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Bacterial cell envelope and extracellular sulfhydryl binding sites: Their roles in metal binding and bioavailability

机译:细菌细胞包络和细胞外巯基结合位点:它们的金属结合和生物利用度的作用

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摘要

Although carboxyl and phosphoryl functional groups within the bacterial cell envelope and on bacterial extracellular polymeric substance (EPS) molecules are the most abundant metal binding sites, recent studies suggest that sulfhydryl sites control the binding of chalcophile and similar elements under environmentally-relevant metal loading conditions. The role of cell surface sulfhydryl sites in metal binding has been demonstrated unambiguously for Zn, Cd, Hg, Cu, Au, and Se. This review article summarizes our current understanding of the nature, concentration, and reactivity of these important metal binding sites, their distribution between the cell envelope and extractable EPS molecules, and their possible role in controlling bacterial bioavailability of some elements. The objective of the review is to summarize the relatively few studies that have focussed on bacterial sulfhydryl sites, and to identify areas in which future research may be most productive.
机译:虽然细菌细胞包膜内的羧基和磷酰基官能团和细菌细胞外聚合物物质(EPS)分子是最丰富的金属结合位点,但最近的研究表明巯基位点在环境相关金属负载条件下对烷烃和类似元素的结合进行了控制 。 对于Zn,Cd,Hg,Cu,Au和Se,明确地证明了细胞表面巯基位点在金属结合中的作用。 该审查文章总结了我们目前对这些重要的金属结合位点的性质,浓度和反应性的理解,它们在细胞包膜和可提取的EPS分子之间的分布以及它们在控制某些元素的细菌生物利用度方面的可能作用。 审查的目的是总结一下侧重于细菌磺酰基地的研究,并确定未来研究可能最富有成效的地区。

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