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The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395

Phaeobacter inhibens DSM 17395, a model organism for marine Roseobacter group, was studied for its response to its own antimicrobial compound tropodithietic acid (TDA). TDA biosynthesis is encoded on the largest extrachromosomal element of P. inhibens, the 262 kb plasmid, whose curation leads to an...

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Autores principales: Will, Sabine Eva, Neumann-Schaal, Meina, Heydorn, Raymond Leopold, Bartling, Pascal, Petersen, Jörn, Schomburg, Dietmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421792/
https://www.ncbi.nlm.nih.gov/pubmed/28481933
http://dx.doi.org/10.1371/journal.pone.0177295
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author Will, Sabine Eva
Neumann-Schaal, Meina
Heydorn, Raymond Leopold
Bartling, Pascal
Petersen, Jörn
Schomburg, Dietmar
author_facet Will, Sabine Eva
Neumann-Schaal, Meina
Heydorn, Raymond Leopold
Bartling, Pascal
Petersen, Jörn
Schomburg, Dietmar
author_sort Will, Sabine Eva
collection PubMed
description Phaeobacter inhibens DSM 17395, a model organism for marine Roseobacter group, was studied for its response to its own antimicrobial compound tropodithietic acid (TDA). TDA biosynthesis is encoded on the largest extrachromosomal element of P. inhibens, the 262 kb plasmid, whose curation leads to an increased growth and biomass yield. In this study, the plasmid-cured strain was compared to the wild-type strain and to transposon mutants lacking single genes of the TDA biosynthesis. The data show that the growth inhibition of the wild-type strain can be mainly attributed to the TDA produced by P. inhibens itself. Oxygen uptake rates remained constant in all strains but the growth rate dropped in the wild-type which supports the recently proposed mode of TDA action. Metabolome analysis showed no metabolic alterations that could be attributed directly to TDA. Taken together, the growth of P. inhibens is limited by its own antibacterial compound due to a partial destruction of the proton gradient which leads to a higher energetic demand. The universal presence of TDA biosynthesis in genome-sequenced isolates of the genus Phaeobacter shows that there must be a high benefit of TDA for P. inhibens in its ecological niche despite the drawback on its metabolism.
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spelling pubmed-54217922017-05-14 The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395 Will, Sabine Eva Neumann-Schaal, Meina Heydorn, Raymond Leopold Bartling, Pascal Petersen, Jörn Schomburg, Dietmar PLoS One Research Article Phaeobacter inhibens DSM 17395, a model organism for marine Roseobacter group, was studied for its response to its own antimicrobial compound tropodithietic acid (TDA). TDA biosynthesis is encoded on the largest extrachromosomal element of P. inhibens, the 262 kb plasmid, whose curation leads to an increased growth and biomass yield. In this study, the plasmid-cured strain was compared to the wild-type strain and to transposon mutants lacking single genes of the TDA biosynthesis. The data show that the growth inhibition of the wild-type strain can be mainly attributed to the TDA produced by P. inhibens itself. Oxygen uptake rates remained constant in all strains but the growth rate dropped in the wild-type which supports the recently proposed mode of TDA action. Metabolome analysis showed no metabolic alterations that could be attributed directly to TDA. Taken together, the growth of P. inhibens is limited by its own antibacterial compound due to a partial destruction of the proton gradient which leads to a higher energetic demand. The universal presence of TDA biosynthesis in genome-sequenced isolates of the genus Phaeobacter shows that there must be a high benefit of TDA for P. inhibens in its ecological niche despite the drawback on its metabolism. Public Library of Science 2017-05-08 /pmc/articles/PMC5421792/ /pubmed/28481933 http://dx.doi.org/10.1371/journal.pone.0177295 Text en © 2017 Will et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited.
spellingShingle Research Article
Will, Sabine Eva
Neumann-Schaal, Meina
Heydorn, Raymond Leopold
Bartling, Pascal
Petersen, Jörn
Schomburg, Dietmar
The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title_full The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title_fullStr The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title_full_unstemmed The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title_short The limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in Phaeobacter inhibens DSM 17395
title_sort limits to growth – energetic burden of the endogenous antibiotic tropodithietic acid in phaeobacter inhibens dsm 17395
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421792/
https://www.ncbi.nlm.nih.gov/pubmed/28481933
http://dx.doi.org/10.1371/journal.pone.0177295
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