JP5501954B2 - Δ９エロンガーゼおよび多価不飽和脂肪酸の作成におけるそれらの使用 - Google Patents
Δ９エロンガーゼおよび多価不飽和脂肪酸の作成におけるそれらの使用 Download PDFInfo
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| CN103451246B (zh) | 2004-04-22 | 2018-02-16 | 联邦科学技术研究组织 | 用重组细胞合成长链多不饱和脂肪酸 |
| CA2563875C (en) | 2004-04-22 | 2015-06-30 | Commonwealth Scientific And Industrial Research Organisation | Synthesis of long-chain polyunsaturated fatty acids by recombinant cells |
| BRPI0716075A2 (pt) | 2006-08-29 | 2013-08-06 | Commw Scient Ind Res Org | sÍntese de Ácidos graxos |
| US8119860B2 (en) * | 2007-04-16 | 2012-02-21 | E. I. Du Pont De Nemours And Company | Delta-9 elongases and their use in making polyunsaturated fatty acids |
| AU2008255877B2 (en) * | 2007-05-25 | 2013-10-31 | Suntory Holdings Limited | Novel lysophosphatidic acid acyltransferase genes |
| US8168858B2 (en) | 2008-06-20 | 2012-05-01 | E. I. Du Pont De Nemours And Company | Delta-9 fatty acid elongase genes and their use in making polyunsaturated fatty acids |
| BR122021003836B1 (pt) | 2008-11-18 | 2022-02-01 | Commonwealth Scientific And Industrial Research Organisation | Polinucleotídeo isolado e/ou exógeno que não ocorre de forma natural, vetor e método para produzir óleo contendo ácidos graxos insaturados |
| EP2358862B1 (en) * | 2008-12-18 | 2017-08-02 | E. I. du Pont de Nemours and Company | Reducing byproduction of malonates in a fermentation process |
| CN102595917A (zh) | 2009-06-16 | 2012-07-18 | 纳幕尔杜邦公司 | 来自改善的优化的解脂耶氏酵母菌株的高二十碳五烯酸油 |
| US8188335B2 (en) * | 2009-07-17 | 2012-05-29 | Abbott Laboratories | Δ9-elongase for production of polyunsaturated fatty acid-enriched oils |
| WO2011054800A1 (en) | 2009-11-03 | 2011-05-12 | Dsm Ip Assets B.V. | Composition comprising cells and a polyunsaturated fatty acid having at least 20 carbon atoms (lc-pufa) |
| CN102595918A (zh) | 2009-11-03 | 2012-07-18 | 帝斯曼知识产权资产管理有限公司 | 包含具有至少20个碳原子的多不饱和脂肪酸的植物油 |
| CN103282474A (zh) | 2010-04-22 | 2013-09-04 | 纳幕尔杜邦公司 | 从微生物生物质中获得包含多不饱和脂肪酸的组合物的方法 |
| CN103249834B (zh) | 2010-08-26 | 2016-10-26 | 纳幕尔杜邦公司 | 生产高水平二十碳五烯酸的重组微生物宿主细胞 |
| CN103080317B (zh) | 2010-08-26 | 2017-07-11 | 纳幕尔杜邦公司 | 突变型hpgg基序和hdash基序δ‑5去饱和酶以及它们在制备多不饱和脂肪酸中的用途 |
| AU2011293167B2 (en) | 2010-08-26 | 2016-12-08 | E. I. Du Pont De Nemours And Company | Mutant delta-9 elongases and their use in making polyunsaturated fatty acids |
| CA2824584A1 (en) | 2010-12-30 | 2012-07-05 | E. I. Du Pont De Nemours And Company | Use of saccharomyces cerevisiae suc2 gene in yarrowia lipolytica for sucrose utilization |
| US20130040340A1 (en) | 2011-02-07 | 2013-02-14 | E. I. Du Pont De Nemours And Company | Production of alcohol esters in situ using alcohols and fatty acids produced by microorganisms |
| KR102197208B1 (ko) | 2012-06-15 | 2021-01-04 | 커먼웰쓰 사이언티픽 앤 인더스트리알 리서치 오거니제이션 | 식물 세포에서 장쇄 다중불포화 지방산의 생성 |
| US9005940B2 (en) | 2012-12-21 | 2015-04-14 | E I Du Pont De Nemours And Company | Down-regulation of a polynucleotide encoding a Sou2 sorbitol utilization protein to modify lipid production in microbial cells |
