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Microbiotechnology in Cosmetics, Pharmaceuticals and Food

A special issue of Processes (ISSN 2227-9717). This special issue belongs to the section "Biological Processes and Systems".

Deadline for manuscript submissions: closed (28 February 2025) | Viewed by 21120

Special Issue Editor


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Guest Editor
Organic, Biochemical and Food Department, Gheorghe Asachi Technical University of Iasi, 700050 Iasi, Romania
Interests: microbiotechnology; separations; biosorption; microencapsulation
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Microorganisms are the most important group of organisms on our planet, conquering almost every conceivable space on Earth. Microbiological processes play significant roles in the current and future food, cosmetic and pharmaceutical global industries. This Special Issue focuses on research studies devoted to the discovery, study, mechanistic understanding and exploitation of microorganisms in food, cosmetic and pharmaceutical domains.

The most important contribution of microbiology to the pharmaceutical industry is the development of antibiotics and vaccines, drugs and bio products (through microorganism genetic manipulations), but it is also important in quality control in pharmaceutical laboratories.

Of particular biotechnological interest are secondary metabolites that can function as ion-scavenging or quorum-sensing metabolites or act as antimicrobials, with applications in pharmaceuticals and cosmetics. The most innovative developments and advancements in the biotechnological production of antibiotics, drugs and vitamins with emphasis on the technical aspects of biotechnological processes are of increasing interest in the food and pharmaceutical industries.

The microbial contamination of food and cosmetic products is a matter of great importance to the industry, and it can become a major cause of both product and economic losses. The design of preservative systems that provide good protection to cosmetic and food products against microbial contamination is extremely important, as contamination can result in the conversion of these goods into products that are hazardous to consumers. Research into new molecules with biocide action but also good compatibility (from a toxicological point of view), the synergism and antagonism analysis of preservative blends and the search for fast, reliable methods to detect microbial contamination is of great interest in the cosmetic industry.

This Special Issue welcomes fundamental research and applied investigations in all of these areas of focus.

Dr. Alexandra Cristina Blaga
Guest Editor

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Processes is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2400 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • metabolic engineering
  • novel biochemical pathways
  • microbial interactions
  • secondary metabolite
  • antibiotics
  • antimicrobials
  • probiotics
  • microbial contamination

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Published Papers (7 papers)

