Characterization of the ferrous iron transporter Feo in Vibrio cholerae

描述（由申请人提供）：铁参与各种细胞反应，是几乎所有生物体的必需元素。铁的获取对于病原菌是有问题的，其必须与宿主竞争有限量的可用铁，并且细菌通常表达对其三价铁或含铁配体特异性的高亲和力转运系统。FeO是原核生物中主要的亚铁转运系统。它广泛分布于真细菌和古细菌中，表明它是一种非常古老的铁转运蛋白。此外，FeoB蛋白具有与真核G蛋白相似的GTdR和GDI结构域，并且Feo可能代表现代G蛋白的原始祖先。尽管其普遍存在的性质和潜在的作用，在细菌的发病机制，很少有人知道它的结构，运输机制和生物学作用。因此，它是至关重要的，以表征这种蛋白质和它的作用，亚铁运输。 这些研究将在病原体霍乱弧菌，人类发病率和死亡率的主要原因。霍乱弧菌是这些研究的理想模型，因为我们有试剂和遗传工具来回答关于FeO的基本问题。此外，我们可以扩展这些研究，以包括Feo在宿主定植和疾病中的作用，这将为开发阻断霍乱弧菌感染的新方法奠定基础。 我们的第一个具体目标是使用遗传和生物化学方法来表征FeO结构及其运输机制。这些研究将有助于确定FeO转运蛋白的基本蛋白组分以及每个蛋白质中的关键区域和氨基酸。基于这些结果，我们将能够测试模型的FeO结构和功能。我们的第二个具体目标是表征辅助亚铁转运蛋白VciB。这可能会提供深入了解FeO如何获得其亚铁配体在周质。第三，我们将确定feo操纵子表达的调控机制，并确定其在宿主体内的表达模式。这些数据将提供有关致病细菌如何协调其铁转运基因表达的新信息，以最佳利用可用的铁源，并将有助于定义细菌在宿主中遇到的环境信号。

DESCRIPTION (provided by applicant): Iron participates in a wide variety of cellular reactions and is an essential element for nearly all organisms. Iron acquisition is problematic for pathogenic bacteria, which must compete with the host for limited amounts of available iron, and bacteria typically express high affinity transport systems that are specific for their ferric or ferous iron ligands. Feo is the major ferrous iron transport system in prokaryotic organisms. It is widely distributed in eubacteria and in the Archaea, suggesting that it is a very ancient class of iron transporter. Further, the FeoB protein has GTPase and GDI domains similar to eukaryotic G proteins, and Feo may represent a primitive ancestor of modern G proteins. Despite its ubiquitous nature and potential role in bacterial pathogenesis, little is known about its structure, mechanism of transport, and biological role. Thus, it is critical to characterize this protein and its role in ferrous iron transport. These studies will be done in the pathogen Vibrio cholerae, a major cause of human morbidity and mortality. V. cholerae is an ideal model for these studies as we have the reagents and genetic tools to answer basic questions about Feo. Further, we can extend these studies to include questions about the role of Feo in host colonization and disease, which will lay the groundwork for developing new methods of blocking infection by V. cholerae. Our first specific aim is to use genetic and biochemical approaches to characterize Feo structure and its mechanism of transport. These studies will help define the essential protein components of the Feo transporter and the critical regions and amino acids within each protein. Based on these results, we will be able to test models for Feo structure and function. Our second specific aim is to characterize the accessory ferrous iron transport protein, VciB. This may provide insight into how Feo obtains its ferrous iron ligand in the periplasm. Third, we will define the mechanism of regulation of expression of the feo operon and determine its pattern of expression when the bacteria are within the host. These data will provide new information about how pathogenic bacteria coordinate the expression of their iron transport genes to allow optimal utilization of available iron sources and will also help define the environmental signals the bacteria encounter in the host.