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Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria

Iron–sulfur (Fe–S) clusters are ancient and ubiquitous cofactors and are involved in many important biological processes. Unlike the non-photosynthetic bacteria, cyanobacteria have developed the sulfur utilization factor (SUF) mechanism as their main assembly pathway for Fe–S clusters, supplemented...

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Autor principal: Gao, Fudan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058544/
https://www.ncbi.nlm.nih.gov/pubmed/32184761
http://dx.doi.org/10.3389/fmicb.2020.00165
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author Gao, Fudan
author_facet Gao, Fudan
author_sort Gao, Fudan
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description Iron–sulfur (Fe–S) clusters are ancient and ubiquitous cofactors and are involved in many important biological processes. Unlike the non-photosynthetic bacteria, cyanobacteria have developed the sulfur utilization factor (SUF) mechanism as their main assembly pathway for Fe–S clusters, supplemented by the iron–sulfur cluster and nitrogen-fixing mechanisms. The SUF system consists of cysteine desulfurase SufS, SufE that can enhance SufS activity, SufBC(2)D scaffold complex, carrier protein SufA, and regulatory repressor SufR. The S source for the Fe–S cluster assembly mainly originates from L-cysteine, but the Fe donor remains elusive. This minireview mainly focuses on the biogenesis pathway of the Fe–S clusters in cyanobacteria and its relationship with iron homeostasis. Future challenges of studying Fe–S clusters in cyanobacteria are also discussed.
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spelling pubmed-70585442020-03-17 Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria Gao, Fudan Front Microbiol Microbiology Iron–sulfur (Fe–S) clusters are ancient and ubiquitous cofactors and are involved in many important biological processes. Unlike the non-photosynthetic bacteria, cyanobacteria have developed the sulfur utilization factor (SUF) mechanism as their main assembly pathway for Fe–S clusters, supplemented by the iron–sulfur cluster and nitrogen-fixing mechanisms. The SUF system consists of cysteine desulfurase SufS, SufE that can enhance SufS activity, SufBC(2)D scaffold complex, carrier protein SufA, and regulatory repressor SufR. The S source for the Fe–S cluster assembly mainly originates from L-cysteine, but the Fe donor remains elusive. This minireview mainly focuses on the biogenesis pathway of the Fe–S clusters in cyanobacteria and its relationship with iron homeostasis. Future challenges of studying Fe–S clusters in cyanobacteria are also discussed. Frontiers Media S.A. 2020-02-28 /pmc/articles/PMC7058544/ /pubmed/32184761 http://dx.doi.org/10.3389/fmicb.2020.00165 Text en Copyright © 2020 Gao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Gao, Fudan
Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title_full Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title_fullStr Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title_full_unstemmed Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title_short Iron–Sulfur Cluster Biogenesis and Iron Homeostasis in Cyanobacteria
title_sort iron–sulfur cluster biogenesis and iron homeostasis in cyanobacteria
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058544/
https://www.ncbi.nlm.nih.gov/pubmed/32184761
http://dx.doi.org/10.3389/fmicb.2020.00165
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