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Identification of the varR Gene as a Transcriptional Regulator of Virginiamycin S Resistance in Streptomyces virginiae

机译:鉴定varR基因作为弗吉尼亚链霉菌弗吉尼亚霉素S抗性的转录调节因子

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摘要

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.
机译:在编码链霉菌素S(VS)特异性转运蛋白的varS基因下游的维链霉菌89 bp处鉴定到一个名为varR(用于弗吉尼亚抗生素抗性调节剂)的基因。推导的varR产物与具有保守的螺旋-转-螺旋-DNA结合基序的TetR家族的阻遏物显示出高度同源性。纯化的重组VarR蛋白在体外以二聚体形式存在,并且对varS启动子区域显示出清晰的DNA结合活性。 VS的存在取消了这种结合,表明VarR以VS依赖性的方式调节varS的转录。 Northern印迹分析表明,varR与上游varS共转录为2.4-kb转录本,并且VS充当双顺反子转录的诱导物。 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。

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