GB1017794A - Process for producing 5-ribonucleotides - Google Patents

Process for producing 5-ribonucleotides

Info

Publication number
GB1017794A
GB1017794A GB1201264A GB1201264A GB1017794A GB 1017794 A GB1017794 A GB 1017794A GB 1201264 A GB1201264 A GB 1201264A GB 1201264 A GB1201264 A GB 1201264A GB 1017794 A GB1017794 A GB 1017794A
Authority
GB
United Kingdom
Prior art keywords
acid
nucleotide
sodium
culture
suitable amount
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.)
Expired
Application number
GB1201264A
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Publication of GB1017794A publication Critical patent/GB1017794A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/26Preparation of nitrogen-containing carbohydrates
    • C12P19/28N-glycosides
    • C12P19/30Nucleotides
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/26Preparation of nitrogen-containing carbohydrates
    • C12P19/28N-glycosides
    • C12P19/30Nucleotides
    • C12P19/32Nucleotides having a condensed ring system containing a six-membered ring having two N-atoms in the same ring, e.g. purine nucleotides, nicotineamide-adenine dinucleotide

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

51-Inosinic acid, 51-xanthylic acid and 51-guanylic acid are obtained by contacting an enzyme source of bacterial origin, having nucleoside phosphotransferase activity for producing 51-nucleotide from the corresponding nucleoside and a phosphate donor, with a solution containing the corresponding nucleoside and a 51-nucleotide other than that to be synthesized, allowing biochemical phosphorylation to take place to produce the desired 51-nucleotide while maintaining the pH of the solution in the alkaline range, preferably between 7.0 and 10.0, the accumulated 51-ribonucleotide may be recovered by a conventional procedure. The production of the 51-nucleotide may be promoted by the addition of cupric and/or arsenic salts, the most suitable concentration of metallic salt being from 10- 3 to 10- 2 mole. Bacteria which have the ability to synthesize 51-nucleotide from the corresponding nucleoside and a phosphate donor include species which belong to the genera Pseudomonas, Serratia, Flavobacterium, Staphylococcus and Achromobacter. 51 - Nucleotides which may be used as the phosphate donor include 51 - adenylic acid, 51 - cytidylic acid, 51 - uridylic acid, 51-desoxyadenylic acid and 51-thymidylic acid. The enzyme source may be prepared by submerged culture, stationary culture or surface culture, preferably at a temperature of from 20 DEG to 37 DEG C. and for an incubation period of from 10 to 60 hours, in a culture medium containing a suitable amount of an organic or inorganic nitrogen source, such as peptone, meat extract, corn steep liquor, yeast extract, dry yeast, hydrolysate of soybean protein or an inorganic ammonium salt, and a suitable amount of carbon source, such as molasses, glucose or hydrolysate of starch, and a suitable amount of inorganic salts. The enzyme source may be in the form of, for example, living bacterial cells, cultured broth, living cell suspensions, dried cells, crude extract or enzyme preparation. Examples are given for the preparation of 51-inosinic acid in the presence of sodium-51-uridylate and copper sulphate or sodium arsenate, and of 51-guanylic acid in the presence of sodium-51-cytidylate or sodium-51-uridylate, and sodium arsenate.
GB1201264A 1963-03-22 1964-03-20 Process for producing 5-ribonucleotides Expired GB1017794A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1344663 1963-03-22

Publications (1)

Publication Number Publication Date
GB1017794A true GB1017794A (en) 1966-01-19

Family

ID=11833346

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1201264A Expired GB1017794A (en) 1963-03-22 1964-03-20 Process for producing 5-ribonucleotides

Country Status (4)

Country Link
CH (1) CH415646A (en)
DE (1) DE1445440A1 (en)
GB (1) GB1017794A (en)
NL (1) NL6402925A (en)

Also Published As

Publication number Publication date
CH415646A (en) 1966-06-30
NL6402925A (en) 1964-09-23
DE1445440A1 (en) 1969-02-13

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