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The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9
Methanobrevibacter millerae SM9 was isolated from the rumen of a sheep maintained on a fresh forage diet, and its genome has been sequenced to provide information on the phylogenetic diversity of rumen methanogens with a view to developing technologies for methane mitigation. It is the first rumen i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987999/ https://www.ncbi.nlm.nih.gov/pubmed/27536339 http://dx.doi.org/10.1186/s40793-016-0171-9 |
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author | Kelly, William J. Pacheco, Diana M. Li, Dong Attwood, Graeme T. Altermann, Eric Leahy, Sinead C. |
author_facet | Kelly, William J. Pacheco, Diana M. Li, Dong Attwood, Graeme T. Altermann, Eric Leahy, Sinead C. |
author_sort | Kelly, William J. |
collection | PubMed |
description | Methanobrevibacter millerae SM9 was isolated from the rumen of a sheep maintained on a fresh forage diet, and its genome has been sequenced to provide information on the phylogenetic diversity of rumen methanogens with a view to developing technologies for methane mitigation. It is the first rumen isolate from the Methanobrevibacter gottschalkii clade to have its genome sequence completed. The 2.54 Mb SM9 chromosome has an average G + C content of 31.8 %, encodes 2269 protein-coding genes, and harbors a single prophage. The overall gene content is comparable to that of Methanobrevibacter ruminantium M1 and the type strain of M. millerae (ZA-10(T)) suggesting that the basic metabolism of these two hydrogenotrophic rumen methanogen species is similar. However, M. millerae has a larger complement of genes involved in methanogenesis including genes for methyl coenzyme M reductase II (mrtAGDB) which are not found in M1. Unusual features of the M. millerae genomes include the presence of a tannase gene which shows high sequence similarity with the tannase from Lactobacillus plantarum, and large non-ribosomal peptide synthase genes. The M. millerae sequences indicate that methane mitigation strategies based on the M. ruminantium M1 genome sequence are also likely to be applicable to members of the M. gottschalkii clade. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40793-016-0171-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4987999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49879992016-08-18 The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 Kelly, William J. Pacheco, Diana M. Li, Dong Attwood, Graeme T. Altermann, Eric Leahy, Sinead C. Stand Genomic Sci Short Genome Report Methanobrevibacter millerae SM9 was isolated from the rumen of a sheep maintained on a fresh forage diet, and its genome has been sequenced to provide information on the phylogenetic diversity of rumen methanogens with a view to developing technologies for methane mitigation. It is the first rumen isolate from the Methanobrevibacter gottschalkii clade to have its genome sequence completed. The 2.54 Mb SM9 chromosome has an average G + C content of 31.8 %, encodes 2269 protein-coding genes, and harbors a single prophage. The overall gene content is comparable to that of Methanobrevibacter ruminantium M1 and the type strain of M. millerae (ZA-10(T)) suggesting that the basic metabolism of these two hydrogenotrophic rumen methanogen species is similar. However, M. millerae has a larger complement of genes involved in methanogenesis including genes for methyl coenzyme M reductase II (mrtAGDB) which are not found in M1. Unusual features of the M. millerae genomes include the presence of a tannase gene which shows high sequence similarity with the tannase from Lactobacillus plantarum, and large non-ribosomal peptide synthase genes. The M. millerae sequences indicate that methane mitigation strategies based on the M. ruminantium M1 genome sequence are also likely to be applicable to members of the M. gottschalkii clade. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40793-016-0171-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-08-17 /pmc/articles/PMC4987999/ /pubmed/27536339 http://dx.doi.org/10.1186/s40793-016-0171-9 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Genome Report Kelly, William J. Pacheco, Diana M. Li, Dong Attwood, Graeme T. Altermann, Eric Leahy, Sinead C. The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title | The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title_full | The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title_fullStr | The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title_full_unstemmed | The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title_short | The complete genome sequence of the rumen methanogen Methanobrevibacter millerae SM9 |
title_sort | complete genome sequence of the rumen methanogen methanobrevibacter millerae sm9 |
topic | Short Genome Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987999/ https://www.ncbi.nlm.nih.gov/pubmed/27536339 http://dx.doi.org/10.1186/s40793-016-0171-9 |
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