南方医科大学学报 ›› 2004, Vol. 24 ›› Issue (09): 995-997.

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融合表达的副溶血弧菌不耐热性溶血毒素包涵体复性的研究

李志峰, 聂军, 戴迎春, 陈清, 俞守义   

  1. 第一军医大学流行病学教研室, 广东, 广州, 510515
  • 出版日期:2004-09-20 发布日期:2004-09-20
  • 基金资助:
    收稿日期:2003-10-18。
    基金项目:全军“十五”指令性课题(01L050)
    作者简介:李志峰(1970-),男,2003年毕业于第一军医大学,硕士,助研,电话:020-61640114-89129

Renaturation of thermolabile hemolysin inclusion bodies expressed by Vibrio parahaemolyticus

LI Zhi-feng, NIE Jun, DAI Ying-chun, CHEN Qing, YU Shou-yi   

  1. 第一军医大学流行病学教研室, 广东, 广州, 510515
  • Online:2004-09-20 Published:2004-09-20

摘要: 目的 构建融合表达载体,获得具有生物活性的副溶血弧菌不耐热性溶血毒素。方法 克隆tlh基因,构建表达载体pET32a+/tlh,融合表达副溶血弧菌不耐热性溶血毒素,用8 mol/L的尿素溶解包涵体,亲和层析纯化目的蛋白,采取逐步透析、降低蛋白浓度、加入氧化还原剂等复性方法。结果 复性蛋白具有溶血活性及免疫原性。结论 通过克隆tlh基因,构建融合表达载体pET32a+-tlh,采取纯化、复性方法,获得具有融血活性及免疫原性的副溶血弧菌不耐热性溶血毒素。

Abstract: Objective To clone and construct expression vector pET32a+-tlh to acquire biologically functional thermolabile hemolysin of Vibrio parahaemolyticus. Methods tlh gene was cloned and the expression vector pET32a+-tlh constructed. The tlh gene of Vibrio parahaemolyticus was expressed in DE3 in the form of inclusion body, which was resolved in 8 mol/L urea followed by purification of the fusion protein using affinity chromatography and renaturation through gradient dialysis, protein concentration reduction and oxidoreduction. Results and Conclusion The purified and renatured protein possessed hemolytic and immunogenic activities.

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