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Research

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15 pages, 1881 KiB  
Article
Kombucha Fermentation in Coffee: Application of Constant Air Flow Reactor
by Błażej Błaszak, Piotr Dorawa, Paweł Sudoł, Karolina Fabiszak, Martyna Świadek, Klaudia Witucka, Julia Zimnicka, Mateusz Brudnicki, Bartosz Maciejewski, Daniil Bovkun, Marek Cierach, Grażyna Gozdecka and Joanna Szulc
Processes 2024, 12(10), 2159; https://doi.org/10.3390/pr12102159 - 3 Oct 2024
Cited by 1 | Viewed by 1592
Abstract
SCOBY (symbiotic culture of bacteria and yeasts) is an artificially created mixed culture containing selected strains of acetic acid and lactic acid bacteria and yeast which are present in the cellulose membrane. The growing popularity of kombucha consumption and high popularity of coffee [...] Read more.
SCOBY (symbiotic culture of bacteria and yeasts) is an artificially created mixed culture containing selected strains of acetic acid and lactic acid bacteria and yeast which are present in the cellulose membrane. The growing popularity of kombucha consumption and high popularity of coffee creates the possibility of developing coffee-based kombucha production on an industrial scale, which currently does not differ in method from production on a laboratory scale and at home. Therefore, the aim of this work was to determine the possibility of using an alternative method of coffee fermentation using SCOBY, in which the fermentation was carried out in a bioreactor with a constant air flow (rate 2L/min). This study determined the effect of the fermentation method on the processing time, SCOBY mass gain, and selected properties of the fermented coffee beverage. The alternative fermentation method did not negatively affect the properties of the fermented coffee beverage, i.e., caffeine content, colour, polyphenol content, and antioxidant properties, in comparison with the traditional fermentation method. Additionally, it accelerated the fermentation process, shortening it from 8 to 4 days, and in some cases caused an increase in the total polyphenol content and antioxidant activity, almost 10% and over 40%, respectively. The results of this study show a possibility to use alternative methods for coffee fermentation, which can be easily adapted for industrial scale. Variants of fermented and aerated beverages with 4% coffee, and 4 and 5% sugar concentrations stood out among the others as having the best properties and might be introduced to the industry. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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Figure 1
<p>The bioreactor scheme used for coffee fermentation (1—SCOBY, 2—glass bioreactor, 3—air bubbles, 4—air inlet, 5—valve, 6—air pump with an air flow rate 2L/min).</p>
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<p>Change in pH during 4% coffee fermentation (a, b, c…—samples with the same letter in do not differ significantly in the same beverage during fermentation; A, B, C…—samples with the same letter in do not differ significantly between different beverage variants); abbreviations in <a href="#processes-12-02159-t001" class="html-table">Table 1</a>.</p>
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<p>Change in pH during 6% coffee fermentation (a, b, c…—samples with the same letter in do not differ significantly in the same beverage during fermentation; A, B, C…—samples with the same letter in do not differ significantly between different beverage variants); abbreviations in <a href="#processes-12-02159-t001" class="html-table">Table 1</a>.</p>
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<p>Change in TSS during 4% coffee fermentation (a, b, c…—samples with the same letter in do not differ significantly in the same beverage during fermentation; A, B, C…—samples with the same letter in do not differ significantly between different beverage variants); abbreviations in <a href="#processes-12-02159-t001" class="html-table">Table 1</a>.</p>
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<p>Change in TTS during 6% coffee fermentation (a, b, c…—samples with the same letter in do not differ significantly in the same beverage during fermentation; A, B, C…—samples with the same letter in do not differ significantly between different beverage variants); abbreviations in <a href="#processes-12-02159-t001" class="html-table">Table 1</a>.</p>
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12 pages, 5866 KiB  
Article
Effects of Pectinase on Bacterial Succession during Hemp Retting
by Yu Fu, Yan Zhang, Michael S. Allen and Sheldon Q. Shi
Processes 2024, 12(8), 1725; https://doi.org/10.3390/pr12081725 - 16 Aug 2024
Viewed by 1049
Abstract
Pectinase accelerates hemp retting. An elevated temperature during the enzymatic action is favorable for bacterial colonization. Industrial hemp (Cannabis sativa L.) bast fiber was retted in a 40 °C water bath under four different conditions: water retting, pectinase retting, bacterial retting, and [...] Read more.
