ES2336858T3 - Metodo para la produccion de 1,3-propanodiol mediante organismos recombinantes. - Google Patents
Metodo para la produccion de 1,3-propanodiol mediante organismos recombinantes. Download PDFInfo
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- ES2336858T3 ES2336858T3 ES97947395T ES97947395T ES2336858T3 ES 2336858 T3 ES2336858 T3 ES 2336858T3 ES 97947395 T ES97947395 T ES 97947395T ES 97947395 T ES97947395 T ES 97947395T ES 2336858 T3 ES2336858 T3 ES 2336858T3
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- 239000011565 manganese chloride Substances 0.000 description 1
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- 238000005259 measurement Methods 0.000 description 1
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- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 210000002500 microbody Anatomy 0.000 description 1
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- 238000001823 molecular biology technique Methods 0.000 description 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
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- 230000003204 osmotic effect Effects 0.000 description 1
- 230000008723 osmotic stress Effects 0.000 description 1
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- 239000003208 petroleum Substances 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 230000027086 plasmid maintenance Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
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- 229920002635 polyurethane Polymers 0.000 description 1
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- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
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- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
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- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 229960000344 thiamine hydrochloride Drugs 0.000 description 1
- 235000019190 thiamine hydrochloride Nutrition 0.000 description 1
- 239000011747 thiamine hydrochloride Substances 0.000 description 1
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- 238000011426 transformation method Methods 0.000 description 1
- 229940055835 triptone Drugs 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 229960004799 tryptophan Drugs 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
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- 230000003612 virological effect Effects 0.000 description 1
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- 239000002912 waste gas Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
Classifications
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- 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
- C12N9/0004—Oxidoreductases (1.)
-
- 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
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
-
- 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
- C12N9/88—Lyases (4.)
-
- 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
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
- Y10S530/82—Proteins from microorganisms
- Y10S530/823—Lower fungi, e.g. mold
- Y10S530/824—Yeasts
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3060196P | 1996-11-13 | 1996-11-13 | |
| US30601P | 1996-11-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2336858T3 true ES2336858T3 (es) | 2010-04-16 |
Family
ID=21854996
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES97947395T Expired - Lifetime ES2336858T3 (es) | 1996-11-13 | 1997-11-10 | Metodo para la produccion de 1,3-propanodiol mediante organismos recombinantes. |
Country Status (18)
| Country | Link |
|---|---|
| US (3) | US6013494A (OSRAM) |
| EP (2) | EP0942989B1 (OSRAM) |
| JP (2) | JP4327909B2 (OSRAM) |
| KR (1) | KR100509310B1 (OSRAM) |
| CN (2) | CN1236063C (OSRAM) |
| AT (2) | ATE452979T1 (OSRAM) |
| AU (2) | AU733534B2 (OSRAM) |
| BR (2) | BR9712761B1 (OSRAM) |
| CA (2) | CA2269088C (OSRAM) |
| DE (2) | DE69739715D1 (OSRAM) |
| DK (1) | DK0946732T3 (OSRAM) |
| ES (1) | ES2336858T3 (OSRAM) |
| ID (1) | ID21487A (OSRAM) |
| IL (2) | IL129722A0 (OSRAM) |
| MY (1) | MY131754A (OSRAM) |
| NZ (1) | NZ335392A (OSRAM) |
| WO (2) | WO1998021339A1 (OSRAM) |
| ZA (1) | ZA9710194B (OSRAM) |
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|---|---|---|---|---|
| US6428767B1 (en) | 1995-05-12 | 2002-08-06 | E. I. Du Pont De Nemours And Company | Method for identifying the source of carbon in 1,3-propanediol |
