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动物致病真菌对铁的摄取

Iron gathering by zoopathogenic fungi.

作者信息

Howard Dexter H

机构信息

Department of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

出版信息

FEMS Immunol Med Microbiol. 2004 Mar 8;40(2):95-100. doi: 10.1016/S0928-8244(03)00301-8.

Abstract

Iron is a metal required by most microorganisms and is prominently used in the transfer of electrons during metabolism. The gathering of iron is, then, an essential process and its fulfillment becomes a crucial pathogenetic event for zoopathogenic fungi. Iron is rather unavailable because it occurs on the earth's surface in its insoluble ferric form in oxides and hydroxides. In the infected host iron is bound to proteins such as transferrin and ferritin. Solubilization of ferric iron is the major problem confronting microorganisms. This process is achieved by two major mechanisms: ferric reduction and siderophore utilization. Ferric reductase is frequently accompanied by a copper oxidase transport system. There is one example of direct ferric iron transport apparently without prior reduction. Ferric reduction may also be accomplished by low molecular mass compounds. Some fungi have evolved a process of iron acquisition involving the synthesis of iron-gathering compounds called siderophores. Even those fungi that do not synthesize siderophores have developed permeases for transport of such compounds formed by other organisms. Fungi can also reductively release iron from siderophores and transport the ferrous iron often by the copper oxidase transport system. There is a great diversity of iron-gathering mechanisms expressed by pathogenic fungi and such diversity may be found even in a single species.

摘要

铁是大多数微生物所需的一种金属,在新陈代谢过程中显著用于电子传递。因此,铁的聚集是一个必不可少的过程,其实现成为动物致病性真菌的一个关键致病事件。铁相当难以获取,因为它以不溶性三价铁形式存在于地球表面的氧化物和氢氧化物中。在受感染的宿主体内,铁与转铁蛋白和铁蛋白等蛋白质结合。三价铁的溶解是微生物面临的主要问题。这个过程通过两种主要机制实现:三价铁还原和铁载体利用。三价铁还原酶通常伴随着铜氧化酶转运系统。有一个明显未经预先还原的直接三价铁转运的例子。三价铁还原也可以由低分子量化合物完成。一些真菌进化出了一种获取铁的过程,涉及合成称为铁载体的铁聚集化合物。即使是那些不合成铁载体的真菌也已经发展出通透酶来运输其他生物体形成的此类化合物。真菌还可以从铁载体中还原性地释放铁,并通常通过铜氧化酶转运系统运输二价铁。致病真菌表达的铁聚集机制多种多样,甚至在单个物种中也可能发现这种多样性。

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