Vladislava Schulz, Diana Galea, Grit Schleuder, Philipp Strohmeyer, Cornelia Große, Martin Herzberg, Dietrich H Nies
{"title":"铜绿微囊藻中的外排系统 CdfX 能输出 ZntA 无法运输的锌。","authors":"Vladislava Schulz, Diana Galea, Grit Schleuder, Philipp Strohmeyer, Cornelia Große, Martin Herzberg, Dietrich H Nies","doi":"10.1128/jb.00299-24","DOIUrl":null,"url":null,"abstract":"<p><p><i>Cupriavidus metallidurans</i> is able to survive exposure to high concentrations of transition metals, but is also able to grow under metal starvation conditions. A prerequisite of cellular zinc homeostasis is a flow equilibrium combining zinc uptake and efflux processes. The mutant strain ∆e4 of the parental plasmid-free strain AE104 with a deletion of all four chromosomally encoded genes of previously known efflux systems ZntA, CadA, DmeF, and FieF was still able to efflux zinc in a pulse-chase experiment, indicating the existence of a fifth efflux system. The gene <i>cdfX</i>, encoding a protein of the cation diffusion facilitator (CDF) family, is located in proximity to the <i>cadA</i> gene, encoding a P-type ATPase. Deletion of <i>cdfX</i> in the ∆e4 mutant resulted in a further decrease in zinc resistance. Pulse-chase experiments with radioactive <sup>65</sup>Zn(II) and stable-isotope-enriched <sup>67</sup>Zn(II) provided evidence that CdfX was responsible for the residual zinc efflux activity of the mutant strain ∆e4. Reporter gene fusions with <i>cdfX-lacZ</i> indicated that the MerR-type regulator ZntR, the main regulator of <i>zntA</i> expression, was responsible for zinc- and cadmium-dependent upregulation of <i>cdfX</i> expression, especially in mutant cells lacking one or both of the previously characterized efflux systems, ZntA and CadA. Expression of <i>zntR</i> also proved to be controlled by ZntR itself as well as by zinc and cadmium availability. These data indicate that the <i>cdfX-cadA</i> region provides <i>C. metallidurans</i> with a backup system for the zinc-cadmium-exporting P-type ATPase ZntA, with CdfX exporting zinc and CadA cadmium.IMPORTANCEBacteria have evolved the ability to supply the important trace element zinc to zinc-dependent proteins, despite external zinc concentrations varying over a wide range. Zinc homeostasis can be understood as adaptive layering of homeostatic systems, allowing coverage from extreme starvation to extreme resistance. Central to zinc homeostasis is a flow equilibrium of zinc comprising uptake and efflux reactions, which adjusts the cytoplasmic zinc content. This report describes what happens when an imbalance in zinc and cadmium concentrations impairs the central inner-membrane zinc efflux system for zinc by competitive inhibition for this exporter. The problem is solved by activation of Cd-exporting CadA or Zn-exporting CdfX as additional efflux systems.</p>","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":" ","pages":"e0029924"},"PeriodicalIF":2.7000,"publicationDate":"2024-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11580412/pdf/","citationCount":"0","resultStr":"{\"title\":\"The efflux system CdfX exports zinc that cannot be transported by ZntA in <i>Cupriavidus metallidurans</i>.\",\"authors\":\"Vladislava Schulz, Diana Galea, Grit Schleuder, Philipp Strohmeyer, Cornelia Große, Martin Herzberg, Dietrich H Nies\",\"doi\":\"10.1128/jb.00299-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Cupriavidus metallidurans</i> is able to survive exposure to high concentrations of transition metals, but is also able to grow under metal starvation conditions. A prerequisite of cellular zinc homeostasis is a flow equilibrium combining zinc uptake and efflux processes. The mutant strain ∆e4 of the parental plasmid-free strain AE104 with a deletion of all four chromosomally encoded genes of previously known efflux systems ZntA, CadA, DmeF, and FieF was still able to efflux zinc in a pulse-chase experiment, indicating the existence of a fifth efflux system. The gene <i>cdfX</i>, encoding a protein of the cation diffusion facilitator (CDF) family, is located in proximity to the <i>cadA</i> gene, encoding a P-type ATPase. Deletion of <i>cdfX</i> in the ∆e4 mutant resulted in a further decrease in zinc resistance. Pulse-chase experiments with radioactive <sup>65</sup>Zn(II) and stable-isotope-enriched <sup>67</sup>Zn(II) provided evidence that CdfX was responsible for the residual zinc efflux activity of the mutant strain ∆e4. Reporter gene fusions with <i>cdfX-lacZ</i> indicated that the MerR-type regulator ZntR, the main regulator of <i>zntA</i> expression, was responsible for zinc- and cadmium-dependent upregulation of <i>cdfX</i> expression, especially in mutant cells lacking one or both of the previously characterized efflux systems, ZntA and CadA. Expression of <i>zntR</i> also proved to be controlled by ZntR itself as well as by zinc