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A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem
A nearly complete genome sequence of Candidatus ‘Acetothermum autotrophicum’, a presently uncultivated bacterium in candidate division OP1, was revealed by metagenomic analysis of a subsurface thermophilic microbial mat community. Phylogenetic analysis based on the concatenated sequences of proteins...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267732/ https://www.ncbi.nlm.nih.gov/pubmed/22303444 http://dx.doi.org/10.1371/journal.pone.0030559 |
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author | Takami, Hideto Noguchi, Hideki Takaki, Yoshihiro Uchiyama, Ikuo Toyoda, Atsushi Nishi, Shinro Chee, Gab-Joo Arai, Wataru Nunoura, Takuro Itoh, Takehiko Hattori, Masahira Takai, Ken |
author_facet | Takami, Hideto Noguchi, Hideki Takaki, Yoshihiro Uchiyama, Ikuo Toyoda, Atsushi Nishi, Shinro Chee, Gab-Joo Arai, Wataru Nunoura, Takuro Itoh, Takehiko Hattori, Masahira Takai, Ken |
author_sort | Takami, Hideto |
collection | PubMed |
description | A nearly complete genome sequence of Candidatus ‘Acetothermum autotrophicum’, a presently uncultivated bacterium in candidate division OP1, was revealed by metagenomic analysis of a subsurface thermophilic microbial mat community. Phylogenetic analysis based on the concatenated sequences of proteins common among 367 prokaryotes suggests that Ca. ‘A. autotrophicum’ is one of the earliest diverging bacterial lineages. It possesses a folate-dependent Wood-Ljungdahl (acetyl-CoA) pathway of CO(2) fixation, is predicted to have an acetogenic lifestyle, and possesses the newly discovered archaeal-autotrophic type of bifunctional fructose 1,6-bisphosphate aldolase/phosphatase. A phylogenetic analysis of the core gene cluster of the acethyl-CoA pathway, shared by acetogens, methanogens, some sulfur- and iron-reducers and dechlorinators, supports the hypothesis that the core gene cluster of Ca. ‘A. autotrophicum’ is a particularly ancient bacterial pathway. The habitat, physiology and phylogenetic position of Ca. ‘A. autotrophicum’ support the view that the first bacterial and archaeal lineages were H(2)-dependent acetogens and methanogenes living in hydrothermal environments. |
format | Online Article Text |
id | pubmed-3267732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32677322012-02-02 A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem Takami, Hideto Noguchi, Hideki Takaki, Yoshihiro Uchiyama, Ikuo Toyoda, Atsushi Nishi, Shinro Chee, Gab-Joo Arai, Wataru Nunoura, Takuro Itoh, Takehiko Hattori, Masahira Takai, Ken PLoS One Research Article A nearly complete genome sequence of Candidatus ‘Acetothermum autotrophicum’, a presently uncultivated bacterium in candidate division OP1, was revealed by metagenomic analysis of a subsurface thermophilic microbial mat community. Phylogenetic analysis based on the concatenated sequences of proteins common among 367 prokaryotes suggests that Ca. ‘A. autotrophicum’ is one of the earliest diverging bacterial lineages. It possesses a folate-dependent Wood-Ljungdahl (acetyl-CoA) pathway of CO(2) fixation, is predicted to have an acetogenic lifestyle, and possesses the newly discovered archaeal-autotrophic type of bifunctional fructose 1,6-bisphosphate aldolase/phosphatase. A phylogenetic analysis of the core gene cluster of the acethyl-CoA pathway, shared by acetogens, methanogens, some sulfur- and iron-reducers and dechlorinators, supports the hypothesis that the core gene cluster of Ca. ‘A. autotrophicum’ is a particularly ancient bacterial pathway. The habitat, physiology and phylogenetic position of Ca. ‘A. autotrophicum’ support the view that the first bacterial and archaeal lineages were H(2)-dependent acetogens and methanogenes living in hydrothermal environments. Public Library of Science 2012-01-27 /pmc/articles/PMC3267732/ /pubmed/22303444 http://dx.doi.org/10.1371/journal.pone.0030559 Text en Takami et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Takami, Hideto Noguchi, Hideki Takaki, Yoshihiro Uchiyama, Ikuo Toyoda, Atsushi Nishi, Shinro Chee, Gab-Joo Arai, Wataru Nunoura, Takuro Itoh, Takehiko Hattori, Masahira Takai, Ken A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title | A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title_full | A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title_fullStr | A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title_full_unstemmed | A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title_short | A Deeply Branching Thermophilic Bacterium with an Ancient Acetyl-CoA Pathway Dominates a Subsurface Ecosystem |
title_sort | deeply branching thermophilic bacterium with an ancient acetyl-coa pathway dominates a subsurface ecosystem |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3267732/ https://www.ncbi.nlm.nih.gov/pubmed/22303444 http://dx.doi.org/10.1371/journal.pone.0030559 |
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