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A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus

Methoxylated aromatic compounds (MACs) are important components of lignin found in significant amounts in the subsurface. Recently, the methanogenic archaeon Methermicoccus shengliensis was shown to be able to use a variety of MACs during methoxydotrophic growth. After a molecular survey, we found t...

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Autores principales: Welte, Cornelia U., de Graaf, Rob, Dalcin Martins, Paula, Jansen, Robert S., Jetten, Mike S. M., Kurth, Julia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359953/
https://www.ncbi.nlm.nih.gov/pubmed/33913565
http://dx.doi.org/10.1111/1462-2920.15546
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author Welte, Cornelia U.
de Graaf, Rob
Dalcin Martins, Paula
Jansen, Robert S.
Jetten, Mike S. M.
Kurth, Julia M.
author_facet Welte, Cornelia U.
de Graaf, Rob
Dalcin Martins, Paula
Jansen, Robert S.
Jetten, Mike S. M.
Kurth, Julia M.
author_sort Welte, Cornelia U.
collection PubMed
description Methoxylated aromatic compounds (MACs) are important components of lignin found in significant amounts in the subsurface. Recently, the methanogenic archaeon Methermicoccus shengliensis was shown to be able to use a variety of MACs during methoxydotrophic growth. After a molecular survey, we found that the hyperthermophilic non‐methanogenic archaeon Archaeoglobus fulgidus also encodes genes for a bacterial‐like demethoxylation system. In this study, we performed growth and metabolite analysis, and used transcriptomics to investigate the response of A. fulgidus during growth on MACs in comparison to growth on lactate. We observed that A. fulgidus converts MACs to their hydroxylated derivatives with CO(2) as the main product and sulfate as electron acceptor. Furthermore, we could show that MACs improve the growth of A. fulgidus in the presence of organic substrates such as lactate. We also found evidence that other archaea such as Bathyarchaeota, Lokiarchaeota, Verstraetearchaeota, Korarchaeota, Helarchaeota and Nezhaarchaeota encode a demethoxylation system. In summary, we here describe the first non‐methanogenic archaeon with the ability to grow on MACs indicating that methoxydotrophic archaea might play a so far underestimated role in the global carbon cycle.
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spelling pubmed-83599532021-08-17 A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus Welte, Cornelia U. de Graaf, Rob Dalcin Martins, Paula Jansen, Robert S. Jetten, Mike S. M. Kurth, Julia M. Environ Microbiol Special Issue Articles Methoxylated aromatic compounds (MACs) are important components of lignin found in significant amounts in the subsurface. Recently, the methanogenic archaeon Methermicoccus shengliensis was shown to be able to use a variety of MACs during methoxydotrophic growth. After a molecular survey, we found that the hyperthermophilic non‐methanogenic archaeon Archaeoglobus fulgidus also encodes genes for a bacterial‐like demethoxylation system. In this study, we performed growth and metabolite analysis, and used transcriptomics to investigate the response of A. fulgidus during growth on MACs in comparison to growth on lactate. We observed that A. fulgidus converts MACs to their hydroxylated derivatives with CO(2) as the main product and sulfate as electron acceptor. Furthermore, we could show that MACs improve the growth of A. fulgidus in the presence of organic substrates such as lactate. We also found evidence that other archaea such as Bathyarchaeota, Lokiarchaeota, Verstraetearchaeota, Korarchaeota, Helarchaeota and Nezhaarchaeota encode a demethoxylation system. In summary, we here describe the first non‐methanogenic archaeon with the ability to grow on MACs indicating that methoxydotrophic archaea might play a so far underestimated role in the global carbon cycle. John Wiley & Sons, Inc. 2021-05-05 2021-07 /pmc/articles/PMC8359953/ /pubmed/33913565 http://dx.doi.org/10.1111/1462-2920.15546 Text en © 2021 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Issue Articles
Welte, Cornelia U.
de Graaf, Rob
Dalcin Martins, Paula
Jansen, Robert S.
Jetten, Mike S. M.
Kurth, Julia M.
A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title_full A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title_fullStr A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title_full_unstemmed A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title_short A novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon Archaeoglobus fulgidus
title_sort novel methoxydotrophic metabolism discovered in the hyperthermophilic archaeon archaeoglobus fulgidus
topic Special Issue Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359953/
https://www.ncbi.nlm.nih.gov/pubmed/33913565
http://dx.doi.org/10.1111/1462-2920.15546
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