JP5755884B2 - 第一級アルコールを産生する生物 - Google Patents
第一級アルコールを産生する生物 Download PDFInfo
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- JP5755884B2 JP5755884B2 JP2010549897A JP2010549897A JP5755884B2 JP 5755884 B2 JP5755884 B2 JP 5755884B2 JP 2010549897 A JP2010549897 A JP 2010549897A JP 2010549897 A JP2010549897 A JP 2010549897A JP 5755884 B2 JP5755884 B2 JP 5755884B2
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Families Citing this family (81)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8110670B2 (en) | 2006-05-19 | 2012-02-07 | Ls9, Inc. | Enhanced production of fatty acid derivatives |
| US20100242345A1 (en) | 2006-05-19 | 2010-09-30 | LS9, Inc | Production of fatty acids & derivatives thereof |
| US9080187B2 (en) * | 2007-05-17 | 2015-07-14 | The Board Of Trustees Of The University Of Illinois | Methods and compositions for producing solvents |
| CA2712779C (en) | 2008-01-22 | 2021-03-16 | Genomatica, Inc. | Methods and organisms for utilizing synthesis gas or other gaseous carbon sources and methanol |
| CA3081506A1 (en) | 2008-03-05 | 2009-09-11 | Genomatica, Inc. | Long chain alcohol-producing organisms |
| MX350285B (es) | 2008-05-16 | 2017-09-04 | Reg Life Sciences Llc | Métodos y composiciones para producir hidrocarburos. |
| US8129154B2 (en) | 2008-06-17 | 2012-03-06 | Genomatica, Inc. | Microorganisms and methods for the biosynthesis of fumarate, malate, and acrylate |
| US8647642B2 (en) | 2008-09-18 | 2014-02-11 | Aviex Technologies, Llc | Live bacterial vaccines resistant to carbon dioxide (CO2), acidic PH and/or osmolarity for viral infection prophylaxis or treatment |
| ES2550467T3 (es) | 2008-10-07 | 2015-11-10 | REG Life Sciences, LLC | Métodos y composiciones para producir aldehídos grasos |
| ES2505115T3 (es) * | 2008-10-28 | 2014-10-09 | Ls9, Inc. | Métodos para producir alcoholes grasos |
| WO2010057022A1 (en) * | 2008-11-14 | 2010-05-20 | Genomatica, Inc. | Microorganisms for the production of methyl ethyl ketone and 2-butanol |
| EP2376619A4 (en) * | 2008-12-15 | 2012-07-04 | Greenlight Biosciences Inc | METHODS FOR CONTROLLING FLOWS IN METABOLIC PATHWAYS |
| WO2010071697A1 (en) | 2008-12-16 | 2010-06-24 | Genomatica, Inc. | Microorganisms and methods for conversion of syngas and other carbon sources to useful products |
| CN102459622B (zh) | 2009-04-27 | 2020-08-18 | 基因组股份公司 | 脂肪酸酯的产生 |
| BRPI1015461A2 (pt) * | 2009-04-29 | 2015-09-01 | Eudes De Crecy | Organismo evolucionariamente modificado, método de produção do organismo e de produto final, fábrica de biocombustível, método para produzir um produto de biocombustível. |
| WO2010144746A2 (en) * | 2009-06-10 | 2010-12-16 | Genomatica, Inc. | Microorganisms and methods for carbon-efficient biosynthesis of mek and 2-butanol |
| EP2277989A1 (en) | 2009-07-24 | 2011-01-26 | Technische Universiteit Delft | Fermentative glycerol-free ethanol production |
| CN109136161A (zh) | 2009-12-10 | 2019-01-04 | 基因组股份公司 | 合成气或其他气态碳源和甲醇转化为1,3-丁二醇的方法和有机体 |
| US8637286B2 (en) | 2010-02-23 | 2014-01-28 | Genomatica, Inc. | Methods for increasing product yields |
| EP2546331B1 (en) | 2010-03-09 | 2019-07-03 | Mitsui Chemicals, Inc. | Highly productive isopropyl alcohol-producing bacterium |
| US20110250663A1 (en) | 2010-04-08 | 2011-10-13 | Ls9, Inc. | Methods and compositions related to fatty alcohol biosynthetic enzymes |
| US20110269201A1 (en) * | 2010-04-30 | 2011-11-03 | Qteros, Inc. | Redirected bioenergetics in recombinant cellulolytic clostridium microorganisms |
| BR112012028290B1 (pt) | 2010-05-05 | 2021-02-02 | Lallemand Hungary Liquidity Management Llc. | levedura recombinante, processo para converter biomassa em etanol e meio de fermentação compreendendo dita levedura |
| CA2797786C (en) | 2010-05-07 | 2020-09-22 | Greenlight Biosciences, Inc. | Methods for control of flux in metabolic pathways through enzyme relocation |
| JP5852648B2 (ja) | 2010-07-15 | 2016-02-03 | ザ プロクター アンド ギャンブルカンパニー | 鎖端付近分枝型化合物(nearterminal−branchedcompound)を含む組成物及びその製造方法 |
| CA2807561C (en) | 2010-08-06 | 2022-04-12 | Mascoma Corporation | Production of malonyl-coa derived products via anaerobic pathways |
| ES2839424T3 (es) | 2010-08-31 | 2021-07-05 | Greenlight Biosciences Inc | Métodos para control de flujo en vías metabólicas mediante manipulación de proteasas |
| EP2655612B1 (en) * | 2010-12-23 | 2017-07-19 | Shell Internationale Research Maatschappij B.V. | Gene disruptants producing fatty acyl-coa derivatives |
| EP2673369B1 (en) | 2011-02-07 | 2017-04-05 | William Marsh Rice University | Reverse beta oxidation pathway |
| CA2827658A1 (en) | 2011-02-17 | 2012-08-23 | The Procter & Gamble Company | Bio-based linear alkylphenyl sulfonates |
