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Complexities of complex II: Sulfide metabolism in vivo
High levels of H(2)S produced by gut microbiota can block oxygen utilization by inhibiting mitochondrial complex IV. Kumar et al. have shown how cells respond to this inhibition by using the mitochondrial sulfide oxidation pathway and reverse electron transport. The reverse activity of mitochondrial...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844276/ https://www.ncbi.nlm.nih.gov/pubmed/35101450 http://dx.doi.org/10.1016/j.jbc.2022.101661 |
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author | Cecchini, Gary |
author_facet | Cecchini, Gary |
author_sort | Cecchini, Gary |
collection | PubMed |
description | High levels of H(2)S produced by gut microbiota can block oxygen utilization by inhibiting mitochondrial complex IV. Kumar et al. have shown how cells respond to this inhibition by using the mitochondrial sulfide oxidation pathway and reverse electron transport. The reverse activity of mitochondrial complex II (succinate-quinone oxidoreductase, i.e., fumarate reduction) generates oxidized coenzyme Q, which is then reduced by the mitochondrial sulfide quinone oxidoreductase to oxidize H(2)S. This newly identified redox circuitry points to the importance of complex II reversal in mitochondria during periods of hypoxia and cellular stress. |
format | Online Article Text |
id | pubmed-8844276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-88442762022-02-25 Complexities of complex II: Sulfide metabolism in vivo Cecchini, Gary J Biol Chem Editors' Pick Highlight High levels of H(2)S produced by gut microbiota can block oxygen utilization by inhibiting mitochondrial complex IV. Kumar et al. have shown how cells respond to this inhibition by using the mitochondrial sulfide oxidation pathway and reverse electron transport. The reverse activity of mitochondrial complex II (succinate-quinone oxidoreductase, i.e., fumarate reduction) generates oxidized coenzyme Q, which is then reduced by the mitochondrial sulfide quinone oxidoreductase to oxidize H(2)S. This newly identified redox circuitry points to the importance of complex II reversal in mitochondria during periods of hypoxia and cellular stress. American Society for Biochemistry and Molecular Biology 2022-01-29 /pmc/articles/PMC8844276/ /pubmed/35101450 http://dx.doi.org/10.1016/j.jbc.2022.101661 Text en © 2022 The Author 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 | Editors' Pick Highlight Cecchini, Gary Complexities of complex II: Sulfide metabolism in vivo |
title | Complexities of complex II: Sulfide metabolism in vivo |
title_full | Complexities of complex II: Sulfide metabolism in vivo |
title_fullStr | Complexities of complex II: Sulfide metabolism in vivo |
title_full_unstemmed | Complexities of complex II: Sulfide metabolism in vivo |
title_short | Complexities of complex II: Sulfide metabolism in vivo |
title_sort | complexities of complex ii: sulfide metabolism in vivo |
topic | Editors' Pick Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844276/ https://www.ncbi.nlm.nih.gov/pubmed/35101450 http://dx.doi.org/10.1016/j.jbc.2022.101661 |
work_keys_str_mv | AT cecchinigary complexitiesofcomplexiisulfidemetabolisminvivo |