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A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui

BACKGROUND: Acetogenic bacteria are able to use CO(2) as terminal electron acceptor of an anaerobic respiration, thereby producing acetate with electrons coming from H(2). Due to this feature, acetogens came into focus as platforms to produce biocommodities from waste gases such as H(2) + CO(2) and/...

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Autores principales: Hess, Verena, Poehlein, Anja, Weghoff, Marie Charlotte, Daniel, Rolf, Müller, Volker
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320612/
https://www.ncbi.nlm.nih.gov/pubmed/25523312
http://dx.doi.org/10.1186/1471-2164-15-1139
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author Hess, Verena
Poehlein, Anja
Weghoff, Marie Charlotte
Daniel, Rolf
Müller, Volker
author_facet Hess, Verena
Poehlein, Anja
Weghoff, Marie Charlotte
Daniel, Rolf
Müller, Volker
author_sort Hess, Verena
collection PubMed
description BACKGROUND: Acetogenic bacteria are able to use CO(2) as terminal electron acceptor of an anaerobic respiration, thereby producing acetate with electrons coming from H(2). Due to this feature, acetogens came into focus as platforms to produce biocommodities from waste gases such as H(2) + CO(2) and/or CO. A prerequisite for metabolic engineering is a detailed understanding of the mechanisms of ATP synthesis and electron-transfer reactions to ensure redox homeostasis. Acetogenesis involves the reduction of CO(2) to acetate via soluble enzymes and is coupled to energy conservation by a chemiosmotic mechanism. The membrane-bound module, acting as an ion pump, was of special interest for decades and recently, an Rnf complex was shown to couple electron flow from reduced ferredoxin to NAD(+) with the export of Na(+) in Acetobacterium woodii. However, not all acetogens have rnf genes in their genome. In order to gain further insights into energy conservation of non-Rnf-containing, thermophilic acetogens, we sequenced the genome of Thermoanaerobacter kivui. RESULTS: The genome of Thermoanaerobacter kivui comprises 2.9 Mbp with a G + C content of 35% and 2,378 protein encoding orfs. Neither autotrophic growth nor acetate formation from H(2) + CO(2) was dependent on Na(+) and acetate formation was inhibited by a protonophore, indicating that H(+) is used as coupling ion for primary bioenergetics. This is consistent with the finding that the c subunit of the F(1)F(O) ATP synthase does not have the conserved Na(+) binding motif. A search for potential H(+)-translocating, membrane-bound protein complexes revealed genes potentially encoding two different proton-reducing, energy-conserving hydrogenases (Ech). CONCLUSIONS: The thermophilic acetogen T. kivui does not use Na(+) but H(+) for chemiosmotic ATP synthesis. It does not contain cytochromes and the electrochemical proton gradient is most likely established by an energy-conserving hydrogenase (Ech). Its thermophilic nature and the efficient conversion of H(2) + CO(2) make T. kivui an interesting acetogen to be used for the production of biocommodities in industrial micobiology. Furthermore, our experimental data as well as the increasing number of sequenced genomes of acetogenic bacteria supported the new classification of acetogens into two groups: Rnf- and Ech-containing acetogens.
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spelling pubmed-43206122015-02-08 A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui Hess, Verena Poehlein, Anja Weghoff, Marie Charlotte Daniel, Rolf Müller, Volker BMC Genomics Research Article BACKGROUND: Acetogenic bacteria are able to use CO(2) as terminal electron acceptor of an anaerobic respiration, thereby producing acetate with electrons coming from H(2). Due to this feature, acetogens came into focus as platforms to produce biocommodities from waste gases such as H(2) + CO(2) and/or CO. A prerequisite for metabolic engineering is a detailed understanding of the mechanisms of ATP synthesis and electron-transfer reactions to ensure redox homeostasis. Acetogenesis involves the reduction of CO(2) to acetate via soluble enzymes and is coupled to energy conservation by a chemiosmotic mechanism. The membrane-bound module, acting as an ion pump, was of special interest for decades and recently, an Rnf complex was shown to couple electron flow from reduced ferredoxin to NAD(+) with the export of Na(+) in Acetobacterium woodii. However, not all acetogens have rnf genes in their genome. In order to gain further insights into energy conservation of non-Rnf-containing, thermophilic acetogens, we sequenced the genome of Thermoanaerobacter kivui. RESULTS: The genome of Thermoanaerobacter kivui comprises 2.9 Mbp with a G + C content of 35% and 2,378 protein encoding orfs. Neither autotrophic growth nor acetate formation from H(2) + CO(2) was dependent on Na(+) and acetate formation was inhibited by a protonophore, indicating that H(+) is used as coupling ion for primary bioenergetics. This is consistent with the finding that the c subunit of the F(1)F(O) ATP synthase does not have the conserved Na(+) binding motif. A search for potential H(+)-translocating, membrane-bound protein complexes revealed genes potentially encoding two different proton-reducing, energy-conserving hydrogenases (Ech). CONCLUSIONS: The thermophilic acetogen T. kivui does not use Na(+) but H(+) for chemiosmotic ATP synthesis. It does not contain cytochromes and the electrochemical proton gradient is most likely established by an energy-conserving hydrogenase (Ech). Its thermophilic nature and the efficient conversion of H(2) + CO(2) make T. kivui an interesting acetogen to be used for the production of biocommodities in industrial micobiology. Furthermore, our experimental data as well as the increasing number of sequenced genomes of acetogenic bacteria supported the new classification of acetogens into two groups: Rnf- and Ech-containing acetogens. BioMed Central 2014-12-18 /pmc/articles/PMC4320612/ /pubmed/25523312 http://dx.doi.org/10.1186/1471-2164-15-1139 Text en © Hess et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Research Article
Hess, Verena
Poehlein, Anja
Weghoff, Marie Charlotte
Daniel, Rolf
Müller, Volker
A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title_full A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title_fullStr A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title_full_unstemmed A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title_short A genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium Thermoanaerobacter kivui
title_sort genome-guided analysis of energy conservation in the thermophilic, cytochrome-free acetogenic bacterium thermoanaerobacter kivui
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320612/
https://www.ncbi.nlm.nih.gov/pubmed/25523312
http://dx.doi.org/10.1186/1471-2164-15-1139
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