| JP5815750B2 (ja) | 2011-02-17 | 2015-11-17 | ザ プロクター アンド ギャンブルカンパニー | C10〜c13アルキルフェニルスルホネートの混合物を含む組成物 |
| WO2012118933A1 (en) * | 2011-03-01 | 2012-09-07 | Rutgers, The State University Of New Jersey | Genetically engineered microbes and uses thereof |
| CN102174419B (zh) * | 2011-03-24 | 2013-04-03 | 南京工业大学 | 一株米根霉菌株及其诱变筛选方法和发酵生产富马酸的方法 |
| AU2012273005A1 (en) * | 2011-06-22 | 2013-05-09 | Genomatica, Inc. | Microorganism for producing primary alcohols and related compounds and methods related thereto |
| WO2013003432A1 (en) * | 2011-06-29 | 2013-01-03 | Genomatica, Inc. | Microorganisms for producing succinate and methods related thereto |
| MX348706B (es) | 2011-07-12 | 2017-06-26 | Scientist Of Fortune Sa | Microorganismo recombinante para la produccion de metabolitos utiles. |
| CA2880785A1 (en) | 2011-08-03 | 2013-02-07 | REG Life Sciences, LLC | Production of fatty acids and derivatives thereof having improved aliphatic chain length and saturation characteristics |
| CN103998600A (zh) | 2011-09-07 | 2014-08-20 | 威廉马什莱斯大学 | 通过反向脂肪酸氧化的官能化羧酸和醇 |
| WO2013036787A2 (en) | 2011-09-09 | 2013-03-14 | Greenlight Biosciences, Inc. | Cell-free preparation of carbapenems |
| DE102012207921A1 (de) | 2012-05-11 | 2013-11-14 | Evonik Industries Ag | Mehrstufiges Syntheseverfahren mit Synthesegas |
| KR101464656B1 (ko) | 2012-06-15 | 2014-12-02 | 한국생명공학연구원 | 발효산물 고생성능을 가지는 변이 미생물 및 이를 이용한 발효산물의 제조방법 |
| WO2014004616A2 (en) * | 2012-06-26 | 2014-01-03 | Gevo, Inc. | Engineered yeast with improved growth under low aeration |
| WO2014016328A1 (en) * | 2012-07-25 | 2014-01-30 | Total Marketing Services | Genetically engineered micro-organisms for production of fatty acids |
| US20140051136A1 (en) | 2012-08-10 | 2014-02-20 | Opx Biotechnologies, Inc. | Micoorganisms and Methods for the Production of Fatty Acids and Fatty Acid Derived Products |
| EP2906705A4 (en) * | 2012-10-15 | 2016-09-07 | Genomatica Inc | MICRO-ORGANISMS AND METHOD FOR PRODUCING FAT-ALCOHOLS OF SPECIFIC LENGTH AND RELATED COMPOUNDS |
| JP2016504034A (ja) | 2012-12-21 | 2016-02-12 | グリーンライト バイオサイエンシーズ インコーポレーテッドGreenlight Biosciences,Inc. | メタンを燃料、ピルビン酸またはイソブタノールに変換する無細胞システム |
| JP2014193153A (ja) * | 2013-02-28 | 2014-10-09 | Euglena Co Ltd | ユーグレナへの遺伝子導入方法 |
| BR112015020827A2 (pt) * | 2013-02-28 | 2017-10-10 | Euglena Co Ltd | método para a introdução de gene em euglena, e transformante do mesmo |
| US9267158B2 (en) | 2013-03-14 | 2016-02-23 | Intrexon Corporation | Biological production of multi-carbon compounds from methane |
| WO2014146026A1 (en) | 2013-03-15 | 2014-09-18 | Opx Biotechnologies, Inc. | Bioproduction of chemicals |
| EP2971021A4 (en) | 2013-03-15 | 2016-12-21 | Genomatica Inc | MICROORGANISMS AND METHOD FOR THE PRODUCTION OF BUTADIENE AND RELATED COMPOUNDS BY FORMATASSIMILATION |
| US11408013B2 (en) | 2013-07-19 | 2022-08-09 | Cargill, Incorporated | Microorganisms and methods for the production of fatty acids and fatty acid derived products |
| WO2015010103A2 (en) | 2013-07-19 | 2015-01-22 | Opx Biotechnologies, Inc. | Microorganisms and methods for the production of fatty acids and fatty acid derived products |
| SG11201600898YA (en) | 2013-08-05 | 2016-03-30 | Greenlight Biosciences Inc | Engineered proteins with a protease cleavage site |
| CN103571764B (zh) * | 2013-08-26 | 2015-06-10 | 天津科技大学 | 一种高产中链脂肪酸乙酯的酿酒酵母工程菌及其构建方法 |
| WO2015057154A2 (en) * | 2013-10-18 | 2015-04-23 | Biopetrolia Ab | ENGINEERING OF ACETYL-CoA METABOLISM IN YEAST |
| EP4296364B1 (en) | 2013-12-03 | 2025-12-03 | Genomatica, Inc. | Microorganisms and methods for improving product yields on methanol using acetyl-coa synthesis |
| EP3087174B1 (en) | 2013-12-27 | 2020-05-13 | Genomatica, Inc. | Methods and organisms with increased carbon flux efficiencies |
| JP6034332B2 (ja) | 2014-05-30 | 2016-11-30 | トヨタ自動車株式会社 | 組換え微生物及び当該組換え微生物を用いた物質製造方法 |
| JP6189793B2 (ja) | 2014-05-30 | 2017-08-30 | トヨタ自動車株式会社 | 組換え微生物及び当該組換え微生物を用いた物質製造方法 |
| EP3470840B1 (en) | 2014-06-12 | 2021-03-03 | Hyglos Invest GmbH | Unmasking endotoxins in solution |
| ES2942896T3 (es) | 2014-06-12 | 2023-06-07 | Biomerieux Deutschland Gmbh | Desenmascaramiento de endotoxinas en disolución |
| EP2993228B1 (en) | 2014-09-02 | 2019-10-09 | Cargill, Incorporated | Production of fatty acid esters |
| CN120624582A (zh) | 2014-09-18 | 2025-09-12 | 基因组股份公司 | 具有提高的能源效率的非天然微生物 |
| EP3277808A4 (en) | 2015-03-30 | 2019-05-22 | Greenlight Biosciences, Inc. | ACELLULAR PRODUCTION OF RIBONUCLEIC ACID |
| EP3283615A4 (en) * | 2015-04-15 | 2018-09-05 | William Marsh Rice University | Iterative platform for the synthesis of alpha functionalized products |
| US11319562B2 (en) | 2015-04-15 | 2022-05-03 | Ramon Gonzalez | Modified fatty acid biosynthesis with ACP-dependent thiolases |
