Bacterial Approaches for Assembling Iron-Sulfur Proteins

被引:53
作者
Esquilin-Lebron, Karla [1 ]
Dubrac, Sarah [2 ]
Barras, Frederic [2 ]
Boyd, Jeffrey M. [1 ]
机构
[1] Rutgers State Univ, Dept Biochem & Microbiol, New Brunswick, NJ USA
[2] Univ Paris, CNRS UMR 2001, Dept Microbiol, SAMe Unit, Paris, France
基金
美国国家科学基金会;
关键词
bacteria; iron-sulfur cluster; iron; sulfide; SUF; ISC; NIF; genetic regulation; iron regulation; iron utilization; metalloproteins; metalloregulation; sulfur; S CLUSTER BIOGENESIS; ESCHERICHIA-COLI; SALMONELLA-ENTERICA; OXIDATIVE STRESS; 4FE-4S CLUSTERS; CYSTEINE DESULFURASE; NITRIC-OXIDE; SUF OPERON; MONOTHIOL GLUTAREDOXIN; CRYSTAL-STRUCTURE;
D O I
10.1128/mBio.02425-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
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 anti-pathogen target.
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页数:17
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