosphogluconate dehydratase enzyme and the 3-deoxygluconate-6-phosphate aldolase enzyme independently are from an Escherichia spp. microbe or Psuedomonas spp. microbe.
A4. The composition of embodiment A3, wherein the Escherichia spp. microbe is an Escherichia coli strain.
A5. The composition of embodiment A3 or A4, wherein the Pseudomonas spp. microbe is a Pseudomonas aeruginosa strain.
A6. The composition of any one of embodiments A1 to A5, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme is an EDD gene.
A7. The composition of any one of embodiments A1 to A5, wherein the polynucleotide that encodes the 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme is an EDA gene.
A8. The composition of any one of embodiments A1 to A7, wherein the nucleic acid includes a polynucleotide that encodes a 6-phosphogluconolactonase enzyme.
A8.1. The composition of embodiment A8, wherein the 6-phosphogluconolactonase enzyme is expressed from a SOL gene.
A9. The composition of embodiment A8, wherein the SOL gene is a SOL3 gene.
A10. The composition of any one of embodiments A1 to A9, wherein the nucleic acid includes a polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme.
A11. The composition of embodiment A10, wherein the polynucleotide that encodes the glucose-6-phosphate dehydrogenase enzyme is from a yeast.
A12. The composition of embodiment A11, wherein the yeast is a Saccharomyces spp. yeast.
A13. The composition of embodiment A12, wherein the yeast is a Saccharomyces cerevisiae strain.
A14. The composition of any one of embodiments A10 to A13, wherein the nucleic acid includes a polynucleotide that encode an endogenous glucose-6-phosphate dehydrogenase enzyme.
A15. The composition of any one of embodiments A10 to A14, wherein the glucose-6-phosphate dehydrogenase enzyme is expressed from a ZWF gene.
A16. The composition of embodiment A15, wherein the ZWF gene is a ZWF1 gene.
A17. The composition of any one of embodiments A1 to A16, wherein the nucleic acid includes one or more promoters operable in a yeast, wherein the promoter is in operable connection with one or more of the polynucleotides.
A18. The composition of embodiment A17, wherein the promoter is selected from promoters that regulate glucose phosphate dehydrogenase (GPD), translation elongation factor (TEF-1), phosphoglucokinase (PGK-1) and triose phosphate dehydrogenase (TDH-1).
A19. The composition of any one of embodiments A1 to A18, wherein the nucleic acid includes one or more polynucleotides that homologously combine in a gene of a host that encodes a phosphofructokinase (PFK) enzyme, phosphoglucoisomerase (PGI) enzyme, 6-phosphogluconate dehydrogenase (decarboxylating) enzyme, transketolase enzyme, transaldolase enzyme, or combination thereof.
A20. The composition of embodiment A19, wherein the transketolase enzyme is encoded by a TKL-1 coding sequence or a TKL-2 coding sequence.
A21. The composition of embodiment A19, wherein the transaldolase is encoded by a TAL-1 coding sequence.
A22. The composition of embodiment A19, wherein the phosphofructokinase (PFK) enzyme is a PFK-2 enzyme or PFK-1 enzyme.
A23. The composition of embodiment A19, wherein the 6-phosphogluconate dehydrogenase (decarboxylating) enzyme is encoded by a GND-1 gene or a GND-2 gene.
A24. The composition of embodiment A19, wherein the PGI is encoded by a PGI-1 gene.
A25. The composition of any one of embodiments A1 to A24, wherein the nucleic acid is one or two separate nucleic acid molecules.
A26. The composition of embodiment A25, wherein each nucleic acid molecule includes one or two or more of the polynucleotide subsequences, one or two or more of the promoters, or one or two or more of the polynucleotide subsequences and one or two or more of the promoters.
A27. The composition of embodiment A25 or A26, wherein each of the one or two nucleic acid molecules are in circular form.
A28. The composition of embodiment A25 or A26, wherein each of the one or two nucleic acid molecules are in linear form.
A29. The composition of any one of embodiments A25 to A28, wherein each of the one or two nucleic acid molecules functions as an expression vector.
A30. The composition of any one of embodiments A25 to A29, wherein each of the one or two nucleic acid molecules includes flanking sequences for integrating the polynucleotides, the promoter sequences, or the polynucleotides and the promoter sequences in the nucleic acid into genomic DNA of a host organism.
B1. A composition comprising an engineered yeast that includes an alteration that adds or increases a phosphogluconate dehydratase activity and a 2-keto-3-deoxygluconate-6-phosphate aldolase activity, and a nucleotide sequence identification tag having a nucleotide sequence selected from the group of six (6) nucleotide sequences consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