and cadmium availability. These data indicate that the <i>cdfX-cadA</i> region provides <i>C. metallidurans</i> with a backup system for the zinc-cadmium-exporting P-type ATPase ZntA, with CdfX exporting zinc and CadA cadmium.IMPORTANCEBacteria have evolved the ability to supply the important trace element zinc to zinc-dependent proteins, despite external zinc concentrations varying over a wide range. Zinc homeostasis can be understood as adaptive layering of homeostatic systems, allowing coverage from extreme starvation to extreme resistance. Central to zinc homeostasis is a flow equilibrium of zinc comprising uptake and efflux reactions, which adjusts the cytoplasmic zinc content. This report describes what happens when an imbalance in zinc and cadmium concentrations impairs the central inner-membrane zinc efflux system for zinc by competitive inhibition for this exporter. The problem is solved by activation of Cd-exporting CadA or Zn-exporting CdfX as additional efflux systems.</p>\",\"PeriodicalId\":15107,\"journal\":{\"name\":\"Journal of Bacteriology\",\"volume\":\" \",\"pages\":\"e0029924\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-11-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11580412/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Bacteriology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/jb.00299-24\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/10/30 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/jb.00299-24","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/10/30 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
铜绿微囊藻(Cupriavidus metallidurans)不仅能在高浓度过渡金属环境中存活,还能在金属饥饿条件下生长。细胞锌平衡的一个先决条件是锌吸收和流出过程的流动平衡。亲本无质粒菌株 AE104 的突变菌株 ∆e4 缺失了以前已知的外排系统 ZntA、CadA、DmeF 和 FieF 的所有四个染色体编码基因,但在脉冲追逐实验中仍能外排锌,这表明存在第五个外排系统。编码阳离子扩散促进因子(CDF)家族蛋白的基因 cdfX 位于编码 P 型 ATP 酶的 cadA 基因附近。在 ∆e4 突变体中缺失 cdfX 会导致抗锌性进一步下降。用放射性 65Zn(II) 和稳定同位素富集的 67Zn(II) 进行的脉冲追逐实验证明,CdfX 是突变株 ∆e4 剩余锌外流活性的原因。与 cdfX-lacZ 融合的报告基因表明,MerR 型调节因子 ZntR(zntA 表达的主要调节因子)负责锌和镉依赖性 cdfX 表达的上调,尤其是在缺乏一种或两种先前表征的外排系统 ZntA 和 CadA 的突变细胞中。事实证明,zntR 的表达也受 ZntR 本身以及锌和镉供应的控制。这些数据表明,ccfX-cadA 区域为 C. metallidurans 提供了锌镉外排 P 型 ATP 酶 ZntA 的备用系统,其中 CdfX 外排锌,CadA 外排镉。锌稳态可理解为稳态系统的适应性分层,可从极度饥饿覆盖到极度抵抗。锌平衡的核心是锌的流动平衡,包括吸收和流出反应,从而调整细胞质中的锌含量。本报告描述了当锌和镉浓度失衡时,锌的中央内膜锌外排系统受到竞争性抑制的影响。通过激活镉输出的 CadA 或锌输出的 CdfX 作为额外的外排系统,问题得以解决。
The efflux system CdfX exports zinc that cannot be transported by ZntA in Cupriavidus metallidurans.
Cupriavidus metallidurans is able to survive exposure to high concentrations of transition metals, but is also able to grow under metal starvation conditions. A prerequisite of cellular zinc homeostasis is a flow equilibrium combining zinc uptake and efflux processes. The mutant strain ∆e4 of the parental plasmid-free strain AE104 with a deletion of all four chromosomally encoded genes of previously known efflux systems ZntA, CadA, DmeF, and FieF was still able to efflux zinc in a pulse-chase experiment, indicating the existence of a fifth efflux system. The gene cdfX, encoding a protein of the cation diffusion facilitator (CDF) family, is located in proximity to the cadA gene, encoding a P-type ATPase. Deletion of cdfX in the ∆e4 mutant resulted in a further decrease in zinc resistance. Pulse-chase experiments with radioactive 65Zn(II) and stable-isotope-enriched 67Zn(II) provided evidence that CdfX was responsible for the residual zinc efflux activity of the mutant strain ∆e4. Reporter gene fusions with cdfX-lacZ indicated that the MerR-type regulator ZntR, the main regulator of zntA expression, was responsible for zinc- and cadmium-dependent upregulation of cdfX expression, especially in mutant cells lacking one or both of the previously characterized efflux systems, ZntA and CadA. Expression of zntR also proved to be controlled by ZntR itself as well as by zinc and cadmium availability. These data indicate that the cdfX-cadA region provides C. metallidurans with a backup system for the zinc-cadmium-exporting P-type ATPase ZntA, with CdfX exporting zinc and CadA cadmium.IMPORTANCEBacteria have evolved the ability to supply the important trace element zinc to zinc-dependent proteins, despite external zinc concentrations varying over a wide range. Zinc homeostasis can be understood as adaptive layering of homeostatic systems, allowing coverage from extreme starvation to extreme resistance. Central to zinc homeostasis is a flow equilibrium of zinc comprising uptake and efflux reactions, which adjusts the cytoplasmic zinc content. This report describes what happens when an imbalance in zinc and cadmium concentrations impairs the central inner-membrane zinc efflux system for zinc by competitive inhibition for this exporter. The problem is solved by activation of Cd-exporting CadA or Zn-exporting CdfX as additional efflux systems.
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.