Pectinase accelerates hemp retting. An elevated temperature during the enzymatic action is favorable for bacterial colonization. Industrial hemp (Cannabis sativa L.) bast fiber was retted in a 40 °C water bath under four different conditions: water retting, pectinase retting, bacterial retting, and bacterial retting with the presence of pectinase. Bacterial communities were sampled from the retting liquid of each condition at the beginning of retting and on days 1, 3, and 5. The bacterial successions were identified by 16S rRNA gene metagenomic sequencing. The results showed that Bacillaceae dominated the hemp retting conditions containing 1% (m/v) pectinase, suggesting that pectinase can manipulate the bacterial community succession by changing the nutrients available to bacteria through the breakdown of pectin. Micromorphological analysis also observed the degradation of a gum-like substance and the aggregation of bacteria with the addition of pectinase. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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<p>Schematic diagram of the bacterial retting strategy of hemp bast.</p>
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<p>Experimental plan.</p>
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<p>pH changes during four retting processes. The retting conditions with the involvement of pectinase rapidly turn acidic.</p>
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<p>SEM micrographs of hemp fiber sampled from day 1 (<b>a</b>,<b>c</b>,<b>e</b>,<b>g</b>) and day 5 (<b>b</b>,<b>d</b>,<b>f</b>,<b>h</b>) of four retting schedules (R1–R4), where a and b are from R1, c and d are from R2, e and f are from R3, and g and h are from R4. Fibers were wrapped by gummy substance (<b>a</b>), and retting schedule R1 did not remove the gummy substance (<b>b</b>). The gummy substance was removed partially (<b>c</b>,<b>e</b>) at the beginning of schedules R2 and R3. Bacteria colonized and adhered to the fiber surfaces after 5 days of retting for both R2 and R3 (<b>d</b>,<b>f</b>). Bacteria were not enriched on fiber for retting schedule R4 (<b>g</b>,<b>h</b>).</p>
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<p>Principal coordinate analysis (PCoA) based on unweighted and weighted UniFrac distances. Unweighted PCoA (<b>a</b>) showed the clustering of bacterial communities at the beginning of retting. The microbial communities showed clustering in the presence and absence of pectinase. Weighted PCoA (<b>b</b>) indicated that the bacterial communities in the presence of pectinase were similar after 3 days of hemp retting. Each point represents a sample.</p>
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<p>Relative abundances of the phylum-level (<b>a</b>) and family-level (<b>b</b>) bacterial community compositions during retting. Only bacterial phyla with relative abundances &gt;1% and bacterial families with relative abundances &gt;5% are shown.</p>
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<p>Reducing sugar analysis with DNS method indicated that a small amount of pectinase (1% <span class="html-italic">w</span>/<span class="html-italic">v</span>) could degrade the pectin at the beginning of retting. The reducing sugar concentration within 24 h was slightly higher than that from the water retting. As the Bacillaceae accumulated for 72 h (Day 3), the reducing sugar concentration reached its peak.</p>
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13 pages, 2776 KiB  
Article
Effects of Olive Oil and Tween 80 on Production of Lipase by Yarrowia Yeast Strains
by Gizella Sipiczki, Stefan Savo Micevic, Csilla Kohari-Farkas, Edina Szandra Nagy, Quang D. Nguyen, Attila Gere and Erika Bujna
Processes 2024, 12(6), 1206; https://doi.org/10.3390/pr12061206 - 12 Jun 2024
Cited by 3 | Viewed by 1796
Abstract
Lipase is one of the most commonly used biocatalysts in the food, pharmaceutical and cosmetic industries, and can be produced by Yarrowia lipolytica yeast. Despite the intensive studies of lipase from Yarrowia, there are still many open questions regarding the enzyme secretion [...] Read more.
Lipase is one of the most commonly used biocatalysts in the food, pharmaceutical and cosmetic industries, and can be produced by Yarrowia lipolytica yeast. Despite the intensive studies of lipase from Yarrowia, there are still many open questions regarding the enzyme secretion process, especially by new isolates of this genus as well as the effect of substrates or surfactants, or both on the production of lipase. This research focused on the effect of olive oil and surfactant Tween 80 including the optimisation of the concentration of these compounds on the production of lipase by some novel Yarrowia isolates. Moreover, the optimal environmental parameters (pH, temperature) of crude enzyme synthetised by Yarrowia strains were determined. All investigated strains were able to produce lipase in both intracellular and extracellular fractions. The extracellular lipase activities were higher than the intracellular ones (Y. divulgata Y.02062 and Yarrowia lipolytica 854/4 147 U/L, 80 U/L and 474 U/L, 122 U/L, respectively). In the case of extracellular lipase, supplementing olive oil and Tween 80 enhanced significantly the synthesis and secretion of the enzyme. The lipase activity can even be enhanced by 20 times higher from 25 U/L to 474 U/L in the case of Yarrowia lipolytica 854/4 strain. In the case of intracellular, supplementation