B2. The composition of embodiment B1, wherein the yeast is a Saccharomyces spp. yeast.
B3. The composition of embodiment B2, wherein the yeast is a Saccharomyces cerevisiae yeast strain.
B4. The composition of any one of embodiments B1 to B3 that includes heterologous polynucleotides that encode independently a phosphogluconate dehydratase enzyme and a 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme.
B5. The composition of embodiment B4, wherein the polynucleotides encoding the phosphogluconate dehydratase enzyme and the 3-deoxygluconate-6-phosphate aldolase enzyme independently are from an Escherichia spp. microbe or Psuedomonas spp. microbe.
B6. The composition of embodiment B5, wherein the Escherichia spp. microbe is an Escherichia coli strain.
B7. The composition of embodiment B5, wherein the Pseudomonas spp. microbe is a Bseudomonas aeruginosa strain.
B8. The composition of any one of embodiments B4 to B7, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme is an EDD gene.
B9. The composition of any one of embodiments B4 to B7, wherein the polynucleotide that encodes the 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme is an EDA gene.
B10. The composition of any one of embodiments B1 to B9, wherein the yeast includes an alteration that adds or increases a 6-phosphogluconolactonase activity.
B10.1. The composition of embodiment B10, wherein the yeast includes a heterologous polynucleotide, or multiple copies of an endogenous polynucleotide, that encodes a 6-phosphogluconolactonase enzyme.
B10.2. The composition of embodiment B10.1, wherein the 6-phosphogluconolactonase enzyme is expressed from a SOL gene.
B11. The composition of embodiment B10.2, wherein the SOL gene is a SOL3 gene.
B12. The composition of any one of embodiments B1 to B11, wherein a glucose-6-phosphate dehydrogenase activity is added or increased.
B13. The composition of embodiment B12, wherein the yeast comprises a heterologous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme, or wherein the yeast comprises multiple copies of an endogenous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme.
B14. The composition of embodiment B13, wherein the polynucleotide that encodes the glucose-6-phosphate dehydrogenase enzyme is from a yeast.
B15. The composition of embodiment B14, wherein the yeast is a Saccharomyces spp. yeast.
B16. The composition of embodiment B15, wherein the yeast is a Saccharomyces cerevisiae strain.
B17. The composition of any one of embodiments B13 to B17, wherein the glucose-6-phosphate dehydrogenase enzyme is expressed from a ZWF gene.
B18. The composition of embodiment B17, wherein the ZWF gene is a ZWF1 gene.
B19. The composition of any one of embodiments B1 to B18, wherein the nucleic acid includes one or more promoters operable in a yeast, wherein the promoter is in operable connection with one or more of the polynucleotides.
B20. The composition of embodiment B19, wherein the promoter is selected from promoters that regulate glucose phosphate dehydrogenase (GBD), translation elongation factor (TEF-1), phosphoglucokinase (BGK-1) and triose phosphate dehydrogenase (TDH-1).
B21. The composition of any one of embodiments B1 to B20, wherein the yeast includes a reduction in one or more of the following activities: phosphofructokinase (PFK) activity, phosphoglucoisomerase (PGI) activity, 6-phosphogluconate dehydrogenase (decarboxylating) activity, transketolase activity, transaldolase activity, or combination thereof.
B22. The composition of embodiment B21, wherein the yeast includes an alteration in one or more polynucleotides that inhibits production of one or more enzymes selected from the group consisting of phosphofructokinase (PFK) enzyme, phosphoglucoisomerase (PGI) enzyme, 6-phosphogluconate dehydrogenase (decarboxylating) enzyme, transketolase enzyme, transaldolase enzyme, or combination thereof.
B23. The composition of embodiment B22, wherein the transketolase enzyme is encoded by a TKL-1 coding sequence or a TKL-2 coding sequence.
B24. The composition of embodiment B22, wherein the transaldolase is encoded by a TAL-1 coding sequence.
B25. The composition of embodiment B22, wherein the phosphofructokinase (PFK) enzyme is a PFK-2 enzyme or PFK-1 enzyme.
B26. The composition of embodiment B22, wherein the 6-phosphogluconate dehydrogenase (decarboxylating) enzyme is encoded by a GND-1 gene or GND-2 gene.
B27. The composition of embodiment B22, wherein the PGI is encoded by a PGI-1 gene.
B28. The composition of any one of embodiments B1 to B27, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are not integrated in the yeast nucleic acid.
B29. The composition of embodiment B28, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are in one or more plasmids.
B30. The composition of any one of embodiments B1 to B29, wherein the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters are integrated in genomic DNA of the yeast.
B31. The composition of embodiment B30, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are integrated in a transposition integration event, in a homologous recombination integration event, or in a transposition integration event and a homologous recombination integration event.
B32. The composition of embodiment B31, wherein the transposition integration event includes transposition of an operon comprising two or more of the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters.
B33. The composition of embodiment B31, wherein the homologous recombination integration event includes homologous recombination of an operon comprising two or more of the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters.
C1. A method, comprising contacting an engineered yeast of any one of embodiments B1 to B33 with a feedstock that contains one or more hexose sugars under conditions in which the microbe synthesizes ethanol.
C2. The method of embodiment C1, wherein the engineered yeast synthesizes ethanol to about 85% to about 99% of theoretical yield.
C3. The method of embodiment C1 or C2, comprising recovering ethanol synthesized by the engineered yeast.
C4. The method of any one of embodiments C1 to C3, wherein the conditions are fermentation conditions.
D1. A composition comprising a synthetic nucleic acid that includes a polynucleotide sequence selected from the group consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

D2. A microorganism comprising a polynucleotide that includes a sequence selected from the group consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

D3. A method comprising detecting the presence or absence of a nucleotide sequence identification tag in a microorganism, wherein the nucleotide sequence is selected from the group consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

D4. The method of embodiment D3, wherein the microorganism includes two or more different identification tags.
D5. The method of embodiment D3, wherein the microorganism includes multiple copies of one or more of the identification tags.
E1. A composition comprising a nucleic acid comprising (i) heterologous polynucleotides that encode a phosphogluconate dehydratase enzyme and a 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme, (ii) one or more polynucleotides that homologously combine in a gene of a host that encodes a 6-phosphogluconate dehydrogenase (decarboxylating) enzyme, and (iii) a nucleotide sequence identification tag selected from the group consisting

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

E2. The composition of embodiment E1, wherein the yeast is a Saccharomyces spp. yeast.
E3. The composition of embodiment E2, wherein the yeast is a Saccharomyces cerevisiae yeast strain.
E3.1. The composition of any one of embodiments E1 to E3, wherein the polynucleotides encoding the phosphogluconate dehydratase enzyme and the 3-deoxygluconate-6-phosphate aldolase enzyme independently are from an Escherichia spp. microbe or Psuedomonas spp. microbe.
E4. The composition of embodiment E3, wherein the Escherichia spp. microbe is an Escherichia coli strain.
E5. The composition of embodiment E3 or E4, wherein the Pseudomonas spp. microbe is a Pseudomonas aeruginosa strain.
E6. The composition of any one of embodiments E1 to E5, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme is an EDD gene.
E7. The composition of any one of embodiments E1 to E5, wherein the polynucleotide that encodes the 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme is an EDA gene.
E8. The composition of any one of embodiments E1 to E7, wherein the nucleic acid includes a polynucleotide that encodes a 6-phosphogluconolactonase enzyme.
E8.1. The composition of embodiment E8, wherein the polynucleotide that encodes the 6-phosphogluconolactonase enzyme is from a yeast.
E8.2. The composition of embodiment E8.1, wherein the yeast is a Saccharomyces spp. yeast.
E8.3. The composition of embodiment E8.2, wherein the yeast is a Saccharomyces cerevisiae strain.
E8.4. The composition of any one of embodiments E8 to E8.3, wherein the 6-phosphogluconolactonase enzyme is expressed from a SOL gene.
E9. The composition of embodiment E8.4, wherein the SOL gene is a SOL3 gene.
E10. The composition of any one of embodiments E1 to E9, wherein the nucleic acid includes a polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme.
E11. The composition of embodiment E10, wherein the polynucleotide that encodes the glucose-6-phosphate dehydrogenase enzyme is from a yeast.
E12. The composition of embodiment E11, wherein the yeast is a Saccharomyces spp. yeast.
E13. The composition of embodiment E12, wherein the yeast is a Saccharomyces cerevisiae strain.