| US10676723B2 (en) | 2015-05-11 | 2020-06-09 | David Gordon Bermudes | Chimeric protein toxins for expression by therapeutic bacteria |
| CN105331647B (zh) * | 2015-07-03 | 2019-02-22 | 赣南师范大学 | 一种微生物体内合成脂肪醇乙酸酯的方法 |
| US10301653B2 (en) * | 2015-07-06 | 2019-05-28 | Wisconsin Alumni Research Foundation | Microorganisms that co-consume glucose with non-glucose carbohydrates and methods of use |
| CN115322261A (zh) | 2015-10-30 | 2022-11-11 | 基因组股份公司 | 甲醇脱氢酶融合蛋白 |
| RU2018138975A (ru) | 2016-04-06 | 2020-05-12 | Гринлайт Байосайенсис, Инк. | Бесклеточная продукция рибонуклеиновой кислоты |
| US11129906B1 (en) | 2016-12-07 | 2021-09-28 | David Gordon Bermudes | Chimeric protein toxins for expression by therapeutic bacteria |
| US11180535B1 (en) | 2016-12-07 | 2021-11-23 | David Gordon Bermudes | Saccharide binding, tumor penetration, and cytotoxic antitumor chimeric peptides from therapeutic bacteria |
| WO2018129275A1 (en) | 2017-01-06 | 2018-07-12 | Greenlight Biosciences, Inc. | Cell-free production of sugars |
| CN110494566A (zh) | 2017-02-02 | 2019-11-22 | 嘉吉公司 | 产生c6-c10脂肪酸衍生物的经遗传修饰的细胞 |
| WO2019075167A1 (en) | 2017-10-11 | 2019-04-18 | Greenlight Biosciences, Inc. | METHODS AND COMPOSITIONS FOR THE PRODUCTION OF NUCLEOSIDE TRIPHOSPHATE AND RIBONUCLEIC ACID |
| US20210079334A1 (en) | 2018-01-30 | 2021-03-18 | Genomatica, Inc. | Fermentation systems and methods with substantially uniform volumetric uptake rate of a reactive gaseous component |
| US11541105B2 (en) | 2018-06-01 | 2023-01-03 | The Research Foundation For The State University Of New York | Compositions and methods for disrupting biofilm formation and maintenance |
| CA3103377A1 (en) | 2018-06-26 | 2020-01-02 | Genomatica, Inc. | Engineered microorganisms with g3p---> 3pg enzyme and/or fructose-1,6-bisphosphatase including those having synthetic or enhanced methylotrophy |
| WO2023178261A1 (en) * | 2022-03-16 | 2023-09-21 | Genomatica, Inc. | Microbial production of z3-hexenol, z3-hexenal and z3-hexenyl acetate |
Family Cites Families (180)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3513209A (en) * | 1968-08-19 | 1970-05-19 | Du Pont | Method of making 1,4-cyclohexadiene |
| US4076948A (en) * | 1968-10-10 | 1978-02-28 | El Paso Products Company | Process for treatment of adipic acid mother liquor |
| GB1230276A (enExample) | 1968-12-09 | 1971-04-28 | ||
| US3965182A (en) * | 1969-10-02 | 1976-06-22 | Ethyl Corporation | Preparation of aniline from phenol and ammonia |
| JPS506776Y1 (enExample) | 1969-12-27 | 1975-02-26 | ||
| JPS4831084B1 (enExample) | 1970-09-04 | 1973-09-26 | ||
| GB1344557A (en) | 1972-06-23 | 1974-01-23 | Mitsubishi Petrochemical Co | Process for preparing 1,4-butanediol |
| JPS506776A (enExample) | 1973-05-28 | 1975-01-23 | ||
| DE2455617C3 (de) * | 1974-11-23 | 1982-03-18 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von Butandiol und/oder Tetrahydrofuran über die Zwischenstufe des γ-Butyrolactons |
| DE2501499A1 (de) | 1975-01-16 | 1976-07-22 | Hoechst Ag | Verfahren zur herstellung von butandiol-(1.4) |
| US4344002A (en) | 1978-02-22 | 1982-08-10 | Supertex, Inc. | Detection circuit and structure therefor |
| US4301077A (en) * | 1980-12-22 | 1981-11-17 | Standard Oil Company | Process for the manufacture of 1-4-butanediol and tetrahydrofuran |
| IT1190783B (it) | 1981-04-29 | 1988-02-24 | Davy Mckee Oil & Chem | Processo per l'idrogenolisi di esteri di acidi carbossilici |
| US4652685A (en) * | 1985-11-15 | 1987-03-24 | General Electric Company | Hydrogenation of lactones to glycols |
| US5143834A (en) * | 1986-06-11 | 1992-09-01 | Glassner David A | Process for the production and purification of succinic acid |
| US5168055A (en) * | 1986-06-11 | 1992-12-01 | Rathin Datta | Fermentation and purification process for succinic acid |
| ES2036188T3 (es) * | 1986-06-11 | 1993-05-16 | Michigan Biotechnology Institute | Un procedimiento para la produccion de acido succinico por fermentacion anaerobia. |
| US5182199A (en) * | 1987-05-27 | 1993-01-26 | Hartley Brian S | Thermophilic ethanol production in a two-stage closed system |
| WO1989010410A1 (fr) * | 1988-04-27 | 1989-11-02 | Daicel Chemical Industries, Ltd. | Procede de preparation de 1,3-butanediol optiquement actif |
| DE69020555T2 (de) * | 1989-04-27 | 1995-11-02 | Biocontrol Systems Inc | Fällungstest für mikroorganismen. |
| US5192673A (en) * | 1990-04-30 | 1993-03-09 | Michigan Biotechnology Institute | Mutant strain of C. acetobutylicum and process for making butanol |
| US5079143A (en) * | 1990-05-02 | 1992-01-07 | The Upjohn Company | Method of indentifying compounds useful as antiparasitic drugs |
