Transgenic expression of a phytochrome a gene
    1.
    发明申请
    Transgenic expression of a phytochrome a gene 有权
    植物色素a基因的转基因表达

    公开(公告)号:US20040268443A1

    公开(公告)日:2004-12-30

    申请号:US10834786

    申请日:2004-04-29

    CPC classification number: C12N15/8261 Y02A40/146

    Abstract: An isolated nucleic acid construct including a nucleic acid molecule encoding a light-labile, phytochrome A, a light-inducible promoter which is 5null to the nucleic acid molecule encoding a light-labile, phytochrome A, and a terminator region which is 3null to the nucleic acid molecule encoding a light-labile, phytochrome A is disclosed. Methods for regulating a plant's canopy architecture and regulating a plant's seed yield, which involve transgenic plants or transgenic plant seeds including an isolated nucleic acid construct according to the present invention, are also disclosed.

    Inducible promoter
    3.
    发明申请
    Inducible promoter 失效
    诱导启动子

    公开(公告)号:US20040248303A1

    公开(公告)日:2004-12-09

    申请号:US10760752

    申请日:2004-01-20

    CPC classification number: C12N15/8281 C07K14/415 C12N15/8282

    Abstract: The Arabidopsis NI16 gene was isolated in a yeast 2-hybrid screen via its interaction with the NIM1 protein and encodes a protein involved in the regulation of SAR gene expression in plants. NI16 is strongly induced in NIM1-overexpressing plants treated with benzo(1,2,3)thiadiazole-7-carbothioic acid S-methyl ester (BTH). The nucleic acid sequence of the Arabidopsis NI16 promoter is disclosed herein.

    Abstract translation: 通过与NIM1蛋白的相互作用,在酵母2-杂交筛选中分离拟南芥NI16基因,并编码参与植物中SAR基因表达调控的蛋白质。 NI16在用苯并(1,2,3)噻二唑-7-硫代硫酸S-甲酯(BTH)处理的NIM1过表达植物中强烈诱导。 本文公开了拟南芥NI16启动子的核酸序列。

    Engineering beta-ketoacyl ACP synthase for novel substrate specificity
    4.
    发明申请
    Engineering beta-ketoacyl ACP synthase for novel substrate specificity 审中-公开
    工程β-酮酰胆碱ACP合酶用于新颖的底物特异性

    公开(公告)号:US20040216185A1

    公开(公告)日:2004-10-28

    申请号:US10851894

    申请日:2004-05-24

    CPC classification number: C12N9/1029 C12N15/8247 C12P7/6409 C12P7/6463

    Abstract: Methods of altering substrate specificity of beta-ketoacyl-ACP synthase, and engineered beta-ketoacyl-ACP synthases so produced are provided. DNA sequences and constructs for expression of engineered beta-ketoacyl-ACP synthases, as well as the novel beta-ketoacyl-ACP synthases produced therefrom are also provided. Such DNA sequences may be used for expression of the engineered beta-ketoacyl-ACP synthases in host cells, particularly seed cells of oilseed crop plants, for the modification of fatty acid composition.

    Abstract translation: 提供了改变β-酮酰基-ACP合成酶底物特异性的方法和如此制备的工程化β-酮酰基-ACP合成酶。 还提供了用于表达工程化β-酮酸酰-ACP合酶的DNA序列和构建体,以及由其产生的新型β-酮酰基-ACP合成酶。 这样的DNA序列可用于在宿主细胞,特别是油菜作物植物的种子细胞中表达改造的β-酮酸酰-ACP合酶,用于改变脂肪酸组成。

    Expression of spider silk proteins in higher plants
    7.
    发明申请
    Expression of spider silk proteins in higher plants 有权
    蜘蛛丝蛋白在高等植物中的表达

    公开(公告)号:US20040210956A1

    公开(公告)日:2004-10-21

    申请号:US10479638

    申请日:2004-05-05

    CPC classification number: C07K14/43518 C12N15/8257

    Abstract: The present invention relates to the fields of molecular biology and plant biology. Specifically, the invention is directed to the methods for expressing spider silk proteins in plants and the synthesis and purification of spider silk proteins therefrom.

    Abstract translation: 本发明涉及分子生物学和植物生物学领域。 具体地说,本发明涉及在植物中表达蜘蛛丝蛋白的方法以及从其中合成和提纯蜘蛛丝蛋白。

    Pathogen induced promoters
    9.
    发明申请
    Pathogen induced promoters 审中-公开
    病原体诱导的启动子

    公开(公告)号:US20040205841A1

    公开(公告)日:2004-10-14

    申请号:US10638464

    申请日:2003-08-12

    CPC classification number: C12N15/8282 C12N15/8239

    Abstract: Pathogen-inducible plant promoters are identified. The promoters control expression of nullhypersensitive responsenull proteins, including a protease inhibitor, an isocitrate lyase, and a glycoprotein. Heterologous gene sequences are produced by operably linking a promoter according to the present invention with a gene to be expressed in a transformed plant. Transformed plants are made by transforming a vector with a heterologous gene according to the present invention and then transforming the plant with the transformed vector. The transformed plants are capable of expressing a pre-selected protein in response to challenge by a plant pathogen, for example tobacco blue moldnullP. tabacina.

    Abstract translation: 确定病原体诱导型植物启动子。 启动子控制“过敏反应”蛋白质的表达,包括蛋白酶抑制剂,异柠檬酸裂解酶和糖蛋白。 通过将根据本发明的启动子与在转化植物中表达的基因可操作地连接来产生异源基因序列。 通过用根据本发明的异源基因转化载体然后用转化的载体转化植物来制备转化的植物。 转化的植物能够响应于植物病原体(例如烟草蓝霉素-P)的攻击而表达预先选择的蛋白质。 tabacina

    HBV mutations associated with reduced susceptibility to adefovir
    10.
    发明申请
    HBV mutations associated with reduced susceptibility to adefovir 审中-公开
    与阿德福韦敏感性降低相关的HBV突变

    公开(公告)号:US20040194155A1

    公开(公告)日:2004-09-30

    申请号:US10678443

    申请日:2003-10-01

    Abstract: Applicants have identified 5 mutants associated with hepatitis B virus resistance to adefovir, a nucleotide analogue antiviral drug widely employed in the therapy of hepatitis B. In accord with this invention, reverse transcriptase mutants rtN236T, rtA181V, rtA181T and their corresponding surface antigen mutants sL173F and sL172trunc are provided. The mutant proteins, antibodies thereto and nucleic acids encoding the mutants have diagnostic value in monitoring and adjusting patient therapy with adefovir and in the therapy of patients infected with the mutants.

    Abstract translation: 申请人已经确定了与乙型肝炎病毒抗性相关的5种突变体,阿德福韦,广泛用于乙型肝炎治疗的核苷酸类似物抗病毒药物。根据本发明,逆转录酶突变体rtN236T,rtA181V,rtA181T及其相应的表面抗原突变体sL173F和 提供sL172trunc。 突变蛋白,其抗体和编码突变体的核酸在监测和调整阿德福韦的患者治疗以及感染突变体的患者的治疗方面具有诊断价值。

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