《中国畜牧兽医》 ›› 2016, Vol. 43 ›› Issue (12): 3135-3140.doi: 10.16431/j.cnki.1671-7236.2016.12.008

• 生物技术 • 上一篇    下一篇

鹿结核分枝杆菌MPB70蛋白的表达与免疫原性鉴定

王晓龙1, 卢天成1, 王秀然1, 杨艳玲2   

  1. 1. 吉林农业大学生命科学学院, 长春 130118;
    2. 中国农业科学院特产研究所, 长春 130112
  • 收稿日期:2016-05-12 出版日期:2016-12-20 发布日期:2016-12-22
  • 通讯作者: 杨艳玲 E-mail:yangyanling12280@sina.com
  • 作者简介:王晓龙(1991-),男,吉林榆树人,硕士生,研究方向:微生物资源开发与利用,E-mail:15004314273@163.com
  • 基金资助:

    吉林省科技攻关项目(20140204070NY)

Expression of MPB70 Protein and Identification the Immunogenicity of Deer Mycobacterium tuberculosis

WANG Xiao-long1, LU Tian-cheng1, WANG Xiu-ran1, YANG Yan-ling2   

  1. 1. College of Life Science, Jilin Agricultural University, Changchun 130118, China;
    2. Institute of Special Animal and Plant Sciences, Chinese Academy of Agricultural Sciences, Changchun 130112, China
  • Received:2016-05-12 Online:2016-12-20 Published:2016-12-22

摘要:

本研究以分离的鹿结核分枝杆菌DNA为模板扩增免疫原性蛋白MPB70基因,获得约590 bp片段,并将其克隆,构建原核表达载体pET-30a-MPB70,将重组质粒转入大肠杆菌BL21(DE3),经IPTG诱导后纯化和SDS-PAGE分析,在20 ku处可见特异性蛋白条带。利用鹿结核阳性血清进行Western blotting鉴定,原核表达的融合蛋白可与鹿结核阳性血清抗体结合,并出现特异的免疫反应。该蛋白可作为特异性抗原进行鹿结核病的检测,从而为鹿结核病诊断方法的研究奠定基础。

关键词: 结核分枝杆菌; MPB70基因; 原核表达

Abstract:

In this study,the immunogenicity protein MPB70 gene was amplified from Mycobacterium tuberculosis genome DNA which separated from deer, and about 590 bp fragment was obtained. Then the fragment was cloned and constructed prokaryotic expression vector of pET-30a-MPB70, and the recombinant plasmid was put into E. coli BL21(DE3).Purified after IPTG induction, and analyzed by SDS-PAGE, a specificity protein band was observed at 20 ku. Using the deer serum positive of tuberculosis in Western blotting, the fusion protein could be combined with deer serum positive of tuberculosis antibody and arise specific immune response. The protein could be used as a specific antigen to test the deer tuberculosis. The study laid a foundation for further studying the deer tuberculosis appraisal method.

Key words: Mycobacterium tuberculosis; MPB70 gene; prokaryotic expression

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