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JPS6443194A - Plasmid and escherichia-coli transformed therewith - Google Patents

Plasmid and escherichia-coli transformed therewith

Info

Publication number
JPS6443194A
JPS6443194A JP20052487A JP20052487A JPS6443194A JP S6443194 A JPS6443194 A JP S6443194A JP 20052487 A JP20052487 A JP 20052487A JP 20052487 A JP20052487 A JP 20052487A JP S6443194 A JPS6443194 A JP S6443194A
Authority
JP
Japan
Prior art keywords
plasmid
thermostable
mentioned
dna
afore
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP20052487A
Other languages
Japanese (ja)
Other versions
JP2602840B2 (en
Inventor
Yonekazu Sakamoto
Masao Kageyama
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Unitika Ltd
Original Assignee
Unitika Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unitika Ltd filed Critical Unitika Ltd
Priority to JP20052487A priority Critical patent/JP2602840B2/en
Publication of JPS6443194A publication Critical patent/JPS6443194A/en
Application granted granted Critical
Publication of JP2602840B2 publication Critical patent/JP2602840B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004Oxidoreductases (1.)
    • C12N9/0012Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
    • C12N9/0014Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on the CH-NH2 group of donors (1.4)
    • C12N9/0016Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on the CH-NH2 group of donors (1.4) with NAD or NADP as acceptor (1.4.1)

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Molecular Biology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

PURPOSE:To produce a thermostable alanine dehydrogenase, by linking a thermostable dehydrogenase gene having a specific mol. wt. or below to a vector plasmid, introducing the resultant recombinant plasmid into Escherichia coli and cultivating the obtained transformant strain in a culture medium. CONSTITUTION:A chromosomic DNA of Bacillus.sterothermophilus IFO12550 strain is digested with a restriction enzyme SalI to provide a DNA fragment, which is then linked to a plasmid pBR322 treated with the SalI with a T4 ligase to afford a plasmid pICR3. An exogenote region of the above-mentioned plasmid is subsequently taken out and introduced into an M13 phage vector to determine a DNA base sequence. A DNA fragment, capable of coding an alanine dehydrogenase and having <=2 megadaltons is obtained on the basis of the afore-mentioned sequence and linked to a plasmid pKK223-3 by ligase treatment to afford pICR330. The afore-mentioned plasmid is then introduced into Escherichia coli and the resultant transformant strain is cultivated in a culture medium to provide the aimed thermostable enzyme.
JP20052487A 1987-08-10 1987-08-10 Plasmids and Escherichia coli transformed therewith Expired - Lifetime JP2602840B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20052487A JP2602840B2 (en) 1987-08-10 1987-08-10 Plasmids and Escherichia coli transformed therewith

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20052487A JP2602840B2 (en) 1987-08-10 1987-08-10 Plasmids and Escherichia coli transformed therewith

Publications (2)

Publication Number Publication Date
JPS6443194A true JPS6443194A (en) 1989-02-15
JP2602840B2 JP2602840B2 (en) 1997-04-23

Family

ID=16425743

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20052487A Expired - Lifetime JP2602840B2 (en) 1987-08-10 1987-08-10 Plasmids and Escherichia coli transformed therewith

Country Status (1)

Country Link
JP (1) JP2602840B2 (en)

Also Published As

Publication number Publication date
JP2602840B2 (en) 1997-04-23

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