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| 鸡传染性支气管炎病毒(IBV)ZZ2004株核衣壳蛋白基因的克隆及原核表达 | |
| 引用本文： | 贺会利,徐敏,余娟,魏小兵,闫艺婷,勾肖晶,刘兴友.鸡传染性支气管炎病毒(IBV)ZZ2004株核衣壳蛋白基因的克隆及原核表达[J].中国畜牧兽医,2014,41(9):15-20. |
| 作者姓名： | 贺会利 徐敏 余娟 魏小兵 闫艺婷 勾肖晶 刘兴友 |
| 作者单位： | 1. 河南科技学院动物科学学院, 河南新乡 453003; 2. 畜禽智能化清洁生产河南省工程实验室, 河南新乡 453003; 3. 动物病毒病防控与药残分析河南省重点学科开放实验室, 河南新乡 453003 |
| 基金项目： | 国家自然科学基金（30771601）；河南省高校科技创新人才支持计划（2009HASTIT010）。 |
| 摘 要： | 本研究旨在克隆并表达鸡传染性支气管炎病毒（IBV）的核衣壳蛋白（N）。根据IBV ZZ2004株的N基因设计1对引物，提取IBV ZZ2004株的RNA，利用RT-PCR技术扩增大小约1.23 kb的片段，将其插入克隆载体pGEM-T构建pGEM-T-N。将pGEM-T-N用EcoRⅠ和XhoⅠ进行双酶切，将酶切后的N基因片段克隆到表达载体pGEX-6P-1，转入大肠杆菌BL21（DE3）菌中，经IPTG诱导表达，进行SDS-PAGE电泳，结果显示外源基因获得了表达且为可溶性蛋白；Western blotting检测结果显示N蛋白可与相应的IBV ZZ2004阳性血清发生特异性反应，结果表明N蛋白有一定的生物活性。本研究为IBV诊断试剂盒及新型IBV重组亚单位疫苗研制奠定基础。 |
| 关 键 词： | 鸡传染性支气管炎病毒(IBV) 核衣壳蛋白 克隆 可溶性表达 |
| 收稿时间： | 2014-04-30 |
Cloning and Prokaryotic Expression of Nucleoprotein Gene of Infectious Bronchitis Virus (IBV)ZZ2004 Strain |
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| HE Hui-li,XU Min,YU Juan,WEI Xiao-bing,YAN Yi-ting,GOU Xiao-jing,LIU Xing-you.Cloning and Prokaryotic Expression of Nucleoprotein Gene of Infectious Bronchitis Virus (IBV)ZZ2004 Strain[J].China Animal Husbandry & Veterinary Medicine,2014,41(9):15-20. | |
| Authors: | HE Hui-li XU Min YU Juan WEI Xiao-bing YAN Yi-ting GOU Xiao-jing LIU Xing-you |
| Institution: | 1. School of Animal Science, Henan University of Science and Technology, Xinxiang 453003, China; 2. Henan Higher Education Engineering Discipline Intelligent Cleaner Production of Livestock, Xinxiang 453003, China; 3. Animal Viral Disease Control and Residual Analysis Henan Higher Education Key Discipline Open Laboratory, Xinxiang 453003, China |
| Abstract: | This experiment was conducted to clone and express the nucleoprotein (N) gene of infectious bronchitis virus (IBV). A pair of specific primers was designed and synthesized according to the published sequence of IBV ZZ2004. RNA of IBV ZZ2004 strain was extracted and the fragment of about 1.23 kb was amplified by RT-PCR, which was correct fragment.The fragment was inserted into the cloning vector pGEM-T to construct pGEM-T-N, and nucleotide sequence was determined by dideoxy-mediated chain termination method. The pGEM-T-N was excised by EcoR Ⅰ and Xho Ⅰ, and inserted into the expression plasmid pGEX-6P-1 to obtain the recombinant expression vector pGEX-6P-1-N, which was used to transform into E.coli BL21 (DE3) competent cells. Then the recombinant pGEX-6P-1-N was induced by IPTG, SDS-PAGE and Western blotting results confirmed that the gene had been expressed in recombinant pGEX-6P-1-N, and the protein was soluble. The expression product could specially react to the anti-sera of IBV which showed that N protein had some biological activity. This study had laid a solid foundation for production of diagnostic reagents for testing IB and new type IB gene engineering vaccines. |
| Keywords: | infectious bronchitis virus(IBV) nucleoprotein cloning soluble expression |
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