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The role of sulfhydryl sites in metal binding onto bacterial cells.

机译:巯基位点在金属结合到细菌细胞上的作用。

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摘要

Bacteria can adsorb a wide range of metals through interactions with their abundant cell envelope binding sites, thereby strongly affecting the speciation, distribution, bioavailability and mobility of metals in these systems. Besides carboxyl, phosphoryl, and amine groups, the sulfhydryl sites have also been identified recently as potential metal binding sites, but the exact role of sulfhydryl sites has not yet been extensively studied. The research presented in this dissertation focuses on the role played by sulfhydryl sites in metal adsorption onto bacteria. Chapter 2 presents an approach to determine the concentrations and acidity constant values of sulfhydryl sites within bacterial cell envelopes, and the approach is applied to a range of bacterial species. Chapter 3 focuses on understanding the adsorption and desorption of Cd onto bacterial sulfhydryl sites, and the work results in the first determination of a thermodynamic stability constant value for a metal-sulfhydryl bacterial complex. Chapter 4 presents work that determines the distribution of sulfhydryl sites within cell envelopes, with a focus on the concentrations of sulfhydryl sites on EPS molecules.;The results in Chapters 2 and 3 demonstrate that the measured concentration of sulfhydryl sites is lower than those of the more abundant carboxyl and phosphoryl sites within cell envelopes, but that the concentration of sulfhydryl sites is high enough to control the binding of chalcophilic metals onto bacteria under low metal-loading conditions due to the high affinity of these sites to bind chalcophilic metals. In Chapter 3, I developed a surface complexation model based on the calculated stability constants of Cd-sulfhydryl and Cd-non-sulfhydryl bacterial complexes that successfully accounts for the adsorption of Cd onto Shewanella oneidensis as a function of pH and metal loading. The distributions of sulfhydryl sites within cell envelopes determined in Chapter 4 vary significantly between Shewanella oneidensis and Pseudomonas putida, likely resulting in the different Cd resistance that was measured between these two bacterial species. The research presented in this dissertation significantly improves our understanding of the controls on metal adsorption onto bacteria, especially under environmentally-relevant low metal loading conditions, and thereby can lead to improved models of the transport and global cycling of metals.
机译:细菌可以通过与它们丰富的细胞包膜结合位点相互作用来吸附各种金属,从而强烈影响这些系统中金属的形态,分布,生物利用度和迁移率。除羧基,磷酰基和胺基外,巯基位点最近也已被确定为潜在的金属结合位点,但巯基位点的确切作用尚未得到广泛研究。本文的研究重点是巯基在金属吸附细菌上的作用。第2章介绍了一种确定细菌细胞包膜中巯基位点的浓度和酸度常数的方法,该方法适用于一系列细菌。第3章着重于了解Cd在细菌巯基位点上的吸附和解吸,并且该工作首次确定了金属-巯基细菌配合物的热力学稳定性常数。第4章介绍确定细胞包膜中巯基位点分布的工作,着重于EPS分子上巯基位点的浓度;第2章和第3章的结果表明,测得的巯基位点浓度低于那些在细胞膜中有更多丰富的羧基和磷酰基位点,但是巯基位点的浓度足够高,足以控制嗜酸性金属在低金属负载条件下与细菌的结合,因为这些位点对嗜酸性金属的亲和力很高。在第3章中,我基于计算出的Cd-巯基和Cd-非巯基细菌复合物的稳定常数,开发了一种表面络合模型,该常数成功地说明了Cd在Shewanella oneidensis上的吸附随pH和金属负载的变化。在第四章中确定的细胞包膜中巯基位点的分布在沙瓦氏假单胞菌和恶臭假单胞菌之间存在显着差异,这可能导致在这两种细菌之间测得的不同的Cd抗性。这篇论文提出的研究极大地增进了我们对金属吸附到细菌上的控制的理解,特别是在与环境有关的低金属负载条件下,从而可以改善金属的运输和整体循环模型。

著录项

  • 作者

    Yu, Qiang.;

  • 作者单位

    University of Notre Dame.;

  • 授予单位 University of Notre Dame.;
  • 学科 Geochemistry.;Environmental science.;Environmental geology.
  • 学位 Ph.D.
  • 年度 2015
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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