Cargando…
Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph
Proteorhodopsins (PRs) are retinal-binding photoproteins that mediate light-driven proton translocation across prokaryotic cell membranes. Despite their abundance, wide distribution and contribution to the bioenergy budget of the marine photic zone, an understanding of PR function and physiological...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380642/ https://www.ncbi.nlm.nih.gov/pubmed/22741028 http://dx.doi.org/10.1371/journal.pone.0038749 |
_version_ | 1782236320164216832 |
---|---|
author | Wang, Zheng O'Shaughnessy, Thomas J. Soto, Carissa M. Rahbar, Amir M. Robertson, Kelly L. Lebedev, Nikolai Vora, Gary J. |
author_facet | Wang, Zheng O'Shaughnessy, Thomas J. Soto, Carissa M. Rahbar, Amir M. Robertson, Kelly L. Lebedev, Nikolai Vora, Gary J. |
author_sort | Wang, Zheng |
collection | PubMed |
description | Proteorhodopsins (PRs) are retinal-binding photoproteins that mediate light-driven proton translocation across prokaryotic cell membranes. Despite their abundance, wide distribution and contribution to the bioenergy budget of the marine photic zone, an understanding of PR function and physiological significance in situ has been hampered as the vast majority of PRs studied to date are from unculturable bacteria or culturable species that lack the tools for genetic manipulation. In this study, we describe the presence and function of a horizontally acquired PR and retinal biosynthesis gene cluster in the culturable and genetically tractable bioluminescent marine bacterium Vibrio campbellii. Pigmentation analysis, absorption spectroscopy and photoinduction assays using a heterologous over-expression system established the V. campbellii PR as a functional green light absorbing proton pump. In situ analyses comparing PR expression and function in wild type (WT) V. campbellii with an isogenic ΔpR deletion mutant revealed a marked absence of PR membrane localization, pigmentation and light-induced proton pumping in the ΔpR mutant. Comparative photoinduction assays demonstrated the distinct upregulation of pR expression in the presence of light and PR-mediated photophosphorylation in WT cells that resulted in the enhancement of cellular survival during respiratory stress. In addition, we demonstrate that the master regulator of adaptive stress response and stationary phase, RpoS1, positively regulates pR expression and PR holoprotein pigmentation. Taken together, the results demonstrate facultative phototrophy in a classical marine organoheterotrophic Vibrio species and provide a salient example of how this organism has exploited lateral gene transfer to further its adaptation to the photic zone. |
format | Online Article Text |
id | pubmed-3380642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33806422012-06-27 Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph Wang, Zheng O'Shaughnessy, Thomas J. Soto, Carissa M. Rahbar, Amir M. Robertson, Kelly L. Lebedev, Nikolai Vora, Gary J. PLoS One Research Article Proteorhodopsins (PRs) are retinal-binding photoproteins that mediate light-driven proton translocation across prokaryotic cell membranes. Despite their abundance, wide distribution and contribution to the bioenergy budget of the marine photic zone, an understanding of PR function and physiological significance in situ has been hampered as the vast majority of PRs studied to date are from unculturable bacteria or culturable species that lack the tools for genetic manipulation. In this study, we describe the presence and function of a horizontally acquired PR and retinal biosynthesis gene cluster in the culturable and genetically tractable bioluminescent marine bacterium Vibrio campbellii. Pigmentation analysis, absorption spectroscopy and photoinduction assays using a heterologous over-expression system established the V. campbellii PR as a functional green light absorbing proton pump. In situ analyses comparing PR expression and function in wild type (WT) V. campbellii with an isogenic ΔpR deletion mutant revealed a marked absence of PR membrane localization, pigmentation and light-induced proton pumping in the ΔpR mutant. Comparative photoinduction assays demonstrated the distinct upregulation of pR expression in the presence of light and PR-mediated photophosphorylation in WT cells that resulted in the enhancement of cellular survival during respiratory stress. In addition, we demonstrate that the master regulator of adaptive stress response and stationary phase, RpoS1, positively regulates pR expression and PR holoprotein pigmentation. Taken together, the results demonstrate facultative phototrophy in a classical marine organoheterotrophic Vibrio species and provide a salient example of how this organism has exploited lateral gene transfer to further its adaptation to the photic zone. Public Library of Science 2012-06-07 /pmc/articles/PMC3380642/ /pubmed/22741028 http://dx.doi.org/10.1371/journal.pone.0038749 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Wang, Zheng O'Shaughnessy, Thomas J. Soto, Carissa M. Rahbar, Amir M. Robertson, Kelly L. Lebedev, Nikolai Vora, Gary J. Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title | Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title_full | Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title_fullStr | Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title_full_unstemmed | Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title_short | Function and Regulation of Vibrio campbellii Proteorhodopsin: Acquired Phototrophy in a Classical Organoheterotroph |
title_sort | function and regulation of vibrio campbellii proteorhodopsin: acquired phototrophy in a classical organoheterotroph |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380642/ https://www.ncbi.nlm.nih.gov/pubmed/22741028 http://dx.doi.org/10.1371/journal.pone.0038749 |
work_keys_str_mv | AT wangzheng functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT oshaughnessythomasj functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT sotocarissam functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT rahbaramirm functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT robertsonkellyl functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT lebedevnikolai functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph AT voragaryj functionandregulationofvibriocampbelliiproteorhodopsinacquiredphototrophyinaclassicalorganoheterotroph |