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Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes

Brevibacillus massiliensis strain phR is an obligately aerobic microbe that was isolated from human feces. Here, we show that it readily takes up tungsten (W), a metal previously associated only with anaerobes. The W is incorporated into an oxidoreductase enzyme (BmWOR) that was purified from native...

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Autores principales: Thorgersen, Michael P., Schut, Gerrit J., Poole, Farris L., Haja, Dominik K., Putumbaka, Saisuki, Mycroft, Harriet I., de Vries, Willem J., Adams, Michael W. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424855/
https://www.ncbi.nlm.nih.gov/pubmed/36051760
http://dx.doi.org/10.3389/fmicb.2022.965625
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author Thorgersen, Michael P.
Schut, Gerrit J.
Poole, Farris L.
Haja, Dominik K.
Putumbaka, Saisuki
Mycroft, Harriet I.
de Vries, Willem J.
Adams, Michael W. W.
author_facet Thorgersen, Michael P.
Schut, Gerrit J.
Poole, Farris L.
Haja, Dominik K.
Putumbaka, Saisuki
Mycroft, Harriet I.
de Vries, Willem J.
Adams, Michael W. W.
author_sort Thorgersen, Michael P.
collection PubMed
description Brevibacillus massiliensis strain phR is an obligately aerobic microbe that was isolated from human feces. Here, we show that it readily takes up tungsten (W), a metal previously associated only with anaerobes. The W is incorporated into an oxidoreductase enzyme (BmWOR) that was purified from native biomass. BmWOR consists of a single 65 kDa subunit and contains a single W-pyranopterin cofactor and a single [4Fe-4S] cluster. It exhibited high aldehyde-oxidizing activity with very high affinities (apparent K(m) < 6 μM) for aldehydes common in the human gut and in cooked foods, including furfural, propionaldehyde, benzaldehyde and tolualdehyde, suggesting that BmWOR plays a key role in their detoxification. B. massiliensis converted added furfural to furoic acid when grown in the presence of W, but not in the presence of the analogous element molybdenum. B. massiliensis ferredoxin (BmFd) served as the electron acceptor (apparent K(m) < 5 μM) for BmWOR suggesting it is the physiological electron carrier. Genome analysis revealed a Fd-dependent rather than NADH-dependent Complex I, suggesting that WOR not only serves a detoxification role but its aldehyde substrates could also serve as a source of energy. BmWOR is the first tungstoenzyme and the first member of the WOR family to be obtained from a strictly aerobic microorganism. Remarkably, BmWOR oxidized furfural in the presence of air (21% O(2), v/v) but only if BmFd was also present. BmWOR is the first characterized member of the Clade 83 WORs, which are predominantly found in extremely halophilic and aerobic archaea (Clade 83A), with many isolated from food sources, while the remaining bacterial members (Clade 83B) include both aerobes and anaerobes. The potential advantages for microbes found in foods and involved in human gut health that harbor O(2)-resistant WORs, including in Bacillus and Brevibacillus based-probiotics, are discussed.
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spelling pubmed-94248552022-08-31 Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes Thorgersen, Michael P. Schut, Gerrit J. Poole, Farris L. Haja, Dominik K. Putumbaka, Saisuki Mycroft, Harriet I. de Vries, Willem J. Adams, Michael W. W. Front Microbiol Microbiology Brevibacillus massiliensis strain phR is an obligately aerobic microbe that was isolated from human feces. Here, we show that it readily takes up tungsten (W), a metal previously associated only with anaerobes. The W is incorporated into an oxidoreductase enzyme (BmWOR) that was purified from native biomass. BmWOR consists of a single 65 kDa subunit and contains a single W-pyranopterin cofactor and a single [4Fe-4S] cluster. It exhibited high aldehyde-oxidizing activity with very high affinities (apparent K(m) < 6 μM) for aldehydes common in the human gut and in cooked foods, including furfural, propionaldehyde, benzaldehyde and tolualdehyde, suggesting that BmWOR plays a key role in their detoxification. B. massiliensis converted added furfural to furoic acid when grown in the presence of W, but not in the presence of the analogous element molybdenum. B. massiliensis ferredoxin (BmFd) served as the electron acceptor (apparent K(m) < 5 μM) for BmWOR suggesting it is the physiological electron carrier. Genome analysis revealed a Fd-dependent rather than NADH-dependent Complex I, suggesting that WOR not only serves a detoxification role but its aldehyde substrates could also serve as a source of energy. BmWOR is the first tungstoenzyme and the first member of the WOR family to be obtained from a strictly aerobic microorganism. Remarkably, BmWOR oxidized furfural in the presence of air (21% O(2), v/v) but only if BmFd was also present. BmWOR is the first characterized member of the Clade 83 WORs, which are predominantly found in extremely halophilic and aerobic archaea (Clade 83A), with many isolated from food sources, while the remaining bacterial members (Clade 83B) include both aerobes and anaerobes. The potential advantages for microbes found in foods and involved in human gut health that harbor O(2)-resistant WORs, including in Bacillus and Brevibacillus based-probiotics, are discussed. Frontiers Media S.A. 2022-08-16 /pmc/articles/PMC9424855/ /pubmed/36051760 http://dx.doi.org/10.3389/fmicb.2022.965625 Text en Copyright © 2022 Thorgersen, Schut, Poole, Haja, Putumbaka, Mycroft, de Vries and Adams. https://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
Thorgersen, Michael P.
Schut, Gerrit J.
Poole, Farris L.
Haja, Dominik K.
Putumbaka, Saisuki
Mycroft, Harriet I.
de Vries, Willem J.
Adams, Michael W. W.
Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title_full Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title_fullStr Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title_full_unstemmed Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title_short Obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
title_sort obligately aerobic human gut microbe expresses an oxygen resistant tungsten-containing oxidoreductase for detoxifying gut aldehydes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9424855/
https://www.ncbi.nlm.nih.gov/pubmed/36051760
http://dx.doi.org/10.3389/fmicb.2022.965625
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