| DE69132472T2 (de) | 1990-10-15 | 2001-03-15 | Daicel Chemical Industries, Ltd. | Verfahren zur Herstellung von optisch aktivem 1,3-Butandiol |
| US5173429A (en) * | 1990-11-09 | 1992-12-22 | The Board Of Trustees Of The University Of Arkansas | Clostridiumm ljungdahlii, an anaerobic ethanol and acetate producing microorganism |
| IL100572A (en) | 1991-01-03 | 1997-01-10 | Lepetit Spa | Amides of antibiotic ge 2270 factors their preparation and pharmaceutical compositions containing them |
| US5416020A (en) * | 1992-09-29 | 1995-05-16 | Bio-Technical Resources | Lactobacillus delbrueckii ssp. bulgaricus strain and fermentation process for producing L-(+)-lactic acid |
| US5807722A (en) * | 1992-10-30 | 1998-09-15 | Bioengineering Resources, Inc. | Biological production of acetic acid from waste gases with Clostridium ljungdahlii |
| US6136577A (en) * | 1992-10-30 | 2000-10-24 | Bioengineering Resources, Inc. | Biological production of ethanol from waste gases with Clostridium ljungdahlii |
| FR2702492B1 (fr) * | 1993-03-12 | 1995-05-24 | Rhone Poulenc Chimie | Procédé de production par fermentation d'acide itaconique. |
| US5487987A (en) * | 1993-09-16 | 1996-01-30 | Purdue Research Foundation | Synthesis of adipic acid from biomass-derived carbon sources |
| US5521075A (en) | 1994-12-19 | 1996-05-28 | Michigan Biotechnology Institute | Method for making succinic acid, anaerobiospirillum succiniciproducens variants for use in process and methods for obtaining variants |
| US5504004A (en) * | 1994-12-20 | 1996-04-02 | Michigan Biotechnology Institute | Process for making succinic acid, microorganisms for use in the process and methods of obtaining the microorganisms |
| US5700934A (en) * | 1995-03-01 | 1997-12-23 | Dsm N.V. | Process for the preparation of epsilon-caprolactam and epsilon-caprolactam precursors |
| US5478952A (en) * | 1995-03-03 | 1995-12-26 | E. I. Du Pont De Nemours And Company | Ru,Re/carbon catalyst for hydrogenation in aqueous solution |
| US5863782A (en) | 1995-04-19 | 1999-01-26 | Women's And Children's Hospital | Synthetic mammalian sulphamidase and genetic sequences encoding same |
| US5686276A (en) * | 1995-05-12 | 1997-11-11 | E. I. Du Pont De Nemours And Company | Bioconversion of a fermentable carbon source to 1,3-propanediol by a single microorganism |
| FR2736927B1 (fr) * | 1995-07-18 | 1997-10-17 | Rhone Poulenc Fibres & Polymer | Enzymes a activite amidase, outils genetiques et microorganismes hotes permettant leur obtention et procede d'hydrolyse mettant en oeuvre lesdites enzymes |
| US5573931A (en) * | 1995-08-28 | 1996-11-12 | Michigan Biotechnology Institute | Method for making succinic acid, bacterial variants for use in the process, and methods for obtaining variants |
| US5869301A (en) * | 1995-11-02 | 1999-02-09 | Lockhead Martin Energy Research Corporation | Method for the production of dicarboxylic acids |
| US5770435A (en) * | 1995-11-02 | 1998-06-23 | University Of Chicago | Mutant E. coli strain with increased succinic acid production |
| IL125910A0 (en) * | 1996-02-27 | 1999-04-11 | Univ Michigan State | Cloning and expression of the gene encoding thermoanaerobacter ethanolicus 39e secondary-alcohol dehydrogenase and enzyme biochemical characterization |
| US5958745A (en) * | 1996-03-13 | 1999-09-28 | Monsanto Company | Methods of optimizing substrate pools and biosynthesis of poly-β-hydroxybutyrate-co-poly-β-hydroxyvalerate in bacteria and plants |
| JP4101295B2 (ja) | 1996-07-01 | 2008-06-18 | バイオエンジニアリング・リソーシズ・インコーポレーテツド | 廃ガスからの酢酸の生物学的生産 |
| KR100459818B1 (ko) * | 1996-09-02 | 2004-12-03 | 이. 아이. 두퐁 드 느무르 앤드 컴퍼니 | ε-카프로락탐의 제조방법 |
| WO1998036078A1 (en) * | 1997-02-13 | 1998-08-20 | James Madison University | Methods of making polyhydroxyalkanoates comprising 4-hydroxybutyrate monomer units |
| US6274790B1 (en) * | 1997-04-14 | 2001-08-14 | The University Of British Columbia | Nucleic acids encoding a plant enzyme involved in very long chain fatty acid synthesis |
| KR19990013007A (ko) * | 1997-07-31 | 1999-02-25 | 박원훈 | 형질전환된 대장균 ss373(kctc 8818p)과 이를 이용한숙신산의 생산방법 |
| JPH11103863A (ja) * | 1997-10-08 | 1999-04-20 | Nippon Shokubai Co Ltd | マレイン酸異性化酵素遺伝子 |
| US6280986B1 (en) * | 1997-12-01 | 2001-08-28 | The United States Of America As Represented By The Secretary Of Agriculture | Stabilization of pet operon plasmids and ethanol production in bacterial strains lacking lactate dehydrogenase and pyruvate formate lyase activities |
| US20030087381A1 (en) * | 1998-04-13 | 2003-05-08 | University Of Georgia Research Foundation, Inc. | Metabolically engineered organisms for enhanced production of oxaloacetate-derived biochemicals |
