Alimentary Pharmabiotic Centre and Department of Microbiology, Bioscience Institute, National University of Ireland, Cork, Ireland.
Appl Environ Microbiol. 2012 Oct;78(19):7032-41. doi: 10.1128/AEM.01776-12. Epub 2012 Jul 27.
This work reports on the identification and molecular characterization of a two-component regulatory system (2CRS), encoded by serRK, which is believed to control the expression of the ser(2003) locus in Bifidobacterium breve UCC2003. The ser(2003) locus consists of two genes, Bbr_1319 (sagA) and Bbr_1320 (serU), which are predicted to encode a hypothetical membrane-associated protein and a serpin-like protein, respectively. The response regulator SerR was shown to bind to the promoter region of ser(2003), and the probable recognition sequence of SerR was determined by a combinatorial approach of in vitro site-directed mutagenesis coupled to transcriptional fusion and electrophoretic mobility shift assays (EMSAs). The importance of the serRK 2CRS in the response of B. breve to protease-mediated induction was confirmed by generating a B. breve serR insertion mutant, which was shown to exhibit altered ser(2003) transcriptional induction patterns compared to the parent strain, UCC2003. Interestingly, the analysis of a B. breve serU mutant revealed that the SerRK signaling pathway appears to include a SerU-dependent autoregulatory loop.
本研究报告了一个双组份调控系统(2CRS)的鉴定和分子特征,该系统由 serRK 编码,被认为控制双歧杆菌短双歧亚种 UCC2003 中 ser(2003)基因座的表达。ser(2003)基因座由两个基因,Bbr_1319(sagA)和 Bbr_1320(serU)组成,分别预测编码一个假设的膜相关蛋白和一个丝氨酸蛋白酶抑制剂样蛋白。结果表明,应答调节因子 SerR 与 ser(2003)的启动子区域结合,SerR 的可能识别序列通过体外定向诱变与转录融合和电泳迁移率变动分析(EMSA)的组合方法确定。通过生成双歧杆菌短双歧亚种 serR 插入突变体,证实了 serRK 2CRS 在双歧杆菌对蛋白酶介导的诱导反应中的重要性,与亲本菌株 UCC2003 相比,该突变体表现出改变的 ser(2003)转录诱导模式。有趣的是,对双歧杆菌短双歧亚种 serU 突变体的分析表明,SerRK 信号通路似乎包括一个 SerU 依赖性的自身调控环。