How Is Fe-S Cluster Formation Regulated?

被引:60
|
作者
Mettert, Erin L. [1 ]
Kiley, Patricia J. [1 ]
机构
[1] Univ Wisconsin Madison, Dept Biomol Chem, Sch Med & Publ Hlth, Madison, WI 53706 USA
来源
关键词
Ion-sulfer; Fe-S; regulation; homeostasis; Isc pathway; Suf pathway; IRON-SULFUR CLUSTERS; MOLECULAR CHAPERONE SYSTEM; FRATAXIN HOMOLOG CYAY; ESCHERICHIA-COLI; OXIDATIVE STRESS; HYDROGEN-PEROXIDE; CYSTEINE DESULFURASE; BACTERIAL FRATAXIN; SCAFFOLD PROTEIN; GENE-EXPRESSION;
D O I
10.1146/annurev-micro-091014-104457
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Iron-sulfur (Fe-S) clusters are fundamental to numerous biological processes in most organisms, but these protein cofactors can be prone to damage by various oxidants (e.g., O-2, reactive oxygen species, and reactive nitrogen species) and toxic levels of certain metals (e.g., cobalt and copper). Furthermore, their synthesis can also be directly influenced by the level of available iron in the environment. Consequently, the cellular need for Fe-S cluster biogenesis varies with fluctuating growth conditions. To accommodate changes in Fe-S demand, microorganisms employ diverse regulatory strategies to tailor Fe-S cluster biogenesis according to their surroundings. Here, we review the mechanisms that regulate Fe-S cluster formation in bacteria, primarily focusing on control of the Isc and Suf Fe-S cluster biogenesis systems in the model bacterium Escherichia coli.
引用
收藏
页码:505 / 526
页数:22
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