计算生物学
固氮
基因
细菌蛋白
化学
基因组
硫黄
星团(航天器)
纳米技术
生物
生物化学
细菌
遗传学
材料科学
计算机科学
有机化学
程序设计语言
作者
Karla Esquilin-Lebron,Sarah Dubrac,Frédéric Barras,Jeffrey M. Boyd
出处
期刊:MBio
[American Society for Microbiology]
日期:2021-12-21
卷期号:12 (6)
被引量:5
标识
DOI:10.1128/mbio.02425-21
摘要
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.
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