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产气荚膜梭菌肠毒素基因原核表达载体的构建
引用本文:唐源,赵健湖,罗阿东,王开功,周碧君,文明.产气荚膜梭菌肠毒素基因原核表达载体的构建[J].贵州农业科学,2009,37(7).
作者姓名:唐源  赵健湖  罗阿东  王开功  周碧君  文明
作者单位:1. 贵州大学,动物科学学院,贵州,贵阳,550025
2. 贵州大学,职业技术学院,贵州,贵阳,550003
3. 贵州大学,动物科学学院,贵州,贵阳,550025;贵州大学动物疫病研究所,贵州,贵阳,550025
基金项目:国家科技部支撑计划,贵州省科技支撑计划项目,贵州省农业厅兽医科技计划项目 
摘    要:以含C型产气荚膜梭菌分离株(CP2)肠毒素基因的克隆载体pMD18-T-cpe为材料,根据产气荚膜梭菌开放阅读框设计合成一对特异性引物,采用PCR技术对其进行扩增,经BamHI和EcoRI双酶切后,从胶上回收目的基因,与经过相同两种内切酶处理的原核表达栽体pET32a连接,转化大肠杆菌DH5a感受态细胞后,提取质粒进行PCR和BamHI/EcoRI双酶切鉴定后测序.结果表明,肠毒素基因已成功地克隆到原核表达栽体上(重组质粒命名为pET32a-cpe),从而构建了产气荚膜梭菌肠毒素基因的原核表达质粒.

关 键 词:产气荚膜梭菌  肠毒素基因  原核表达载体  构建

Construction of Prokaryotic Expression Vector of the Enterotoxin Gene of Clostridium perfringens Type C
TANG Yuan,ZHAO Jian-hu,LUO A-dong,WANG Kai-gong,ZHOU Bi-jun,WEN Ming.Construction of Prokaryotic Expression Vector of the Enterotoxin Gene of Clostridium perfringens Type C[J].Guizhou Agricultural Sciences,2009,37(7).
Authors:TANG Yuan  ZHAO Jian-hu  LUO A-dong  WANG Kai-gong  ZHOU Bi-jun  WEN Ming
Institution:1.College of Animal Science;Guizhou University;Guiyang;Guizhou 550025;2.College of Vocational Education;3.Animal Disease Institute;China
Abstract:A pair of specific primers was designed and synthesized based on the published C.perfringens enterotoxin gene,and amplified the gene from vector pMD18-T-cpe.The PCR products retrieved from 1.0% agarose gel was digested by BamHI and EcoRI and then directly ligased to prokaryotic expression vector pET32a digested by same enzymes.The recombinant plasmid was transferred into competent cells of E.coli DH5a.The recombinant plasmid was identified by PCR and restriction enzyme and then sequenced.The results showed ...
Keywords:Clostridium perfringens  enterotoxin gene  prokaryotic expression vector  construction  
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