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Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans
Anaerobic thermophiles inhabit relic environments that resemble the early Earth. However, the lineage of these modern organisms co-evolved with our planet. Hence, these organisms carry both ancestral and acquired genes and serve as models to reconstruct early metabolism. Based on comparative genomic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441870/ https://www.ncbi.nlm.nih.gov/pubmed/28436819 http://dx.doi.org/10.7554/eLife.18990 |
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author | Giovannelli, Donato Sievert, Stefan M Hügler, Michael Markert, Stephanie Becher, Dörte Schweder, Thomas Vetriani, Costantino |
author_facet | Giovannelli, Donato Sievert, Stefan M Hügler, Michael Markert, Stephanie Becher, Dörte Schweder, Thomas Vetriani, Costantino |
author_sort | Giovannelli, Donato |
collection | PubMed |
description | Anaerobic thermophiles inhabit relic environments that resemble the early Earth. However, the lineage of these modern organisms co-evolved with our planet. Hence, these organisms carry both ancestral and acquired genes and serve as models to reconstruct early metabolism. Based on comparative genomic and proteomic analyses, we identified two distinct groups of genes in Thermovibrio ammonificans: the first codes for enzymes that do not require oxygen and use substrates of geothermal origin; the second appears to be a more recent acquisition, and may reflect adaptations to cope with the rise of oxygen on Earth. We propose that the ancestor of the Aquificae was originally a hydrogen oxidizing, sulfur reducing bacterium that used a hybrid pathway for CO(2) fixation. With the gradual rise of oxygen in the atmosphere, more efficient terminal electron acceptors became available and this lineage acquired genes that increased its metabolic flexibility while retaining ancestral metabolic traits. DOI: http://dx.doi.org/10.7554/eLife.18990.001 |
format | Online Article Text |
id | pubmed-5441870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54418702017-05-24 Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans Giovannelli, Donato Sievert, Stefan M Hügler, Michael Markert, Stephanie Becher, Dörte Schweder, Thomas Vetriani, Costantino eLife Genomics and Evolutionary Biology Anaerobic thermophiles inhabit relic environments that resemble the early Earth. However, the lineage of these modern organisms co-evolved with our planet. Hence, these organisms carry both ancestral and acquired genes and serve as models to reconstruct early metabolism. Based on comparative genomic and proteomic analyses, we identified two distinct groups of genes in Thermovibrio ammonificans: the first codes for enzymes that do not require oxygen and use substrates of geothermal origin; the second appears to be a more recent acquisition, and may reflect adaptations to cope with the rise of oxygen on Earth. We propose that the ancestor of the Aquificae was originally a hydrogen oxidizing, sulfur reducing bacterium that used a hybrid pathway for CO(2) fixation. With the gradual rise of oxygen in the atmosphere, more efficient terminal electron acceptors became available and this lineage acquired genes that increased its metabolic flexibility while retaining ancestral metabolic traits. DOI: http://dx.doi.org/10.7554/eLife.18990.001 eLife Sciences Publications, Ltd 2017-04-24 /pmc/articles/PMC5441870/ /pubmed/28436819 http://dx.doi.org/10.7554/eLife.18990 Text en © 2017, Giovannelli et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Giovannelli, Donato Sievert, Stefan M Hügler, Michael Markert, Stephanie Becher, Dörte Schweder, Thomas Vetriani, Costantino Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title | Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title_full | Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title_fullStr | Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title_full_unstemmed | Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title_short | Insight into the evolution of microbial metabolism from the deep-branching bacterium, Thermovibrio ammonificans |
title_sort | insight into the evolution of microbial metabolism from the deep-branching bacterium, thermovibrio ammonificans |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5441870/ https://www.ncbi.nlm.nih.gov/pubmed/28436819 http://dx.doi.org/10.7554/eLife.18990 |
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