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猪瘟病毒E2基因的克隆表达
引用本文:朱文豪,张以芳,徐引弟,王治方,张玉杨,郭成留.猪瘟病毒E2基因的克隆表达[J].河南农业科学,2009(9).
作者姓名:朱文豪  张以芳  徐引弟  王治方  张玉杨  郭成留
作者单位:1. 河南省农业科学院,畜牧兽医研究所,河南,郑州,450002;云南农业大学,动物科技学院,云南,昆明,650201
2. 云南农业大学,动物科技学院,云南,昆明,650201
3. 河南省农业科学院,畜牧兽医研究所,河南,郑州,450002
基金项目:国家自然科学基金项目,河南省农科院专项发展基金 
摘    要:PCR扩增猪瘟病毒(CSFV)定点突变后的E2基因,克隆至原核表达载体质粒pET-28a中,重组质粒pET28a-E2转化BL21(DE3),IPTG诱导,高效表达了E2基因,表达量达菌体总蛋白的25.3%。免疫印迹表明,所表达的蛋白是CSFV特异性的。

关 键 词:猪瘟病毒  E2基因  原核表达

Cloning and Expression of E2 Gene of Classic Swine Fever Virus
ZHU Wen-hao,ZHANG Yi-fang,XU Yin-di,WANG Zhi-fang,ZHANG Yu-yang,GUO Cheng-liu.Cloning and Expression of E2 Gene of Classic Swine Fever Virus[J].Journal of Henan Agricultural Sciences,2009(9).
Authors:ZHU Wen-hao  ZHANG Yi-fang  XU Yin-di  WANG Zhi-fang  ZHANG Yu-yang  GUO Cheng-liu
Institution:1.Institute of Animal Husbandry and Veterinary Research;Henan Academy of Agricultural Sciences;Zhengzhou 450002;China;2.College of Animal Science and Technology;Yunnan Agricultural University;Kunming 650201;China
Abstract:A mutated CSFV E2 gene was amplified by PCR and cloned into pET-28a to construct the prokaryotic expression vector pET28a-E2.The recombinant plasmid was transformed into BL21(DE3) and expressed at high level induced by IPTG.The expressed E2 protein was amounted to 25.3% of the total bacteria proteins.The result of Western-blot showed that the recombinant E2 protein was CSFV-specific.
Keywords:CSFV  E2 gene  Prokaryotic expression  
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