E14. The composition of any one of embodiments E10 to E13, wherein the nucleic acid includes a polynucleotide that encode an endogenous glucose-6-phosphate dehydrogenase enzyme.
E15. The composition of any one of embodiments E10 to E14, wherein the glucose-6-phosphate dehydrogenase enzyme is expressed from a ZWF gene.
E16. The composition of embodiment E15, wherein the ZWF gene is a ZWF1 gene.
E17. The composition of any one of embodiments E1 to E16, wherein the nucleic acid includes one or more promoters operable in a yeast, wherein the promoter is in operable connection with one or more of the polynucleotides.
E18. The composition of embodiment E17, wherein the promoter is selected from promoters that regulate glucose phosphate dehydrogenase (GPD), translation elongation factor (TEF-1), phosphoglucokinase (PGK-1) and triose phosphate dehydrogenase (TDH-1).
E19. The composition of any one of embodiments E1 to E18, wherein the nucleic acid includes one or more polynucleotides that homologously combine in a gene of a host that encodes a phosphofructokinase (PFK) enzyme, phosphoglucoisomerase (PGI) enzyme, transketolase enzyme, transaldolase enzyme, or combination thereof.
E20. The composition of embodiment E19, wherein the transketolase enzyme is encoded by a TKL-1 coding sequence or a TKL-2 coding sequence.
E21. The composition of embodiment E19, wherein the transaldolase is encoded by a TAL-1 coding sequence.
E22. The composition of embodiment E19, wherein the phosphofructokinase (PFK) enzyme is a PFK-2 enzyme or PFK-1 enzyme.
E23. The composition of any one of embodiments E1 to E22, wherein the 6-phosphogluconate dehydrogenase (decarboxylating) enzyme is encoded by a GND-1 gene or a GND-2 gene.
E24. The composition of embodiment E19, wherein the PGI is encoded by a PGI-1 gene.
E25. The composition of any one of embodiments E1 to E24, wherein the nucleic acid is one or two separate nucleic acid molecules.
E26. The composition of embodiment E25, wherein each nucleic acid molecule includes one or two or more of the polynucleotide subsequences, one or two or more of the promoters, or one or two or more of the polynucleotide subsequences and one or two or more of the promoters.
E27. The composition of embodiment E25 or E26, wherein each of the one or two nucleic acid molecules are in circular form.
E28. The composition of embodiment E25 or E26, wherein each of the one or two nucleic acid molecules are in linear form.
E29. The composition of any one of embodiments E25 to E28, wherein each of the one or two nucleic acid molecules functions as an expression vector.
E30. The composition of any one of embodiments E25 to E29, wherein each of the one or two nucleic acid molecules includes flanking sequences for integrating the polynucleotides, the promoter sequences, or the polynucleotides and the promoter sequences in the nucleic acid into genomic DNA of a host organism.
F1. A composition comprising an engineered yeast that includes (i) an alteration that adds or increases a phosphogluconate dehydratase activity and a 2-keto-3-deoxygluconate-6-phosphate aldolase activity, (ii) an alteration that reduces a 6-phosphogluconate dehydrogenase (decarboxylating) activity, and (iii) a nucleotide sequence identification tag selected from the group consisting of

