GB1021962A - Process for preparing 5-nucleotides - Google Patents
Process for preparing 5-nucleotidesInfo
- Publication number
- GB1021962A GB1021962A GB39515/64A GB3951564A GB1021962A GB 1021962 A GB1021962 A GB 1021962A GB 39515/64 A GB39515/64 A GB 39515/64A GB 3951564 A GB3951564 A GB 3951564A GB 1021962 A GB1021962 A GB 1021962A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nucleotide
- enzyme
- purine
- synthesized
- reaction
- 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
Links
- 239000002773 nucleotide Substances 0.000 title abstract 8
- 238000004519 manufacturing process Methods 0.000 title 1
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 abstract 4
- 102000004190 Enzymes Human genes 0.000 abstract 3
- 108090000790 Enzymes Proteins 0.000 abstract 3
- 150000007530 organic bases Chemical class 0.000 abstract 3
- LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 abstract 2
- BVIAOQMSVZHOJM-UHFFFAOYSA-N N(6),N(6)-dimethyladenine Chemical compound CN(C)C1=NC=NC2=C1N=CN2 BVIAOQMSVZHOJM-UHFFFAOYSA-N 0.000 abstract 2
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 abstract 2
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Chemical compound NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 abstract 2
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 abstract 2
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- RWQNBRDOKXIBIV-UHFFFAOYSA-N thymine Chemical compound CC1=CNC(=O)NC1=O RWQNBRDOKXIBIV-UHFFFAOYSA-N 0.000 abstract 2
- MWBWWFOAEOYUST-UHFFFAOYSA-N 2-aminopurine Chemical compound NC1=NC=C2N=CNC2=N1 MWBWWFOAEOYUST-UHFFFAOYSA-N 0.000 abstract 1
- JDBGXEHEIRGOBU-UHFFFAOYSA-N 5-hydroxymethyluracil Chemical compound OCC1=CNC(=O)NC1=O JDBGXEHEIRGOBU-UHFFFAOYSA-N 0.000 abstract 1
- CKOMXBHMKXXTNW-UHFFFAOYSA-N 6-methyladenine Chemical compound CNC1=NC=NC2=C1N=CN2 CKOMXBHMKXXTNW-UHFFFAOYSA-N 0.000 abstract 1
- MSSXOMSJDRHRMC-UHFFFAOYSA-N 9H-purine-2,6-diamine Chemical compound NC1=NC(N)=C2NC=NC2=N1 MSSXOMSJDRHRMC-UHFFFAOYSA-N 0.000 abstract 1
- GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 abstract 1
- 229930024421 Adenine Natural products 0.000 abstract 1
- 241000588986 Alcaligenes Species 0.000 abstract 1
- 241000588722 Escherichia Species 0.000 abstract 1
- 241000589565 Flavobacterium Species 0.000 abstract 1
- UGQMRVRMYYASKQ-UHFFFAOYSA-N Hypoxanthine nucleoside Natural products OC1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 UGQMRVRMYYASKQ-UHFFFAOYSA-N 0.000 abstract 1
- FAIXYKHYOGVFKA-UHFFFAOYSA-N Kinetin Natural products N=1C=NC=2N=CNC=2C=1N(C)C1=CC=CO1 FAIXYKHYOGVFKA-UHFFFAOYSA-N 0.000 abstract 1
- 241000192041 Micrococcus Species 0.000 abstract 1
- NWBJYWHLCVSVIJ-UHFFFAOYSA-N N-benzyladenine Chemical compound N=1C=NC=2NC=NC=2C=1NCC1=CC=CC=C1 NWBJYWHLCVSVIJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 241000588769 Proteus <enterobacteria> Species 0.000 abstract 1
- 241000589516 Pseudomonas Species 0.000 abstract 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
- 241000607720 Serratia Species 0.000 abstract 1
- 241000191940 Staphylococcus Species 0.000 abstract 1
- 229960000643 adenine Drugs 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- -1 alkali metal salt Chemical class 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 238000005842 biochemical reaction Methods 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- 229940104302 cytosine Drugs 0.000 abstract 1
- 238000006911 enzymatic reaction Methods 0.000 abstract 1
- 239000000284 extract Substances 0.000 abstract 1
- 238000004255 ion exchange chromatography Methods 0.000 abstract 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 abstract 1
- 229960001669 kinetin Drugs 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 229940113082 thymine Drugs 0.000 abstract 1
- 229940035893 uracil Drugs 0.000 abstract 1
- 229940075420 xanthine Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/26—Preparation of nitrogen-containing carbohydrates
- C12P19/28—N-glycosides
- C12P19/30—Nucleotides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
- C07H1/02—Phosphorylation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/828—Aerobacter
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/829—Alcaligenes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/848—Escherichia
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/848—Escherichia
- Y10S435/849—Escherichia coli
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/859—Micrococcus
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/873—Proteus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Saccharide Compounds (AREA)
Abstract
