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Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans
BACKGROUND: The Delta-Proteobacterium Desulfotignum phosphitoxidans is a type strain of the genus Desulfotignum, which comprises to date only three species together with D. balticum and D. toluenicum. D. phosphitoxidans oxidizes phosphite to phosphate as its only source of electrons, with either sul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046663/ https://www.ncbi.nlm.nih.gov/pubmed/24180241 http://dx.doi.org/10.1186/1471-2164-14-753 |
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author | Poehlein, Anja Daniel, Rolf Schink, Bernhard Simeonova, Diliana D |
author_facet | Poehlein, Anja Daniel, Rolf Schink, Bernhard Simeonova, Diliana D |
author_sort | Poehlein, Anja |
collection | PubMed |
description | BACKGROUND: The Delta-Proteobacterium Desulfotignum phosphitoxidans is a type strain of the genus Desulfotignum, which comprises to date only three species together with D. balticum and D. toluenicum. D. phosphitoxidans oxidizes phosphite to phosphate as its only source of electrons, with either sulfate or CO(2) as electron acceptor to gain its metabolic energy, which is of exclusive interest. Sequencing of the genome of this bacterium was undertaken to elucidate the genomic basis of this so far unique type of energy metabolism. RESULTS: The genome contains 4,998,761 base pairs and 4646 genes of which 3609 were assigned to a function, and 1037 are without function prediction. Metabolic reconstruction revealed that most biosynthetic pathways of Gram negative, autotrophic sulfate reducers were present. Autotrophic CO(2) assimilation proceeds through the Wood-Ljungdahl pathway. Additionally, we have found and confirmed the ability of the strain to couple phosphite oxidation to dissimilatory nitrate reduction to ammonia, which in itself is a new type of energy metabolism. Surprisingly, only two pathways for uptake, assimilation and utilization of inorganic and organic phosphonates were found in the genome. The unique for D. phosphitoxidans Ptx-Ptd cluster is involved in inorganic phosphite oxidation and an atypical C-P lyase-coding cluster (Phn) is involved in utilization of organophosphonates. CONCLUSIONS: We present the whole genome sequence of the first bacterium able to gain metabolic energy via phosphite oxidation. The data obtained provide initial information on the composition and architecture of the phosphite–utilizing and energy-transducing systems needed to live with phosphite as an unusual electron donor. |
format | Online Article Text |
id | pubmed-4046663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40466632014-06-06 Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans Poehlein, Anja Daniel, Rolf Schink, Bernhard Simeonova, Diliana D BMC Genomics Research Article BACKGROUND: The Delta-Proteobacterium Desulfotignum phosphitoxidans is a type strain of the genus Desulfotignum, which comprises to date only three species together with D. balticum and D. toluenicum. D. phosphitoxidans oxidizes phosphite to phosphate as its only source of electrons, with either sulfate or CO(2) as electron acceptor to gain its metabolic energy, which is of exclusive interest. Sequencing of the genome of this bacterium was undertaken to elucidate the genomic basis of this so far unique type of energy metabolism. RESULTS: The genome contains 4,998,761 base pairs and 4646 genes of which 3609 were assigned to a function, and 1037 are without function prediction. Metabolic reconstruction revealed that most biosynthetic pathways of Gram negative, autotrophic sulfate reducers were present. Autotrophic CO(2) assimilation proceeds through the Wood-Ljungdahl pathway. Additionally, we have found and confirmed the ability of the strain to couple phosphite oxidation to dissimilatory nitrate reduction to ammonia, which in itself is a new type of energy metabolism. Surprisingly, only two pathways for uptake, assimilation and utilization of inorganic and organic phosphonates were found in the genome. The unique for D. phosphitoxidans Ptx-Ptd cluster is involved in inorganic phosphite oxidation and an atypical C-P lyase-coding cluster (Phn) is involved in utilization of organophosphonates. CONCLUSIONS: We present the whole genome sequence of the first bacterium able to gain metabolic energy via phosphite oxidation. The data obtained provide initial information on the composition and architecture of the phosphite–utilizing and energy-transducing systems needed to live with phosphite as an unusual electron donor. BioMed Central 2013-11-02 /pmc/articles/PMC4046663/ /pubmed/24180241 http://dx.doi.org/10.1186/1471-2164-14-753 Text en © Poehlein et al.; licensee BioMed Central Ltd. 2013 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/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Poehlein, Anja Daniel, Rolf Schink, Bernhard Simeonova, Diliana D Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title | Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title_full | Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title_fullStr | Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title_full_unstemmed | Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title_short | Life based on phosphite: a genome-guided analysis of Desulfotignum phosphitoxidans |
title_sort | life based on phosphite: a genome-guided analysis of desulfotignum phosphitoxidans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046663/ https://www.ncbi.nlm.nih.gov/pubmed/24180241 http://dx.doi.org/10.1186/1471-2164-14-753 |
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