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Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase
Shewanella species are facultative anaerobic bacteria that colonize redox-stratified habitats where O(2) and nutrient concentrations fluctuate. The model species Shewanella oneidensis MR-1 possesses genes coding for three terminal oxidases that can perform O(2) respiration: a bd-type quinol oxidase...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728554/ https://www.ncbi.nlm.nih.gov/pubmed/26815910 http://dx.doi.org/10.1038/srep19726 |
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author | Le Laz, Sébastien kpebe, Arlette Bauzan, Marielle Lignon, Sabrina Rousset, Marc Brugna, Myriam |
author_facet | Le Laz, Sébastien kpebe, Arlette Bauzan, Marielle Lignon, Sabrina Rousset, Marc Brugna, Myriam |
author_sort | Le Laz, Sébastien |
collection | PubMed |
description | Shewanella species are facultative anaerobic bacteria that colonize redox-stratified habitats where O(2) and nutrient concentrations fluctuate. The model species Shewanella oneidensis MR-1 possesses genes coding for three terminal oxidases that can perform O(2) respiration: a bd-type quinol oxidase and cytochrome c oxidases of the cbb(3)-type and the A-type. Whereas the bd- and cbb(3)-type oxidases are routinely detected, evidence for the expression of the A-type enzyme has so far been lacking. Here, we investigated the effect of nutrient starvation on the expression of these terminal oxidases under different O(2) tensions. Our results reveal that the bd-type oxidase plays a significant role under nutrient starvation in aerobic conditions. The expression of the cbb(3)-type oxidase is also modulated by the nutrient composition of the medium and increases especially under iron-deficiency in exponentially growing cells. Most importantly, under conditions of carbon depletion, high O(2) and stationary-growth, we report for the first time the expression of the A-type oxidase in S. oneidensis, indicating that this terminal oxidase is not functionally lost. The physiological role of the A-type oxidase in energy conservation and in the adaptation of S. oneidensis to redox-stratified environments is discussed. |
format | Online Article Text |
id | pubmed-4728554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47285542016-02-01 Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase Le Laz, Sébastien kpebe, Arlette Bauzan, Marielle Lignon, Sabrina Rousset, Marc Brugna, Myriam Sci Rep Article Shewanella species are facultative anaerobic bacteria that colonize redox-stratified habitats where O(2) and nutrient concentrations fluctuate. The model species Shewanella oneidensis MR-1 possesses genes coding for three terminal oxidases that can perform O(2) respiration: a bd-type quinol oxidase and cytochrome c oxidases of the cbb(3)-type and the A-type. Whereas the bd- and cbb(3)-type oxidases are routinely detected, evidence for the expression of the A-type enzyme has so far been lacking. Here, we investigated the effect of nutrient starvation on the expression of these terminal oxidases under different O(2) tensions. Our results reveal that the bd-type oxidase plays a significant role under nutrient starvation in aerobic conditions. The expression of the cbb(3)-type oxidase is also modulated by the nutrient composition of the medium and increases especially under iron-deficiency in exponentially growing cells. Most importantly, under conditions of carbon depletion, high O(2) and stationary-growth, we report for the first time the expression of the A-type oxidase in S. oneidensis, indicating that this terminal oxidase is not functionally lost. The physiological role of the A-type oxidase in energy conservation and in the adaptation of S. oneidensis to redox-stratified environments is discussed. Nature Publishing Group 2016-01-27 /pmc/articles/PMC4728554/ /pubmed/26815910 http://dx.doi.org/10.1038/srep19726 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Le Laz, Sébastien kpebe, Arlette Bauzan, Marielle Lignon, Sabrina Rousset, Marc Brugna, Myriam Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title | Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title_full | Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title_fullStr | Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title_full_unstemmed | Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title_short | Expression of terminal oxidases under nutrient-starved conditions in Shewanella oneidensis: detection of the A-type cytochrome c oxidase |
title_sort | expression of terminal oxidases under nutrient-starved conditions in shewanella oneidensis: detection of the a-type cytochrome c oxidase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728554/ https://www.ncbi.nlm.nih.gov/pubmed/26815910 http://dx.doi.org/10.1038/srep19726 |
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