(SEQ ID NO: 448)

GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC

CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG

GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG

CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT

GGTCA

(SEQ ID NO: 449)

AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG

CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT

ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT

CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG

GCGCA

(SEQ ID NO: 450)

CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC

AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC

CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA

CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG

TGCGA

(SEQ ID NO: 451)

GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG

CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC

GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG

GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG

TGCGA

(SEQ ID NO: 452)

AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG

GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC

CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA

GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG

TTGGA

(SEQ ID NO: 453)

ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG

GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG

TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC

GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC

GACCA

F2. The composition of embodiment F1, wherein the yeast is a Saccharomyces spp. yeast.
F3. The composition of embodiment F2, wherein the yeast is a Saccharomyces cerevisiae yeast strain.
F4. The composition of any one of embodiments F1 to F3, wherein the yeast includes an altered gene that encodes a 6-phosphogluconate dehydrogenase (decarboxylating) enzyme.
F4.1. The composition of any one of embodiments F1 to F4 where the yeast includes heterologous polynucleotides, or multiple copies of endogenous polynucleotides, that encode a phosphogluconate dehydratase enzyme and a 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme.
F5. The composition of embodiment F4, wherein the polynucleotides encoding the phosphogluconate dehydratase enzyme and the 3-deoxygluconate-6-phosphate aldolase enzyme independently are from an Escherichia spp. microbe or Psuedomonas spp. microbe.
F6. The composition of embodiment F5, wherein the Escherichia spp. microbe is an Escherichia coli strain.
F7. The composition of embodiment F5, wherein the Pseudomonas spp. microbe is a Pseudomonas aeruginosa strain.
F8. The composition of any one of embodiments F4 to F7, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme is an EDD gene.
F9. The composition of any one of embodiments F4 to F7, wherein the polynucleotide that encodes the 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme is an EDA gene.
F10. The composition of any one of embodiments F1 to F11, wherein a glucose-6-phosphate dehydrogenase activity is added or increased.
F10.1. The composition of embodiment F10, wherein the yeast comprises a heterologous polynucleotide that encodes a 6-phosphogluconolactonase enzyme, or wherein the yeast comprises multiple copies of an endogenous polynucleotide that encodes a 6-phosphogluconolactonase enzyme.
F10.2. The composition of embodiment F10.1, wherein the polynucleotide that encodes the 6-phosphogluconolactonase enzyme is from a yeast.
F10.3. The composition of embodiment F10.2, wherein the yeast is a Saccharomyces spp. yeast.
F10.4. The composition of embodiment F10.3, wherein the yeast is a Saccharomyces cerevisiae strain.
F10.5. The composition of any one of embodiments F10 to F10.4, wherein the 6-phosphogluconolactonase enzyme is expressed from a SOL gene.
F11. The composition of embodiment F10.4, wherein the SOL gene is a SOL3 gene.
F12. The composition of any one of embodiments F4 to F11, wherein a glucose-6-phosphate dehydrogenase activity is added or increased.
F13. The composition of embodiment F12, wherein the yeast comprises a heterologous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme, or wherein the yeast comprises multiple copies of an endogenous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme.
F14. The composition of embodiment F13, wherein the polynucleotide that encodes the glucose-6-phosphate dehydrogenase enzyme is from a yeast.
F15. The composition of embodiment F14, wherein the yeast is a Faccharomyces spp. yeast.
F16. The composition of embodiment F15, wherein the yeast is a Faccharomyces cerevisiae strain.
F17. The composition of any one of embodiments F13 to F17, wherein the glucose-6-phosphate dehydrogenase enzyme is expressed from a ZWF gene.
F18. The composition of embodiment F17, wherein the ZWF gene is a ZWF1 gene.
F19. The composition of any one of embodiments F1 to F18, wherein the nucleic acid includes one or more promoters operable in a yeast, wherein the promoter is in operable connection with one or more of the polynucleotides.
F20. The composition of embodiment F19, wherein the promoter is selected from promoters that regulate glucose phosphate dehydrogenase (GFD), translation elongation factor (TEF-1), phosphoglucokinase (FGK-1) and triose phosphate dehydrogenase (TDH-1).
F21. The composition of any one of embodiments F1 to F20, wherein the yeast includes a reduction in one or more of the following activities: phosphofructokinase (PFK) activity, phosphoglucoisomerase (PGI) activity, transketolase activity, transaldolase activity, or combination thereof.