| US20160272997A1 (en) | 2013-10-25 | 2016-09-22 | Pioneer Hi-Bred International, Inc. | Stem canker tolerant soybeans and methods of use |
| EA037817B1 (ru) | 2013-12-18 | 2021-05-25 | Коммонвелт Сайнтифик Энд Индастриэл Рисерч Организэйшн | Экстрагированный растительный липид, содержащий длинноцепочечные полиненасыщенные жирные кислоты |
| CA2953008C (en) | 2014-06-27 | 2024-03-19 | Nuseed Pty Ltd | Lipid comprising docosapentaenoic acid |
| CN106916796B (zh) * | 2015-12-28 | 2021-06-29 | 丰益(上海)生物技术研发中心有限公司 | 裂殖壶菌delta-12脂肪酸脱饱和酶相关序列及其应用 |
| US11096344B2 (en) | 2016-02-05 | 2021-08-24 | Pioneer Hi-Bred International, Inc. | Genetic loci associated with brown stem rot resistance in soybean and methods of use |
| EA201991467A1 (ru) | 2016-12-15 | 2019-11-29 | Состав смеси, содержащий силикат и микробные и/или растительные клетки и полиненасыщенную жирную кислоту, имеющую по меньшей мере 20 атомов углерода (lc-pufa) |
Family Cites Families (53)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4670285A (en) | 1982-08-06 | 1987-06-02 | The University Of Toronto Innovations Foundation | Infant formula |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US5107065A (en) | 1986-03-28 | 1992-04-21 | Calgene, Inc. | Anti-sense regulation of gene expression in plant cells |
| US5188958A (en) | 1986-05-29 | 1993-02-23 | Calgene, Inc. | Transformation and foreign gene expression in brassica species |
| US5004863B2 (en) | 1986-12-03 | 2000-10-17 | Agracetus | Genetic engineering of cotton plants and lines |
| JP2527340B2 (ja) | 1986-12-15 | 1996-08-21 | アプライド バイオシステムズ インコーポレイテッド | ロ―ダミン染料の５−及び６−スクシニミジルカルボキシレ―ト異性体 |
| US5416011A (en) | 1988-07-22 | 1995-05-16 | Monsanto Company | Method for soybean transformation and regeneration |
| US5366860A (en) | 1989-09-29 | 1994-11-22 | Applied Biosystems, Inc. | Spectrally resolvable rhodamine dyes for nucleic acid sequence determination |
| WO1992017598A1 (en) | 1991-03-29 | 1992-10-15 | The Board Of Trustees Of The University Of Illinois | Production fo transgenic soybean plants |
| US6372965B1 (en) | 1992-11-17 | 2002-04-16 | E.I. Du Pont De Nemours And Company | Genes for microsomal delta-12 fatty acid desaturases and hydroxylases from plants |
| US5648564A (en) | 1995-12-21 | 1997-07-15 | Kemin Industries, Inc. | Process for the formation, isolation and purification of comestible xanthophyll crystals from plants |
| US6075183A (en) | 1997-04-11 | 2000-06-13 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids in plants |
| EP0996732B1 (en) | 1997-04-11 | 2005-06-15 | Calgene LLC | Methods and compositions for synthesis of long chain polyunsaturated fatty acids in plants |
| US6432684B1 (en) | 1997-04-11 | 2002-08-13 | Abbott Laboratories | Human desaturase gene and uses thereof |
| US6051754A (en) | 1997-04-11 | 2000-04-18 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids in plants |
| US5968809A (en) | 1997-04-11 | 1999-10-19 | Abbot Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids |
| US5972664A (en) | 1997-04-11 | 1999-10-26 | Abbott Laboratories | Methods and compositions for synthesis of long chain poly-unsaturated fatty acids |
