中华皮肤科杂志 ›› 2005, Vol. 38 ›› Issue (11): 674-676.

• 论著 • 上一篇    下一篇

淋病奈瑟菌mtrC膜蛋白基因的克隆和表达

陈宏翔, 林能兴, 黄长征, 李家文, 刘厚君, 涂亚庭   

  1. 华中科技大学同济医学院附属协和医院皮肤性病科, 武汉 430022
  • 收稿日期:2004-12-27 发布日期:2005-11-15
  • 基金资助:
    国家自然科学基金资助项目(30371293)

Construction of a Prokaryotic Expression Plasmid Encoding the mtrC Gene of N.gonorrhoeae and Its Expression in E.coli

CHEN Hong-xiang, LIN Neng-xing, HUANG Chang-zheng, LI Jia-wen, LIU Hou-jun, TU Ya-ting   

  1. Department of Dermatology, Wuhan Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China
  • Received:2004-12-27 Published:2005-11-15

摘要: 目的 构建淋病奈瑟菌膜蛋白mtrC表达质粒,探讨淋病奈瑟菌耐药的检测和耐药机制.方法 从淋病奈瑟菌标准株中扩增淋病奈瑟菌膜蛋白mtrC基因片段.酶切后插入pET-28a(+),构建重组表达质粒pET-mtrC.通过质粒双酶切和DNA测序证实该重组质粒构建正确.重组质粒转化入大肠杆菌DE3中.经IPTG诱导表达蛋白.结果 经酶切鉴定和测序分析,质粒构建正确.核苷酸序列与GeneBank(U14993)公布的序列相比较,同源性达到99.5%.通过IPTG诱导,SDS—PAGE可检测到约48500大小的融合蛋白,与预测分子量相同.结论 淋病奈瑟菌膜蛋白mtrC原核表达质粒构建和表达成功,为研究其mtrC外排系统的耐药机制打下基础.

关键词: 奈瑟球菌,淋病, 原核表达, mtrC

Abstract: Objective To construct a prokaryotic expression plasmid pET-28a (+) encoding the multiple transferable resistance C (mtrC) gene of N. gonorrhoeaeand express it inE.coli DE3, in order to provide a model to study the pathogen's resistance mechanisms to antimicrobial hydrophobic agents. Methods The mtrC gene of N. gonorrhoeaewas amplified by polymerase chain reaction from reference strains,cleaved with restriction endonuclease, and then cloned into the prokaryotic expression plasmid pET-28a (+) to construct the recombinant pET-mtrC. This was confirmed by cleavage of restriction endonuclease and DNA sequencing. The recombinant pET-mtrC was transformed intoE.coliDE3 to express the protein MtrC with induction by IPTG. Results The mtrC gene in the recombinant pET-mtrC showed 99.5% homology with the reference sequence in GeneBank (U14993). A 48.5 kD fusion protein was identified by SDS-PAGE. Conclusions The successful construction of a prokaryotic plasmid encoding the mtrC gene of N. gonorrhoeaeand its expression inE.colimay facilitate the development of a monoclonal antibody to the MtrC protein and help to investigate the mechanism of the mtr efflux system of N. gonorrhoeae.

Key words: Neisseria gonorrhoeae, Prokaryotic expression, mtrC