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The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()

Vitamin B(12), cobalamin, is a cobalt-containing ring-contracted modified tetrapyrrole that represents one of the most complex small molecules made by nature. In prokaryotes it is utilised as a cofactor, coenzyme, light sensor and gene regulator yet has a restricted role in assisting only two enzyme...

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Detalles Bibliográficos
Autores principales: Osman, Deenah, Cooke, Anastasia, Young, Tessa R., Deery, Evelyne, Robinson, Nigel J., Warren, Martin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689651/
https://www.ncbi.nlm.nih.gov/pubmed/33096143
http://dx.doi.org/10.1016/j.bbamcr.2020.118896
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author Osman, Deenah
Cooke, Anastasia
Young, Tessa R.
Deery, Evelyne
Robinson, Nigel J.
Warren, Martin J.
author_facet Osman, Deenah
Cooke, Anastasia
Young, Tessa R.
Deery, Evelyne
Robinson, Nigel J.
Warren, Martin J.
author_sort Osman, Deenah
collection PubMed
description Vitamin B(12), cobalamin, is a cobalt-containing ring-contracted modified tetrapyrrole that represents one of the most complex small molecules made by nature. In prokaryotes it is utilised as a cofactor, coenzyme, light sensor and gene regulator yet has a restricted role in assisting only two enzymes within specific eukaryotes including mammals. This deployment disparity is reflected in another unique attribute of vitamin B(12) in that its biosynthesis is limited to only certain prokaryotes, with synthesisers pivotal in establishing mutualistic microbial communities. The core component of cobalamin is the corrin macrocycle that acts as the main ligand for the cobalt. Within this review we investigate why cobalt is paired specifically with the corrin ring, how cobalt is inserted during the biosynthetic process, how cobalt is made available within the cell and explore the cellular control of cobalt and cobalamin levels. The partitioning of cobalt for cobalamin biosynthesis exemplifies how cells assist metalation.
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spelling pubmed-76896512021-01-01 The requirement for cobalt in vitamin B(12): A paradigm for protein metalation() Osman, Deenah Cooke, Anastasia Young, Tessa R. Deery, Evelyne Robinson, Nigel J. Warren, Martin J. Biochim Biophys Acta Mol Cell Res Review Vitamin B(12), cobalamin, is a cobalt-containing ring-contracted modified tetrapyrrole that represents one of the most complex small molecules made by nature. In prokaryotes it is utilised as a cofactor, coenzyme, light sensor and gene regulator yet has a restricted role in assisting only two enzymes within specific eukaryotes including mammals. This deployment disparity is reflected in another unique attribute of vitamin B(12) in that its biosynthesis is limited to only certain prokaryotes, with synthesisers pivotal in establishing mutualistic microbial communities. The core component of cobalamin is the corrin macrocycle that acts as the main ligand for the cobalt. Within this review we investigate why cobalt is paired specifically with the corrin ring, how cobalt is inserted during the biosynthetic process, how cobalt is made available within the cell and explore the cellular control of cobalt and cobalamin levels. The partitioning of cobalt for cobalamin biosynthesis exemplifies how cells assist metalation. Elsevier 2021-01 /pmc/articles/PMC7689651/ /pubmed/33096143 http://dx.doi.org/10.1016/j.bbamcr.2020.118896 Text en © 2020 The Authors http://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 Review
Osman, Deenah
Cooke, Anastasia
Young, Tessa R.
Deery, Evelyne
Robinson, Nigel J.
Warren, Martin J.
The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title_full The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title_fullStr The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title_full_unstemmed The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title_short The requirement for cobalt in vitamin B(12): A paradigm for protein metalation()
title_sort requirement for cobalt in vitamin b(12): a paradigm for protein metalation()
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689651/
https://www.ncbi.nlm.nih.gov/pubmed/33096143
http://dx.doi.org/10.1016/j.bbamcr.2020.118896
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