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    • 3. 发明申请
    • PLANTS WITH INCREASED YIELD
    • 植物增加
    • WO2011061656A1
    • 2011-05-26
    • PCT/IB2010/055028
    • 2010-11-05
    • BASF PLANT SCIENCE COMPANY GmbHSCHÖN, HardyTHIMM, OliverRITTE, GerhardBLÄSING, OliverHENKES, StefanBRUYNSEELS, KoenHATZFELD, YvesFRANKARD, ValerieSANZ MOLINERO, Ana IsabelREUZEAU, ChristopheVANDENABEELE, StevenMCKERSIE, BryanKRISHNA, KolliparraBASF (CHINA) COMPANY LIMITEDDAMMANN, Christian
    • SCHÖN, HardyTHIMM, OliverRITTE, GerhardBLÄSING, OliverHENKES, StefanBRUYNSEELS, KoenHATZFELD, YvesFRANKARD, ValerieSANZ MOLINERO, Ana IsabelREUZEAU, ChristopheVANDENABEELE, StevenMCKERSIE, BryanKRISHNA, KolliparraDAMMANN, Christian
    • C12N15/82A01H1/00C12N15/05C12N5/04C12N5/14
    • C12N15/8261C07K14/415Y02A40/146
    • A method for producing a plant with increased yield as compared to a corresponding wild type plant whereby the method comprises at least the following step: increasing or generating in a plant or a part thereof one or more activities of a polypeptide selected from the group consisting of 2-oxoglutarate-dependent dioxygenase, 3-ketoacyl-CoA thiolase, 3'- phosphoadenosine 5'-phosphate phosphatase, 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase, 5OS chloroplast ribosomal protein L21, 57972199. R01.1 -protein, 60952769. R01.1 - protein, 60S ribosomal protein, ABC transporter family protein, AP2 domain-containing transcription factor, argonaute protein, AT1 G29250.1 -protein, AT1 G53885-protein, AT2G35300-protein, AT3G04620-protein, AT4G01870-protein, AT5G42380-protein, AT5G47440-protein, CDS5394-protein, CDS5401_TRUNCATED-protein, cold response protein, cullin, Cytochrome P450, delta-8 sphingolipid desaturase, galactinol synthase, glutathione-S-transferase, GTPase, haspin-related protein, heat shock protein, heat shock transcription factor, histone H2B, jasmonate-zim-domain protein, mitochondrial asparaginyl- tRNA synthetase, Oligosaccharyltransferase, OS02G44730-protein, Oxygen-evolving enhancer protein, peptidyl-prolyl cis-trans isomerase, peptidyl-prolyl cis-trans isomerase family protein, plastid lipid-associated protein, Polypyrimidine tract binding protein, PRLI- interacting factor, protein kinase, protein kinase family protein, rubisco subunit binding- protein beta subunit, serine acetyltransferase, serine hydroxymethyltransferase, small heat shock protein, S-ribosylhomocysteinase, sugar transporter, Thioredoxin H-type, ubiquitin- conjugating enzyme, ubiquitin-protein ligase, universal stress protein family protein, and Vacuolar protein.
    • 与相应的野生型植物相比,生产具有增加的产量的植物的方法,其中所述方法至少包括以下步骤:在植物或其部分中增加或产生一种或多种选自以下的多肽的活性: 2-氧戊二酸依赖性双加氧酶,3-酮酰基辅酶A硫解酶,3'-磷酸腺苷5'-磷酸磷酸酶,4-二磷酸胞苷-2-C-甲基-D-赤藓糖醇激酶,5OS叶绿体核糖体蛋白L21,57972199。R01.1 蛋白质,60952769.R01.1-蛋白质,60S核糖体蛋白质,ABC转运蛋白家族蛋白质,含AP2结构域的转录因子,argonaute蛋白质,AT1 G29250.1-蛋白质,AT1 G53885-蛋白质,AT2G35300-蛋白质,AT3G04620-蛋白质, AT4G01870蛋白质,AT5G42380蛋白质,AT5G47440蛋白质,CDS5394蛋白质,CDS5401_TRUNCATED蛋白质,冷应答蛋白质,cullin,细胞色素P450,δ-8鞘脂类去饱和酶,肌醇半胱氨酸合酶,谷胱甘肽-S-转移酶,GTP酶, n,热休克蛋白,热休克转录因子,组蛋白H2B,茉莉酸-zim结构域蛋白,线粒体天冬酰胺酰-tRNA合成酶,寡糖转移酶,OS02G44730-蛋白,氧进化增强子蛋白,肽基脯氨酰顺式反式异构酶,肽基脯氨酰 顺反异构酶家族蛋白,质体脂质相关蛋白,聚嘧啶多肽结合蛋白,PRLI相互作用因子,蛋白激酶,蛋白激酶家族蛋白,rubisco亚基结合蛋白β亚基,丝氨酸乙酰转移酶,丝氨酸羟甲基转移酶,小热休克蛋白, S-核糖基聚半胱氨酸酶,糖转运蛋白,硫氧还蛋白H型,泛素结合酶,泛素 - 蛋白连接酶,通用应激蛋白家族蛋白和Vacuolar蛋白。
    • 4. 发明申请
    • PLANTS WITH REDUCED ACTIVITY OF THE STARCH PHOSPHORYLATING ENZYME PHOSPHOGLUCAN, WATER DIKINASE
    • 具有降低活性的植物酶活性磷酸酶水解酶
    • WO2005095618A3
    • 2006-03-02
    • PCT/EP2005002450
    • 2005-03-04
    • BAYER CROPSCIENCE GMBHFROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • FROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • C12N9/00C12N9/12C12N15/82A01H5/00C07K16/40C12N1/21C12N5/10C12N15/01C12N15/11C12N15/54
    • C12N9/00C08B31/066C12N9/1294C12N15/8245
    • The present invention relates to plant cells and plants, which are genetically modified, wherein the genetic modification leads to the reduction of the activity of a starch phosphorylating OKl protein in comparison with corresponding wild type plant cells or wild type plants that have not been genetically modified. The OKl protein acts as a phosphoglucan, water dikinase (PWD) which predominately phosphorylates the C3 position. Genetically modified plants in which the expression of PWD is reduced show a starch excess phenotype. Furthermore, the present invention relates to means and methods for the manufacture of such plant cells and plants. Plant cells and plants of this type synthesise a modified starch. The present invention therefore also relates to the starch synthesised by the plant cells and plants according to the invention, methods for the manufacture of this starch, and the manufacture of starch derivatives of this modified starch, as well as flours containing starches according to the invention. Furthermore, the present invention relates to nucleic acid molecules, which ar suitable for manufacturing plants according to the invention.
    • 本发明涉及遗传修饰的植物细胞和植物,其中与相应的野生型植物细胞或未经遗传修饰的野生型植物相比,遗传修饰导致淀粉磷酸化OK1蛋白的活性降低 。 OK1蛋白作为主要磷酸化C3位置的磷酸葡聚糖,水分激酶(PWD)。 其中PWD表达减少的遗传修饰植物显示淀粉过量表型。 此外,本发明涉及用于制造这种植物细胞和植物的方法和方法。 这种植物细胞和植物合成改性淀粉。 因此,本发明还涉及由根据本发明的植物细胞和植物合成的淀粉,这种淀粉的制造方法,以及该改性淀粉的淀粉衍生物的制造,以及含有本发明淀粉的面粉 。 此外,本发明涉及适合于制造根据本发明的植物的核酸分子。
    • 7. 发明申请
    • PLANTS WITH INCREASED ACTIVITY OF A STARCH PHOSPHORYLATING ENZYME
    • 具有增加淀粉酶活性的植物
    • WO2005095617A3
    • 2006-03-02
    • PCT/EP2005002449
    • 2005-03-04
    • BAYER CROPSCIENCE GMBHFROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • FROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • C12N9/12C12N15/82A01H5/00C12N15/29
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and palnts, which are genetically modified, whereby the genetic modification leads to an increase in the activity of a starch-phosphorylating OK1 protein in comparison to the corresponding wild type plant cells or wild type plants that have not been genetically modified. In addition, the present invention concerns means and methods for the manufacture of such plant cells and plants. These types of plant cells and plants synthesise a modified starch. Therefore, the present invention also concerns the starches synthesised from the plant cells and plants according to the invention, methods for manufacturing these starches, and the manufacture of starch derivatives of these modified starches, as well as flours containing starches according to the invention. Furthermore, the present invention also relates to nucleic acids, coding starch-phosphorylating OK1 proteins, vectors, host cells, plant cells, and plants containing such nucleic acid molecules. In addition, the present invention relates to OK1 proteins that have starch-phosphorylating activity.
    • 本发明涉及遗传修饰的植物细胞和植物,由此遗传修饰导致淀粉磷酸化OK1蛋白的活性与尚未被使用的相应野生型植物细胞或野生型植物相比增加 转基因 此外,本发明涉及用于制造这种植物细胞和植物的方法和方法。 这些类型的植物细胞和植物合成了改性淀粉。 因此,本发明还涉及由根据本发明的植物细胞和植物合成的淀粉,这些淀粉的制造方法以及这些改性淀粉的淀粉衍生物的制备,以及含有本发明淀粉的面粉。 此外,本发明还涉及编码淀粉磷酸化OK1蛋白,载体,宿主细胞,植物细胞和含有这种核酸分子的植物的核酸。 此外,本发明涉及具有淀粉磷酸化活性的OK1蛋白质。
    • 8. 发明申请
    • PLANTS WITH INCREASED ACTIVITY OF A STARCH PHOSPHORYLATING ENZYME
    • 具有增加淀粉酶活性的植物
    • WO2005095617A2
    • 2005-10-13
    • PCT/EP2005/002449
    • 2005-03-04
    • BAYER CROPSCIENCE GMBHFROHBERG, ClausKOETTING, OliverRITTE, GerhardSTEUP, Martin
    • FROHBERG, ClausKOETTING, OliverRITTE, GerhardSTEUP, Martin
    • C12N15/82
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and palnts, which are genetically modified, whereby the genetic modification leads to an increase in the activity of a starch-phosphorylating OK1 protein in comparison to the corresponding wild type plant cells or wild type plants that have not been genetically modified. In addition, the present invention concerns means and methods for the manufacture of such plant cells and plants. These types of plant cells and plants synthesise a modified starch. Therefore, the present invention also concerns the starches synthesised from the plant cells and plants according to the invention, methods for manufacturing these starches, and the manufacture of starch derivatives of these modified starches, as well as flours containing starches according to the invention. Furthermore, the present invention also relates to nucleic acids, coding starch-phosphorylating OK1 proteins, vectors, host cells, plant cells, and plants containing such nucleic acid molecules. In addition, the present invention relates to OK1 proteins that have starch-phosphorylating activity.
    • 本发明涉及遗传修饰的植物细胞和植物,由此遗传修饰导致淀粉磷酸化OK1蛋白的活性与尚未被使用的相应野生型植物细胞或野生型植物相比增加 转基因 此外,本发明涉及用于制造这种植物细胞和植物的方法和方法。 这些类型的植物细胞和植物合成了改性淀粉。 因此,本发明还涉及由根据本发明的植物细胞和植物合成的淀粉,这些淀粉的制造方法以及这些改性淀粉的淀粉衍生物的制备,以及含有本发明淀粉的面粉。 此外,本发明还涉及编码淀粉磷酸化OK1蛋白,载体,宿主细胞,植物细胞和含有该核酸分子的植物的核酸。 此外,本发明涉及具有淀粉磷酸化活性的OK1蛋白质。
    • 9. 发明申请
    • PLANTS WITH INCREASED ACTIVITY OF A STARCH PHOSPHORYLATING ENZYME
    • 具有增加淀粉酶活性的植物
    • WO2005095617A9
    • 2016-11-10
    • PCT/EP2005002449
    • 2005-03-04
    • BAYER CROPSCIENCE GMBHFROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • FROHBERG CLAUSKOETTING OLIVERRITTE GERHARDSTEUP MARTIN
    • C12N15/82A01H5/00C12N9/12C12N15/29
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and palnts, which are genetically modified, whereby the genetic modification leads to an increase in the activity of a starch-phosphorylating OK1 protein in comparison to the corresponding wild type plant cells or wild type plants that have not been genetically modified. In addition, the present invention concerns means and methods for the manufacture of such plant cells and plants. These types of plant cells and plants synthesise a modified starch. Therefore, the present invention also concerns the starches synthesised from the plant cells and plants according to the invention, methods for manufacturing these starches, and the manufacture of starch derivatives of these modified starches, as well as flours containing starches according to the invention. Furthermore, the present invention also relates to nucleic acids, coding starch-phosphorylating OK1 proteins, vectors, host cells, plant cells, and plants containing such nucleic acid molecules. In addition, the present invention relates to OK1 proteins that have starch-phosphorylating activity.
    • 本发明涉及遗传修饰的植物细胞和植物,由此遗传修饰导致淀粉磷酸化OK1蛋白的活性与尚未被使用的相应野生型植物细胞或野生型植物相比增加 转基因 此外,本发明涉及用于制造这种植物细胞和植物的方法和方法。 这些类型的植物细胞和植物合成了改性淀粉。 因此,本发明还涉及由根据本发明的植物细胞和植物合成的淀粉,这些淀粉的制造方法以及这些改性淀粉的淀粉衍生物的制备,以及含有本发明淀粉的面粉。 此外,本发明还涉及编码淀粉磷酸化OK1蛋白,载体,宿主细胞,植物细胞和含有该核酸分子的植物的核酸。 此外,本发明涉及具有淀粉磷酸化活性的OK1蛋白质。