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Synchrotron radiation-based spectroscopic investigation of the electronic and geometric structures of iron-sulfur clusters, particles, and minerals.

机译:基于同步辐射的铁硫团簇,颗粒和矿物的电子和几何结构的光谱研究。

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摘要

Iron-sulfur systems are ubiquitous in biological and geological environments. They range from molecular scale [2Fe-2S] clusters to nanometer scale particles to micrometer scale minerals. Across the length scale, each system has unique structural and functional roles with respect to its environment, such as metalloproteins or hydrothermal vents. Therefore, it is of great interest to understand the electronic and geometric structural properties that give a wide range of reactivity. The main focus of this dissertation is to investigate the possible connections among the different size scales using a primary technique, X-ray absorption spectroscopy (XAS), by gaining an understanding into the relationship between the system size and properties. X-ray absorption spectroscopy is a powerful tool to probe geometric and electronic structures across the entire length scale. In this work, extend x-ray absorption fine structure (EXAFS) analysis method was applied to determine geometric structure of the protein bound, molecular iron-sulfur cluster of HydA. It was found to contain a preformed [4Fe-4S] cluster. This method combined with Fe/S K-edge XANES analysis was applied to spore photoproduct lyase metalloprotein to structurally characterize the [4Fe-4S] cluster and its interaction with SAM. The Fe K-edge EXAFS and Fe/S K-edge XANES provide evidence for a cluster distortion upon interacting with SAM as a new EXAFS feature, indicating the presence of longer Fe-Fe distances and this provides new insights into the structure of radical SAM enzymes. At the nanometer scale, mineral and protein encapsulated particles were investigated with a possible link between molecular and micrometer scale. A reference library of FeS systems was established to describe the variation in bonding and structure. Also, a considerable amount was learned about XAS detection methods, and this was applied to the micrometer scale systems. From EXAFS and XANES analysis, the modified surface of pyrite was revealed to have an intermediate layer of Fe(I)-S phase with a metallic iron surface, and a reaction scheme was proposed. These studies of the different size iron-sulfur systems provide insights into the change in the electronic and geometric structures, and a model was proposed to describe the effects of size on the electronic and geometric structure.
机译:铁-硫系统在生物和地质环境中无处不在。它们的范围从分子级[2Fe-2S]团簇到纳米级颗粒再到微米级矿物。在整个长度范围内,每个系统在其环境方面都具有独特的结构和功能作用,例如金属蛋白或热液喷口。因此,非常感兴趣的是了解赋予广泛反应性的电子和几何结构性质。本文的主要重点是通过了解系统尺寸与性能之间的关系,使用一种主要技术X射线吸收光谱法(XAS)研究不同尺寸尺寸之间的可能联系。 X射线吸收光谱法是在整个长度范围内探测几何和电子结构的强大工具。在这项工作中,采用扩展的X射线吸收精细结构(EXAFS)分析方法来确定与蛋白结合的HydA分子铁硫分子簇的几何结构。发现它包含预制的[4Fe-4S]团簇。将该方法与Fe / S K-edge XANES分析相结合,用于孢子光产物裂解酶金属蛋白的结构表征[4Fe-4S]簇及其与SAM的相互作用。 Fe K-edge EXAFS和Fe / S K-edge XANES提供了证据,表明与SAM相互作用时团簇变形是EXAFS的新功能,表明存在更长的Fe-Fe距离,这为自由基SAM的结构提供了新的见解酶。在纳米级,对矿物质和蛋白质包封的颗粒进行了研究,并在分子级和微米级之间建立了可能的联系。建立了FeS系统的参考库来描述键合和结构的变化。此外,还了解到大量有关XAS检测方法的信息,并将其应用于微米级系统。通过EXAFS和XANES分析,发现黄铁矿的改性表面具有具有金属铁表面的Fe(I)-S相的中间层,并提出了反应方案。这些对不同尺寸的铁硫系统的研究提供了对电子和几何结构变化的见解,并提出了一个模型来描述尺寸对电子和几何结构的影响。

著录项

  • 作者

    Gardenghi, David Jeremiah.;

  • 作者单位

    Montana State University.;

  • 授予单位 Montana State University.;
  • 学科 Chemistry Inorganic.;Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2012
  • 页码 172 p.
  • 总页数 172
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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