ATE401407T1 - Verfahren zur herstellung von cytosin- nukleosidverbindungen - Google Patents
Verfahren zur herstellung von cytosin- nukleosidverbindungenInfo
- Publication number
- ATE401407T1 ATE401407T1 AT02253075T AT02253075T ATE401407T1 AT E401407 T1 ATE401407 T1 AT E401407T1 AT 02253075 T AT02253075 T AT 02253075T AT 02253075 T AT02253075 T AT 02253075T AT E401407 T1 ATE401407 T1 AT E401407T1
- Authority
- AT
- Austria
- Prior art keywords
- cytosine
- producing
- cytosine nucleoside
- nucleoside compounds
- product
- Prior art date
Links
- OPTASPLRGRRNAP-UHFFFAOYSA-N cytosine Natural products NC=1C=CNC(=O)N=1 OPTASPLRGRRNAP-UHFFFAOYSA-N 0.000 title abstract 7
- 229940104302 cytosine Drugs 0.000 title abstract 5
- -1 CYTOSINE NUCLEOSIDE COMPOUNDS Chemical class 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- 239000002777 nucleoside Substances 0.000 title abstract 3
- OQRXBXNATIHDQO-UHFFFAOYSA-N 6-chloropyridine-3,4-diamine Chemical compound NC1=CN=C(Cl)C=C1N OQRXBXNATIHDQO-UHFFFAOYSA-N 0.000 abstract 1
- 241000894006 Bacteria Species 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 102100036286 Purine nucleoside phosphorylase Human genes 0.000 abstract 1
- 239000006227 byproduct Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 108010009099 nucleoside phosphorylase Proteins 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 239000000758 substrate Substances 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
- C12P19/38—Nucleosides
-
- 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.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1077—Pentosyltransferases (2.4.2)
-
- 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
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/52—Genes encoding for enzymes or proenzymes
-
- 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.)
-
- 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
- C12P19/38—Nucleosides
- C12P19/385—Pyrimidine nucleosides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Molecular Biology (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Saccharide Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001134352 | 2001-05-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE401407T1 true ATE401407T1 (de) | 2008-08-15 |
Family
ID=34131298
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT02253075T ATE401407T1 (de) | 2001-05-01 | 2002-05-01 | Verfahren zur herstellung von cytosin- nukleosidverbindungen |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US6858721B2 (de) |
| EP (1) | EP1254959B1 (de) |
| KR (1) | KR100476294B1 (de) |
| CN (1) | CN100546997C (de) |
| AT (1) | ATE401407T1 (de) |
| BR (1) | BR0203343A (de) |
| CA (1) | CA2380804A1 (de) |
| DE (1) | DE60227595D1 (de) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60136209D1 (de) * | 2000-11-06 | 2008-11-27 | Mitsui Chemicals Inc | Verfahren zur herstellung einer nukleosidverbindung |
| CN103509837B (zh) * | 2012-06-28 | 2016-03-09 | 张金荣 | 一种酶法复合化学法制备卡培他滨中间体2’,3’-二-o-乙酰基-5’-脱氧-5-氟胞苷的方法 |
| CN103451255B (zh) * | 2013-03-28 | 2016-03-16 | 南京工业大学 | 次黄嘌呤核苷酸的生产方法 |
| EP2883959A1 (de) | 2013-12-13 | 2015-06-17 | Plasmia Biotech, S.L. | Enzymatische Herstellung von Cytosin-Nukleosidanaloga |
