GB1294769A - Process for producing cytidine diphosphate choline - Google Patents

Process for producing cytidine diphosphate choline

Info

Publication number
GB1294769A
GB1294769A GB5555270A GB5555270A GB1294769A GB 1294769 A GB1294769 A GB 1294769A GB 5555270 A GB5555270 A GB 5555270A GB 5555270 A GB5555270 A GB 5555270A GB 1294769 A GB1294769 A GB 1294769A
Authority
GB
United Kingdom
Prior art keywords
cytidine
choline
cells
diphosphate
genera
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
GB5555270A
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.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Publication of GB1294769A publication Critical patent/GB1294769A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06Pyrimidine radicals
    • C07H19/10Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
    • 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
    • C12P19/305Pyrimidine nucleotides

Landscapes

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

Abstract

1294769 Cytidine diphosphate choline ASAHI KASEI KOGYO KK 23 Nov 1970 [26 Nov 1969] 55552/70 Heading C2P Cytidine diphosphate choline is produced by applying an enzyme, contained in the cells of a micro-organism having a fructose-1,6-diphosphate producing ability from carbohydrates of at least 20% by weight of inorganic phosphate consumption in 5 to 8 hours, to a liquid medium containing 5<SP>1</SP>-cytidylic acid, a salt thereof, cytidine or cytosine, together with choline, a salt thereof or phosphatidyl choline, and a phosphoric acid donor, a carbohydrate and a magnesium salt. The phosphoric acid donor may be sodium phosphate, potassium dihydrogen phosphate or dipotassium hydrogen phosphate, the carbohydrate may be glucose, sucrose, fructose or maltose, and the magnesium salt may be the sulphate or chloride., The enzyme may be used in the form of a culture medium of the microorganism, cells thereof, dried cells, cell extracts or ground cells. Suitable micro-organisms are (a) yeasts of the Brettanomyces, Torulopsis, Candida, Saccharomyces, Zygosaccharomyces, Debaryomyces and Pichia genera, (b) bacteria of the Microbacterium, Corynebacterium and Brevibacterium genera and (c) fungi of the Mucor and Aspergillus genera. The reaction may be carried out at 20-45‹ C. at pH 6 to 9. Small amounts of cytidine-5<SP>1</SP>-triphosphate and cytidine-5<SP>1</SP>-diphosphate may also be produced.
GB5555270A 1969-11-26 1970-11-23 Process for producing cytidine diphosphate choline Expired GB1294769A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9428969A JPS5140159B1 (en) 1969-11-26 1969-11-26

Publications (1)

Publication Number Publication Date
GB1294769A true GB1294769A (en) 1972-11-01

Family

ID=14106086

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5555270A Expired GB1294769A (en) 1969-11-26 1970-11-23 Process for producing cytidine diphosphate choline

Country Status (4)

Country Link
JP (1) JPS5140159B1 (en)
CH (1) CH504530A (en)
FR (1) FR2069340A5 (en)
GB (1) GB1294769A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6387667B1 (en) 1992-01-30 2002-05-14 Kyowa Hakko Kogyo, Co., Ltd. Process for producing cytidine diphosphate choline

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5542623A (en) * 1978-09-19 1980-03-26 Matsushita Electric Ind Co Ltd Small electric cleaner
AT364485B (en) * 1980-06-10 1981-10-27 Franz Lex HAND BRUSH SUCTION UNIT

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE789254A (en) * 1971-09-30 1973-03-26 Synthelabo NEW AMINO-ESTERS
JPS4841555A (en) * 1971-10-01 1973-06-18
JPS537424B2 (en) * 1971-10-08 1978-03-17

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6387667B1 (en) 1992-01-30 2002-05-14 Kyowa Hakko Kogyo, Co., Ltd. Process for producing cytidine diphosphate choline

Also Published As

Publication number Publication date
DE2054785B2 (en) 1975-07-31
FR2069340A5 (en) 1971-09-03
CH504530A (en) 1971-03-15
JPS5140159B1 (en) 1976-11-01
DE2054785A1 (en) 1971-06-03

Similar Documents

Publication Publication Date Title
Muntz The role of potassium and ammonium ions in alcoholic fermentation
Hunsley et al. Yeast Pyruvate Kinase: II. KINETIC PROPERTIES
Meredith et al. Uptake and phosphorylation of 2-deoxy-D-glucose by wild type and respiration-deficient baker's yeast
Bresnick Feedback inhibition of aspartate transcarbamylase in liver and in hepatoma
Weimberg et al. Studies with three bacterial sucrose phosphorylases
Streeter et al. Phosphorylation of ribavirin by deoxyadenosine kinase from rat liver. Differentiation between adenosine and deoxyadenosine kinase
GB1300798A (en) Preparation of cytidine diphosphate choline
GB1294769A (en) Process for producing cytidine diphosphate choline
USRE28886E (en) Method for preparing cytidine diphosphate choline
JP3651036B2 (en) Method for producing nucleoside-5&#39;-phosphate ester
Dietzler et al. Regulation of ADP-glucose synthetase, the rate-limiting enzyme of bacterial glycogen synthesis, by the pleiotropic nucleotides ppGpp and pppGpp
Baugh et al. EFFECTS OF BICARBONATE ON GROWTH OF PASTEURELLA PESTIS II: Carbon Dioxide Fixation Into Oxalacetate by Cell-Free Extracts
US3168446A (en) Production of 5&#39;-nucleotides and of nucleosides
GB1334301A (en) Process for producing inosine
Vesell Formation of human lactate dehydrogenase isozyme patterns in vitro.
Tochikura et al. Studies on Microbial Metabolism of Sugar Nucleotides: Part VI. Fermentative Production of UDP N-Acetylglucosamine from 5′-UMP and Glucosamine by Yeasts
GB1190079A (en) Process for producing Nicotinamide Adenine Dinucleotide
US3717547A (en) Process for producing uridine-5&#39;-diphosphoglucose
GB1366451A (en) Preparation of adenosine 3 5 monophosphoric acid
GB1233127A (en)
Endo et al. A simple procedure for the preparation of UDP-N-acetylglucosamine-14C
Martin et al. Mitochondrial autonomy Studies on the mitochondral glycoprotein: Glucosyl and mitochondrial glycoprotein: Mannosyl transferase enzyme systems of rat liver mitochondria utilizing endogenous acceptors
JPS6314956B2 (en)
Tachiki et al. Glutamine production by coupling with energy transfer: employing yeast cell-free extracts and Gluconobacter glutamine synthetase
GB1161262A (en) A Method for Producing Adenosine Diphosphate and Adenosine Triphosphate

Legal Events

Date Code Title Description
PS Patent sealed
48R Reference inserted (sect. 8/1949)
PCNP Patent ceased through non-payment of renewal fee