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The β-Glucoside (bgl) Operon of Escherichia coli Is Involved in the Regulation of oppA, Encoding an Oligopeptide Transporter

机译:大肠杆菌的β-葡萄糖苷(bgl)操纵子参与调节oppA,编码寡肽转运蛋白。

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摘要

We report that the bgl operon of Escherichia coli, encoding the functions necessary for the uptake and metabolism of aryl-β-glucosides, is involved in the regulation of oligopeptide transport during stationary phase. Global analysis of intracellular proteins from Bgl-positive (Bgl+) and Bgl-negative (Bgl−) strains revealed that the operon exerts regulation on at least 12 downstream target genes. Of these, oppA, which encodes an oligopeptide transporter, was confirmed to be upregulated in the Bgl+ strain. Loss of oppA function results in a partial loss of the growth advantage in stationary-phase (GASP) phenotype of Bgl+ cells. The regulatory effect of the bgl operon on oppA expression is indirect and is mediated via gcvA, the activator of the glycine cleavage system, and gcvB, which regulates oppA at the posttranscriptional level. We show that BglG destabilizes the gcvA mRNA in vivo, leading to reduced expression of gcvA in the stationary phase. Deletion of gcvA results in the downregulation of gcvB and upregulation of oppA and can partially rescue the loss of the GASP phenotype seen in ΔbglG strains. A possible mechanism by which oppA confers a competitive advantage to Bgl+ cells relative to Bgl− cells is discussed.
机译:我们报告说,大肠杆菌的bgl操纵子,编码为摄取和代谢芳基-β-葡萄糖苷所必需的功能,参与了稳定期期间寡肽运输的调控。对来自Bgl阳性(Bgl +)和Bgl阴性(Bgl-)菌株的细胞内蛋白质的全局分析显示,操纵子对至少12个下游靶基因施加调控。其中,编码寡肽转运蛋白的oppA被证实在Bgl +菌株中被上调。 opgA功能的丧失导致Bgl +细胞的固定相(GASP)表型的生长优势部分丧失。 bgl操纵子对oppA表达的调节作用是间接的,并通过甘氨酸裂解系统的活化剂gcvA和在转录后水平调节oppA的gcvB介导。我们显示,BglG会在体内破坏gcvA mRNA的稳定性,从而导致gcvA在固定相中的表达减少。 gcvA的缺失导致gcvB的下调和oppA的上调,并且可以部分挽救在ΔbglG菌株中看到的GASP表型的丧失。讨论了oppA赋予Bgl +细胞相对于Bgl-细胞竞争优势的可能机制。

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