of Tween 80 generally reduces lipase activity except for the Y. lipolytica 1/4 strain, which was affected by two times the increase. The optimised concentration of olive oil and Tween 80 were determined for Y. divulgata Y.02062, Y. divulgata 5257, Y. lipolytica 1/4, and Yarrowia lipolytica 854/4 strains as 1.6% olive oil and 0.09% Tween 80, 1.6% olive oil and 0.06% Tween 80, 1.4% olive oil and 0.09% Tween 80 as well as 1.6% olive oil and 0.065% Tween 80, respectively. The optimum pH and temperature of crude lipases (intra and extracellular) synthetised by the tested Yarrowia lipolytica and Y. divulgata yeast strains were found to be pH 7.2 and 37 °C, respectively. Our results confirmed that the new isolate Y. divulgata is a very promising species for further development for industrial use as Y. lipolytica. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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<p>Extracellular lipase activity of new <span class="html-italic">Yarrowia</span> isolates.</p>
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<p>Extracellular lipase activities produced by <span class="html-italic">Yarrowia</span> strains in different media. OO: olive oil.</p>
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<p>Surface plots of the lipase activity from different strains vs. concentration of olive oil and Tween 80. (<b>A</b>) <span class="html-italic">Y. lipolytica</span> 854/4 strain, (<b>B</b>) <span class="html-italic">Y. lipolytica</span> 1/4 strain, (<b>C</b>) <span class="html-italic">Y. divulgata</span> Y.02062 strain, (<b>D</b>) <span class="html-italic">Y. divulgata</span> 5257 strain.</p>
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<p>Optimum temperature of the extracellular (<b>A</b>) and intracellular (<b>B</b>) lipase enzymes of the four <span class="html-italic">Yarrowia</span> strains.</p>
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<p>Optimum pH of the extracellular (<b>A</b>) and intracellular (<b>B</b>) lipase enzymes of <span class="html-italic">Yarrowia</span> strains.</p>
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20 pages, 1128 KiB  
Article
Improving the Functionality of Yogurt after Fortification with a Synbiotic Combination of a Potential Probiotic and Bacteriocin-Producing Bacteria and Hydnora abyssinica Phytosomes
by Ghoson Daba, Waill Elkhateeb, Tarek Nour Soliman, Asmaa Negm El-Dein and Takeshi Zendo
Processes 2024, 12(4), 727; https://doi.org/10.3390/pr12040727 - 3 Apr 2024
Cited by 6 | Viewed by 1464
Abstract
Functional dairy products are attracting consumers’ attention, as they simultaneously have nutritional and health benefits. Hence, we aimed in this study to fortify a dairy product (yogurt) with phytosomes of extract from Hydnora abyssinica (a holoparasitic plant that has ethnobotanical value) and a [...] Read more.
Functional dairy products are attracting consumers’ attention, as they simultaneously have nutritional and health benefits. Hence, we aimed in this study to fortify a dairy product (yogurt) with phytosomes of extract from Hydnora abyssinica (a holoparasitic plant that has ethnobotanical value) and a potential bacteriocin-producing probiotic lactic acid bacterium (LAB). Goat cheese was screened for LAB with promising antimicrobial activity, and the safety and probiotic potential of the selected isolate were studied. As a result, strain GA5 was selected due to its wide antimicrobial activity that was suggested to be caused by bacteriocin production. Moreover, this strain showed promising stress tolerance, in vitro antioxidant activity (95 ± 2.8%), and hydrophobic potential (87.18 ± 3.43%). Strain GA5 was molecularly identified as Lactiplantibacillus plantarum GA5. On the other hand, a hydromethanolic extract was prepared from H. abyssinica flowers, and its prebiotic potential and polyphenol content were evaluated. This extract was also encapsulated in phytosomes. Then, the physical and morphological characteristics of prepared phytosomes were studied. Yogurt fortified with these ingredients (L. plantarum GA5 together with free H. abyssinica extract or its extract encapsulated in phytosomes) showed higher antioxidant content, viscosity, texture profile, and sensory properties than the control. Furthermore, the yogurt remained unspoiled for over 21 days, indicating that the added ingredients prolonged its shelf life. As far as we know, this is the first study describing the fortification of yogurt with H. abyssinica phytosomes and a potential bacteriocin-producing probiotic LAB. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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Figure 1
<p>An <span class="html-italic">H. abyssinica</span> flower as collected from the soil (<b>a</b>); a longitudinal section of it, showing the osmophore (1), perianth lobe (2), antheral ring (3), androecial chamber (4), and gynoecial chamber (5); (<b>b</b>); and a cross section of an <span class="html-italic">H. abyssinica</span> flower (<b>c</b>).</p>