| US20160312261A1 (en) * | 2015-04-24 | 2016-10-27 | Plasmia Biotech, S.L. | Enzymatic production of cytosinic nucleoside analogues |
| CN105087515B (zh) * | 2015-09-10 | 2018-12-04 | 江南大学 | 一种嘌呤核苷磷酸化酶的制备方法及应用 |
| KR101877120B1 (ko) * | 2016-07-08 | 2018-07-11 | 에스티팜 주식회사 | 생물전환공정을 이용한 2'-데옥시시티딘의 제조방법 |
| CN108265095B (zh) * | 2017-12-13 | 2020-11-24 | 东莞理工学院 | 一种15n稳定性同位素标记5-甲基脱氧胞苷的制备方法 |
| CN114107413B (zh) * | 2021-11-03 | 2023-10-20 | 江苏香地化学有限公司 | 一种酶催化胞嘧啶生产胞苷的方法及应用 |
| CN117106680B (zh) * | 2022-05-17 | 2024-02-23 | 苏州华赛生物工程技术有限公司 | 一种生产胞嘧啶的重组微生物及方法 |
| CN115011653B (zh) * | 2022-07-12 | 2024-07-30 | 苏州华赛生物工程技术有限公司 | 一种生产2′-脱氧胞苷的重组微生物及方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5856779A (ja) | 1981-09-24 | 1983-04-04 | 高野 政晴 | 五節リンクロボツト |
| JPS61135597A (ja) * | 1984-12-06 | 1986-06-23 | Takeda Chem Ind Ltd | シチジンおよびデオキシシチジンの製造法 |
| JPH0763385B2 (ja) | 1987-07-17 | 1995-07-12 | 味の素株式会社 | チミジンの製造方法 |
| JPH0789948B2 (ja) | 1987-08-28 | 1995-10-04 | 味の素株式会社 | 2▲’▼−デオキシシチジンの製造方法 |
| AU631607B2 (en) * | 1989-02-28 | 1992-12-03 | Yamasa Shoyu Kabushiki Kaisha | Production of nucleoside |
| US5075225A (en) * | 1989-04-06 | 1991-12-24 | The Texas A&M University System | Process for the enzymatic synthesis of nucleosides |
| JPH03127986A (ja) | 1989-10-12 | 1991-05-31 | Takara Shuzo Co Ltd | 新規ヌクレオシドホスホリラーゼ |
| US5204466A (en) * | 1990-02-01 | 1993-04-20 | Emory University | Method and compositions for the synthesis of bch-189 and related compounds |
| JP3864357B2 (ja) | 1997-08-04 | 2006-12-27 | 有機合成薬品工業株式会社 | プリンヌクレオシド化合物の製造方法 |
| JP3928676B2 (ja) | 1997-11-14 | 2007-06-13 | 味の素株式会社 | 2’−デオキシアデノシン、2’−デオキシグアノシンの製造法 |
| KR20020006046A (ko) * | 1999-05-13 | 2002-01-18 | 사토 아키오 | 뉴클레오사이드화합물의 제조방법 |
| DE60042209D1 (de) | 1999-08-20 | 2009-06-25 | Pasteur Institut | Enzymatische synthese von deoxyribonucleotiden |
-
2002
- 2002-04-30 CA CA002380804A patent/CA2380804A1/en not_active Abandoned
- 2002-04-30 US US10/134,624 patent/US6858721B2/en not_active Expired - Lifetime
- 2002-05-01 KR KR10-2002-0023995A patent/KR100476294B1/ko not_active Expired - Lifetime
- 2002-05-01 DE DE60227595T patent/DE60227595D1/de not_active Expired - Lifetime
- 2002-05-01 EP EP02253075A patent/EP1254959B1/de not_active Expired - Lifetime
- 2002-05-01 AT AT02253075T patent/ATE401407T1/de not_active IP Right Cessation
- 2002-05-02 BR BR0203343-7A patent/BR0203343A/pt not_active IP Right Cessation
- 2002-05-08 CN CNB021193029A patent/CN100546997C/zh not_active Expired - Lifetime
-
2004
- 2004-10-19 US US10/967,239 patent/US7629457B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| KR20020085798A (ko) | 2002-11-16 |
| EP1254959A2 (de) | 2002-11-06 |
| US20050233420A1 (en) | 2005-10-20 |
| US7629457B2 (en) | 2009-12-08 |
| CN100546997C (zh) | 2009-10-07 |
| BR0203343A (pt) | 2003-06-10 |
| EP1254959B1 (de) | 2008-07-16 |
| EP1254959A3 (de) | 2003-07-09 |
| US6858721B2 (en) | 2005-02-22 |
| CN1392153A (zh) | 2003-01-22 |
| KR100476294B1 (ko) | 2005-03-16 |
| DE60227595D1 (de) | 2008-08-28 |
| US20030207405A1 (en) | 2003-11-06 |
| CA2380804A1 (en) | 2002-11-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |