BR0015641A - Isolated polynucleotide, polynucleotide sequence, isolated polynucleotide complement, isolated nucleic acid molecule, chimeric gene, cell, transgenic plant, cell transformation method, method of producing a transgenic plant, method of producing a polynucleotide fragment, method of altering the level of expression of oleoyl-acp thioesterase in a host cell - Google Patents

Isolated polynucleotide, polynucleotide sequence, isolated polynucleotide complement, isolated nucleic acid molecule, chimeric gene, cell, transgenic plant, cell transformation method, method of producing a transgenic plant, method of producing a polynucleotide fragment, method of altering the level of expression of oleoyl-acp thioesterase in a host cell

Info

Publication number
BR0015641A
BR0015641A BR0015641-8A BR0015641A BR0015641A BR 0015641 A BR0015641 A BR 0015641A BR 0015641 A BR0015641 A BR 0015641A BR 0015641 A BR0015641 A BR 0015641A
Authority
BR
Brazil
Prior art keywords
polynucleotide
cell
isolated
transgenic plant
producing
Prior art date
Application number
BR0015641-8A
Other languages
Portuguese (pt)
Inventor
Stephen M Allen
J Antoni Rafalski
Jennie Bih-Jien Shen
Original Assignee
Du Pont
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.)
Filing date
Publication date
Application filed by Du Pont filed Critical Du Pont
Publication of BR0015641A publication Critical patent/BR0015641A/en

Links

Classifications

    • 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
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8243—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
    • C12N15/8247—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine involving modified lipid metabolism, e.g. seed oil composition
    • 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)

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Nutrition Science (AREA)
  • Plant Pathology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Cell Biology (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Medicinal Chemistry (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Enzymes And Modification Thereof (AREA)

Abstract

"POLINUCLEOTìDEO ISOLADO, SEQuêNCIA DE POLINUCLEOTìDEOS, COMPLEMENTO ISOLADO DO POLINUCLEOTìDEO, MOLéCULA DE áCIDO NUCLéICO ISOLADO, GENE QUIMéRICO, CéLULA, PLANTA TRANSGêNICA, MéTODO DE TRANSFORMAçãO DE UMA CéLULA, MéTODO DE PRODUçãO DE UMA PLANTA TRANSGêNICA, MéTODO DE PRODUçãO DE UM FRAGMENTO DE POLINUCLEOTìDEO, MéTODO DE ALTERAçãO DO NìVEL DE EXPRESSãO DE OLEOIL-ACP TIOESTERASE EM UMA CéLULA HOSPEDEIRA". A presente invenção refere-se a um fragmento de ácido nucléico isolado codificador de uma oleoil-ACP tioesterase. A presente invenção também se refere à construção de um gene quimérico codificador da oleoil-ACP tioesterase, no todo ou em parte, em orientação com sentido ou sem sentido, em que a expressão do gene quimérico resulta na produção de níveis alterados da oleoil-ACP tioesterase em células hospedeiras transformadas."ISOLATED POLYNUCLEOTYDE, POLYNUCLEOTYDE SEQUENCE, ISOLATED COMPLEMENT OF POLYNUCLEOTYDE, ISOLATED NUCLEIC ACID MOLECULE, CHEMICAL GENE, CELL, TRANSGENIC PLANT, A TRANSFORMATION METHOD, A CHEMICAL TRANSFORMATION METHOD , METHOD OF CHANGING THE EXPRESSION LEVEL OF OLEOIL-ACP THIOESTERASE IN A HOST CELL ". The present invention relates to an isolated nucleic acid fragment encoding an oleoyl-ACP thioesterase. The present invention also relates to the construction of a chimeric gene encoding oleoyl-ACP thioesterase, in whole or in part, in meaningful or meaningless orientation, in which the expression of the chimeric gene results in the production of altered levels of oleyl-ACP thioesterase in transformed host cells.

BR0015641-8A 1999-11-24 2000-11-22 Isolated polynucleotide, polynucleotide sequence, isolated polynucleotide complement, isolated nucleic acid molecule, chimeric gene, cell, transgenic plant, cell transformation method, method of producing a transgenic plant, method of producing a polynucleotide fragment, method of altering the level of expression of oleoyl-acp thioesterase in a host cell BR0015641A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16751099P 1999-11-24 1999-11-24
PCT/US2000/032012 WO2001038502A2 (en) 1999-11-24 2000-11-22 Oleoyl-acyl-carrier-protein thioesterases in plants

Publications (1)

Publication Number Publication Date
BR0015641A true BR0015641A (en) 2002-07-09

Family

ID=22607664

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0015641-8A BR0015641A (en) 1999-11-24 2000-11-22 Isolated polynucleotide, polynucleotide sequence, isolated polynucleotide complement, isolated nucleic acid molecule, chimeric gene, cell, transgenic plant, cell transformation method, method of producing a transgenic plant, method of producing a polynucleotide fragment, method of altering the level of expression of oleoyl-acp thioesterase in a host cell

Country Status (8)

Country Link
EP (1) EP1232250A2 (en)
JP (1) JP2004508802A (en)
AU (1) AU1787101A (en)
BR (1) BR0015641A (en)
CA (1) CA2387044A1 (en)
HU (1) HUP0203314A3 (en)
MX (1) MXPA02005178A (en)
WO (1) WO2001038502A2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG10201408475VA (en) 2009-12-18 2015-01-29 Cargill Inc Brassica plants yielding oils with a low total saturated fatty acid content
US9695434B2 (en) 2010-05-25 2017-07-04 Cargill, Incorporated Brassica plants yielding oils with a low alpha linolenic acid content
EP2576765A4 (en) 2010-05-25 2013-12-18 Cargill Inc Brassica plants yielding oils with a low alpha linolenic acid content
FR2966162B1 (en) * 2010-10-15 2014-08-29 Genoplante Valor OBTAINING PLANTS HAVING IMPROVED TOLERANCE TO A WATER DEFICIT

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5512482A (en) * 1990-04-26 1996-04-30 Calgene, Inc. Plant thioesterases
AU7147498A (en) * 1997-05-05 1998-11-27 Dow Agrosciences Llc Nucleotide sequences of maize oleoyl-acp thioesterase and palmitoyl-acp thioesterase genes and their use in the modification of fatty acid content of oil

Also Published As

Publication number Publication date
WO2001038502A3 (en) 2001-12-13
HUP0203314A2 (en) 2003-01-28
JP2004508802A (en) 2004-03-25
CA2387044A1 (en) 2001-05-31
WO2001038502A2 (en) 2001-05-31
AU1787101A (en) 2001-06-04
MXPA02005178A (en) 2003-01-28
EP1232250A2 (en) 2002-08-21
HUP0203314A3 (en) 2005-11-28

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Legal Events

Date Code Title Description
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 6AE7A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: REFERENTE AO DESPACHO PUBLICADO NA RPI 1962 DE 12/08/2008.