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GENETIC ENGINEERING OF RICE FOR RESISTANCE TO SHEATH BLIGHT

机译:水稻抗白叶枯病的遗传工程

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摘要

A 1.1 kb rice genomic DNA fragment, containing a chitinase gene under the control of the CaMV 35S promoter, was cloned into the rice transformation vector pGL2. After transformation of Indica rice protoplasts in the presence of polyethyleneglycol, plants were regenerated, The presence of the chimeric chitinase gene in T0 and T1 transgenic rice plants was detected by Southern blot analysis, Western blot analysis of transgenic plants and their progeny revealed the presence of two proteins with apparent molecular weights of 30 and 35 kDa that reacted with the chitinase antibody. Progeny from the chitinase-positive plants were tested for their resistance to the sheath blight pathogen, Rhizoctonia solani. The degree of resistance displayed by the transgenic plants to this pathogen correlated with the level of chitinase expression.
机译:将包含在CaMV 35S启动子控制下的几丁质酶基因的1.1 kb水稻基因组DNA片段克隆到水稻转化载体pGL2中。在聚乙二醇存在下转化In稻原生质体后,再生植株,通过Southern印迹分析检测T0和T1转基因水稻植株中嵌合几丁质酶基因的存在,转基因植物及其子代的Western印迹分析表明存在与几丁质酶抗体反应的两种表观分子量分别为30和35 kDa的蛋白质。测试来自几丁质酶阳性植物的后代对鞘枯病病原体Rhizoctonia solani的抗性。转基因植物对该病原体表现出的抗性程度与几丁质酶表达水平相关。

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