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Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation

The rhizosphere is a highly competitive environment forcing bacteria to evolve strategies to oppose their enemies. The production of toxic secondary metabolites allows bacteria to counteract predators. In this study, we describe the anti-predator armamentarium of the soil-derived bacterium Pseudomon...

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Autores principales: Pflanze, Sebastian, Mukherji, Ruchira, Ibrahim, Anan, Günther, Markus, Götze, Sebastian, Chowdhury, Somak, Reimer, Lisa, Regestein, Lars, Stallforth, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599466/
https://www.ncbi.nlm.nih.gov/pubmed/37886094
http://dx.doi.org/10.1039/d3sc03335j
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author Pflanze, Sebastian
Mukherji, Ruchira
Ibrahim, Anan
Günther, Markus
Götze, Sebastian
Chowdhury, Somak
Reimer, Lisa
Regestein, Lars
Stallforth, Pierre
author_facet Pflanze, Sebastian
Mukherji, Ruchira
Ibrahim, Anan
Günther, Markus
Götze, Sebastian
Chowdhury, Somak
Reimer, Lisa
Regestein, Lars
Stallforth, Pierre
author_sort Pflanze, Sebastian
collection PubMed
description The rhizosphere is a highly competitive environment forcing bacteria to evolve strategies to oppose their enemies. The production of toxic secondary metabolites allows bacteria to counteract predators. In this study, we describe the anti-predator armamentarium of the soil-derived bacterium Pseudomonas nunensis 4A2e. Based on a genome mining approach, we identified several biosynthetic gene clusters coding for nonribosomal peptide synthetases. Generation of gene deletion mutants of the respective clusters shows a loss of defense capabilities. We isolated the novel lipopeptides keanumycin D and nunapeptins B and C, and fully elucidated their structures by a combination of in-depth mass spectrometry experiments, stable isotope labelling, and chemical synthesis. Additionally, investigation of the quorum sensing-dependent biosynthesis allowed us to elucidate parts of the underlying regulation of the biosynthetic machinery. Ecology-inspired bioassays highlight the role of these peptides as a defence strategy against protozoans and led us to find a previously unknown function against the bacterivorous nematode Oscheius myriophilus.
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spelling pubmed-105994662023-10-26 Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation Pflanze, Sebastian Mukherji, Ruchira Ibrahim, Anan Günther, Markus Götze, Sebastian Chowdhury, Somak Reimer, Lisa Regestein, Lars Stallforth, Pierre Chem Sci Chemistry The rhizosphere is a highly competitive environment forcing bacteria to evolve strategies to oppose their enemies. The production of toxic secondary metabolites allows bacteria to counteract predators. In this study, we describe the anti-predator armamentarium of the soil-derived bacterium Pseudomonas nunensis 4A2e. Based on a genome mining approach, we identified several biosynthetic gene clusters coding for nonribosomal peptide synthetases. Generation of gene deletion mutants of the respective clusters shows a loss of defense capabilities. We isolated the novel lipopeptides keanumycin D and nunapeptins B and C, and fully elucidated their structures by a combination of in-depth mass spectrometry experiments, stable isotope labelling, and chemical synthesis. Additionally, investigation of the quorum sensing-dependent biosynthesis allowed us to elucidate parts of the underlying regulation of the biosynthetic machinery. Ecology-inspired bioassays highlight the role of these peptides as a defence strategy against protozoans and led us to find a previously unknown function against the bacterivorous nematode Oscheius myriophilus. The Royal Society of Chemistry 2023-10-02 /pmc/articles/PMC10599466/ /pubmed/37886094 http://dx.doi.org/10.1039/d3sc03335j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Pflanze, Sebastian
Mukherji, Ruchira
Ibrahim, Anan
Günther, Markus
Götze, Sebastian
Chowdhury, Somak
Reimer, Lisa
Regestein, Lars
Stallforth, Pierre
Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title_full Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title_fullStr Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title_full_unstemmed Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title_short Nonribosomal peptides protect Pseudomonas nunensis 4A2e from amoebal and nematodal predation
title_sort nonribosomal peptides protect pseudomonas nunensis 4a2e from amoebal and nematodal predation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10599466/
https://www.ncbi.nlm.nih.gov/pubmed/37886094
http://dx.doi.org/10.1039/d3sc03335j
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