SU395082A1 - - Google Patents
Info
- Publication number
- SU395082A1 SU395082A1 SU1698592A SU1698592A SU395082A1 SU 395082 A1 SU395082 A1 SU 395082A1 SU 1698592 A SU1698592 A SU 1698592A SU 1698592 A SU1698592 A SU 1698592A SU 395082 A1 SU395082 A1 SU 395082A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- water
- yeast
- adenosine
- acidified
- added
- Prior art date
Links
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 5
- 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 description 4
- 239000000706 filtrate Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000026731 phosphorylation Effects 0.000 description 3
- 238000006366 phosphorylation reaction Methods 0.000 description 3
- 239000001226 triphosphate Substances 0.000 description 3
- 235000011178 triphosphate Nutrition 0.000 description 3
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 3
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229960005305 adenosine Drugs 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000002773 nucleotide Substances 0.000 description 2
- 125000003729 nucleotide group Chemical group 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 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 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 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 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 239000002777 nucleoside Substances 0.000 description 1
- 125000003835 nucleoside group Chemical group 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
Landscapes
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1698592A SU395082A1 (enrdf_load_stackoverflow) | 1971-09-14 | 1971-09-14 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU1698592A SU395082A1 (enrdf_load_stackoverflow) | 1971-09-14 | 1971-09-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU395082A1 true SU395082A1 (enrdf_load_stackoverflow) | 1973-08-28 |
Family
ID=20488341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1698592A SU395082A1 (enrdf_load_stackoverflow) | 1971-09-14 | 1971-09-14 |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU395082A1 (enrdf_load_stackoverflow) |
-
1971
- 1971-09-14 SU SU1698592A patent/SU395082A1/ru active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Avison | The synthesis of acyl phosphates in aqueous solution | |
| Reddy et al. | Primary sequence of U-1 nuclear ribonucleic acid of Novikoff hepatoma ascites cells | |
| Fuente et al. | Induced fit in yeast hexokinase | |
| US4804748A (en) | 7-deaza-2'-deoxyguanosine nucleotides | |
| Imazawa et al. | Facile synthesis of 2'-amino-2'-deoxyribofuranosylpurines | |
| Tazawa et al. | Conformation and interaction of dinucleoside mono-and diphosphates. 3. L-adenylyl-(3'-5')-L-adenosine and L-adenylyl-(2'-5')-L-adenosine | |
| Torres et al. | Regulation of skeletal muscle phosphorylase phosphatase activity. I. Kinetic properties of the active and inactive forms | |
| US2844514A (en) | Process for the production of nucleotides | |
| O'Brien | The synthesis of N-acetyl-α-and N-acetyl-β-D-glucosamine 1-phosphates (2-acetamido-2-deoxy-α-and β-D-glucose 1-phosphates) | |
| GB1300798A (en) | Preparation of cytidine diphosphate choline | |
| SU395082A1 (enrdf_load_stackoverflow) | ||
| US3120511A (en) | Production of a mixture of sodium salts of 5'-inosinic acid and 5'-guanylic acid | |
| Howard et al. | The anomeric specificity of yeast galactokinase | |
| GB1182328A (en) | Production of Guanosine-5'-Phosphate | |
| Prihar et al. | Chemical synthesis of β-L-fucopyranosyl phosphate and β-L-rhamnopyranosyl phosphate | |
| Chou et al. | A kinetic analysis of the phosphorolysis of oligonucleotides by polynucleotide phosphorylase | |
| Séquin et al. | Nucleosides and Nucleotides. Part 2: Synthesis of both anomers of 1‐(5′‐O‐phosphoryl‐2′‐deoxy‐D‐ribofuranosyl)‐2 (1H)‐pyridone [1] | |
| Eckstein et al. | Stereochemistry of the transesterification step of pancreatic ribonuclease | |
| Levene et al. | The ribosephosphoric acid from xanthylic acid | |
| Barker et al. | 747. Biosynthesis of polynucleotides. Part I. The mode of action of ribonuclease | |
| Bennett et al. | 2'-0-(α-Methoxyethyl) nucleoside 5'-diphosphates as single-addition substrates in the synthesis of specific oligoribonucleotides with polynucleotide phosphorylase | |
| Binkley | Organization of enzymes in the synthesis of peptides | |
| SU413188A1 (enrdf_load_stackoverflow) | ||
| Huang | Preparation of 5-Amino-1-β-ribosyl-4-imidazolecarboxamide-5'-phosphate and N-(5-Amino-1-β-D-ribosyl-4-imidazolecarbonyl)-L-aspartic Acid 5'-Phosphate | |
| SU722920A1 (ru) | Способ получени аденозин-5 -трифосфата |