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致病细菌、真菌和原生动物获取磷脂代谢物肌醇的策略:自身合成与摄取。

Strategies for acquiring the phospholipid metabolite inositol in pathogenic bacteria, fungi and protozoa: making it and taking it.

作者信息

Reynolds Todd B

机构信息

Department of Microbiology, University of Tennessee, Knoxville, TN 37996, USA.

出版信息

Microbiology (Reading). 2009 May;155(Pt 5):1386-1396. doi: 10.1099/mic.0.025718-0. Epub 2009 Apr 21.

Abstract

myo-Inositol (inositol) is an essential nutrient that is used for building phosphatidylinositol and its derivatives in eukaryotes and even in some eubacteria such as the mycobacteria. As a consequence, fungal, protozoan and mycobacterial pathogens must be able to acquire inositol in order to proliferate and cause infection in their hosts. There are two primary mechanisms for acquiring inositol. One is to synthesize inositol from glucose 6-phosphate using two sequentially acting enzymes: inositol-3-phosphate synthase (Ino1p) converts glucose 6-phosphate to inositol 3-phosphate, and then inositol monophosphatase (IMPase) dephosphorylates inositol 3-phosphate to generate inositol. The other mechanism is to import inositol from the environment via inositol transporters. Inositol is readily abundant in the bloodstream of mammalian hosts, providing a source from which many pathogens could potentially import inositol. However, despite this abundance of inositol in the host, some pathogens such as the bacterium Mycobacterium tuberculosis and the protist parasite Trypanosoma brucei must be able to make inositol de novo in order to cause disease (M. tuberculosis) or even grow (T. brucei). Other pathogens such as the fungus Candida albicans are equally adept at causing disease by importing inositol or by making it de novo. The role of inositol acquisition in the biology and pathogenesis of the parasite Leishmania and the fungus Cryptococcus are being explored as well. The specific strategies used by these pathogens to acquire inositol while in the host are discussed in relation to each pathogen's unique metabolic requirements.

摘要

肌醇是一种必需营养素,用于在真核生物甚至某些真细菌(如分枝杆菌)中构建磷脂酰肌醇及其衍生物。因此,真菌、原生动物和分枝杆菌病原体必须能够获取肌醇才能在其宿主中增殖并引起感染。获取肌醇有两种主要机制。一种是使用两种顺序作用的酶从6-磷酸葡萄糖合成肌醇:肌醇-3-磷酸合酶(Ino1p)将6-磷酸葡萄糖转化为肌醇3-磷酸,然后肌醇单磷酸酶(IMPase)将肌醇3-磷酸去磷酸化以生成肌醇。另一种机制是通过肌醇转运蛋白从环境中导入肌醇。肌醇在哺乳动物宿主的血液中很丰富,为许多病原体提供了潜在的肌醇来源。然而,尽管宿主中肌醇含量丰富,但一些病原体,如结核分枝杆菌和原生动物寄生虫布氏锥虫,必须能够从头合成肌醇才能致病(结核分枝杆菌)甚至生长(布氏锥虫)。其他病原体,如白色念珠菌,同样擅长通过导入肌醇或从头合成肌醇来致病。肌醇获取在利什曼原虫和新型隐球菌寄生虫的生物学和发病机制中的作用也在探索中。这些病原体在宿主体内获取肌醇所使用的具体策略将根据每种病原体独特的代谢需求进行讨论。

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