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白藜芦醇合酶基因的克隆与植物表达载体的构建 被引量:3

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摘要 目的为获得含有白藜芦醇(Res)的转基因植物,进行了白藜芦醇合酶(RS)基因的克隆、植物表达载体构建的研究。方法以葡萄为材料,从其叶片中提取基因组DNA,并以此DNA为模板,利用PCR法扩增得到RS基因,将此基因连接到克隆载体PGEM-TVector,得到重组载体pT-RS;经酶切及测序鉴定后,将RS基因克隆到植物表达载体pBI121,得到重组载体pBI-RS,用PCR及酶切方法进行鉴定。结果重组质粒pT-RS的测序结果表明,RS基因的片段大小为1.522kb。将此片段正向插入植物表达载体pBI121的CaMV35s启动子和NOS终止子之间,对重组子进行PCR及酶切鉴定,均得到预期大小的片断,证明RSDNA与质粒pBI121已成功连接,植物表达载体pBI-RS构建正确。结论成功扩增得到RS基因及成功构植物表达载体pBI-RS,为RS转基因生菜的研究奠定了基础。
出处 《南方医科大学学报》 CAS CSCD 北大核心 2008年第11期2051-2053,共3页 Journal of Southern Medical University
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