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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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