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Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases

Heme, a near ubiquitous cofactor, is synthesized by most organisms. The essential step of insertion of iron into the porphyrin macrocycle is mediated by the enzyme ferrochelatase. Several ferrochelatases have been characterized, and it has been experimentally shown that a fraction of them contain [2...

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Autores principales: Weerth, R. Sophia, Medlock, Amy E., Dailey, Harry A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529089/
https://www.ncbi.nlm.nih.gov/pubmed/34582890
http://dx.doi.org/10.1016/j.jbc.2021.101017
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author Weerth, R. Sophia
Medlock, Amy E.
Dailey, Harry A.
author_facet Weerth, R. Sophia
Medlock, Amy E.
Dailey, Harry A.
author_sort Weerth, R. Sophia
collection PubMed
description Heme, a near ubiquitous cofactor, is synthesized by most organisms. The essential step of insertion of iron into the porphyrin macrocycle is mediated by the enzyme ferrochelatase. Several ferrochelatases have been characterized, and it has been experimentally shown that a fraction of them contain [2Fe-2S] clusters. It has been suggested that all metazoan ferrochelatases have such clusters, but among bacteria, these clusters have been most commonly identified in Actinobacteria and a few other bacteria. Despite this, the function of the [2Fe-2S] cluster remains undefined. With the large number of sequenced genomes currently available, we comprehensively assessed the distribution of putative [2Fe-2S] clusters throughout the ferrochelatase protein family. We discovered that while rare within the bacterial ferrochelatase family, this cluster is prevalent in a subset of phyla. Of note is that genomic data show that the cluster is not common in Actinobacteria, as is currently thought based on the small number of actinobacterial ferrochelatases experimentally examined. With available physiological data for each genome included, we identified a correlation between the presence of the microbial cluster and aerobic metabolism. Additionally, our analysis suggests that Firmicute ferrochelatases are the most ancient and evolutionarily preceded the Alphaproteobacterial precursor to eukaryotic mitochondria. These findings shed light on distribution and evolution of the [2Fe-2S] cluster in ferrochelatases and will aid in determining the function of the cluster in heme synthesis.
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spelling pubmed-85290892021-10-27 Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases Weerth, R. Sophia Medlock, Amy E. Dailey, Harry A. J Biol Chem Research Article Heme, a near ubiquitous cofactor, is synthesized by most organisms. The essential step of insertion of iron into the porphyrin macrocycle is mediated by the enzyme ferrochelatase. Several ferrochelatases have been characterized, and it has been experimentally shown that a fraction of them contain [2Fe-2S] clusters. It has been suggested that all metazoan ferrochelatases have such clusters, but among bacteria, these clusters have been most commonly identified in Actinobacteria and a few other bacteria. Despite this, the function of the [2Fe-2S] cluster remains undefined. With the large number of sequenced genomes currently available, we comprehensively assessed the distribution of putative [2Fe-2S] clusters throughout the ferrochelatase protein family. We discovered that while rare within the bacterial ferrochelatase family, this cluster is prevalent in a subset of phyla. Of note is that genomic data show that the cluster is not common in Actinobacteria, as is currently thought based on the small number of actinobacterial ferrochelatases experimentally examined. With available physiological data for each genome included, we identified a correlation between the presence of the microbial cluster and aerobic metabolism. Additionally, our analysis suggests that Firmicute ferrochelatases are the most ancient and evolutionarily preceded the Alphaproteobacterial precursor to eukaryotic mitochondria. These findings shed light on distribution and evolution of the [2Fe-2S] cluster in ferrochelatases and will aid in determining the function of the cluster in heme synthesis. American Society for Biochemistry and Molecular Biology 2021-09-25 /pmc/articles/PMC8529089/ /pubmed/34582890 http://dx.doi.org/10.1016/j.jbc.2021.101017 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Weerth, R. Sophia
Medlock, Amy E.
Dailey, Harry A.
Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title_full Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title_fullStr Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title_full_unstemmed Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title_short Ironing out the distribution of [2Fe-2S] motifs in ferrochelatases
title_sort ironing out the distribution of [2fe-2s] motifs in ferrochelatases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529089/
https://www.ncbi.nlm.nih.gov/pubmed/34582890
http://dx.doi.org/10.1016/j.jbc.2021.101017
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