Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost

While wetlands are major sources of biogenic methane (CH4), our understanding of resident microbial metabolism is incomplete, which compromises the prediction of CH4 emissions under ongoing climate change. Here, we employed genome-resolved multi-omics to expand our understanding of methanogenesis in...

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Published in:mSystems
Main Authors: Ellenbogen, J.B., Borton, M.A., McGivern, B.B., Cronin, D.R., Hoyt, D.W., Freire-Zapata, V., McCalley, C.K., Varner, R.K., Crill, P.M., Wehr, R.A., Chanton, J.P., Woodcroft, B.J., Tfaily, M.M., Tyson, G.W., Rich, V.I., Wrighton, K.C.
Other Authors: Department of Environmental Science, University of Arizona, Department of Ecology and Evolutionary Biology, University of Arizona
Format: Article in Journal/Newspaper
Language:English
Published: American Society for Microbiology 2023
Subjects:
Online Access:http://hdl.handle.net/10150/672029
https://doi.org/10.1128/msystems.00698-23
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spelling ftunivarizona:oai:repository.arizona.edu:10150/672029 2024-04-28T08:11:32+00:00 Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost Ellenbogen, J.B. Borton, M.A. McGivern, B.B. Cronin, D.R. Hoyt, D.W. Freire-Zapata, V. McCalley, C.K. Varner, R.K. Crill, P.M. Wehr, R.A. Chanton, J.P. Woodcroft, B.J. Tfaily, M.M. Tyson, G.W. Rich, V.I. Wrighton, K.C. Department of Environmental Science, University of Arizona Department of Ecology and Evolutionary Biology, University of Arizona 2023-12-08 http://hdl.handle.net/10150/672029 https://doi.org/10.1128/msystems.00698-23 en eng American Society for Microbiology Ellenbogen JB, Borton MA, McGivern BB, Cronin DR, Hoyt DW, Freire-Zapata V, McCalley CK, Varner RK, Crill PM, Wehr RA, Chanton JP, Woodcroft BJ, Tfaily MM, Tyson GW, Rich VI, Wrighton KC.2024.Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost. mSystems9:e00698-23.https://doi.org/10.1128/msystems.00698-23 2379-5077 38063415 doi:10.1128/msystems.00698-23 http://hdl.handle.net/10150/672029 mSystems © 2023 Ellenbogen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license. https://creativecommons.org/licenses/by/4.0/ mSystems EMERGE Biology Integration Institute methanogenesis methylotrophy Stordalen Mire Article text 2023 ftunivarizona https://doi.org/10.1128/msystems.00698-23 2024-04-03T14:11:41Z While wetlands are major sources of biogenic methane (CH4), our understanding of resident microbial metabolism is incomplete, which compromises the prediction of CH4 emissions under ongoing climate change. Here, we employed genome-resolved multi-omics to expand our understanding of methanogenesis in the thawing permafrost peatland of Stordalen Mire in Arctic Sweden. In quadrupling the genomic representation of the site's methanogens and examining their encoded metabolism, we revealed that nearly 20% of the metagenome-assembled genomes (MAGs) encoded the potential for methylotrophic methanogenesis. Further, 27% of the transcriptionally active methanogens expressed methylotrophic genes; for Methanosarcinales and Methanobacteriales MAGs, these data indicated the use of methylated oxygen compounds (e.g., methanol), while for Methanomassiliicoccales, they primarily implicated methyl sulfides and methylamines. In addition to methanogenic methylotrophy, >1,700 bacterial MAGs across 19 phyla encoded anaerobic methylotrophic potential, with expression across 12 phyla. Metabolomic analyses revealed the presence of diverse methylated compounds in the Mire, including some known methylotrophic substrates. Active methylotrophy was observed across all stages of a permafrost thaw gradient in Stordalen, with the most frozen non-methanogenic palsa found to host bacterial methylotrophy and the partially thawed bog and fully thawed fen seen to house both methanogenic and bacterial methylotrophic activities. Methanogenesis across increasing permafrost thaw is thus revised from the sole dominance of hydrogenotrophic production and the appearance of acetoclastic at full thaw to consider the co-occurrence of methylotrophy throughout. Collectively, these findings indicate that methanogenic and bacterial methylotrophy may be an important and previously underappreciated component of carbon cycling and emissions in these rapidly changing wetland habitats.IMPORTANCEWetlands are the biggest natural source of atmospheric methane (CH4) ... Article in Journal/Newspaper Arctic Climate change palsa permafrost The University of Arizona: UA Campus Repository mSystems 9 1
institution Open Polar
collection The University of Arizona: UA Campus Repository
op_collection_id ftunivarizona
language English
topic EMERGE Biology Integration Institute
methanogenesis
methylotrophy
Stordalen Mire
spellingShingle EMERGE Biology Integration Institute
methanogenesis
methylotrophy
Stordalen Mire
Ellenbogen, J.B.
