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Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm
Plant rhizosphere soil houses complex microbial communities in which microorganisms are often involved in intraspecies as well as interspecies and inter‐kingdom signalling networks. Some members of these networks can improve plant health thanks to an important diversity of bioactive secondary metabo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415375/ https://www.ncbi.nlm.nih.gov/pubmed/33000552 http://dx.doi.org/10.1111/1751-7915.13598 |
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author | Rieusset, Laura Rey, Marjolaine Muller, Daniel Vacheron, Jordan Gerin, Florence Dubost, Audrey Comte, Gilles Prigent‐Combaret, Claire |
author_facet | Rieusset, Laura Rey, Marjolaine Muller, Daniel Vacheron, Jordan Gerin, Florence Dubost, Audrey Comte, Gilles Prigent‐Combaret, Claire |
author_sort | Rieusset, Laura |
collection | PubMed |
description | Plant rhizosphere soil houses complex microbial communities in which microorganisms are often involved in intraspecies as well as interspecies and inter‐kingdom signalling networks. Some members of these networks can improve plant health thanks to an important diversity of bioactive secondary metabolites. In this competitive environment, the ability to form biofilms may provide major advantages to microorganisms. With the aim of highlighting the impact of bacterial lifestyle on secondary metabolites production, we performed a metabolomic analysis on four fluorescent Pseudomonas strains cultivated in planktonic and biofilm colony conditions. The untargeted metabolomic analysis led to the detection of hundreds of secondary metabolites in culture extracts. Comparison between biofilm and planktonic conditions showed that bacterial lifestyle is a key factor influencing Pseudomonas metabolome. More than 50% of the detected metabolites were differentially produced according to planktonic or biofilm lifestyles, with the four Pseudomonas strains overproducing several secondary metabolites in biofilm conditions. In parallel, metabolomic analysis associated with genomic prediction and a molecular networking approach enabled us to evaluate the impact of bacterial lifestyle on chemically identified secondary metabolites, more precisely involved in microbial interactions and plant‐growth promotion. Notably, this work highlights the major effect of biofilm lifestyle on acyl‐homoserine lactone and phenazine production in P. chlororaphis strains. |
format | Online Article Text |
id | pubmed-7415375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74153752020-08-10 Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm Rieusset, Laura Rey, Marjolaine Muller, Daniel Vacheron, Jordan Gerin, Florence Dubost, Audrey Comte, Gilles Prigent‐Combaret, Claire Microb Biotechnol Research Articles Plant rhizosphere soil houses complex microbial communities in which microorganisms are often involved in intraspecies as well as interspecies and inter‐kingdom signalling networks. Some members of these networks can improve plant health thanks to an important diversity of bioactive secondary metabolites. In this competitive environment, the ability to form biofilms may provide major advantages to microorganisms. With the aim of highlighting the impact of bacterial lifestyle on secondary metabolites production, we performed a metabolomic analysis on four fluorescent Pseudomonas strains cultivated in planktonic and biofilm colony conditions. The untargeted metabolomic analysis led to the detection of hundreds of secondary metabolites in culture extracts. Comparison between biofilm and planktonic conditions showed that bacterial lifestyle is a key factor influencing Pseudomonas metabolome. More than 50% of the detected metabolites were differentially produced according to planktonic or biofilm lifestyles, with the four Pseudomonas strains overproducing several secondary metabolites in biofilm conditions. In parallel, metabolomic analysis associated with genomic prediction and a molecular networking approach enabled us to evaluate the impact of bacterial lifestyle on chemically identified secondary metabolites, more precisely involved in microbial interactions and plant‐growth promotion. Notably, this work highlights the major effect of biofilm lifestyle on acyl‐homoserine lactone and phenazine production in P. chlororaphis strains. John Wiley and Sons Inc. 2020-08-09 /pmc/articles/PMC7415375/ /pubmed/33000552 http://dx.doi.org/10.1111/1751-7915.13598 Text en © 2020 The Authors. Microbial Biotechnology published by Society for Applied Microbiology and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Rieusset, Laura Rey, Marjolaine Muller, Daniel Vacheron, Jordan Gerin, Florence Dubost, Audrey Comte, Gilles Prigent‐Combaret, Claire Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title | Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title_full | Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title_fullStr | Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title_full_unstemmed | Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title_short | Secondary metabolites from plant‐associated Pseudomonas are overproduced in biofilm |
title_sort | secondary metabolites from plant‐associated pseudomonas are overproduced in biofilm |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7415375/ https://www.ncbi.nlm.nih.gov/pubmed/33000552 http://dx.doi.org/10.1111/1751-7915.13598 |
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