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<p>Stress tolerance response (%) of <span class="html-italic">L. plantarum</span> strain GA5 after exposure to some stress conditions, including heat stress by exposure to 55 and 70 °C for 15 min; acidic pH stress at pH (2.5 for 3 and 6 h, pH 3.5 for 3 and 6 h); alkaline pH stress (at pH 9.0 for 3 and 6 h); osmotic stress at 3.0 M NaCl for 3 and 6 h; detergent stress at 0.2% Tween 80 for 24 h; pancreatic enzymes (PE, 0.15%) for 24 h; and bile salts (0.05 and 0.1%) for 24 h. Error bars represent the mean ± SD of three independent experiments.</p>
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<p>Viscosity evaluation of yogurt samples. Control (<b>A</b>); fortified with 0.1% free <span class="html-italic">H. abyssinica</span> phytosomes (<b>B</b>); fortified with 0.2% free <span class="html-italic">H. abyssinica</span> phytosomes (<b>C</b>); fortified with 0.1% nanoencapsulated <span class="html-italic">H. abyssinica</span> phytosomes (<b>D</b>); and fortified with 0.2% nanoencapsulated <span class="html-italic">H. abyssinica</span> phytosomes (<b>E</b>). Error bars represent the mean ± SD of three independent experiments.</p>
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<p>Sensory evaluation of yogurt fortified with <span class="html-italic">H. abyssinica</span> free and its nanoencapsulated phytosomes.</p>
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11 pages, 1275 KiB  
Article
In Vitro Evaluation of Commercial Probiotic Products Containing Streptococcus salivarius K12 by Assessment of Probiotic Viability and Inhibitory Potency against Respiratory Pathogens
by Medana Zamfir, Iulia-Roxana Angelescu and Silvia-Simona Grosu-Tudor
Processes 2023, 11(2), 622; https://doi.org/10.3390/pr11020622 - 18 Feb 2023
Cited by 2 | Viewed by 3085
Abstract
Upper respiratory infections (URI) are the most frequent illnesses, especially in children. The majority of those infections are prescribed broad-spectrum antibiotics, which are associated with various side effects and with the increase in multi-drug-resistant strains. A promising alternative approach is the administration of [...] Read more.
Upper respiratory infections (URI) are the most frequent illnesses, especially in children. The majority of those infections are prescribed broad-spectrum antibiotics, which are associated with various side effects and with the increase in multi-drug-resistant strains. A promising alternative approach is the administration of the probiotic strain Streptococcus salivarius K12 (SSK12) that colonizes the upper respiratory tract (URT) and produces the salivaricins A2 and B, which strongly antagonize the growth of key respiratory pathogens. However, since for food supplements no quality controls of the active probiotic ingredient are mandatory, the efficacy of commercial products containing SSK12 may vary. This study aimed to investigate the in vitro efficacy of several commercial SSK12-containing probiotics, positioned for the prevention of respiratory infections. The parameters evaluated to determine the in vitro efficacy included the viability of the probiotic bacterial strain and the minimum inhibitory dilution (MID) of the probiotic, determined by the agar spot method, against the pathogenic/potential pathogenic bacterial strains Streptococcus pyogenes FF22 and Micrococcus luteus T18. All tests were carried out both 12 and 24 months after manufacturing (AM) for each commercial product. The viability ranged from 9 × 108 to 4.4 × 109 CFU/serving at 12 months AM and from 8.5 × 107 to 2.8 × 109 CFU/serving at 24 months AM. The MID was, in general, positively correlated with the probiotic bacterium viability and varied between the commercial products, ranging from 10−5 to 10−7 at 12 months AM and from 10−4 to 10−7 at 24 months AM. Moreover, the inhibition zones related to the two indicator strains were variable in diameter for different products. The high variation of the in vitro efficacy of commercial products containing SSK12 may explain the different results reported in the literature regarding the clinical benefits of these preparations, and the determination of this parameter may be useful to evaluate the quality of probiotic products containing this bacterial strain. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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Figure 1
<p>Water activity of the analyzed commercial products, measured at 12 and 24 months AM. The results are presented as mean values ± standard deviation.</p>
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<p>Inhibitory activity of Bactoblis<sup>®</sup> (<b>a</b>) and Daily Defence-BLIS K12<sup>TM</sup> (<b>b</b>) at 12 and 24 months AM. The inhibitory activity was determined by the agar spot method, using <span class="html-italic">Micrococcus luteus</span> T18 and <span class="html-italic">Streptococcus pyogenes</span> FF22 as indicator strains. The numbers represent the decimal dilutions of each tested sample.</p>
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<p>Principal component analysis (PCA) of the probiotic products at 12 and 24 months after manufacture (AM). BL = Bactoblis Lozenge; BS = Bactoblis Sachets; DD = Daily Defence; DDJr = Daily Defence Junior; Dif = Difflam; TG = Throat Guard PRO; NF = Now Foods Oral Biotics. The numbers (12/24) indicate the time of testing, namely, 12/24 months AM.</p>
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Review

