Cargando…
Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses
The hyperthermophilic, sulfate-reducing archaeon, Archaeoglobus fulgidus, utilizes CO as an energy source and it is resistant to the toxic effects of high CO concentrations. Herein, transcription profiles were obtained from A. fulgidus during growth with CO and sulfate or thiosulfate, or without an...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543118/ https://www.ncbi.nlm.nih.gov/pubmed/26345487 http://dx.doi.org/10.1155/2015/235384 |
_version_ | 1782386577732796416 |
---|---|
author | Hocking, William P. Roalkvam, Irene Magnussen, Carina Stokke, Runar Steen, Ida H. |
author_facet | Hocking, William P. Roalkvam, Irene Magnussen, Carina Stokke, Runar Steen, Ida H. |
author_sort | Hocking, William P. |
collection | PubMed |
description | The hyperthermophilic, sulfate-reducing archaeon, Archaeoglobus fulgidus, utilizes CO as an energy source and it is resistant to the toxic effects of high CO concentrations. Herein, transcription profiles were obtained from A. fulgidus during growth with CO and sulfate or thiosulfate, or without an electron acceptor. This provided a basis for a model of the CO metabolism of A. fulgidus. The model suggests proton translocation by “Mitchell-type” loops facilitated by Fqo catalyzing a Fd(red):menaquinone oxidoreductase reaction, as the major mode of energy conservation, rather than formate or H(2) cycling during respiratory growth. The bifunctional CODH (cdhAB-2) is predicted to play an ubiquitous role in the metabolism of CO, and a novel nitrate reductase-associated respiratory complex was induced specifically in the presence of sulfate. A potential role of this complex in relation to Fd(red) and APS reduction is discussed. Multiple membrane-bound heterodisulfide reductase (DsrMK) could promote both energy-conserving and non-energy-conserving menaquinol oxidation. Finally, the FqoF subunit may catalyze a Fd(red):F(420) oxidoreductase reaction. In the absence of electron acceptor, downregulation of F(420)H(2) dependent steps of the acetyl-CoA pathway is linked to transient formate generation. Overall, carboxidotrophic growth seems as an intrinsic capacity of A. fulgidus with little need for novel resistance or respiratory complexes. |
format | Online Article Text |
id | pubmed-4543118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-45431182015-09-06 Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses Hocking, William P. Roalkvam, Irene Magnussen, Carina Stokke, Runar Steen, Ida H. Archaea Research Article The hyperthermophilic, sulfate-reducing archaeon, Archaeoglobus fulgidus, utilizes CO as an energy source and it is resistant to the toxic effects of high CO concentrations. Herein, transcription profiles were obtained from A. fulgidus during growth with CO and sulfate or thiosulfate, or without an electron acceptor. This provided a basis for a model of the CO metabolism of A. fulgidus. The model suggests proton translocation by “Mitchell-type” loops facilitated by Fqo catalyzing a Fd(red):menaquinone oxidoreductase reaction, as the major mode of energy conservation, rather than formate or H(2) cycling during respiratory growth. The bifunctional CODH (cdhAB-2) is predicted to play an ubiquitous role in the metabolism of CO, and a novel nitrate reductase-associated respiratory complex was induced specifically in the presence of sulfate. A potential role of this complex in relation to Fd(red) and APS reduction is discussed. Multiple membrane-bound heterodisulfide reductase (DsrMK) could promote both energy-conserving and non-energy-conserving menaquinol oxidation. Finally, the FqoF subunit may catalyze a Fd(red):F(420) oxidoreductase reaction. In the absence of electron acceptor, downregulation of F(420)H(2) dependent steps of the acetyl-CoA pathway is linked to transient formate generation. Overall, carboxidotrophic growth seems as an intrinsic capacity of A. fulgidus with little need for novel resistance or respiratory complexes. Hindawi Publishing Corporation 2015-08-06 /pmc/articles/PMC4543118/ /pubmed/26345487 http://dx.doi.org/10.1155/2015/235384 Text en Copyright © 2015 William P. Hocking et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hocking, William P. Roalkvam, Irene Magnussen, Carina Stokke, Runar Steen, Ida H. Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title | Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title_full | Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title_fullStr | Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title_full_unstemmed | Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title_short | Assessment of the Carbon Monoxide Metabolism of the Hyperthermophilic Sulfate-Reducing Archaeon Archaeoglobus fulgidus VC-16 by Comparative Transcriptome Analyses |
title_sort | assessment of the carbon monoxide metabolism of the hyperthermophilic sulfate-reducing archaeon archaeoglobus fulgidus vc-16 by comparative transcriptome analyses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4543118/ https://www.ncbi.nlm.nih.gov/pubmed/26345487 http://dx.doi.org/10.1155/2015/235384 |
work_keys_str_mv | AT hockingwilliamp assessmentofthecarbonmonoxidemetabolismofthehyperthermophilicsulfatereducingarchaeonarchaeoglobusfulgidusvc16bycomparativetranscriptomeanalyses AT roalkvamirene assessmentofthecarbonmonoxidemetabolismofthehyperthermophilicsulfatereducingarchaeonarchaeoglobusfulgidusvc16bycomparativetranscriptomeanalyses AT magnussencarina assessmentofthecarbonmonoxidemetabolismofthehyperthermophilicsulfatereducingarchaeonarchaeoglobusfulgidusvc16bycomparativetranscriptomeanalyses AT stokkerunar assessmentofthecarbonmonoxidemetabolismofthehyperthermophilicsulfatereducingarchaeonarchaeoglobusfulgidusvc16bycomparativetranscriptomeanalyses AT steenidah assessmentofthecarbonmonoxidemetabolismofthehyperthermophilicsulfatereducingarchaeonarchaeoglobusfulgidusvc16bycomparativetranscriptomeanalyses |