大肠杆菌厌氧铜毒性和铁硫团簇生物发生。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2017-08-01 Print Date: 2017-08-15 DOI:10.1128/AEM.00867-17
Guoqiang Tan, Jing Yang, Tang Li, Jin Zhao, Shujuan Sun, Xiaokang Li, Chuxian Lin, Jianghui Li, Huaibin Zhou, Jianxin Lyu, Huangen Ding
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引用次数: 44

摘要

虽然铜是生物中必需的微量元素,但铜污染地下水已成为所有生物的威胁。然而,铜毒性的细胞机制仍未完全了解。先前的研究表明,铁硫蛋白是好氧条件下大肠杆菌铜毒性的主要靶点之一。在这里,我们报告说,在厌氧条件下,大肠杆菌细胞中的铁硫蛋白对培养基中的铜更敏感。在好氧条件下,在LB (Luria-Bertani)培养基中添加0.2 mM氯化铜(II)对野生型大肠杆菌细胞中的铁硫蛋白几乎没有影响,而在厌氧条件下,同样的铜处理通过阻断细胞中的铁硫团生而使铁硫蛋白失活。重要的是,在好氧或厌氧条件下,大肠杆菌细胞中没有铁硫簇的蛋白质(如富马酸酶C和半胱氨酸脱硫酶)不受铜处理的显著影响,这表明铜可能特异性靶向细胞中的铁硫蛋白。进一步的研究表明,在厌氧条件下,大肠杆菌细胞内铜的积累比在有氧条件下要多,并且铜含量的升高与铁硫簇组装蛋白IscU和IscA结合,有效抑制铁硫簇的生物发生。结果表明,铜介导的铁硫蛋白抑制不需要氧气,铁硫簇生物发生是细胞厌氧铜毒性的主要目标。地下水中的铜污染已成为所有生物的威胁。然而,铜毒性的细胞机制至今尚未完全了解。这里描述的工作揭示了大肠杆菌细胞中的铁硫蛋白在厌氧条件下比在有氧条件下更容易受到培养基中铜的影响。在厌氧条件下,大肠杆菌细胞在细胞内积累了过量的铜,铜通过阻断铁硫簇生物发生特异性地靶向铁硫蛋白。由于铁硫蛋白参与多种重要的生理过程,铜对铁硫簇生物发生的抑制会破坏多种细胞功能,最终抑制细胞生长。本研究结果说明了厌氧条件下细菌细胞内铜毒性与铁硫簇生物发生之间的新相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anaerobic Copper Toxicity and Iron-Sulfur Cluster Biogenesis in Escherichia coli.

Anaerobic Copper Toxicity and Iron-Sulfur Cluster Biogenesis in Escherichia coli.

Anaerobic Copper Toxicity and Iron-Sulfur Cluster Biogenesis in Escherichia coli.

Anaerobic Copper Toxicity and Iron-Sulfur Cluster Biogenesis in Escherichia coli.

While copper is an essential trace element in biology, pollution of groundwater from copper has become a threat to all living organisms. Cellular mechanisms underlying copper toxicity, however, are still not fully understood. Previous studies have shown that iron-sulfur proteins are among the primary targets of copper toxicity in Escherichia coli under aerobic conditions. Here, we report that, under anaerobic conditions, iron-sulfur proteins in E. coli cells are even more susceptible to copper in medium. Whereas addition of 0.2 mM copper(II) chloride to LB (Luria-Bertani) medium has very little or no effect on iron-sulfur proteins in wild-type E. coli cells under aerobic conditions, the same copper treatment largely inactivates iron-sulfur proteins by blocking iron-sulfur cluster biogenesis in the cells under anaerobic conditions. Importantly, proteins that do not have iron-sulfur clusters (e.g., fumarase C and cysteine desulfurase) in E. coli cells are not significantly affected by copper treatment under aerobic or anaerobic conditions, indicating that copper may specifically target iron-sulfur proteins in cells. Additional studies revealed that E. coli cells accumulate more intracellular copper under anaerobic conditions than under aerobic conditions and that the elevated copper content binds to the iron-sulfur cluster assembly proteins IscU and IscA, which effectively inhibits iron-sulfur cluster biogenesis. The results suggest that the copper-mediated inhibition of iron-sulfur proteins does not require oxygen and that iron-sulfur cluster biogenesis is the primary target of anaerobic copper toxicity in cells.IMPORTANCE Copper contamination in groundwater has become a threat to all living organisms. However, cellular mechanisms underlying copper toxicity have not been fully understood up to now. The work described here reveals that iron-sulfur proteins in Escherichia coli cells are much more susceptible to copper in medium under anaerobic conditions than they are under aerobic conditions. Under anaerobic conditions, E. coli cells accumulate excess intracellular copper, which specifically targets iron-sulfur proteins by blocking iron-sulfur cluster biogenesis. Since iron-sulfur proteins are involved in diverse and vital physiological processes, inhibition of iron-sulfur cluster biogenesis by copper disrupts multiple cellular functions and ultimately inhibits cell growth. The results from this study illustrate a new interplay between intracellular copper toxicity and iron-sulfur cluster biogenesis in bacterial cells under anaerobic conditions.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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