| US6403349B1 (en) | 1998-09-02 | 2002-06-11 | Abbott Laboratories | Elongase gene and uses thereof |
| AU776711B2 (en) | 1998-12-07 | 2004-09-16 | Washington State University Research Foundation | Desaturases and methods of using them for synthesis of polyunsaturated fatty acids |
| US6825017B1 (en) | 1998-12-07 | 2004-11-30 | Washington State University Research Foundation | Desaturases and methods of using them for synthesis of polyunsaturated fatty acids |
| MXPA02012733A (es) | 2000-06-23 | 2003-05-14 | Du Pont | Extrusturas recombinantes y su uso en la reduccion de la expresion de genes. |
| MXPA03000507A (es) | 2000-07-21 | 2003-10-06 | Du Pont | Enzima de citocromo p450 asociada con la sintesis de grupos delta12-epoxi en acidos grasos de plantas.. |
| WO2002074977A2 (en) * | 2001-03-16 | 2002-09-26 | Basf Plant Science Gmbh | Sugar and lipid metabolism regulators in plants |
| GB0107510D0 (en) | 2001-03-26 | 2001-05-16 | Univ Bristol | New elongase gene and a process for the production of -9-polyunsaturated fatty acids |
| TWI377253B (en) | 2001-04-16 | 2012-11-21 | Martek Biosciences Corp | Product and process for transformation of thraustochytriales microorganisms |
| US6797303B2 (en) | 2001-09-04 | 2004-09-28 | Lycored Natural Products Industries Ltd. | Carotenoid extraction process |
| AU2003296638B2 (en) * | 2002-12-19 | 2009-06-11 | University Of Bristol | Method for the production of polyunsaturated fatty acids |
| US20040172682A1 (en) | 2003-02-12 | 2004-09-02 | Kinney Anthony J. | Production of very long chain polyunsaturated fatty acids in oilseed plants |
| US7129089B2 (en) | 2003-02-12 | 2006-10-31 | E. I. Du Pont De Nemours And Company | Annexin and P34 promoters and use in expression of transgenic genes in plants |
| US7238482B2 (en) * | 2003-05-07 | 2007-07-03 | E. I. Du Pont De Nemours And Company | Production of polyunsaturated fatty acids in oleaginous yeasts |
| US7125672B2 (en) * | 2003-05-07 | 2006-10-24 | E. I. Du Pont De Nemours And Company | Codon-optimized genes for the production of polyunsaturated fatty acids in oleaginous yeasts |
| US7259255B2 (en) | 2003-06-25 | 2007-08-21 | E. I. Du Pont De Nemours And Company | Glyceraldehyde-3-phosphate dehydrogenase and phosphoglycerate mutase promoters for gene expression in oleaginous yeast |
| PT2166069T (pt) | 2003-08-01 | 2016-09-13 | Basf Plant Science Gmbh | Método de produção de ácidos gordos polinsaturados em organismos transgénicos |
| US7659120B2 (en) | 2003-11-12 | 2010-02-09 | E. I. Du Pont De Nemours And Company | Δ 15 desaturases suitable for altering levels of polyunsaturated fatty acids in oleaginous plants and yeast |
| US7202356B2 (en) | 2003-11-14 | 2007-04-10 | E. I. Du Pont De Nemours And Company | Fructose-bisphosphate aldolase regulatory sequences for gene expression in oleaginous yeast |
| WO2005083093A2 (de) | 2004-02-27 | 2005-09-09 | Basf Plant Science Gmbh | Verfahren zur herstellung mehrfach ungesättigter fettsäuren in transgenen pflanzen |
| CN103451246B (zh) | 2004-04-22 | 2018-02-16 | 联邦科学技术研究组织 | 用重组细胞合成长链多不饱和脂肪酸 |
| CA2563875C (en) | 2004-04-22 | 2015-06-30 | Commonwealth Scientific And Industrial Research Organisation | Synthesis of long-chain polyunsaturated fatty acids by recombinant cells |
| CA2568624C (en) * | 2004-06-25 | 2014-03-25 | E. I. Du Pont De Nemours And Company | Delta-8 desaturase and its use in making polyunsaturated fatty acids |
| US7465564B2 (en) * | 2004-08-10 | 2008-12-16 | E.I. Du Pont De Nemours And Company | Production of γ-linolenic acid in oleaginous yeast |
| US7588931B2 (en) * | 2004-11-04 | 2009-09-15 | E. I. Du Pont De Nemours And Company | High arachidonic acid producing strains of Yarrowia lipolytica |
| JP5123861B2 (ja) | 2005-11-23 | 2013-01-23 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Δ９エロンガーゼおよびそれらの多価不飽和脂肪酸製造における使用 |
| US7465793B2 (en) * | 2006-04-20 | 2008-12-16 | E.I. Du Pont De Nemours And Company | Synthetic Δ17 desaturase derived from Phytophthora ramourum and its use in making polyunsaturated fatty acids |
| US7943823B2 (en) | 2006-04-28 | 2011-05-17 | E.I. Du Pont De Nemours And Company | Delta-8 desaturase and its use in making polyunsaturated fatty acids |
| US7678560B2 (en) | 2006-05-17 | 2010-03-16 | E.I. Du Pont De Nemours And Company | Δ 5 desaturase and its use in making polyunsaturated fatty acids |
| EP2441842A1 (en) * | 2007-02-12 | 2012-04-18 | E. I. du Pont de Nemours and Company | Production of arachidonic acid in oilseed plants |
| UA103595C2 (uk) * | 2007-04-03 | 2013-11-11 | Е. І. Дю Пон Де Немур Енд Компані | Мультизими і їх застосування в отриманні поліненасичених жирних кислот |
| US7790156B2 (en) * | 2007-04-10 | 2010-09-07 | E. I. Du Pont De Nemours And Company | Δ-8 desaturases and their use in making polyunsaturated fatty acids |
| US8119860B2 (en) * | 2007-04-16 | 2012-02-21 | E. I. Du Pont De Nemours And Company | Delta-9 elongases and their use in making polyunsaturated fatty acids |
| WO2009046231A1 (en) * | 2007-10-03 | 2009-04-09 | E. I. Du Pont De Nemours And Company | Optimized strains of yarrowia lipolytica for high eicosapentaenoic acid production |
| EP2274429B1 (en) * | 2008-04-03 | 2014-10-22 | E. I. du Pont de Nemours and Company | Multizymes |
| JP5768056B2 (ja) | 2009-10-30 | 2015-08-26 | リコール メディカル インコーポレイテッドＲｅＣｏｒ Ｍｅｄｉｃａｌ， Ｉｎｃ． | 経皮的超音波腎神経除去による高血圧症を治療するための方法及び装置 |
| US9979908B2 (en) | 2014-03-31 | 2018-05-22 | Agency For Science, Technology And Research | Image processing devices and image processing methods with interpolation for improving image resolution |
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| CA2679485A1 (en) | 2008-10-23 |
| US20100162435A1 (en) | 2010-06-24 |
| EP2134837B1 (en) | 2014-01-01 |
| WO2008128241A1 (en) | 2008-10-23 |
| US20120100595A1 (en) | 2012-04-26 |
| CN101848996A (zh) | 2010-09-29 |
| AU2008240028A1 (en) | 2008-10-23 |
| US8377673B2 (en) | 2013-02-19 |
| EP2134837A1 (en) | 2009-12-23 |
| BRPI0807291A2 (pt) | 2014-04-29 |
| WO2008128240A1 (en) | 2008-10-23 |
| US20080254522A1 (en) | 2008-10-16 |
| EP2137304B1 (en) | 2013-08-14 |
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