核糖开关控制的 TerC 家族转运体 Alx 可调节碱性 pH 值下大肠杆菌细胞内的锰浓度。

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2024-07-25 Epub Date: 2024-06-13 DOI:10.1128/jb.00168-24
Ravish Sharma, Tatiana V Mishanina
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引用次数: 0

摘要

细胞使用过渡金属离子作为生物大分子的结构成分和酶促反应的辅助因子,因此过渡金属离子是不可或缺的细胞成分。生物体通过调节导入和导出金属离子的蛋白质的表达来优化金属离子浓度,以满足细胞的需要,这种调节方式通常与金属离子浓度有关。核糖开关是 mRNA 的 5'- 非翻译区,会发生构象变化,促进或抑制下游基因的表达,通常是对配体的反应。细菌核糖开关 yybP-ykoY 家族有一个与锰离子(Mn2+)结合的共轭结构域。在大肠杆菌中,yybP-ykoY 核糖开关先于两个不同基因的表达并对其进行调控:mntP 和 alx,前者根据遗传学证据编码 Mn2+ 导出器,后者编码一种假定的金属离子转运体,其同源配体目前尚存在疑问。高浓度 Mn2+ 和碱性 pH 都会上调 alx 的表达。通过金属离子测量和基因表达研究,我们证明培养基碱化会增加细胞质锰池,进而增强 alx 的表达。Alx 介导的 Mn2+ 输出可防止细胞锰的毒性积累,在碱性 pH 值下输出活性最大。我们在预测的 Alx 跨膜片段中找到了一组酸性残基,它们在 Mn2+ 的导出过程中起着关键作用。我们认为,Alx 介导的 Mn2+ 输出是一种主要的保护机制,可对细胞质中的锰含量进行微调,尤其是在碱性应激期间。重要意义 细菌在遇到某些环境应激时会使用巧妙的方法来调整基因表达,例如人体肠道部分区域的碱性 pH 值和高浓度的过渡金属离子锰。细菌调节基因表达的一种方法是通过信使 RNA 的 5'- 非翻译区(称为核糖开关),这些核糖开关与配体结合,从而开启/关闭基因的表达。在这项工作中,我们研究了大肠杆菌中受 yybP-ykoY 核糖开关调控的两个基因 alx 和 mntP 在碱性 pH 和高浓度 Mn2+ 条件下的作用和调控。这项工作凸显了细菌适应环境的复杂方式,即利用核糖调节机制在不同环境因素中维持 Mn2+ 的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A riboswitch-controlled TerC family transporter Alx tunes intracellular manganese concentration in Escherichia coli at alkaline pH.

Cells use transition metal ions as structural components of biomolecules and cofactors in enzymatic reactions, making transition metal ions integral cellular components. Organisms optimize metal ion concentration to meet cellular needs by regulating the expression of proteins that import and export that metal ion, often in a metal ion concentration-dependent manner. One such regulation mechanism is via riboswitches, which are 5'-untranslated regions of an mRNA that undergo conformational changes to promote or inhibit the expression of the downstream gene, commonly in response to a ligand. The yybP-ykoY family of bacterial riboswitches shares a conserved aptamer domain that binds manganese ions (Mn2+). In Escherichia coli, the yybP-ykoY riboswitch precedes and regulates the expression of two different genes: mntP, which based on genetic evidence encodes an Mn2+ exporter, and alx, which encodes a putative metal ion transporter whose cognate ligand is currently in question. The expression of alx is upregulated by both elevated concentrations of Mn2+ and alkaline pH. With metal ion measurements and gene expression studies, we demonstrate that the alkalinization of media increases the cytoplasmic manganese pool, which, in turn, enhances alx expression. The Alx-mediated Mn2+ export prevents the toxic buildup of the cellular manganese, with the export activity maximal at alkaline pH. We pinpoint a set of acidic residues in the predicted transmembrane segments of Alx that play a critical role in Mn2+ export. We propose that Alx-mediated Mn2+ export serves as a primary protective mechanism that fine tunes the cytoplasmic manganese content, especially during alkaline stress.IMPORTANCEBacteria use clever ways to tune gene expression upon encountering certain environmental stresses, such as alkaline pH in parts of the human gut and high concentration of a transition metal ion manganese. One way by which bacteria regulate the expression of their genes is through the 5'-untranslated regions of messenger RNA called riboswitches that bind ligands to turn expression of genes on/off. In this work, we have investigated the roles and regulation of alx and mntP, the two genes in Escherichia coli regulated by the yybP-ykoY  riboswitches, in alkaline pH and high concentration of Mn2+. This work highlights the intricate ways through which bacteria adapt to their surroundings, utilizing riboregulatory mechanisms to maintain Mn2+ levels amidst varying environmental factors.

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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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