Jump to: Research

11 pages, 1542 KiB  
Review
Pyridazinic Bioisosteres with Potential Applications in Medicinal Chemistry and Agriculture
by Roxana Angela Tucaliuc, Violeta Mangalagiu and Ionel I. Mangalagiu
Processes 2023, 11(8), 2306; https://doi.org/10.3390/pr11082306 - 1 Aug 2023
Cited by 3 | Viewed by 2034
Abstract
Bioisosteres are substituents or groups (atoms, ions, or molecules) with similar chemical or physical properties, and which usually have similar biological properties. Pyridazine and its derivatives are invaluable scaffolds in medicinal chemistry, having a large variety of activities such as antibacterial, antifungal, antimalarial, [...] Read more.
Bioisosteres are substituents or groups (atoms, ions, or molecules) with similar chemical or physical properties, and which usually have similar biological properties. Pyridazine and its derivatives are invaluable scaffolds in medicinal chemistry, having a large variety of activities such as antibacterial, antifungal, antimalarial, anticancer, antituberculosis, antihypertensive, etc. Also, the pyridazine core is of high interest in agriculture, being used as a growth factor for plants, herbicides, etc. This study aims to review our previous contributions related to antimicrobials and the germination and seedling capabilities of some seeds and plants of some pyridazine classical and nonclassical bioisosteres. So, we present herein the synthesis (under conventional thermal heating and microwave irradiation) and spectral characterization of seven series of pyridazine bioisosteres, the in vitro antimicrobial activity (against different strains of Gram-positive and Gram-negative bacteria and fungi), and the biologic effect on wheat germination and seedling growth. Some pyridazine bioisosteres proved to have very good activity against pathogenic bacterial strains, with some spectacular results. Overall, nonclassical bioisosteres prove to have better antibacterial and antifungal activity compared with classical bioisosteres. The pyridazine bioisosteres may influence the wheat germination rate, seedling growth, height, and weight of the plantlets. Feasible explanations for this behaviour were furnished. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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Scheme 1

Scheme 1
<p>The synthesis of α-bromacetophenone pyridazine salts <b>3a</b>–<b>c</b> classical bioisosteres and their ylides <b>4a</b>–<b>c,</b> generated in situ.</p>
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<p>The synthesis of pyridazine classical bioisostere cycloadducts <b>5a</b>–<b>c</b> to <b>8a</b>–<b>c</b> (via cycloaddition reactions with symmetrically substituted dipolarophiles).</p>
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<p>The synthesis of pyridazine classical bioisosteres cycloadducts <b>9a</b>–<b>c</b> to <b>11a</b>–<b>c</b> (via cycloaddition reactions with non-symmetrically substituted dipolarophiles).</p>
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<p>The synthesis of trifluoromethyl-pyrrolo-pyridazine nonclassical bioisostere cycloadducts <b>12a</b>–<b>c</b> to <b>14a</b>–<b>c</b> (via cycloaddition reaction with symmetrically and non-symmetrically substituted dipolarophiles containing trifloromethyl groups).</p>
Full article ">
13 pages, 1348 KiB  
Review
Strain Development, Substrate Utilization, and Downstream Purification of Vitamin C
by Alexandra Tucaliuc, Ana Cîșlaru, Lenuţa Kloetzer and Alexandra Cristina Blaga
Processes 2022, 10(8), 1595; https://doi.org/10.3390/pr10081595 - 12 Aug 2022
Cited by 8 | Viewed by 8793
Abstract
Vitamin C, C6H8O6, is a water-soluble vitamin that is widespread in nature. It is an essential nutrient involved in many biological processes in the living organisms: it enhances collagen biosynthesis, ensures the optimal functioning of enzymes and [...] Read more.
Vitamin C, C6H8O6, is a water-soluble vitamin that is widespread in nature. It is an essential nutrient involved in many biological processes in the living organisms: it enhances collagen biosynthesis, ensures the optimal functioning of enzymes and the immune system, has a major role in lipid and iron metabolism, and it enhances the biosynthesis of l-carnitine. Due to its antioxidant activity, vitamin C can neutralize the tissue-damaging effects of free radicals. Vitamin C is being related to the prevention of cancer and cardiovascular diseases. This review includes current information on the biosynthesis of ascorbic acid, as new methods are now challenging the traditional Reichstein process for vitamin C’s industrial-scale production. Different strains were analyzed in correlation with their ability to synthesize ascorbic acid, and several separation techniques were investigated for a more effective production of vitamin C. Full article
(This article belongs to the Special Issue Microbiotechnology in Cosmetics, Pharmaceuticals and Food)
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Graphical abstract