| EP2194122B1 (en) * | 1998-04-13 | 2015-12-02 | The University Of Georgia Research Foundation, Inc. | Pyruvate carboxylase overexpression for enhanced production of oxaloacetate-derived biochemicals in microbial cells |
| US6159738A (en) * | 1998-04-28 | 2000-12-12 | University Of Chicago | Method for construction of bacterial strains with increased succinic acid production |
| DE19820652A1 (de) | 1998-05-08 | 1999-11-11 | Basf Ag | Kationische Rutheniumkomplexe, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US6432686B1 (en) | 1998-05-12 | 2002-08-13 | E. I. Du Pont De Nemours And Company | Method for the production of 1,3-propanediol by recombinant organisms comprising genes for vitamin B12 transport |
| US6444784B1 (en) * | 1998-05-29 | 2002-09-03 | Exxonmobil Research & Engineering Company | Wax crystal modifiers (LAW657) |
| US6187569B1 (en) | 1998-07-02 | 2001-02-13 | E. I. Du Pont De Nemours And Company | Microbial production of terephthalic acid and isophthalic acid |
| DE19856136C2 (de) * | 1998-12-04 | 2002-10-24 | Pasteur Institut | Verfahren und Vorrichtung zur Selektion beschleunigter Proliferation lebender Zellen in Suspension |
| EP1147229A2 (en) * | 1999-02-02 | 2001-10-24 | Bernhard O. Palsson | Methods for identifying drug targets based on genomic sequence data |
| US6686310B1 (en) * | 1999-02-09 | 2004-02-03 | E. I. Du Pont De Nemours And Company | High surface area sol-gel route prepared hydrogenation catalysts |
| US6365376B1 (en) * | 1999-02-19 | 2002-04-02 | E. I. Du Pont De Nemours And Company | Genes and enzymes for the production of adipic acid intermediates |
| EP1159435A1 (en) * | 1999-03-05 | 2001-12-05 | Monsanto Technology LLC | Multigene expression vectors for the biosynthesis of products via multienzyme biological pathways |
| DE60030403D1 (de) | 1999-08-30 | 2006-10-12 | Wisconsin Alumni Res Found | Herstellung von 3-hydroxypropionsäure in rekombinanten organismen |
| US6852517B1 (en) * | 1999-08-30 | 2005-02-08 | Wisconsin Alumni Research Foundation | Production of 3-hydroxypropionic acid in recombinant organisms |
| US6660857B2 (en) * | 2000-02-03 | 2003-12-09 | Dsm N.V. | Process for the preparation of ε-caprolactam |
| US6878861B2 (en) | 2000-07-21 | 2005-04-12 | Washington State University Research Foundation | Acyl coenzyme A thioesterases |
| PT1303629E (pt) * | 2000-07-25 | 2006-10-31 | Emmaus Foundation Inc | Metodos para aumentar a producao de etanol a partir da fermantacao microbiana |
| US7233567B1 (en) * | 2000-09-22 | 2007-06-19 | Nortel Networks Limited | Apparatus and method for supporting multiple traffic redundancy mechanisms |
| WO2002042418A2 (en) | 2000-11-20 | 2002-05-30 | Cargill, Incorporated | 3-hydroxypropionic acid and other organic compounds |
| CN1249239C (zh) * | 2000-11-22 | 2006-04-05 | 加吉尔·道聚合物公司 | 合成有机产物的方法和材料 |
| CN1358841A (zh) | 2000-12-11 | 2002-07-17 | 云南省微生物研究所 | 云南链霉菌 |
| CN1491282A (zh) * | 2000-12-28 | 2004-04-21 | 丰田自动车株式会社 | 异戊二烯醇的制备方法 |
| US7711490B2 (en) | 2001-01-10 | 2010-05-04 | The Penn State Research Foundation | Method and system for modeling cellular metabolism |
| US7127379B2 (en) | 2001-01-31 | 2006-10-24 | The Regents Of The University Of California | Method for the evolutionary design of biochemical reaction networks |
| US20030059792A1 (en) * | 2001-03-01 | 2003-03-27 | Palsson Bernhard O. | Models and methods for determining systemic properties of regulated reaction networks |
| US6743610B2 (en) * | 2001-03-30 | 2004-06-01 | The University Of Chicago | Method to produce succinic acid from raw hydrolysates |
| WO2002090312A1 (en) | 2001-05-07 | 2002-11-14 | Cargill, Incorporated | Process for preparing carboxylic acids and derivatives thereof |
| JP4630486B2 (ja) | 2001-05-28 | 2011-02-09 | ダイセル化学工業株式会社 | 新規な(r)−2,3−ブタンジオール脱水素酵素、その製造方法、及びこれを利用した光学活性アルコールの製造方法 |
| WO2003010322A1 (en) | 2001-07-20 | 2003-02-06 | Youming Zhang | Improved rect or recet cloning and subcloning method |
| CA2356540A1 (en) | 2001-08-30 | 2003-02-28 | Emory University | Expressed dna sequences involved in mitochondrial functions |
| CA2466133A1 (en) * | 2001-11-02 | 2003-05-15 | Rice University | Recycling system for manipulation of intracellular nadh availability |
| BR0307010A (pt) * | 2002-01-18 | 2006-04-11 | Cargill Inc | alanina 2,3-aminomutase |
| JPWO2003066863A1 (ja) | 2002-02-06 | 2005-06-02 | 昭和電工株式会社 | α−置換−α,β−不飽和カルボニル化合物の還元酵素遺伝子 |
| JP2005520517A (ja) | 2002-03-18 | 2005-07-14 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 高い溶媒および温度安定性を有するアルコールデヒドロゲナーゼ |
| US20030224363A1 (en) | 2002-03-19 | 2003-12-04 | Park Sung M. | Compositions and methods for modeling bacillus subtilis metabolism |
| EP1495321A4 (en) | 2002-03-29 | 2006-10-25 | Genomatica Inc | HUMAN METABOLISM MODELS AND ASSOCIATED METHODS |
