JPS57166992A - Preparation of adenosine-5'-triphosphate - Google Patents
Preparation of adenosine-5'-triphosphateInfo
- Publication number
- JPS57166992A JPS57166992A JP56053681A JP5368181A JPS57166992A JP S57166992 A JPS57166992 A JP S57166992A JP 56053681 A JP56053681 A JP 56053681A JP 5368181 A JP5368181 A JP 5368181A JP S57166992 A JPS57166992 A JP S57166992A
- Authority
- JP
- Japan
- Prior art keywords
- adenosine
- glycolytic
- cultured
- triphosphate
- dried
- 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
Links
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 title abstract 4
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 title abstract 4
- 229960001456 adenosine triphosphate Drugs 0.000 title abstract 3
- 230000002414 glycolytic effect Effects 0.000 abstract 4
- 241000894006 Bacteria Species 0.000 abstract 2
- 102000004190 Enzymes Human genes 0.000 abstract 2
- 108090000790 Enzymes Proteins 0.000 abstract 2
- 241000588724 Escherichia coli Species 0.000 abstract 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 abstract 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 abstract 2
- 230000001580 bacterial effect Effects 0.000 abstract 2
- -1 e.g. Substances 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 239000002243 precursor Substances 0.000 abstract 2
- 239000000758 substrate Substances 0.000 abstract 2
- 239000002126 C01EB10 - Adenosine Substances 0.000 abstract 1
- UDMBCSSLTHHNCD-UHFFFAOYSA-N Coenzym Q(11) Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1O UDMBCSSLTHHNCD-UHFFFAOYSA-N 0.000 abstract 1
- 108010073254 Colicins Proteins 0.000 abstract 1
- 229930091371 Fructose Natural products 0.000 abstract 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 abstract 1
- 239000005715 Fructose Substances 0.000 abstract 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- 102000001105 Phosphofructokinases Human genes 0.000 abstract 1
- 108010069341 Phosphofructokinases Proteins 0.000 abstract 1
- 108700015934 Triose-phosphate isomerases Proteins 0.000 abstract 1
- 229960005305 adenosine Drugs 0.000 abstract 1
- UDMBCSSLTHHNCD-KQYNXXCUSA-N adenosine 5'-monophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O UDMBCSSLTHHNCD-KQYNXXCUSA-N 0.000 abstract 1
- 229950006790 adenosine phosphate Drugs 0.000 abstract 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract 1
- 239000012295 chemical reaction liquid Substances 0.000 abstract 1
- 238000012258 culturing Methods 0.000 abstract 1
- 238000010353 genetic engineering Methods 0.000 abstract 1
- 239000008103 glucose Substances 0.000 abstract 1
- 229910001425 magnesium ion Inorganic materials 0.000 abstract 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 abstract 1
- 235000019341 magnesium sulphate Nutrition 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 235000015097 nutrients Nutrition 0.000 abstract 1
- 239000008055 phosphate buffer solution Substances 0.000 abstract 1
- 239000013612 plasmid Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/12—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/90—Isomerases (5.)
