Department of Biochemistry and Microbiology, Rutgers, the State University of New Jersey, New Brunswick, New Jersey, USA.
Institut Pasteurgrid.428999.7, Université de Paris, CNRS UMR 2001, Department of Microbiology, SAMe Unit, Paris, France.
mBio. 2021 Dec 21;12(6):e0242521. doi: 10.1128/mBio.02425-21. Epub 2021 Nov 16.
Building iron-sulfur (Fe-S) clusters and assembling Fe-S proteins are essential actions for life on Earth. The three processes that sustain life, photosynthesis, nitrogen fixation, and respiration, require Fe-S proteins. Genes coding for Fe-S proteins can be found in nearly every sequenced genome. Fe-S proteins have a wide variety of functions, and therefore, defective assembly of Fe-S proteins results in cell death or global metabolic defects. Compared to alternative essential cellular processes, there is less known about Fe-S cluster synthesis and Fe-S protein maturation. Moreover, new factors involved in Fe-S protein assembly continue to be discovered. These facts highlight the growing need to develop a deeper biological understanding of Fe-S cluster synthesis, holo-protein maturation, and Fe-S cluster repair. Here, we outline bacterial strategies used to assemble Fe-S proteins and the genetic regulation of these processes. We focus on recent and relevant findings and discuss future directions, including the proposal of using Fe-S protein assembly as an antipathogen target.
在地球上,构建铁硫(Fe-S)簇并组装 Fe-S 蛋白是生命活动的必要步骤。支撑生命的三个过程,光合作用、固氮作用和呼吸作用,都需要 Fe-S 蛋白。几乎在每个测序的基因组中都可以找到编码 Fe-S 蛋白的基因。Fe-S 蛋白具有广泛的功能,因此,Fe-S 蛋白组装的缺陷会导致细胞死亡或全局代谢缺陷。与替代的必要细胞过程相比,人们对 Fe-S 簇合成和 Fe-S 蛋白成熟过程的了解较少。此外,新的参与 Fe-S 蛋白组装的因素仍在不断被发现。这些事实突出表明,人们越来越需要深入了解 Fe-S 簇合成、全蛋白成熟和 Fe-S 簇修复的生物学。在这里,我们概述了细菌组装 Fe-S 蛋白的策略以及这些过程的遗传调控。我们重点介绍了最近的相关发现,并讨论了未来的方向,包括提议将 Fe-S 蛋白组装用作抗病原体的靶标。