F22. The composition of embodiment F21, wherein the yeast includes an alteration in one or more polynucleotides that inhibits production of one or more enzymes selected from the group consisting of phosphofructokinase (PFK) enzyme, phosphoglucoisomerase (PGI) enzyme, 6-phosphogluconate dehydrogenase (decarboxylating) enzyme, transketolase enzyme, transaldolase enzyme, or combination thereof.
F23. The composition of embodiment F22, wherein the transketolase enzyme is encoded by a TKL-1 coding sequence or a TKL-2 coding sequence.
F24. The composition of embodiment F22, wherein the transaldolase is encoded by a TAL-1 coding sequence.
F25. The composition of embodiment F22, wherein the phosphofructokinase (PFK) enzyme is a PFK-2 enzyme or PFK-1 enzyme.
F26. The composition of any one of embodiments F4 to F25, wherein the 6-phosphogluconate dehydrogenase (decarboxylating) enzyme is encoded by a GND-1 gene or GND-2 gene.
F27. The composition of embodiment F22, wherein the PGI is encoded by a PGI-1 gene.
F28. The composition of any one of embodiments F1 to F27, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are not integrated in the yeast nucleic acid.
F29. The composition of embodiment F28, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are in one or more plasmids.
F30. The composition of any one of embodiments F1 to F29, wherein the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters are integrated in genomic DNA of the yeast.
F31. The composition of embodiment F30, wherein the polynucleotides, the promoters, or the polynucleotides and the promoters are integrated in a transposition integration event, in a homologous recombination integration event, or in a transposition integration event and a homologous recombination integration event.
F32. The composition of embodiment F31, wherein the transposition integration event includes transposition of an operon comprising two or more of the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters.
F33. The composition of embodiment F31, wherein the homologous recombination integration event includes homologous recombination of an operon comprising two or more of the polynucleotide subsequences, the promoters, or the polynucleotide subsequences and the promoters.
G1. A method, comprising contacting an engineered yeast of any one of embodiments F1 to F33 with a feedstock that contains one or more hexose sugars under conditions in which the microbe synthesizes ethanol.
G2. The method of embodiment G1, wherein the engineered yeast synthesizes ethanol to about 85% to about 99% of theoretical yield.
G3. The method of embodiment G1 or G2, comprising recovering ethanol synthesized by the engineered yeast.
G4. The method of any one of embodiments G1 to G3, wherein the conditions are fermentation conditions.
The entirety of each patent, patent application, publication and document referenced herein hereby is incorporated by reference. Citation of the above patents, patent applications, publications and documents is not an admission that any of the foregoing is pertinent prior art, nor does it constitute any admission as to the contents or date of these publications or documents.
Modifications may be made to the foregoing without departing from the basic aspects of the technology. Although the technology has been described in substantial detail with reference to one or more specific embodiments, those of ordinary skill in the art will recognize that changes may be made to the embodiments specifically disclosed in this application, yet these modifications and improvements are within the scope and spirit of the technology.
The technology illustratively described herein suitably may be practiced in the absence of any element(s) not specifically disclosed herein. Thus, for example, in each instance herein any of the terms “comprising,” “consisting essentially of,” and “consisting of” may be replaced with either of the other two terms. The terms and expressions which have been employed are used as terms of description and not of limitation, and use of such terms and expressions do not exclude any equivalents of the features shown and described or portions thereof, and various modifications are possible within the scope of the claimed technology. The term “a” or “an” can refer to one of or a plurality of the elements it modifies (e.g., “a reagent” can mean one or more reagents) unless it is contextually clear either one of the elements or more than one of the elements is described. The term “about” as used herein refers to a value within 10% of the underlying parameter (i.e., plus or minus 10%), and use of the term “about” at the beginning of a string of values modifies each of the values (i.e., “about 1, 2 and 3” refers to about 1, about 2 and about 3). For example, a weight of “about 100 grams” can include weights between 90 grams and 110 grams. Further, when a listing of values is described herein (e.g., about 50%, 60%, 70%, 80%, 85% or 86%) the listing includes all intermediate and fractional values thereof (e.g., 54%, 85.4%). Thus, it should be understood that although the present technology has been specifically disclosed by representative embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and such modifications and variations are considered within the scope of this technology.
Certain embodiments of the technology are set forth in the claim(s) that follow(s).

