首页> 外文会议>International Conference on Biomedical and Biological Engineering >Cloning and Expression of cry9Ea10 Gene from Bacillus Thuringiensis Strain GZ2 Isolated from Infected Hyphantria Cunea Larvae
【24h】

Cloning and Expression of cry9Ea10 Gene from Bacillus Thuringiensis Strain GZ2 Isolated from Infected Hyphantria Cunea Larvae

机译:从感染的菌丝氏菌幼虫分离的Bacillus thuringiensis菌株GZ2克隆和表达Cry9ea10基因

获取原文

摘要

A novel Bacillus thuringiensis (Bt) strain GZ2, was isolated from infected Hyphantria cunealarvae. The bioassay results showed that GZ2 had insecticidal activity to H.cunea larvae. The genotypes of GZ2 were identified by PCR-RFLP method. GZ2 was identified to harbor cry9Ea10 gene and the full length of cry9Ea10 was cloned and sequenced. The engineering strain of Bt carrying cry9Ea10gene wasconstructed successfully. SDS-PAGE analysis confirmed that the expression of cry9Ea10 as ~130kDa protein. And Cry9Ea10 protein produced by Bt engineeringstra inexhibited a high toxicity to H.cunealarvae.
机译:新的芽孢杆菌(BT)菌株GZ2,被来自受感染的菌丝Cunarvae分离。生物测定结果表明,GZ2对H.Cunea幼虫有杀虫活性。通过PCR-RFLP方法鉴定GZ2的基因型。 GZ2被鉴定为Harb Cry9ea10基因,并且克隆并测序的全长Cry9ea10。 BT携带Cry9ea10gene的工程应变成功呈现。 SDS-PAGE分析证实,Cry9ea10表达为〜130kda蛋白。 BT Engineeriantstra产生的Cry9ea10蛋白缺乏对H.Cunealarvae的高毒性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号