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    • 1. 发明申请
    • Methods for identifying inhibitors of chlorophyll synthase
    • 鉴定叶绿素合酶抑制剂的方法
    • US20050130118A1
    • 2005-06-16
    • US10737014
    • 2003-12-16
    • Abubakr AslamkhanLining GuoRao MulpuriNeil HoffmanSusanne KjemtrupJocelyn KearneyCory ChristensenKeith DavisAdel ZayedRobert AscenziDouglas Boyes
    • Abubakr AslamkhanLining GuoRao MulpuriNeil HoffmanSusanne KjemtrupJocelyn KearneyCory ChristensenKeith DavisAdel ZayedRobert AscenziDouglas Boyes
    • C12Q1/00G01N33/573
    • G01N33/573
    • The present inventors have discovered that antisense suppression of a chlorophyll synthase (CS) gene results in plants exhibiting one or more of chlorosis, reduced growth, and altered development. Thus, the present inventors have discovered that the protein encoded by the CS gene is essential for normal plant growth and development, and is useful as a target for the identification of compounds as antibiotics and herbicides, especially herbicides. The present invention is directed to methods for identifying inhibitors of a CS enzyme by incubating a CS polypeptide with a chlorophyllide and a phopholipid substrate in the presence and absence of a test compound under conditions suitable for the CS enzyme activity, adding a solution to the incubation reactions comprising a water immiscible organic solvent, a water-soluble alcohol, and a water-soluble dye that absorbs in the range of one or both the excitation and emission wavelength ranges of the chlorophyllide substrate, and measuring the fluorescence of the incubation reactions at from about 650 to 750 nm, using from about 425 to 445 nm as excitation wavelength, wherein a decrease in the fluorescence in the presence of the test compound indicates that the compound is a CS inhibitor.
    • 本发明人已经发现,叶绿素合酶(CS)基因的反义抑制导致植物表现出一种或多种褪绿,生长减少和改变发育。 因此,本发明人已经发现,由CS基因编码的蛋白质对于正常的植物生长和发育是必需的,并且可用作鉴定作为抗生素和除草剂,特别是除草剂的化合物的靶标。 本发明涉及通过在适合于CS酶活性的条件下,在存在和不存在测试化合物的情况下,将CS多肽与叶绿素和磷脂底物一起温育来鉴定CS酶抑制剂的方法,向培养基中加入溶液 包括与水不溶混的有机溶剂,水溶性醇和在所述叶绿素底物的激发和发射波长范围中的一个或两个的范围内吸收的水溶性染料的反应,以及测量从 约650至750nm,使用约425至445nm作为激发波长,其中在测试化合物存在下荧光的降低表明该化合物是CS抑制剂。
    • 10. 发明申请
    • Methods And Compositions For Analyzing Ahasl Genes
    • 用于分析Ahasl基因的方法和组合
    • US20130289264A1
    • 2013-10-31
    • US13527103
    • 2012-06-19
    • Chengyan ZHAORobert AscenziBijay K. Singh
    • Chengyan ZHAORobert AscenziBijay K. Singh
    • C12Q1/68
    • C12Q1/6876C12Q1/6895C12Q2600/156
    • The invention relates to methods and compositions for analyzing plant acetohydroxy acid synthase large subunit (AHASL) genes. In particular, the invention relates to methods for the detection of wild-type AHASL alleles and mutant AHASL alleles that encode imidazolinone-tolerant AHASL proteins. The methods involve the use of PCR amplification and novel compositions comprising allele-specific and gene-specific primers to detect the presence of mutant and/or wild-type alleles present at the individual AHASL genes of a plant. Specifically, the methods and compositions are useful for analyzing the three AHASL genes of Triticum aestivum and the two AHASL genes of Triticum turgidum ssp. durum.
    • 本发明涉及用于分析植物乙酰羟酸合酶大亚基(AHASL)基因的方法和组合物。 特别地,本发明涉及检测野生型AHASL等位基因的方法和编码咪唑啉酮耐受性AHASL蛋白的突变型AHASL等位基因。 所述方法包括使用PCR扩增和包含等位基因特异性和基因特异性引物的新型组合来检测存在于植物个体AHASL基因的突变体和/或野生型等位基因的存在。 具体地说,该方法和组合物可用于分析小麦Triticum aestivum的三种AHASL基因和Twiticum turgidum ssp的两种AHASL基因。 硬粒小麦