| US20050287655A1 (en) * | 2002-05-10 | 2005-12-29 | Kyowa Hakko Kogyo Co., Ltd. | Process for producing mevalonic acid |
| US7856317B2 (en) * | 2002-06-14 | 2010-12-21 | Genomatica, Inc. | Systems and methods for constructing genomic-based phenotypic models |
| JP4402587B2 (ja) | 2002-06-14 | 2010-01-20 | ディーエスエム アイピー アセッツ ビー.ブイ. | α−H−α−アミノ酸アミドラセマーゼ活性を有するポリペプチドおよびそれをコードする核酸 |
| US7826975B2 (en) | 2002-07-10 | 2010-11-02 | The Penn State Research Foundation | Method for redesign of microbial production systems |
| WO2004018621A2 (en) | 2002-07-10 | 2004-03-04 | The Penn State Research Foundation | Method for determining gene knockout strategies |
| US7413878B2 (en) * | 2002-07-15 | 2008-08-19 | Kosan Biosciences, Inc. | Recombinant host cells expressing atoAD and capable of making a polyketide using a starter unit |
| CN100471946C (zh) * | 2002-10-04 | 2009-03-25 | 纳幕尔杜邦公司 | 高产量生物生产1,3-丙二醇的方法 |
| WO2004035009A2 (en) | 2002-10-15 | 2004-04-29 | The Regents Of The University Of California | Methods and systems to identify operational reaction pathways |
| WO2004044210A2 (en) * | 2002-11-06 | 2004-05-27 | University Of Florida | Materials and methods for the efficient production of acetate and other products |
| BRPI0406756A (pt) | 2003-01-13 | 2005-12-20 | Cargill Inc | Método para fabricação de agentes quìmicos industriais |
| US7432091B2 (en) * | 2003-02-24 | 2008-10-07 | Research Institute Of Innovative Technology For The Earth | Highly efficient hydrogen production method using microorganism |
| RU2268300C2 (ru) | 2003-04-07 | 2006-01-20 | Закрытое акционерное общество "Научно-исследовательский институт Аджиномото-Генетика" | СПОСОБ ПОЛУЧЕНИЯ L-АМИНОКИСЛОТ С ИСПОЛЬЗОВАНИЕМ БАКТЕРИЙ, ОБЛАДАЮЩИХ ПОВЫШЕННОЙ ЭКСПРЕССИЕЙ ГЕНА pckA |
| JP4451393B2 (ja) | 2003-07-29 | 2010-04-14 | 財団法人地球環境産業技術研究機構 | コリネ型細菌形質転換体及びそれを用いるジカルボン酸の製造方法 |
| US7927859B2 (en) * | 2003-08-22 | 2011-04-19 | Rice University | High molar succinate yield bacteria by increasing the intracellular NADH availability |
| WO2005026349A1 (ja) * | 2003-09-17 | 2005-03-24 | Mitsubishi Chemical Corporation | 非アミノ有機酸の製造方法 |
| WO2005026338A1 (en) | 2003-09-18 | 2005-03-24 | Ciba Specialty Chemicals Holding Inc. | Alcohol dehydrogenases with increased solvent and temperature stability |
| FR2862068B1 (fr) | 2003-11-06 | 2007-10-12 | Metabolic Explorer Sa | Souches de microorganismes optimisees pour des voies de biosyntheses consommatrices de nadph |
| US7244610B2 (en) * | 2003-11-14 | 2007-07-17 | Rice University | Aerobic succinate production in bacteria |
| FR2864967B1 (fr) * | 2004-01-12 | 2006-05-19 | Metabolic Explorer Sa | Microorganisme evolue pour la production de 1,2-propanediol |
| BRPI0506942B1 (pt) | 2004-01-19 | 2015-07-28 | Dsm Ip Assets B.V. | Síntese bioquímica de ácido 6-amino capróico |
| US7608700B2 (en) | 2004-03-08 | 2009-10-27 | North Carolina State University | Lactobacillus acidophilus nucleic acid sequences encoding stress-related proteins and uses therefor |
| DE102004029112B4 (de) | 2004-06-11 | 2007-06-21 | Julich Chiral Solutions Gmbh | Alkoholdehydrogenase zur stereoselektiven Gewinnung von Hydroxyverbindungen |
| DE102004031177A1 (de) | 2004-06-29 | 2006-01-19 | Henkel Kgaa | Neue Geruchsstoffe bildende Genprodukte von Bacillus licheniformis und darauf aufbauende verbesserte biotechnologische Produktionsverfahren |
| US7262046B2 (en) * | 2004-08-09 | 2007-08-28 | Rice University | Aerobic succinate production in bacteria |
| BRPI0514734B1 (pt) | 2004-08-27 | 2018-02-06 | Rice University | VARIEDADE BACTERIANA DE E. Coli MODIFICADA |
| ES2444785T3 (es) * | 2004-09-09 | 2014-02-26 | Research Institute Of Innovative Technology For The Earth | Fragmento de ADN que tiene función promotora |
| US20060073577A1 (en) * | 2004-09-17 | 2006-04-06 | San Ka-Yiu | High succinate producing bacteria |
| US20070022497A1 (en) * | 2004-10-08 | 2007-01-25 | Basf Plant Science Gmbh | Trans-2-enoyl-coa reductase gene of euglena gracilis |
| US7569380B2 (en) * | 2004-12-22 | 2009-08-04 | Rice University | Simultaneous anaerobic production of isoamyl acetate and succinic acid |
| JP2006204255A (ja) | 2005-01-31 | 2006-08-10 | Canon Inc | アセチル−CoAアシルトランスフェラーゼ遺伝子破壊ポリヒドロキシアルカノエート生産菌、またこれを利用したポリヒドロキシアルカノエート生産方法 |
| WO2006109312A2 (en) | 2005-04-15 | 2006-10-19 | Vascular Biogenics Ltd. | Compositions containing beta 2-glycoprotein i-derived peptides for the prevention and/or treatment of vascular disease |
| US8187842B2 (en) | 2005-06-20 | 2012-05-29 | Archer Daniels Midland Company | Altered glyoxylate shunt for improved production of aspartate-derived amino acids and chemicals |
| KR100676160B1 (ko) * | 2005-08-19 | 2007-02-01 | 한국과학기술원 | 말릭효소를 코딩하는 유전자로 형질전환된 재조합 미생물 및 이를 이용한 숙신산의 제조방법 |
