ATE472606T1 - Biokatalytische herstellung von (meth- )acrylsäureestern - Google Patents

Biokatalytische herstellung von (meth- )acrylsäureestern

Info

Publication number: ATE472606T1
Authority: AT; Austria
Prior art keywords: meth; coa; acrylic acid; biocatalyst; acrylyl
Prior art date: 2005-09-19

Application number

AT06793437T

Other languages

English (en)

Inventor

Kenneth Charles Symes

Simon Andrew Collier

Yvonne Christine Armitage

Rajesh Mistry

Robert Baranyai

Original Assignee

Basf Se

Priority date (The priority date 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 date listed.)

2005-09-19

Filing date

2006-09-12

Publication date

2010-07-15

2006-09-12 Application filed by Basf Se filed Critical Basf Se

2010-07-15 Application granted granted Critical

2010-07-15 Publication of ATE472606T1 publication Critical patent/ATE472606T1/de

Links

CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 title abstract 3
230000002210 biocatalytic effect Effects 0.000 title abstract 2
102000004190 Enzymes Human genes 0.000 abstract 5
108090000790 Enzymes Proteins 0.000 abstract 5
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 3
239000011942 biocatalyst Substances 0.000 abstract 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
102000004357 Transferases Human genes 0.000 abstract 2
108090000992 Transferases Proteins 0.000 abstract 2
238000006243 chemical reaction Methods 0.000 abstract 2
230000000694 effects Effects 0.000 abstract 2
238000000034 method Methods 0.000 abstract 2
239000007858 starting material Substances 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
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 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
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
150000001298 alcohols Chemical class 0.000 abstract 1
230000015572 biosynthetic process Effects 0.000 abstract 1
239000003054 catalyst Substances 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
150000002148 esters Chemical class 0.000 abstract 1
125000002524 organometallic group Chemical group 0.000 abstract 1
150000003839 salts Chemical class 0.000 abstract 1
239000000126 substance Substances 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Zoology (AREA)
Life Sciences & Earth Sciences (AREA)
Wood Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Microbiology (AREA)
General Chemical & Material Sciences (AREA)
Biotechnology (AREA)
Health & Medical Sciences (AREA)
Biochemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Enzymes And Modification Thereof (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

AT06793437T 2005-09-19 2006-09-12 Biokatalytische herstellung von (meth- )acrylsäureestern ATE472606T1 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP05108603		2005-09-19
PCT/EP2006/066260 WO2007039415A1 (en)	2005-09-19	2006-09-12	Biocatalytic manufacturing of (meth)acrylic esters

Publications (1)

Publication Number	Publication Date
ATE472606T1 true ATE472606T1 (de)	2010-07-15

Family

ID=36655084

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
AT06793437T ATE472606T1 (de)	2005-09-19	2006-09-12	Biokatalytische herstellung von (meth- )acrylsäureestern

Country Status (9)

Country	Link
US (1)	US7901915B2 (de)
EP (1)	EP1926822B1 (de)
CN (1)	CN101268196B (de)
AT (1)	ATE472606T1 (de)
AU (1)	AU2006298893B2 (de)
BR (1)	BRPI0616207A2 (de)
CA (1)	CA2622537C (de)
DE (1)	DE602006015208D1 (de)
WO (1)	WO2007039415A1 (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DK2262901T3 (en)	2008-03-05	2019-01-21	Genomatica Inc	ORGANISMS PRODUCING PRIMARY ALCOHOL
WO2009135074A2 (en)	2008-05-01	2009-11-05	Genomatica, Inc.	Microorganisms for the production of methacrylic acid
DE102009003035A1 (de) *	2009-05-12	2010-11-18	Basf Se	Verfahren zur Herstellung von urethangruppenhaltigen (Meth)acrylsäureestern
US8445244B2 (en) *	2010-02-23	2013-05-21	Genomatica, Inc.	Methods for increasing product yields
BR112013025226A2 (pt) *	2011-04-01	2018-09-11	Genomatica Inc	micro-organismos para produzir ácido metacrílico e ésteres de metacrilato e métodos relacionados a eles
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
US11814664B2 (en)	2013-05-24	2023-11-14	Genomatica, Inc.	Microorganisms and methods for producing (3R)-hydroxybutyl (3R)-hydroxybutyrate
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
WO2016034691A1 (en) *	2014-09-03	2016-03-10	Syngip Bv	Recombinant microorganism producing alkenes from acetyl-coa
US11913054B2 (en) *	2016-03-30	2024-02-27	Basf Se	Fermentative production of n-butylacrylate using alcohol acyl transferase enzymes
CN111269848B (zh) *	2019-12-30	2022-03-18	浙江工业大学	赤红球菌jj-3及其在降解丙烯酸中的应用
CN111041015B (zh) *	2019-12-31	2022-03-18	浙江工业大学	一种高温下制备(r)-(+)-n-乙酰基-1-甲基-3-苯丙胺的方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR970009154B1 (ko)	1994-02-26	1997-06-07	주식회사 유공	효소에 의한 기상(氣狀) 에스테르화 반응
FR2757179B1 (fr)	1996-12-13	1999-01-08	Coatex Sa	Procede de preparation d'amides de l'acide acrylique ou methacrylique
WO2000071738A1 (en)	1999-05-21	2000-11-30	Cargill Dow Llc	Methods and materials for the synthesis of organic products
BR0115877A (pt)	2000-11-20	2003-10-07	Cargill Inc	ácido 3-hidroxipropiÈnico e outros compostos orgánicos
BR0115558A (pt)	2000-11-22	2004-08-17	Cargill Dow Polymers Llc	ácido nucleico isolado, construção de expressão recombinante, célula de levedura transformada com a construção de expressão recombinante, e, método para produzir ácido lático

2006
- 2006-09-12 DE DE602006015208T patent/DE602006015208D1/de active Active
- 2006-09-12 WO PCT/EP2006/066260 patent/WO2007039415A1/en not_active Ceased
- 2006-09-12 EP EP06793437A patent/EP1926822B1/de not_active Not-in-force
- 2006-09-12 US US11/991,446 patent/US7901915B2/en not_active Expired - Fee Related
- 2006-09-12 BR BRPI0616207-0A patent/BRPI0616207A2/pt active Search and Examination
- 2006-09-12 AU AU2006298893A patent/AU2006298893B2/en not_active Ceased
- 2006-09-12 CA CA2622537A patent/CA2622537C/en not_active Expired - Fee Related
- 2006-09-12 CN CN200680034257.2A patent/CN101268196B/zh not_active Expired - Fee Related
- 2006-09-12 AT AT06793437T patent/ATE472606T1/de not_active IP Right Cessation

Also Published As

Publication number	Publication date
CA2622537A1 (en)	2007-04-12
AU2006298893B2 (en)	2011-08-04
CA2622537C (en)	2013-12-10
CN101268196A (zh)	2008-09-17
US20090130729A1 (en)	2009-05-21
EP1926822B1 (de)	2010-06-30
CN101268196B (zh)	2014-03-12
BRPI0616207A2 (pt)	2011-06-14
AU2006298893A1 (en)	2007-04-12
WO2007039415A1 (en)	2007-04-12
DE602006015208D1 (de)	2010-08-12
EP1926822A1 (de)	2008-06-04
US7901915B2 (en)	2011-03-08

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Legal Events

Date	Code	Title	Description
2010-12-15	RER	Ceased as to paragraph 5 lit. 3 law introducing patent treaties