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中国农学通报 ›› 2013, Vol. 29 ›› Issue (11): 55-59.doi: 10.11924/j.issn.1000-6850.2012-3302

所属专题: 生物技术

• 水产 渔业 • 上一篇    下一篇

溶藻弧菌HY9901转运蛋白TolB的原核表达及条件优化和纯化

周泽军 庞欢瑛 丁燏 简纪常 吴灶和   

  • 收稿日期:2012-10-07 修回日期:2012-10-22 出版日期:2013-04-15 发布日期:2013-04-15
  • 基金资助:
    国家重点基础研究发展计划;国家自然科学基金;广东省教育厅育苗基金

Purification and Optimization of Prokaryotic Expression of Translocation Protein TolB Gene from Vibrio alginolyticus Strain HY9901

  • Received:2012-10-07 Revised:2012-10-22 Online:2013-04-15 Published:2013-04-15

摘要: 为研究溶藻弧菌(Vibrio alginolyticus) HY9901转运蛋白TolB作为疫苗候选抗原的可能性,根据已发表的溶藻弧菌HY9901转运蛋白TolB序列(JQ846501),设计1对带酶切位点的引物,PCR扩增tolB基因,然后经酶切、连接等步骤,构建tolB基因的原核表达载体pET-TolB,并对其IPTG浓度、诱导时间、温度、洗脱浓度进行优化,以期获得较大量的目的蛋白。结果表明:IPTG诱导后经SDS-PAGE与Western-blot分析,成功表达了溶藻弧菌HY9901株TolB蛋白,分子量与预期相符,且表达的蛋白以包涵体的形式存在;TolB蛋白在大肠杆菌中诱导表达的优化条件为:0.2 mmol/L IPTG,37℃诱导4 h;最佳咪唑洗脱浓度为400 mmol/L。这些结果为进一步研究目的蛋白的免疫原性和疫苗制备奠定基础。

关键词: 花色苷, 花色苷

Abstract: To investigate the possibility of TolB from Vibrio alginolyticus HY9901 as a candidate antigen for vaccine production, the tolB gene was amplified by using a pair of primer according to the published tolB gene sequence (JQ846501), and then followed by digestion, connection; the prokaryotic expression vector pET-TolB of tolB gene was constructed. Then the IPTG concentration, induction time, temperature, elution concentration of the pET-TolB was optimized to obtain a relatively large amount of the target protein. The result showed that, the TolB protein was successfully expressed after being inducted with IPTG and SDS-PAGE, Western-blot analysis. The molecular weight of TolB protein was in line with expectation, and the expressed protein existed in the form of inclusion body. The optimization condition of inducible expression for TolB protein in Escherichia coli was optimized at 37℃ for 4 hours, with 0.2 mmol/L IPTG. The best elution concentration of imidazole was 400 mmol/L. These results laid a foundation for further studies on the protein immunogenecity and vaccine preparation.

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