| KR100679638B1 (ko) * | 2005-08-19 | 2007-02-06 | 한국과학기술원 | 포메이트 디하이드로게나제 d 또는 e를 코딩하는 유전자로 형질전환된 미생물 및 이를 이용한 숙신산의 제조방법 |
| AU2006287257A1 (en) | 2005-09-09 | 2007-03-15 | Genomatica, Inc. | Methods and organisms for the growth-coupled production of succinate |
| EP1926822B1 (en) | 2005-09-19 | 2010-06-30 | Basf Se | Biocatalytic manufacturing of (meth)acrylic esters |
| US9297028B2 (en) * | 2005-09-29 | 2016-03-29 | Butamax Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
| NZ566406A (en) * | 2005-10-26 | 2012-04-27 | Butamax Advanced Biofuels Llc | Fermentive production of four carbon alcohols |
| DE102006017760A1 (de) | 2006-03-24 | 2007-09-27 | Ufz-Umweltforschungszentrum Leipzig-Halle Gmbh | Verfahren zur enzymatischen Herstellung von 2-Hydroxy-2-methylcarbonsäuren |
| MY157798A (en) | 2006-05-01 | 2016-07-29 | Univ Florida | Ethanol production in non-recombination hosts |
| US8206970B2 (en) * | 2006-05-02 | 2012-06-26 | Butamax(Tm) Advanced Biofuels Llc | Production of 2-butanol and 2-butanone employing aminobutanol phosphate phospholyase |
| EP2157170B1 (en) * | 2006-05-19 | 2014-01-15 | LS9, Inc. | Production of fatty acids and derivatives thereof |
| US8110670B2 (en) | 2006-05-19 | 2012-02-07 | Ls9, Inc. | Enhanced production of fatty acid derivatives |
| US20100242345A1 (en) | 2006-05-19 | 2010-09-30 | LS9, Inc | Production of fatty acids & derivatives thereof |
| DE102006025821A1 (de) | 2006-06-02 | 2007-12-06 | Degussa Gmbh | Ein Enzym zur Herstellung von Mehylmalonatsemialdehyd oder Malonatsemialdehyd |
| WO2008013996A2 (en) * | 2006-07-27 | 2008-01-31 | Gevo Inc. | Engineered microorganisms for increasing product yield in biotransformations, related methods and systems |
| RU2311231C1 (ru) | 2006-08-15 | 2007-11-27 | ООО "Объединенный центр исследований и разработок" | Катализатор для получения эфиров акриловой кислоты по реакции метатезиса диалкилмалеатов (варианты) и каталитическая композиция на его основе |
| US8030045B2 (en) | 2006-08-30 | 2011-10-04 | Cargill, Incorporated | Beta-alanine/alpha-ketoglutarate aminotransferase for 3-hydroxypropionic acid production |
| US20100036174A1 (en) * | 2006-10-31 | 2010-02-11 | Lourina Madeleine Raamsdonk | Butanol production in a eukaryotic cell |
| WO2008143704A2 (en) * | 2006-12-01 | 2008-11-27 | Gevo, Inc. | Engineered microorganisms for producing n-butanol and related methods |
| US8017364B2 (en) | 2006-12-12 | 2011-09-13 | Butamax(Tm) Advanced Biofuels Llc | Solvent tolerant microorganisms |
| CA2715092A1 (en) * | 2006-12-21 | 2008-07-03 | Gevo, Inc. | Butanol production by metabolically engineered yeast |
| CN101903513B (zh) | 2007-01-12 | 2013-08-21 | 科罗拉多大学董事会法人 | 增强微生物对产生的有机化学物质的耐受性的组合物和方法 |
| PL389665A1 (pl) * | 2007-02-09 | 2010-07-05 | The Regents of the University of CaliforniaThe Regents of the University of California | Wytwarzanie biopaliwa przez rekombinowane mikroorganizmy |
| WO2008113041A2 (en) | 2007-03-14 | 2008-09-18 | Ls9, Inc. | Process for producing low molecular weight hydrocarbons from renewable resources |
| TWI568847B (zh) * | 2007-03-16 | 2017-02-01 | 奇諾麥提卡公司 | 用於1,4-丁二醇及其前驅物之生物合成的組合物及方法 |
| BRPI0809345A2 (pt) | 2007-03-28 | 2014-10-07 | Ls9 Inc | Células recombinantes, composições produzidas por estas, métodos para produzir derivados de ácidos graxos em uma célula recombinante, para aumentar a produção de derivados de ácidos graxos em uma célula recombinante, construto recombinante, vetores, métodos para aumentar a produção de derivados de ácidos graxos em uma célula hospedeira de produção, para produzir derivados de ácidos graxos, derivados de ácidos graxos, composições de biocombustível. |
| US20100159546A1 (en) * | 2007-03-30 | 2010-06-24 | Aristos Aristidou | Metabolic engineering of yeasts for the production of 1-butanol |
| WO2008130995A2 (en) | 2007-04-18 | 2008-10-30 | E. I. Du Pont De Nemours And Company | Fermentive production of isobutanol using highly active ketol-acid reductoisomerase enzymes |
| US20080293125A1 (en) * | 2007-04-18 | 2008-11-27 | Gevo, Inc. | Engineered microorganisms for producing isopropanol |
| US20080293060A1 (en) | 2007-04-23 | 2008-11-27 | Ls9, Inc. | Methods and Compositions for Identification of Hydrocarbon Response, Transport and Biosynthesis Genes |
| US20080274522A1 (en) * | 2007-05-02 | 2008-11-06 | Bramucci Michael G | Method for the production of 2-butanone |
| US8426174B2 (en) | 2007-05-02 | 2013-04-23 | Butamax(Tm) Advanced Biofuels Llc | Method for the production of 2-butanol |
| US9080187B2 (en) | 2007-05-17 | 2015-07-14 | The Board Of Trustees Of The University Of Illinois | Methods and compositions for producing solvents |
