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Methanethiol-dependent dimethylsulfide production in soil environments
Dimethylsulfide (DMS) is an environmentally important trace gas with roles in sulfur cycling, signalling to higher organisms and in atmospheric chemistry. DMS is believed to be predominantly produced in marine environments via microbial degradation of the osmolyte dimethylsulfoniopropionate (DMSP)....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607357/ https://www.ncbi.nlm.nih.gov/pubmed/28763056 http://dx.doi.org/10.1038/ismej.2017.105 |
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author | Carrión, Ornella Pratscher, Jennifer Curson, Andrew R J Williams, Beth T Rostant, Wayne G Murrell, J Colin Todd, Jonathan D |
author_facet | Carrión, Ornella Pratscher, Jennifer Curson, Andrew R J Williams, Beth T Rostant, Wayne G Murrell, J Colin Todd, Jonathan D |
author_sort | Carrión, Ornella |
collection | PubMed |
description | Dimethylsulfide (DMS) is an environmentally important trace gas with roles in sulfur cycling, signalling to higher organisms and in atmospheric chemistry. DMS is believed to be predominantly produced in marine environments via microbial degradation of the osmolyte dimethylsulfoniopropionate (DMSP). However, significant amounts of DMS are also generated from terrestrial environments, for example, peat bogs can emit ~6 μmol DMS m(−2) per day, likely via the methylation of methanethiol (MeSH). A methyltransferase enzyme termed ‘MddA’, which catalyses the methylation of MeSH, generating DMS, in a wide range of bacteria and some cyanobacteria, may mediate this process, as the mddA gene is abundant in terrestrial metagenomes. This is the first study investigating the functionality of MeSH-dependent DMS production (Mdd) in a wide range of aerobic environments. All soils and marine sediment samples tested produced DMS when incubated with MeSH. Cultivation-dependent and cultivation-independent methods were used to assess microbial community changes in response to MeSH addition in a grassland soil where 35.9% of the bacteria were predicted to contain mddA. Bacteria of the genus Methylotenera were enriched in the presence of MeSH. Furthermore, many novel Mdd(+) bacterial strains were isolated. Despite the abundance of mddA in the grassland soil, the Mdd pathway may not be a significant source of DMS in this environment as MeSH addition was required to detect DMS at only very low conversion rates. |
format | Online Article Text |
id | pubmed-5607357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56073572017-10-01 Methanethiol-dependent dimethylsulfide production in soil environments Carrión, Ornella Pratscher, Jennifer Curson, Andrew R J Williams, Beth T Rostant, Wayne G Murrell, J Colin Todd, Jonathan D ISME J Original Article Dimethylsulfide (DMS) is an environmentally important trace gas with roles in sulfur cycling, signalling to higher organisms and in atmospheric chemistry. DMS is believed to be predominantly produced in marine environments via microbial degradation of the osmolyte dimethylsulfoniopropionate (DMSP). However, significant amounts of DMS are also generated from terrestrial environments, for example, peat bogs can emit ~6 μmol DMS m(−2) per day, likely via the methylation of methanethiol (MeSH). A methyltransferase enzyme termed ‘MddA’, which catalyses the methylation of MeSH, generating DMS, in a wide range of bacteria and some cyanobacteria, may mediate this process, as the mddA gene is abundant in terrestrial metagenomes. This is the first study investigating the functionality of MeSH-dependent DMS production (Mdd) in a wide range of aerobic environments. All soils and marine sediment samples tested produced DMS when incubated with MeSH. Cultivation-dependent and cultivation-independent methods were used to assess microbial community changes in response to MeSH addition in a grassland soil where 35.9% of the bacteria were predicted to contain mddA. Bacteria of the genus Methylotenera were enriched in the presence of MeSH. Furthermore, many novel Mdd(+) bacterial strains were isolated. Despite the abundance of mddA in the grassland soil, the Mdd pathway may not be a significant source of DMS in this environment as MeSH addition was required to detect DMS at only very low conversion rates. Nature Publishing Group 2017-10 2017-08-01 /pmc/articles/PMC5607357/ /pubmed/28763056 http://dx.doi.org/10.1038/ismej.2017.105 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Carrión, Ornella Pratscher, Jennifer Curson, Andrew R J Williams, Beth T Rostant, Wayne G Murrell, J Colin Todd, Jonathan D Methanethiol-dependent dimethylsulfide production in soil environments |
title | Methanethiol-dependent dimethylsulfide production in soil environments |
title_full | Methanethiol-dependent dimethylsulfide production in soil environments |
title_fullStr | Methanethiol-dependent dimethylsulfide production in soil environments |
title_full_unstemmed | Methanethiol-dependent dimethylsulfide production in soil environments |
title_short | Methanethiol-dependent dimethylsulfide production in soil environments |
title_sort | methanethiol-dependent dimethylsulfide production in soil environments |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5607357/ https://www.ncbi.nlm.nih.gov/pubmed/28763056 http://dx.doi.org/10.1038/ismej.2017.105 |
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