| 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 |
| ID21487A (id) * | 1996-11-13 | 1999-06-17 | Du Pont | Metoda pembuatan 1,3 - propandiol dengan organisme rekombinan |
| BR9712942B1 (pt) | 1996-11-13 | 2010-09-21 | método para a produção de glicerol e célula hospedeira de e. coli transformada. | |
| JP4570775B2 (ja) * | 1997-12-02 | 2010-10-27 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 組換え生物によるグリセロールの産生方法 |
| GB9806762D0 (en) * | 1998-03-31 | 1998-05-27 | Neutec Pharma Plc | Treatment and diagnosis of staphylococcal infections |
| US7074608B1 (en) | 1998-05-12 | 2006-07-11 | E. I. Du Pont De Nemours And Company | Method for the production of 1,3-propanediol by recombinant organisms comprising genes for coenzyme B12 synthesis |
| 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 |
| ATE385521T1 (de) | 1998-08-04 | 2008-02-15 | Metabolix Inc | Herstellung von polyhydroxyalkanoaten aus polyolen |
| US6468773B1 (en) * | 1999-05-19 | 2002-10-22 | Genencor International, Inc. | Mutant 1,3-propandiol dehydrogenase |
| FR2796081B1 (fr) | 1999-07-09 | 2003-09-26 | Agronomique Inst Nat Rech | Procede de preparation du 1,3-propanediol par un micro-organisme recombinant en l'absence de coenzyme b12 ou de l'un de ses precurseurs |
| EP1586647A1 (en) * | 1999-08-18 | 2005-10-19 | E.I. du Pont de Nemours and Company | Process for the biological production of 1,3-propanediol with high titer |
| US6514733B1 (en) * | 1999-08-18 | 2003-02-04 | E. I. Du Pont De Nemours And Company | Process for the biological production of 1,3-propanediol with high titer |
| DE60030403D1 (de) * | 1999-08-30 | 2006-10-12 | Wisconsin Alumni Res Found | Herstellung von 3-hydroxypropionsäure in rekombinanten organismen |
| US6803218B1 (en) | 1999-09-24 | 2004-10-12 | Genencor Intl., Inc. | Enzymes which dehydrate glycerol |
| FR2800751B1 (fr) | 1999-11-09 | 2003-08-29 | Roquette Freres | Procede de production de 1,3 propanediol par voie fermentaire |
| FR2801058B1 (fr) | 1999-11-16 | 2002-01-18 | Roquette Freres | Procede de purification du 1,3-propanediol a partir d'un milieu de fermentation |
| US6617478B2 (en) | 2000-11-29 | 2003-09-09 | Samsung Electronics Co., Ltd. | Process for preparing a 1,3-alkandiol from 3-hydroxyester |
| EP1211234A3 (en) | 2000-11-29 | 2003-11-26 | Samsung Electronics Co., Ltd. | Process for preparing 1,3-alkandiols from 3-hydroxyesters |
| BR0307010A (pt) * | 2002-01-18 | 2006-04-11 | Cargill Inc | alanina 2,3-aminomutase |
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| JP4756861B2 (ja) | 2002-08-16 | 2011-08-24 | ジェネンコー・インターナショナル・インク | 新規なハイプロクレアジェコリーナｃｂｈ１セルラーゼ |
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| WO2004044210A2 (en) | 2002-11-06 | 2004-05-27 | University Of Florida | Materials and methods for the efficient production of acetate and other products |
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| WO2004085611A2 (en) * | 2003-03-21 | 2004-10-07 | The Research Foundation Of State University Of New York | Model for mutually exclusive domain folding molecular switch |
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| EP1625224B1 (en) * | 2003-05-06 | 2010-07-28 | E.I. Du Pont De Nemours And Company | Purification of biologically-produced 1,3-propanediol |
| US7056439B2 (en) * | 2003-05-06 | 2006-06-06 | Tate & Lyle Ingredidents Americas, Inc. | Process for producing 1, 3-propanediol |
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| BRPI0611855A2 (pt) * | 2005-06-16 | 2010-10-05 | Wabash Technologies Inc | conjunto de pedal com um mecanismo de histerese |
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| ATE85813T1 (de) * | 1988-12-12 | 1993-03-15 | Unilever Nv | Verfahren zur mikrobiologischen herstellung von 1,3-propandiol aus glycerin. |
| US5599689A (en) * | 1995-05-12 | 1997-02-04 | E. I. Du Pont De Nemours And Company | Process for making 1,3-propanediol from carbohydrates using mixed microbial cultures |
| US5633362A (en) * | 1995-05-12 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Production of 1,3-propanediol from glycerol by recombinant bacteria expressing recombinant diol dehydratase |
| 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 |
| ID21487A (id) | 1996-11-13 | 1999-06-17 | Du Pont | Metoda pembuatan 1,3 - propandiol dengan organisme rekombinan |
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