Graphical abstract
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<p>Ascorbic acid structure: (<b>a</b>) <span class="html-small-caps">l</span>-ascorbic acid (vitamin C), and (<b>b</b>) <span class="html-small-caps">d</span>-ascorbic acid Adapted with permission from Ref. [<a href="#B7-processes-10-01595" class="html-bibr">7</a>].</p>
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<p>Electron delocalization of an ascorbate anion. Adapted with permission from Ref. [<a href="#B8-processes-10-01595" class="html-bibr">8</a>].</p>
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<p>Aerobic degradation of vitamin C. Adapted with permission from Ref. [<a href="#B7-processes-10-01595" class="html-bibr">7</a>].</p>
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<p>Applications of vitamin C [<a href="#B9-processes-10-01595" class="html-bibr">9</a>].</p>
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<p>Reichstein method of vitamin C production. (<b>A</b>) <span class="html-small-caps">d</span>-glucose, (<b>B</b>) <span class="html-small-caps">d</span>-sorbitol, (<b>C</b>) <span class="html-small-caps">l</span>-sorbose, (<b>D</b>) 2,3,4,6-di-isopropylidene-<span class="html-small-caps">l</span>-xylo-2-hexofuranose, (<b>E</b>) 2-keto-<span class="html-small-caps">l</span>-gulonic acid, and (<b>F</b>) vitamin C. Step 1 is a reduction process with 100% yield, step 2 is an oxidation process with a yield between 60–95% using <span class="html-italic">Acetobacter suboxydans</span>, and steps 3 to 6 are oxidation processes with 80%, 90%, and 75% yields, respectively. In addition, <span class="html-italic">Pseudomonas</span> strains can be used for the first oxidation step.</p>
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<p>Representation of the two-step fermentation process.</p>
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<p>Biosynthesis of vitamin C in plants and <span class="html-small-caps">d</span>-erythroascorbic acid in yeasts. (<b>A</b>)—<span class="html-small-caps">d</span>-glucose, (<b>B</b>)—<span class="html-small-caps">d</span>-arabinose, (<b>C</b>)—<span class="html-small-caps">d</span>-arabinono-1,4-lactone, (<b>D</b>)—<span class="html-small-caps">d</span>-erythroascorbic acid, (<b>E</b>)—<span class="html-small-caps">l</span>-galactose, (<b>F</b>)—<span class="html-small-caps">l</span>-galactono-1,4-lactone, and (<b>G</b>)—vitamin C. In plants, galactose (obtained from glucose by the subsequent action of the following enzymes: hexokinase, hexose phosphate isomerase, phosphomannose isomerase, phosphomannose mutase, GDP-mannose pyrophosphorylase, and GDP-mannose-3,5-epimerase) is converted by <span class="html-small-caps">l</span>-galactose dehydrogenase into <span class="html-small-caps">l</span>-galactono-1,4-lactone and by <span class="html-small-caps">l</span>-galactono-1,4-lactone dehydrogenase into vitamin C. In yeast cells, a five-carbon analogue of vitamin C is synthesized by the action of the following enzymes: <span class="html-small-caps">d</span>-arabinose dehydrogenase and <span class="html-small-caps">d</span>-arabinono-1,4-lactone oxidase.</p>
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<p>Representation of the production and separation processes of vitamin C.</p>
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