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H3N2亚型SIV核蛋白基因的克隆及在大肠杆菌中的表达
朱春平1,2, 李 燕1, 吴亚丽,等1
1.河南农业大学 牧医工程学院;2.中国兽医药品监察所
摘要:
【目的】克隆和表达H3N2型猪流感病毒(SIV) A/swine/Henan/1/2010(H3N2)的核蛋白(NP)基因,为制备NP抗体和SIV基因工程疫苗奠定基础。【方法】提取SIV A/swine/Henan/1/2010(H3N2)的RNA,用RT-PCR扩增NP基因,将其定向克隆到pET-28a(+)原核表达载体,构建重组表达载体,并将其转化入大肠杆菌Rosetta中表达,用SDS-PAGE和Western blotting检测表达产物,同时考察IPTG不同浓度(0.2,0.4,0.6,0.8,1.0 mmol/L)和不同诱导时间(2,4,6,8 h)对重组NP蛋白表达量的影响。【结果】克隆到1 512 bp的NP基因,与预期的核蛋白基因大小一致,共编码498个氨基酸;构建的重组表达载体在大肠杆菌Rosetta中表达出了分子质量约60 ku的重组核蛋白,其主要以包涵体的形式存在。IPTG不同诱导浓度和不同诱导时间对重组NP蛋白表达量的影响均较小。【结论】克隆和表达了H3N2亚型猪流感病毒的核蛋白基因。
关键词:  猪流感病毒  核蛋白  H3N2亚型  大肠杆菌
DOI:
分类号:
基金项目:国家农业科技成果转化资金项目(2012GB2D000273);河南省科技成果转化计划项目(122201110027)
Clone of nucleoprotein gene of influenza A virus (H3N2) and its expression in Escherichia coli
ZHU Chun-ping,LI Yan,WU Ya-li,et al
Abstract:
【Objective】The nucleoprotein (NP) gene from swine influenza virus (SIV) A/swine/Henan/1/2010 (H3N2) was cloned and expressed to lay foundation for the preparation of NP antibody and genetic engineering vaccine of SIV.【Method】The total RNA of SIV A/swine/Henan/1/2010(H3N2) was extracted.The NP gene was amplified from the total RNA by using RT-PCR and it was inserted into prokaryotic expression vector pET-28a(+) to construct recombinant expression vector.Then the vector was transformed and expressed in Escherichia coli Rosetta.The expressed protein was detected by SDS-PAGE and Western blotting,and the expression levels of recombinant NP protein under different IPTG concentrations (0.2,0.4,0.6,0.8,and 1.0 mmol/L) and different induction times (2,4,6,and 8 h) were determined.【Result】The cloned NP gene (1 512 bp) was consistent with the expected nucleoprotein gene,encoding 498 amino acids.Recombinant expression vector expressed in E.coli Rosetta as recombinant nucleoprotein with the relative molecular weight of ~60 ku and mainly in the form of inclusion bodies.The expression level of recombinant NP protein was slightly influenced by IPTG concentration and induction time.【Conclusion】H3N2 swine influenza virus nucleoprotein gene was successfully cloned and expressed.
Key words:  SIV  nucleoprotein  H3N2  Escherichia coli