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Expression of the Multidrug Resistance Transporter NorA from Staphylococcus aureus Is Modified by a Two-Component Regulatory System

机译:金黄色葡萄球菌的多药耐药转运蛋白NorA的表达是由两组分调节系统修改的。

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摘要

To dissect genetically the regulation of NorA, a multidrug transporter of Staphylococcus aureus, we analyzed the differential expression of the norA promoter using a transcriptional fusion with a β-lactamase reporter gene. Expression studies with an arlS mutant revealed that the norA promoter is ArlS dependent. The arlR-arlS locus was shown to code for a two-component regulatory system. The protein ArlR has strong similarity to response regulators, and ArlS has strong similarity to protein histidine kinases. We have also analyzed the 350-bp region upstream of the Shine-Dalgarno sequence of norA by gel mobility shift experiments. It was shown that only the 115-bp region upstream of the promoter was necessary for multiple binding of an 18-kDa protein. From transcriptional fusions, we have localized four different putative boxes of 6 bp, which appear to play a role in the binding of the 18-kDa protein and in the up-regulation of norA expression in the presence of the arlS mutation. Furthermore, the gel mobility shift of the 18-kDa protein was modified in the presence of the arlS mutation, and the arlS mutation altered the growth-phase regulation of NorA. These results indicate that expression of norA is modified by a two-component regulatory system.
机译:为了从基因上解剖金黄色葡萄球菌的多药转运蛋白NorA的调控,我们使用与β-内酰胺酶报告基因的转录融合物分析了norA启动子的差异表达。用arlS突变体进行的表达研究表明norA启动子是ArlS依赖性的。显示arlR-arlS基因座编码为两组分调节系统。蛋白质ArlR与应答调节剂有很强的相似性,而ArlS与蛋白质组氨酸激酶有很强的相似性。我们还通过凝胶迁移率迁移实验分析了norA的Shine-Dalgarno序列上游350 bp区域。结果表明,18kDa蛋白的多重结合仅需要启动子上游的115bp区域。从转录融合中,我们已经定位了四个6 bp的不同推定框,它们在18 kDa蛋白的结合以及存在arlS突变的norA表达的上调中似乎起着作用。此外,在存在arlS突变的情况下,18-kDa蛋白的凝胶迁移率发生改变,而arlS突变改变了NorA的生长期调控。这些结果表明,norA的表达被两组分调节系统修饰。

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