Borton, M.A.
McGivern, B.B.
Cronin, D.R.
Hoyt, D.W.
Freire-Zapata, V.
McCalley, C.K.
Varner, R.K.
Crill, P.M.
Wehr, R.A.
Chanton, J.P.
Woodcroft, B.J.
Tfaily, M.M.
Tyson, G.W.
Rich, V.I.
Wrighton, K.C.
Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
topic_facet EMERGE Biology Integration Institute
methanogenesis
methylotrophy
Stordalen Mire
description While wetlands are major sources of biogenic methane (CH4), our understanding of resident microbial metabolism is incomplete, which compromises the prediction of CH4 emissions under ongoing climate change. Here, we employed genome-resolved multi-omics to expand our understanding of methanogenesis in the thawing permafrost peatland of Stordalen Mire in Arctic Sweden. In quadrupling the genomic representation of the site's methanogens and examining their encoded metabolism, we revealed that nearly 20% of the metagenome-assembled genomes (MAGs) encoded the potential for methylotrophic methanogenesis. Further, 27% of the transcriptionally active methanogens expressed methylotrophic genes; for Methanosarcinales and Methanobacteriales MAGs, these data indicated the use of methylated oxygen compounds (e.g., methanol), while for Methanomassiliicoccales, they primarily implicated methyl sulfides and methylamines. In addition to methanogenic methylotrophy, >1,700 bacterial MAGs across 19 phyla encoded anaerobic methylotrophic potential, with expression across 12 phyla. Metabolomic analyses revealed the presence of diverse methylated compounds in the Mire, including some known methylotrophic substrates. Active methylotrophy was observed across all stages of a permafrost thaw gradient in Stordalen, with the most frozen non-methanogenic palsa found to host bacterial methylotrophy and the partially thawed bog and fully thawed fen seen to house both methanogenic and bacterial methylotrophic activities. Methanogenesis across increasing permafrost thaw is thus revised from the sole dominance of hydrogenotrophic production and the appearance of acetoclastic at full thaw to consider the co-occurrence of methylotrophy throughout. Collectively, these findings indicate that methanogenic and bacterial methylotrophy may be an important and previously underappreciated component of carbon cycling and emissions in these rapidly changing wetland habitats.IMPORTANCEWetlands are the biggest natural source of atmospheric methane (CH4) ...
author2 Department of Environmental Science, University of Arizona
Department of Ecology and Evolutionary Biology, University of Arizona
format Article in Journal/Newspaper
author Ellenbogen, J.B.
Borton, M.A.
McGivern, B.B.
Cronin, D.R.
Hoyt, D.W.
Freire-Zapata, V.
McCalley, C.K.
Varner, R.K.
Crill, P.M.
Wehr, R.A.
Chanton, J.P.
Woodcroft, B.J.
Tfaily, M.M.
Tyson, G.W.
Rich, V.I.
Wrighton, K.C.
author_facet Ellenbogen, J.B.
Borton, M.A.
McGivern, B.B.
Cronin, D.R.
Hoyt, D.W.
Freire-Zapata, V.
McCalley, C.K.
Varner, R.K.
Crill, P.M.
Wehr, R.A.
Chanton, J.P.
Woodcroft, B.J.
Tfaily, M.M.
Tyson, G.W.
Rich, V.I.
Wrighton, K.C.
author_sort Ellenbogen, J.B.
title Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
title_short Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
title_full Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
title_fullStr Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
title_full_unstemmed Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost
title_sort methylotrophy in the mire: direct and indirect routes for methane production in thawing permafrost
publisher American Society for Microbiology
publishDate 2023
url http://hdl.handle.net/10150/672029
https://doi.org/10.1128/msystems.00698-23
genre Arctic
Climate change
palsa
permafrost
genre_facet Arctic
Climate change
palsa
permafrost
op_source mSystems
op_relation Ellenbogen JB, Borton MA, McGivern BB, Cronin DR, Hoyt DW, Freire-Zapata V, McCalley CK, Varner RK, Crill PM, Wehr RA, Chanton JP, Woodcroft BJ, Tfaily MM, Tyson GW, Rich VI, Wrighton KC.2024.Methylotrophy in the Mire: direct and indirect routes for methane production in thawing permafrost. mSystems9:e00698-23.https://doi.org/10.1128/msystems.00698-23
2379-5077
38063415
doi:10.1128/msystems.00698-23
http://hdl.handle.net/10150/672029
mSystems
op_rights © 2023 Ellenbogen et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
https://creativecommons.org/licenses/by/4.0/
op_doi https://doi.org/10.1128/msystems.00698-23
container_title mSystems
container_volume 9
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