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)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56053681A JPH0698014B2 (ja) | 1981-04-08 | 1981-04-08 | アデノシン−５′−三リン酸の製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56053681A JPH0698014B2 (ja) | 1981-04-08 | 1981-04-08 | アデノシン−５′−三リン酸の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57166992A true JPS57166992A (en) | 1982-10-14 |
| JPH0698014B2 JPH0698014B2 (ja) | 1994-12-07 |
Family
ID=12949555
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56053681A Expired - Lifetime JPH0698014B2 (ja) | 1981-04-08 | 1981-04-08 | アデノシン−５′−三リン酸の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0698014B2 (ja) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60102195A (ja) * | 1983-11-05 | 1985-06-06 | Wako Sangyo Kk | アデノシン−５’−三燐酸の製造法 |
| WO1998048031A1 (fr) * | 1997-04-18 | 1998-10-29 | Yamasa Corporation | Procede de production d'adenosine 5'-triphosphate et utilisation de ladite substance |
| JPWO2021246522A1 (ja) * | 2020-06-05 | 2021-12-09 |
-
1981
- 1981-04-08 JP JP56053681A patent/JPH0698014B2/ja not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60102195A (ja) * | 1983-11-05 | 1985-06-06 | Wako Sangyo Kk | アデノシン−５’−三燐酸の製造法 |
| WO1998048031A1 (fr) * | 1997-04-18 | 1998-10-29 | Yamasa Corporation | Procede de production d'adenosine 5'-triphosphate et utilisation de ladite substance |
| JPWO2021246522A1 (ja) * | 2020-06-05 | 2021-12-09 | ||
| WO2021246522A1 (ja) * | 2020-06-05 | 2021-12-09 | 国立大学法人神戸大学 | 耐熱性組換え宿主、耐熱性組換え宿主の製造方法、宿主に耐熱性を付与する方法、及び有用物質を生産する方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0698014B2 (ja) | 1994-12-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Axelrod et al. | A biochemical lesion in congenital, non-obstructive, non-haemolytic jaundice | |
| Weiss | Enzymatic incorporation of ribonucleoside triphosphates into the interpolynucleotide linkages of ribonucleic acid | |
| Brockman et al. | Metabolism of uracil and 5-fluorouracil by drug-sensitive and by drug-resistant bacteria | |
| Umezawa et al. | Phosphorylative inactivation of aminoglycosidic antibiotics by Escherichia coli carrying R factor | |
| Preiss et al. | Enzymatic synthesis of nicotinamide mononucleotide | |
| MacNutt | The enzymically catalysed transfer of the deoxyribosyl group from one purine or pyrimidine to another | |
| Hershey et al. | A competitive inhibitor of the GTP reaction in protein synthesis | |
| Biswas et al. | Release of repressor control of ribonucleotide reductase by thymine starvation | |
| de Verdier et al. | Alternative pathways of thymine and uracil metabolism in the liver and hepatoma | |
| Li et al. | A highly efficient galactokinase from Bifidobacterium infantis with broad substrate specificity | |
| KR20020048930A (ko) | 데옥시리보뉴클레오시드의 효소적 합성 | |
| Zou et al. | Substrate specificity of galactokinase from Streptococcus pneumoniae TIGR4 towards galactose, glucose, and their derivatives | |
| US4331662A (en) | Methods for the treatment of viral infections | |
| Taran et al. | Enzymatic transglycosylation of natural and modified nucleosides by immobilized thermostable nucleoside phosphorylases from Geobacillus stearothermophilus | |
| JPH02231091A (ja) | フルクトース―１，６―二リン酸の製造法 | |
| Keenan et al. | The characterisation of a galactokinase from Streptomyces coelicolor | |
| Rapaport et al. | Relationship of the first step in protein synthesis to ppGpp: formation of A (5') ppp (5') Gpp. | |
| JPS57166992A (en) | Preparation of adenosine-5'-triphosphate | |
| Mikhailopulo et al. | Synthesis of 2-chloro-2′-deoxyadenosine by microbiological transglycosylation | |
| Zaitseva et al. | Chemical-enzymatic synthesis of 3′-amino-2′, 3′-dideoxy-β-D-ribofuranosides of natural heterocyclic bases and their 5′-monophosphates | |
| CN110885812A (zh) | 一种酶法制备尿苷酸的方法 | |
| US4141972A (en) | Purine nucleoside 5'-phosphate (mono, di or tri) 3'(2')-diphosphates and processes for their preparation | |
| TW201732039A (zh) | 新型多磷酸鹽依存性葡萄糖激酶與使用其製備葡萄糖-6-磷酸的方法 | |
| EP0566140B1 (en) | Method for producing dinucleoside polyphosphate, nucleoside polyphosphate or derivatives thereof | |
| CN113122593A (zh) | 一种利用多聚磷酸盐制备核苷三磷酸和脱氧核苷三磷酸的方法 |