首页> 美国卫生研究院文献>Journal of Bacteriology >Copper Efflux Is Induced during Anaerobic Amino Acid Limitation in Escherichia coli To Protect Iron-Sulfur Cluster Enzymes and Biogenesis
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Copper Efflux Is Induced during Anaerobic Amino Acid Limitation in Escherichia coli To Protect Iron-Sulfur Cluster Enzymes and Biogenesis

机译:在大肠杆菌中限制厌氧氨基酸含量的过程中诱导铜流出以保护铁硫簇酶和生物发生。

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摘要

Adaptation to changing environments is essential to bacterial physiology. Here we report a unique role of the copper homeostasis system in adapting Escherichia coli to its host-relevant environment of anaerobiosis coupled with amino acid limitation. We found that expression of the copper/silver efflux pump CusCFBA was significantly upregulated during anaerobic amino acid limitation in E. coli without the supplement of exogenous copper. Inductively coupled plasma mass spectrometry analysis of the total intracellular copper content combined with transcriptional assay of the PcusC-lacZ reporter in the presence of specific Cu(I) chelators indicated that anaerobic amino acid limitation led to the accumulation of free Cu(I) in the periplasmic space of E. coli, resulting in Cu(I) toxicity. Cells lacking cusCFBA and another copper transporter, copA, under this condition displayed growth defects and reduced ATP production during fumarate respiration. Ectopic expression of the Fe-S cluster enzyme fumarate reductase (Frd), or supplementation with amino acids whose biosynthesis involves Fe-S cluster enzymes, rescued the poor growth of ΔcusC cells. Yet, Cu(I) treatment did not impair the Frd activity in vitro. Further studies revealed that the alternative Fe-S cluster biogenesis system Suf was induced during the anaerobic amino acid limitation, and ΔcusC enhanced this upregulation, indicating the impairment of the Fe-S cluster assembly machinery and the increased Fe-S cluster demands under this condition. Taken together, we conclude that the copper efflux system CusCFBA is induced during anaerobic amino acid limitation to protect Fe-S cluster enzymes and biogenesis from the endogenously originated Cu(I) toxicity, thus facilitating the physiological adaptation of E. coli.
机译:适应不断变化的环境对于细菌生理至关重要。在这里,我们报告铜稳态系统在使大肠杆菌适应其与主机相关的厌氧菌环境以及氨基酸限制的环境中的独特作用。我们发现铜/银外排泵CusCFBA的表达在大肠杆菌中的厌氧氨基酸限制过程中显着上调,而无需添加外源铜。在特定Cu(I)螯合剂存在下,对总细胞内铜含量的电感耦合等离子体质谱分析与PcusC-lacZ报告基因的转录分析相结合,表明厌氧氨基酸的限制导致游离Cu(I)的积累大肠杆菌的周质空间,导致Cu(I)毒性。在这种条件下,缺乏cusCFBA和另一种铜转运蛋白copA的细胞在富马酸盐呼吸期间显示出生长缺陷并降低了ATP的产生。 Fe-S簇酶富马酸还原酶(Frd)的异位表达,或补充其生物合成涉及Fe-S簇酶的氨基酸,可以挽救ΔcusC细胞的不良生长。但是,Cu(I)处理并未损害Frd的体外活性。进一步的研究表明,在厌氧氨基酸限制过程中诱导了替代性的Fe-S簇生物发生系统Suf,ΔcusC增强了这种上调,表明在这种条件下Fe-S簇组装机制受损,Fe-S簇需求增加。两者合计,我们得出结论,铜排泄系统CusCFBA是在厌氧氨基酸限制过程中诱导的,以保护Fe-S簇酶和生物发生免受内源性Cu(I)毒性的影响,从而促进大肠杆菌的生理适应性。

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