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鸭Ⅰ型肝炎病毒VP1基因片段的克隆与表达载体的构建
引用本文:赵瑞宏,张丹俊,潘孝成,程宝艳,胡晓苗.鸭Ⅰ型肝炎病毒VP1基因片段的克隆与表达载体的构建[J].中国畜牧兽医,2010,37(7):67-69.
作者姓名:赵瑞宏  张丹俊  潘孝成  程宝艳  胡晓苗
作者单位:(安徽省农业科学院畜牧兽医研究所,合肥 230031)
基金项目:院长青年创新基金,国家科技支撑计划项目 
摘    要:为研究鸭肝炎病毒VP1基因在大肠杆菌中的表达情况,根据鸭肝炎病毒核苷酸序列设计1对外引物和1对含有EcoRⅠ和SalⅠ酶切位点的内引物。以内外引物进行PCR扩增,将所得PCR产物回收,以相同的限制性内切酶酶切目的基因和表达载体pET-32a后构建重组表达载体,并转入宿主菌BL21和Rosseta,经酶切、PCR和测序鉴定,证明VP1基因正确插入了表达载体。用不同浓度的IPTG诱导VP1基因的表达,收集菌液进行SDS-PAGE电泳,结果表明,VP1基因片段在大肠杆菌Rosseta和BL21中均难以表达。

关 键 词:鸭肝炎病毒R85952株  VP1基因  克隆  表达  

Cloning of VP1 Gene Fragments of Duck Hepatitis Virus Type I and Construction of its Expression Plasmid
ZHAO Rui-hong,ZHANG Dan-jun,PAN Xiao-cheng,CHENG Bao-yan,HU Xiao-miao.Cloning of VP1 Gene Fragments of Duck Hepatitis Virus Type I and Construction of its Expression Plasmid[J].China Animal Husbandry & Veterinary Medicine,2010,37(7):67-69.
Authors:ZHAO Rui-hong  ZHANG Dan-jun  PAN Xiao-cheng  CHENG Bao-yan  HU Xiao-miao
Abstract:To study the expression of the duck hepatitis virus 1(DHV1) VP1 gene in E.coli ,one outer primer pair and one inter primer pair containing EcoR Ⅰ and Sal Ⅰ according to complete genome of DHV1 were designed. PCR products were re cycled by outer and inter primer pair .The PCR products and pET-32a vector were digested by EcoR Ⅰ and Sal Ⅰ to construct the recombinant plasmids.Then the recombinant plasmids were transfected into E.coli BL21 and Rosseta. After digestion, PCR and sequencing the target gene were insert expression vector correctly. With different concentrations of IPTG induced bacteria express VP1 gene, the bacterias were collected and examined by SDS-PAGE.The results showed that the VP1 gene fragments hard to express in E.coli Rosseta and BL21.
Keywords:duck hepatitis virus R85952 strain  VP1 gene  cloning  expression
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