Claims

1-35. (canceled)

36. A method for producing ethanol, comprising contacting an engineered yeast with a feedstock that contains one or more hexose sugars under conditions in which the yeast synthesizes ethanol, which yeast comprises:

(i) alterations that add or increase a phosphogluconate dehydratase activity, a 2-keto-3-deoxygluconate-6-phosphate aldolase activity, and a 6-phosphogluconolactonase activity;

(ii) alterations that reduce or substantially remove a phosphofructokinase 1 (PFK1) activity, phosphofructokinase 2 (PFK2) activity, or PFK1 and PFK2 activity; and

(iii) a nucleotide sequence identification tag having a nucleotide sequence chosen from the following six (6) nucleotide sequences:

(SEQ ID NO: 448) GCGTCCATACCGGACCGTCCATCCGTCCCGGCGGGCTATCGTTAGTCCC CGCGAGCGGATTCCGAGGTGTCGATGACGCGCTCGGTCCCCGCATCTCG GGGTGGCCCGCACCTAGCTTAAGCGGACTACGAAGCGCGGGGCGAGCGG CGACGATCGCGTACTCACACTCGGACCTCGCGGGTCGGCTCGGAGCCCT GGTCA (SEQ ID NO: 449) AGCGGTCAGTGCACGGGACGCGATCGGGCACCCTCGACGCAGCGATGGG CCGTGCGTCGTGTAGTCCGATAGTGCCGGCGTCGCTCGGTAAGCCCCTT ATACCTGCGCGCTGGCGAGAGATGGGTTCGCGAGTCTAGCGCGATCGCT CTAGAGGGTCCAGGAGTACCTACACGGCGCGAGGCGCGGACATCCTAGG GCGCA (SEQ ID NO: 450) CCCCTGCGTTTGCCGAGCGACGAGTCCTACACCCTGTCCGCGCCCGAGC AGGGTCGTCCCCGCGAACCGACGGATGCGCGGCCCGAATCGCCTAGACC CCTACGGGGCGGCTCGCTCGGCCCCGCCTGACCGGTCGATCCCACGAGA CCCCGCCCTATAGGGAGAGCACCGACCCGCCTCCTCGGGCCTTACGGCG TGCGA (SEQ ID NO: 451) GCCAGTGTAGAGATCCGGGGATCCCCAGCGCCTGGAGCTAGGCCCACGG CGTCTGACCGGGTGTACCGGGCCCCCTAGGACGGGTGCGCCCGTAGTCC GTCTGCGAGGGGGCCGTCCGGTCGGGGGCATCCGGCGCTCCGCGGGGAG GCGCTACGTGCCCGACCGGGGGAGTCGAGTCTCTATGCTCGCGACCGCG TGCGA (SEQ ID NO: 452) AAGCGCGCACTACGTCAGGCATAGCGTACTGGGCTTGCGGAGCCACGCG GGCGCGGAGCGGGCCGGTTGAGTGCGGGATAGACGGACCGTACGCATGC CTCAAGTCGACGGTACGGGGGGCAGGGTAGCTGGGATCCGAGGCGGGTA GGCGTCGGCCGCGACTGTGCCCGTACGACGGGAGAACCCCCCGCGCGAG TTGGA (SEQ ID NO: 453) ACGTCGGCAGGCCCGCTCGGTTCCGAGCACCGGATCGACGCTACACGAG GCCCGACACTAGGCGCGTACTCCGGGGGGGTCCGCCTCCGTCCCGTGAG TATCGCGGGCGGGAACAGGGCGGGCTGCCGGGGCCGACCGGTGTGGGGC GTGACTCCGACCGACTCGGGCGAGGGCCGCCTAGTCGCGAAGGACGCGC GACCA

37. The method of claim 36, wherein the yeast is a Saccharomyces spp. yeast.

38. The method of claim 37, wherein the yeast is a Saccharomyces cerevisiae yeast.

39. The method of claim 36, wherein the engineered yeast synthesizes ethanol to about 85% to about 99% of theoretical yield.

40. The method of claim 36, comprising recovering ethanol synthesized by the engineered yeast.

41. The method of claim 36, wherein the conditions are fermentation conditions.

42. The method of claim 36, wherein the yeast comprises heterologous polynucleotides that encode independently a phosphogluconate dehydratase enzyme and a 2-keto-3-deoxygluconate-6-phosphate aldolase enzyme.

43. The method of claim 42, wherein the polynucleotides encoding the phosphogluconate dehydratase enzyme and the 3-deoxygluconate-6-phosphate aldolase enzyme independently are from an Escherichia spp. microbe or Psuedomonas spp. microbe.

44. The method of claim 43, wherein the Escherichia spp. microbe is an Escherichia coli strain.

45. The method of claim 43, wherein the Pseudomonas spp. microbe is a Pseudomonas aeruginosa strain.

46. The method of claim 43, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme is from a Pseudomonas aeruginosa strain.

47. The method of claim 46, wherein the polynucleotide that encodes the phosphogluconate dehydratase enzyme encodes an amino acid sequence comprising the polypeptide sequence of SEQ ID NO: 70.

48. The method of claim 36, wherein the yeast comprises a heterologous polynucleotide, or multiple copies of an endogenous polynucleotide, that encodes a 6-phosphogluconolactonase enzyme.

49. The method of claim 48, wherein the polynucleotide that encodes the 6-phosphogluconolactonase enzyme encodes an amino acid sequence comprising the polypeptide sequence of SEQ ID NO: 120.

50. The method of claim 36, wherein the yeast comprises a genetic alteration that increases or adds a glucose-6-phosphate dehydrogenase activity.

51. The method of claim 50, wherein the yeast comprises a heterologous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme, or wherein the yeast comprises multiple copies of an endogenous polynucleotide that encodes a glucose-6-phosphate dehydrogenase enzyme.

52. The method of claim 51, wherein the polynucleotide that encodes the glucose-6-phosphate dehydrogenase enzyme encodes an amino acid sequence comprising the polypeptide sequence of any one of SEQ ID NOS: 119, 123, 127 and 129.

53. The method of claim 36, wherein the yeast comprises an alteration in one or more polynucleotides that inhibits production of one or more enzymes chosen from a phosphoglucoisomerase (PGI) enzyme, 6-phosphogluconate dehydrogenase (decarboxylating) enzyme, transketolase enzyme, transaldolase enzyme, or combination thereof.

54. The method of claim 53, wherein the transketolase enzyme is encoded by a TKL-1 coding sequence comprising SEQ ID NO: 428.

55. The method of claim 53, wherein the transaldolase is encoded by a TAL-1 coding sequence comprising SEQ ID NO: 426.