Namwat W, Lee C K, Kinoshita H, Yamada Y, Nihira T
Department of Biotechnology, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Bacteriol. 2001 Mar;183(6):2025-31. doi: 10.1128/JB.183.6.2025-2031.2001.
A gene designated varR (for virginiae antibiotic resistance regulator) was identified in Streptomyces virginiae 89 bp downstream of a varS gene encoding a virginiamycin S (VS)-specific transporter. The deduced varR product showed high homology to repressors of the TetR family with a conserved helix-turn-helix DNA binding motif. Purified recombinant VarR protein was present as a dimer in vitro and showed clear DNA binding activity toward the varS promoter region. This binding was abolished by the presence of VS, suggesting that VarR regulates transcription of varS in a VS-dependent manner. Northern blot analysis revealed that varR was cotranscribed with upstream varS as a 2.4-kb transcript and that VS acted as an inducer of bicistronic transcription. Deletion analysis of the varS promoter region clarified two adjacent VarR binding sites in the varS promoter.
在弗吉尼亚链霉菌中,一个名为varR(弗吉尼亚抗生素抗性调节因子)的基因在编码维吉尼亚霉素S(VS)特异性转运蛋白的varS基因下游89 bp处被鉴定出来。推导的VarR产物与TetR家族的阻遏物具有高度同源性,带有保守的螺旋-转角-螺旋DNA结合基序。纯化的重组VarR蛋白在体外以二聚体形式存在,并对varS启动子区域表现出明显的DNA结合活性。VS的存在消除了这种结合,这表明VarR以VS依赖的方式调节varS的转录。Northern印迹分析显示,varR与上游的varS共转录为一个2.4 kb的转录本,并且VS作为双顺反子转录的诱导剂。varS启动子区域的缺失分析明确了varS启动子中两个相邻的VarR结合位点。