ATE451467T1 - Biokatalytische herstellung von (meth)acyrlylcholin oder 2-(n,n- dimethylamino)ethyl-(meth)acrylat - Google Patents
Biokatalytische herstellung von (meth)acyrlylcholin oder 2-(n,n- dimethylamino)ethyl-(meth)acrylatInfo
- Publication number
- ATE451467T1 ATE451467T1 AT05716966T AT05716966T ATE451467T1 AT E451467 T1 ATE451467 T1 AT E451467T1 AT 05716966 T AT05716966 T AT 05716966T AT 05716966 T AT05716966 T AT 05716966T AT E451467 T1 ATE451467 T1 AT E451467T1
- Authority
- AT
- Austria
- Prior art keywords
- meth
- dimethylamino
- acrylate
- coa
- acyrlylcholine
- Prior art date
Links
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 title abstract 2
- 230000002210 biocatalytic effect Effects 0.000 title abstract 2
- 108090000790 Enzymes Proteins 0.000 abstract 2
- 102000004190 Enzymes Human genes 0.000 abstract 2
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 abstract 2
- POODSGUMUCVRTR-IEXPHMLFSA-N acryloyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C=C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 POODSGUMUCVRTR-IEXPHMLFSA-N 0.000 abstract 2
- 239000011942 biocatalyst Substances 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- NPALUEYCDZWBOV-NDZSKPAWSA-N methacrylyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C(=C)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 NPALUEYCDZWBOV-NDZSKPAWSA-N 0.000 abstract 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 108010058699 Choline O-acetyltransferase Proteins 0.000 abstract 1
- 102100023460 Choline O-acetyltransferase Human genes 0.000 abstract 1
- RGJOEKWQDUBAIZ-IBOSZNHHSA-N CoASH Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCS)O[C@H]1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-IBOSZNHHSA-N 0.000 abstract 1
- 102000005870 Coenzyme A Ligases Human genes 0.000 abstract 1
- 108010011449 Long-chain-fatty-acid-CoA ligase Proteins 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 abstract 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 abstract 1
- ZSLZBFCDCINBPY-ZSJPKINUSA-N acetyl-CoA Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@@H](O)C(=O)NCCC(=O)NCCSC(=O)C)O[C@H]1N1C2=NC=NC(N)=C2N=C1 ZSLZBFCDCINBPY-ZSJPKINUSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229960001231 choline Drugs 0.000 abstract 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 1
- RGJOEKWQDUBAIZ-UHFFFAOYSA-N coenzime A Natural products OC1C(OP(O)(O)=O)C(COP(O)(=O)OP(O)(=O)OCC(C)(C)C(O)C(=O)NCCC(=O)NCCS)OC1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005516 coenzyme A Substances 0.000 abstract 1
- 229940093530 coenzyme a Drugs 0.000 abstract 1
- KDTSHFARGAKYJN-UHFFFAOYSA-N dephosphocoenzyme A Natural products OC1C(O)C(COP(O)(=O)OP(O)(=O)OCC(C)(C)C(O)C(=O)NCCC(=O)NCCS)OC1N1C2=NC=NC(N)=C2N=C1 KDTSHFARGAKYJN-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229940055076 parasympathomimetics choline ester Drugs 0.000 abstract 1
- 150000003248 quinolines Chemical class 0.000 abstract 1
- 238000003786 synthesis reaction Methods 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/001—Amines; Imines
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0406217.0A GB0406217D0 (en) | 2004-03-19 | 2004-03-19 | Biocatalytic manufacturing of (meth)acrylyicholine or 2- (N, N-dimethylamino) ethyl (meth)acrylate |
| PCT/EP2005/051046 WO2005090586A1 (en) | 2004-03-19 | 2005-03-09 | Biocatalytic manufacturing of (meth)acrylylcholine or 2-(n,n-dimethylamino)ethyl (meth)acrylate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE451467T1 true ATE451467T1 (de) | 2009-12-15 |
Family
ID=32118033
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT05716966T ATE451467T1 (de) | 2004-03-19 | 2005-03-09 | Biokatalytische herstellung von (meth)acyrlylcholin oder 2-(n,n- dimethylamino)ethyl-(meth)acrylat |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7754455B2 (de) |
| EP (1) | EP1725671B1 (de) |
| CN (1) | CN1934262B (de) |
| AT (1) | ATE451467T1 (de) |
| AU (1) | AU2005224378B2 (de) |
| BR (1) | BRPI0508971A (de) |
| CA (1) | CA2558189C (de) |
| DE (1) | DE602005018176D1 (de) |
| DK (1) | DK1725671T3 (de) |
| GB (1) | GB0406217D0 (de) |
| WO (1) | WO2005090586A1 (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8625565B2 (en) | 2009-10-06 | 2014-01-07 | Intel Corporation | Millimeter-wave communication station and method for multiple-access beamforming in a millimeter-wave communication network |
| BR112015004355A8 (pt) * | 2012-09-10 | 2018-01-02 | Mitsubishi Rayon Co | Método para produção de ácido metacrílico e/ou éster do mesmo |
| ES2689477T3 (es) * | 2012-09-10 | 2018-11-14 | Mitsubishi Chemical Corporation | Método para producir éster del ácido metacrílico |
| JP6296512B2 (ja) * | 2014-03-07 | 2018-03-20 | 公立大学法人 富山県立大学 | メタクリル酸エステルの製造方法および新規メタクリル酸エステル合成酵素 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0479889A (ja) * | 1990-07-20 | 1992-03-13 | Mitsui Toatsu Chem Inc | アクリル酸またはメタクリル酸のアルキルアミノアルキルエステルの製造方法 |
-
2004
- 2004-03-19 GB GBGB0406217.0A patent/GB0406217D0/en not_active Ceased
-
2005
- 2005-03-09 DE DE602005018176T patent/DE602005018176D1/de not_active Expired - Lifetime
- 2005-03-09 CN CN2005800087381A patent/CN1934262B/zh not_active Expired - Fee Related
- 2005-03-09 BR BRPI0508971-9A patent/BRPI0508971A/pt not_active Application Discontinuation
- 2005-03-09 DK DK05716966.6T patent/DK1725671T3/da active
- 2005-03-09 US US10/591,775 patent/US7754455B2/en not_active Expired - Fee Related
- 2005-03-09 CA CA2558189A patent/CA2558189C/en not_active Expired - Fee Related
- 2005-03-09 WO PCT/EP2005/051046 patent/WO2005090586A1/en not_active Ceased
- 2005-03-09 AT AT05716966T patent/ATE451467T1/de not_active IP Right Cessation
- 2005-03-09 EP EP05716966A patent/EP1725671B1/de not_active Expired - Lifetime
- 2005-03-09 AU AU2005224378A patent/AU2005224378B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0508971A (pt) | 2007-08-28 |
| EP1725671B1 (de) | 2009-12-09 |
| CA2558189C (en) | 2013-07-02 |
| DE602005018176D1 (de) | 2010-01-21 |
| US7754455B2 (en) | 2010-07-13 |
| AU2005224378A1 (en) | 2005-09-29 |
| CN1934262B (zh) | 2012-01-11 |
| WO2005090586A1 (en) | 2005-09-29 |
| EP1725671A1 (de) | 2006-11-29 |
| AU2005224378B2 (en) | 2010-05-27 |
| US20070238156A1 (en) | 2007-10-11 |
| CN1934262A (zh) | 2007-03-21 |
| GB0406217D0 (en) | 2004-04-21 |
| CA2558189A1 (en) | 2005-09-29 |
| DK1725671T3 (da) | 2010-04-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |