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    • 1. 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
    • US20120017333A1
    • 2012-01-19
    • US13174228
    • 2011-06-30
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMARTIN STEUP
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMARTIN STEUP
    • A01H5/00C12N15/54C12N15/63C12N1/15C12N15/82C12N1/21C12N1/19C12N5/10C12Q1/68
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and plants, 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,其中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造,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。
    • 2. 发明申请
    • Plants with Increased Yield (NUE)
    • 提高产量的植物(NUE)
    • US20110321197A1
    • 2011-12-29
    • US13125433
    • 2009-10-02
    • Hardy SchönOliver ThimmGerhard RitteOliver BläsingKoen BruynseelsYves HatzfeldValerie FrankardAna Isabel Sanz MolineroChristophe ReuzeauSteven Vandenabeele
    • Hardy SchönOliver ThimmGerhard RitteOliver BläsingKoen BruynseelsYves HatzfeldValerie FrankardAna Isabel Sanz MolineroChristophe ReuzeauSteven Vandenabeele
    • A01H1/06C12N15/63C12P21/00C12N9/88C12N9/12C12N9/10C12N9/00C12N9/04C12N9/16C12N9/22C12N9/90C07K2/00C07K16/40C07K16/14C07K16/12C12N5/10A01H5/00C12Q1/68G01N33/53C12Q1/02C12Q1/28C12Q1/32C12Q1/48C12Q1/44C12Q1/42C08B30/04A01C14/00C07H21/00
    • C12N15/8273C12N15/8261Y02A40/146
    • 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 selected from the group consisting of 17.6 kDa class I heat shock protein, 26.5 kDa class I small heat shock protein, 26S protease subunit, 2-Cys peroxiredoxin, 3-dehydroquinate synthase, 5-keto-D-gluconate-5-reductase, asparagine synthetase A, aspartate 1-decar-boxylase precursor, ATP-dependent RNA helicase, B0567-protein, B1088-protein, B1289-protein, B2940-protein, calnexin homolog, CDS5399-protein, chromatin structure-remodeling complex protein, D-amino acid dehydrogenase, D-arabinono-1,4-lac-tone oxidase, Delta 1-pyrroline-5-carboxylate reductase, glycine cleavage complex lipoylprotein, ketodeoxygluconokinase, lipoyl synthase, low-molecular-weight heat-shock protein, Microsomal cytochrome b reductase, mitochondrial ribosomal protein, mitotic check point protein, monodehydroascorbate reductase, paraquat-inducible protein B, phosphatase, Phosphoglucosamine mutase, protein disaggregation chaperone, protein kinase, pyruvate decarboxylase, recA family protein, rhodanese-related sulfurtransferase, ribonuclease P protein component, ribosome modulation factor, sensory histidine kinase, serine hydroxymethyltransferase, SLL1280-protein, SLL1797-protein, small membrane lipoprotein, Small nucleolar ribonucleoprotein complex subunit, Sulfatase, transcription initiation factor subunit, tretraspanin, tRNA ligase, xyloglucan galactosyltransferase, YKL130C-protein, YLR443W-protein, YML096W-protein, and zinc finger family protein-activity.
    • 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17.6kDa类的活性 I热休克蛋白,26.5 kDa I类小热休克蛋白,26S蛋白酶亚基,2-Cys过氧化还原蛋白,3-脱氢秋水仙素合成酶,5-酮-D-葡萄糖酸-5-还原酶,天冬酰胺合成酶A,天冬氨酸1-脱羧基酶 前体,ATP依赖性RNA解旋酶,B0567-蛋白,B1088-蛋白,B1289-蛋白,B2940蛋白,钙粘蛋白同源物,CDS5399-蛋白,染色质结构重塑复合蛋白,D-氨基酸脱氢酶,D-阿拉伯聚糖-1, 4-lac-色素氧化酶,1α-吡咯啉-5-羧酸还原酶,甘氨酸裂解复合物脂酰蛋白,酮脱氧葡萄糖激酶,脂酰基合成酶,低分子量热休克蛋白,微粒体细胞色素b还原酶,线粒体核糖体蛋白,有丝分裂检测点 nt蛋白,单脱氢抗坏血酸还原酶,百草枯诱导蛋白B,磷酸酶,磷酸葡糖胺变位酶,蛋白质分解伴侣蛋白,蛋白激酶,丙酮酸脱羧酶,recA家族蛋白,硫酸相关硫转移酶,核糖核酸酶P蛋白组分,核糖体调节因子,感觉组氨酸激酶,丝氨酸 羟基甲基转移酶,SLL1280蛋白,SLL1797蛋白,小膜脂蛋白,小核仁核糖核蛋白复合子亚基,硫酸酯酶,转录起始因子亚基,tretraspanin,tRNA连接酶,木葡聚糖半乳糖基转移酶,YKL130C-蛋白,YLR443W蛋白,YML096W蛋白和锌指 家庭蛋白质活性。
    • 3. 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
    • US20110027447A1
    • 2011-02-03
    • US12774420
    • 2010-05-05
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMATIN STEUP
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMATIN STEUP
    • A23L1/10C08B31/00C12P19/04C12N9/12B02C11/00
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and plants, 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,其中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。
    • 7. 发明授权
    • Plants with increased activity of a starch phosphorylating enzyme
    • 具有增加淀粉磷酸化酶活性的植物
    • US07772463B2
    • 2010-08-10
    • US10591428
    • 2005-03-04
    • Claus FrohbergOliver KoettingGerhard RitteMartin Steup
    • Claus FrohbergOliver KoettingGerhard RitteMartin Steup
    • C12N15/82C12N15/00C12N15/29C12N15/52C12N15/63A01H5/00
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and plants, 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 synthesize a modified starch. Therefore, the present invention also concerns the starches synthesized 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,其中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。
    • 8. 发明授权
    • Plants with increased activity of a starch phosphorylating enzyme
    • 具有增加淀粉磷酸化酶活性的植物
    • US08895804B2
    • 2014-11-25
    • US13174228
    • 2011-06-30
    • Claus FrohbergOliver KoettingGerhard RitteMartin Steup
    • Claus FrohbergOliver KoettingGerhard RitteMartin Steup
    • C12N15/82C12N15/00C12N15/29C12N15/63A01H5/00B02C9/00C12N9/12
    • B02C9/00C12N9/12C12N9/1205C12N15/8245
    • The present invention relates to plant cells and plants, 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 synthesize a modified starch. Therefore, the present invention also concerns the starches synthesized 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,其中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造,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。
    • 10. 发明申请
    • Plants with Reduced Activity of a Starch Phosphorylating Enzyme
    • 具有淀粉磷酸化酶活性降低的植物
    • US20110269195A1
    • 2011-11-03
    • US13033495
    • 2011-02-23
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMARTIN STEUP
    • CLAUS FROHBERGOLIVER KOETTINGGERHARD RITTEMARTIN STEUP
    • C12P19/04C08B31/00
    • 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 OK1 protein in comparison with corresponding wild type plant cells or wild type plants that have not been genetically modified. 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 are 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,其中遗传修饰导致淀粉磷酸化OK1蛋白的活性降低,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较 。 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。