节点文献

苏云金杆菌杀虫晶体蛋白基因cry1A的克隆及特征分析

Cloning and characterization analysis of insecticidal crystal protein gene cry1 A from Bacillus thuringiensis

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 钟万芳蔡平钟阎文昭裴炎

【Author】 ZHONG Wan-fang~(1,3),CAI Ping-zhong~(1,2),YAN Wen-zhao~(1,2),PEI Yan~3(1.Biotechnological Breeding Center,Sichuan Academy of Agricultural Sciences,Chengdu 610066,China;2.Institute of Biotechnology and Nuclear Technology,Sichuan Academy of Agricultural Sciences,Chengdu 610066,China;3.Biotechnological Research Center,Southwest Agricultrual University,Chongqing 400716,China)

【机构】 四川省农业科学院生物技术育种中心西南农业大学生物技术中心 四川成都 610066西南农业大学生物技术中心重庆北碚 400716四川成都 610066四川省农业科学院生物技术核技术研究所四川成都 610066重庆北碚 400716

【摘要】 苏云金芽孢杆菌猝倒亚种(Bacillusthuringiensissubsp.sotto)对鳞翅目幼虫有高毒力。根据cry1A类基因序列设计特异引物,应用PCR技术从该菌株中扩增得到一大小约为3 6kb的DNA片段。将获得的片段克隆至pGEM7zf中并转化大肠杆菌DH5α。在ABIPRISM377自动测序仪上对其5′及3′端进行部分测序,结果表明其核苷酸序列与cry1A基因高度同源。

【Abstract】 Bacillus thuringiensis subsp.sotto is highly toxic to lepidopetera larvae.Using computer analysis of cry1A gene sequences,a pair of specific primers was designed.With the primers,PCR was performed and about 3.6kb fragments were obtained from Bacillus thuringiensis subsp.sotto.The fragments were ligated into the cloning vector pGEM7zf and then transformed into E.coli DH5α.Partial sequencing was done to the 5′-end and 3′-end by ABI PRISM 377 DNA suquencer.The result revealed its high homology with cry1A genes.

【基金】 四川省生物技术重点资助项目
  • 【文献出处】 西南农业学报 ,Southwest China Journal of Agricultural Sciences , 编辑部邮箱 ,2004年01期
  • 【分类号】Q78
  • 【被引频次】3
  • 【下载频次】191
节点文献中: