JIA Qi-jun, MENG Xiao-lin*, XU Jin-ping, WANG Jian and LU Wei. Expression of Envelope Protein VP19 of Penaeus monodon WSSV in E.coli and the Effect against WSSV[J]. Virologica Sinica, 2006, 21(6): 585-588.
Citation: JIA Qi-jun, MENG Xiao-lin*, XU Jin-ping, WANG Jian, LU Wei. Expression of Envelope Protein VP19 of Penaeus monodon WSSV in E.coli and the Effect against WSSV .VIROLOGICA SINICA, 2006, 21(6) : 585-588.

对虾白斑综合症病毒囊膜蛋白VP19的融合表达及其抗病毒感染作用

  • 根据GenBank上WSSV囊膜蛋白基因vp 19的序列,设计并合成引物,PCR扩增得到vp19基因并克隆到pGEM‐T载体中,经过BamHⅠ/Hind Ⅲ酶切、连接并将vp19插入到pET32b表达载体中。用重组质粒pET32b-vp19转化大肠杆菌Origami(DE3)pLysS,在IPTG诱导下,融合蛋白Trx-VP19以可溶性的形式得到表达,经SDS-PAGE和Western-blot检测显示其分子量与预期的大小相符合。目的蛋白经Ni2+柱纯化并定量后分别直接注射鳌虾和包被饲料投喂鳌虾。实验结果表明注射Trx-VP19可以提高鳌虾个体抗WSSV感染力的作用。

Expression of Envelope Protein VP19 of Penaeus monodon WSSV in E.coli and the Effect against WSSV

  • The vp19 gene of White spot syndrome virus (WSSV) was amplified by PCR with specific primers and subcloned into the prokaryotic expression vector pET32b to get the recombinant plasmid pET32b-vp19. A positive plasmid was transformed into the host cell Origami(DE3)pLysS and the target gene was successfully expressed as a fusion protoen when induced with IPTG. The molecular weight of the engineered protein was about 37kDa as demonstrated by SDS-PAGE and Western-blot. The engineered protein Trx-VP19 purified by Ni2+-column chromatography was injected into crayfish or used as a supplement to feed crayfish. Crayfish vaccinated by intramuscular injection with Trx-VP19 showed lower cumulative mortality due to WSSV compared to vaccination with bacteria expressing the empty vectors.

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    Expression of Envelope Protein VP19 of Penaeus monodon WSSV in E.coli and the Effect against WSSV

    • 1. State Key Laboratory of Virology, Wuhan University, Wuhan 430072, China

    Abstract: The vp19 gene of White spot syndrome virus (WSSV) was amplified by PCR with specific primers and subcloned into the prokaryotic expression vector pET32b to get the recombinant plasmid pET32b-vp19. A positive plasmid was transformed into the host cell Origami(DE3)pLysS and the target gene was successfully expressed as a fusion protoen when induced with IPTG. The molecular weight of the engineered protein was about 37kDa as demonstrated by SDS-PAGE and Western-blot. The engineered protein Trx-VP19 purified by Ni2+-column chromatography was injected into crayfish or used as a supplement to feed crayfish. Crayfish vaccinated by intramuscular injection with Trx-VP19 showed lower cumulative mortality due to WSSV compared to vaccination with bacteria expressing the empty vectors.

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