51-Nucleotides are prepared by contacting an enzyme source, having ribose-51-phosphate transferring activity for producing 51-nucleotide from the corresponding organic base and a 51-nucleotide, with a solution containing the corresponding organic base and a 51-nucleotide other than that to be synthesized, and allowing biochemical reaction to take place to produce the desired 51-nucleotide. Suitable microorganisms which can be used are enzyme sources which belong to the genera Pseudomonas, Alcaligenes, Serratia, Flavobacterium, Micrococcus, Staphylococcus, Proteus, Aerobacter, and Escherichia. The organic bases which may be used are the purine and pyrimidine bases such as purine, adenine, hypoxanthine, xanthine, guanine, 2-aminopurine, 2,6-diaminopurine, 6-dimethyl aminopurine, benzyladenine, 6-methylaminopurine, kinetin, uracil, 5-hydroxy-methyluracil, cytosine, thymine and barbituric acid. The enzyme reaction may be carried out in aqueous medium of a pH of from 5 to 10 and a temperature of from 30 DEG to 60 DEG C. and the synthesized 51-nucleotide isolated from the reaction mixture by such methods as ion exchange chromatography or precipitation. 51-nucleotide may suitably be obtained as crude crystals in the form of the alkali metal salt. The enzyme source can be admixed with the reaction mixture in the form of cultured broth, living cells, dried cells or cell extracts.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5080363 | 1963-09-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1021962A true GB1021962A (en) | 1966-03-09 |
Family
ID=12868921
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB39515/64A Expired GB1021962A (en) | 1963-09-27 | 1964-09-28 | Process for preparing 5-nucleotides |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3296087A (en) |
| DE (1) | DE1445456A1 (en) |
| FR (1) | FR1550952A (en) |
| GB (1) | GB1021962A (en) |
| NL (1) | NL6411078A (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1285477B (en) * | 1964-05-19 | 1968-12-19 | Kyowa Hakko Kogyo Kk | Process for the preparation of 5'-guanyl acid |
| US3408206A (en) * | 1965-01-11 | 1968-10-29 | Ajinomoto Kk | 5'-nucleotides seasoning agents |
| US3458398A (en) * | 1965-07-20 | 1969-07-29 | Kyowa Hakko Kogyo Kk | Process for producing inosinic acid |
| US3457254A (en) * | 1965-10-09 | 1969-07-22 | Asahi Chemical Ind | Process for preparing nucleosides |
| GB1184133A (en) * | 1967-03-18 | 1970-03-11 | Kyowa Hakko Kogyo Kk | Process for producing 5'-Inosinic Acid and 5'-Guanylic Acid Nucleotides |
| JPS59161398A (en) * | 1983-03-02 | 1984-09-12 | Mitsui Toatsu Chem Inc | Method and apparatus for incising deoxyribonucleic acid |
-
1964
- 1964-09-23 NL NL6411078A patent/NL6411078A/xx unknown
- 1964-09-24 US US399082A patent/US3296087A/en not_active Expired - Lifetime
- 1964-09-25 DE DE19641445456 patent/DE1445456A1/en active Pending
- 1964-09-28 GB GB39515/64A patent/GB1021962A/en not_active Expired
- 1964-09-28 FR FR1550952D patent/FR1550952A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE1445456A1 (en) | 1968-12-19 |
| FR1550952A (en) | 1968-12-27 |
| NL6411078A (en) | 1965-03-29 |
| US3296087A (en) | 1967-01-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MacNutt | The enzymically catalysed transfer of the deoxyribosyl group from one purine or pyrimidine to another | |
| SU437288A1 (en) | Method for preparing thiophosphate nucleoside di-or-triphosphate analogues | |
| Acs et al. | Biological and biochemical properties of the analogue antibiotic tubercidin | |
| Simon et al. | Calf intestine adenosine deaminase. Substrate specificity | |
| Bresnick | Feedback inhibition of aspartate transcarbamylase in liver and in hepatoma | |
| Young | The biosynthesis of the vitamins thiamin, riboflavin, and folic acid | |
| Elstner et al. | The biosynthesis of the nucleoside antibiotics: IX. Purification and properties of guanosine triphosphate 8-formylhydrolase that catalyzes production of formic acid from the ureido carbon of guanosine triphosphate | |
| GB1021962A (en) | Process for preparing 5-nucleotides | |
| Baugh et al. | Biosynthesis of riboflavine in Corynebacterium species: the purine precursor | |
| Zinchenko et al. | Synthesis of 9-(β-D-arabinofuranosyl) guanine using whole cells of Escherichia coli | |
| US4141972A (en) | Purine nucleoside 5'-phosphate (mono, di or tri) 3'(2')-diphosphates and processes for their preparation | |
| GB1163103A (en) | Ribofuranosyl Purine Derivatives | |
| Moore et al. | Utilization of uracil by a strain of Escherichia coli | |
| US4371613A (en) | Method for producing purine arabinosides | |
| Marsh et al. | Purification of trans-N-glycosidase of Thermobacter acidophilus: inhibition of enzyme by 6-azathymidine | |
| MITSUDA et al. | Biochemical Studies on Pteridines in Plants III. Biogenesis of Folic Acid in Green Leaves; Inhibitors Acting on the Biosynthetic Pathway for the Formation of Dihydropteroic Acid from Guanylic Acid | |
| US4594320A (en) | Process for producing 3-deoxyguanosine | |
| CA1120876A (en) | Method for producing purine arabinosides | |
| GB1063952A (en) | A process for producing purine-ribosides | |
| Sakai et al. | Metabolisms of Nucleosides in Bacteria: Part IV. Pyrimidine Nucleoside Phosphorylase in Erwinia carotovora and Corynebacterium sepedonicum Part V. Purine Nucleoside Phosphorylases in Erwina carotovoia and Corynebactcrium sepedonicum | |
| US3806413A (en) | Process for producing ribosides of 1h-pyrazolo (3,4-d) pyrimidines | |
| JPS6314956B2 (en) | ||
| GB1063951A (en) | A process for producing purine ribosides or deoxyribosides | |
| Ochi et al. | BIOSYNTHESIS OF FORMYCIN FORMATION OF FORMYCIN FROM FORMYCIN B | |
| US3879260A (en) | Process for production of ribosides of nucleic acid base derivatives and analogues thereof |