| US9200299B2 (en) | 2007-05-22 | 2015-12-01 | REG Life Sciences, LLC | Genetically engineered cell encoding ole amino acid motifs in a carbon source producing aliphatic ketones or olefins |
| KR101504618B1 (ko) | 2007-06-01 | 2015-03-23 | 솔라짐, 인코포레이티드 | 미생물에서 오일의 생성 |
| KR20100049012A (ko) | 2007-06-15 | 2010-05-11 | 에보니크 데구사 게엠베하 | 비타민 b12 시스템이 탈조절된 미생물 |
| US20100199548A1 (en) | 2007-07-06 | 2010-08-12 | Ls9, Inc. | Systems and methods for the production of fatty esters |
| EP2017344A1 (en) | 2007-07-20 | 2009-01-21 | Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO | Production of itaconic acid |
| US20100205857A1 (en) | 2007-07-23 | 2010-08-19 | Einte-Karst Dijk | Butanol production in a eukaryotic cell |
| WO2009013158A1 (en) * | 2007-07-23 | 2009-01-29 | Dsm Ip Assets B.V. | Butanol production in a eukaryotic cell |
| PL2173881T3 (pl) * | 2007-07-23 | 2017-05-31 | Dsm Ip Assets B.V. | Acetylo-coa wytwarzający enzymy w drożdżach |
| US8285554B2 (en) * | 2007-07-27 | 2012-10-09 | Dsp Group Limited | Method and system for dynamic aliasing suppression |
| US7947483B2 (en) * | 2007-08-10 | 2011-05-24 | Genomatica, Inc. | Methods and organisms for the growth-coupled production of 1,4-butanediol |
| KR101042242B1 (ko) | 2007-09-07 | 2011-06-17 | 한국과학기술원 | 1,4-부탄디올 생성능을 가지는 변이체 및 이를 이용한1,4-부탄디올의 제조방법 |
| CN101903530A (zh) | 2007-10-12 | 2010-12-01 | 加利福尼亚大学董事会 | 被改造以产生异丙醇的微生物 |
| WO2009085278A1 (en) | 2007-12-21 | 2009-07-09 | Ls9, Inc. | Methods and compositions for producing olefins |
| CA2712779C (en) | 2008-01-22 | 2021-03-16 | Genomatica, Inc. | Methods and organisms for utilizing synthesis gas or other gaseous carbon sources and methanol |
| WO2009103026A1 (en) | 2008-02-15 | 2009-08-20 | Gevo, Inc. | Engineered microorganisms for producing isopropanol |
| US20090246842A1 (en) | 2008-02-15 | 2009-10-01 | Gevo, Inc. | Engineered microorganisms for producing propanol |
| US7981647B2 (en) | 2008-03-03 | 2011-07-19 | Joule Unlimited, Inc. | Engineered CO2 fixing microorganisms producing carbon-based products of interest |
| CA3081506A1 (en) * | 2008-03-05 | 2009-09-11 | Genomatica, Inc. | Long chain alcohol-producing organisms |
| SI2252698T1 (en) | 2008-03-11 | 2018-04-30 | Genomatica, Inc. | SYNTHESIS ADIPAT ESTRA OR TIOESTRA |
| TW200951103A (en) | 2008-03-11 | 2009-12-16 | Dsm Ip Assets Bv | Preparation of 6-aminocaproic acid from α-ketopimelic acid |
| US7799545B2 (en) | 2008-03-27 | 2010-09-21 | Genomatica, Inc. | Microorganisms for the production of adipic acid and other compounds |
| WO2009131040A1 (ja) | 2008-04-25 | 2009-10-29 | 財団法人地球環境産業技術研究機構 | イソプロパノール生産能を有するコリネ型細菌の形質転換体 |
| MX350285B (es) | 2008-05-16 | 2017-09-04 | Reg Life Sciences Llc | Métodos y composiciones para producir hidrocarburos. |
| US8129154B2 (en) * | 2008-06-17 | 2012-03-06 | Genomatica, Inc. | Microorganisms and methods for the biosynthesis of fumarate, malate, and acrylate |
| WO2010022090A1 (en) | 2008-08-18 | 2010-02-25 | Ls9, Inc. | Systems and methods for the production of mixed fatty esters |
| WO2010022763A1 (en) | 2008-08-25 | 2010-03-04 | Metabolic Explorer | Method for the preparation of 2-hydroxy-isobutyrate |
| US8357826B2 (en) * | 2008-10-16 | 2013-01-22 | Karl Kharas | Methods and apparatus for synthesis of alcohols from syngas |
| ES2505115T3 (es) * | 2008-10-28 | 2014-10-09 | Ls9, Inc. | Métodos para producir alcoholes grasos |
| US9090898B2 (en) | 2008-12-12 | 2015-07-28 | Metabolix, Inc. | Green process and compositions for producing poly(5HV) and 5 carbon chemicals |
| CN102459622B (zh) | 2009-04-27 | 2020-08-18 | 基因组股份公司 | 脂肪酸酯的产生 |
| US9101598B2 (en) | 2011-11-30 | 2015-08-11 | Merial, Inc. | Recombinant Gallid herpesvirus 3 (MDV serotype 2) vectors expressing antigens of avian pathogens and uses thereof |
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| WO2009111672A1 (en) | 2009-09-11 |
| US11613767B2 (en) | 2023-03-28 |
| CA2717586C (en) | 2020-08-11 |
| US20190309329A1 (en) | 2019-10-10 |
| PL2262901T3 (pl) | 2019-04-30 |
| JP2014100147A (ja) | 2014-06-05 |
| DK2262901T3 (en) | 2019-01-21 |
| CA3081506A1 (en) | 2009-09-11 |
| SI2262901T1 (sl) | 2019-02-28 |
| EP2262901A4 (en) | 2014-07-16 |
| EP3450550A1 (en) | 2019-03-06 |
| EP2262901A1 (en) | 2010-12-22 |
| BRPI0909690A2 (pt) | 2019-02-26 |
| US20210108232A1 (en) | 2021-04-15 |
| US10208320B2 (en) | 2019-02-19 |
| US20090275097A1 (en) | 2009-11-05 |
| ES2703775T3 (es) | 2019-03-12 |
| CA2717586A1 (en) | 2009-09-11 |
| US20120040426A1 (en) | 2012-02-16 |
| US7977084B2 (en) | 2011-07-12 |
| EP2262901B1 (en) | 2018-11-21 |
| JP2011512848A (ja) | 2011-04-28 |
| US20160355845A1 (en) | 2016-12-08 |
| ZA201007065B (en) | 2011-07-27 |
| US9260729B2 (en) | 2016-02-16 |
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