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作 者:刘成宏[1] 金扩世[2] 金宁一[2] 鲁会军[2] 贾雷立[2] 陈义锋[1] 金明兰[1] 姜鲲[1]
机构地区:[1]吉林大学农学部畜牧兽医学院,长春130062 [2]军事医学科学院军事兽医研究所,长春130062
出 处:《中国生物制品学杂志》2007年第2期73-76,共4页Chinese Journal of Biologicals
基 金:吉林省科技计划发展项目(20040560)
摘 要:目的构建鸡新城疫(ND)强毒株多裂解位点串联基因表达载体,为建立NDV强弱毒株的ELISA鉴别方法奠定基础。方法人工合成一段包含4种不同NDV强毒株裂解位点的基因Fe(F prote in multitude epi-position),其中各裂解位点之间用Linker(GGGGS)使其串联,然后进行2倍和4倍拷贝,并定向克隆至原核表达质粒pET-28a(+)中,构建重组表达质粒pET-28a(+)/2Fe和pET-28a(+)/4Fe,进行表达和Western blot鉴定。结果构建的原核表达重组质粒pET-28a(+)/2Fe和pET-28 a(+)/4Fe测序正确。Western blot检测结果表明,2Fe、4Fe蛋白均与新城疫强毒株F48E9阳性血清呈阳性反应,而与新城疫弱毒株V4阳性血清呈阴性反应。结论已成功构建NDV强毒株F蛋白裂解位点串联基因表达载体,为建立NDV强弱毒株的ELISA鉴别方法提供理论依据。Objective To construct the prokaryotic expression vector for F protein schizolysis site gene cascade of virulent Newcastle disease virus(NDV) strain and lay a foundation of differentiation of virulent and low virulent NDV strains by ELISA. Methotis Synthesize a gene fragment Fe ( F protein multitude epi-position) containing 4 different schizolysis sites of virulent NDV strains, of which the sites were linked through a linker GGGGS. Copy Fe gene for 2 and 4 times,then clone the obtained 2Fe and 4Fe genes directly into pmkaryotic expression vector pET-28a( + ) respectively. Transform the constructed recombinant plasmids pET-28a( + )/2Fe and pET-28a( + )/4Fe to E. coil BL21 (DE3) respectively and identify the expressed products by Western blot. Results Sequencing results proved that recombinant plasmids pET-28a( + )/2Fe and pET-28a( + )/4Fe were correctly constructed. Western blot shooed specific reaction of expressed 2Fe and 4Fe proteins with F48E9 positive sera but no reaction with V4 positive sera. Conclusion A prokaryotic expression vector for F pretein schizolysis site gene cascade of virulent NDV strain was successfully constructad,which provided a theoretical basis for differentiation of virulent and low virtdent NDV strains by ELISA.
分 类 号:S852.65[农业科学—基础兽医学]
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