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Bioactive secondary metabolites with multiple activities from a fungal endophyte

In order to replace particularly biohazardous nematocides, there is a strong drive to finding natural product‐based alternatives with the aim of containing nematode pests in agriculture. The metabolites produced by the fungal endophyte Fusarium oxysporum 162 when cultivated on rice media were isolat...

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Autores principales: Bogner, Catherine W., Kamdem, Ramsay S.T., Sichtermann, Gisela, Matthäus, Christian, Hölscher, Dirk, Popp, Jürgen, Proksch, Peter, Grundler, Florian M.W., Schouten, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270730/
https://www.ncbi.nlm.nih.gov/pubmed/27990770
http://dx.doi.org/10.1111/1751-7915.12467
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author Bogner, Catherine W.
Kamdem, Ramsay S.T.
Sichtermann, Gisela
Matthäus, Christian
Hölscher, Dirk
Popp, Jürgen
Proksch, Peter
Grundler, Florian M.W.
Schouten, Alexander
author_facet Bogner, Catherine W.
Kamdem, Ramsay S.T.
Sichtermann, Gisela
Matthäus, Christian
Hölscher, Dirk
Popp, Jürgen
Proksch, Peter
Grundler, Florian M.W.
Schouten, Alexander
author_sort Bogner, Catherine W.
collection PubMed
description In order to replace particularly biohazardous nematocides, there is a strong drive to finding natural product‐based alternatives with the aim of containing nematode pests in agriculture. The metabolites produced by the fungal endophyte Fusarium oxysporum 162 when cultivated on rice media were isolated and their structures elucidated. Eleven compounds were obtained, of which six were isolated from a Fusarium spp. for the first time. The three most potent nematode‐antagonistic compounds, 4‐hydroxybenzoic acid, indole‐3‐acetic acid (IAA) and gibepyrone D had LC (50) values of 104, 117 and 134 μg ml(−1), respectively, after 72 h. IAA is a well‐known phytohormone that plays a role in triggering plant resistance, thus suggesting a dual activity, either directly, by killing or compromising nematodes, or indirectly, by inducing defence mechanisms against pathogens (nematodes) in plants. Such compounds may serve as important leads in the development of novel, environmental friendly, nematocides.
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spelling pubmed-52707302017-02-01 Bioactive secondary metabolites with multiple activities from a fungal endophyte Bogner, Catherine W. Kamdem, Ramsay S.T. Sichtermann, Gisela Matthäus, Christian Hölscher, Dirk Popp, Jürgen Proksch, Peter Grundler, Florian M.W. Schouten, Alexander Microb Biotechnol Research Articles In order to replace particularly biohazardous nematocides, there is a strong drive to finding natural product‐based alternatives with the aim of containing nematode pests in agriculture. The metabolites produced by the fungal endophyte Fusarium oxysporum 162 when cultivated on rice media were isolated and their structures elucidated. Eleven compounds were obtained, of which six were isolated from a Fusarium spp. for the first time. The three most potent nematode‐antagonistic compounds, 4‐hydroxybenzoic acid, indole‐3‐acetic acid (IAA) and gibepyrone D had LC (50) values of 104, 117 and 134 μg ml(−1), respectively, after 72 h. IAA is a well‐known phytohormone that plays a role in triggering plant resistance, thus suggesting a dual activity, either directly, by killing or compromising nematodes, or indirectly, by inducing defence mechanisms against pathogens (nematodes) in plants. Such compounds may serve as important leads in the development of novel, environmental friendly, nematocides. John Wiley and Sons Inc. 2016-12-19 /pmc/articles/PMC5270730/ /pubmed/27990770 http://dx.doi.org/10.1111/1751-7915.12467 Text en © 2016 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology. This is an open access article under the terms of the Creative Commons Attribution (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
Bogner, Catherine W.
Kamdem, Ramsay S.T.
Sichtermann, Gisela
Matthäus, Christian
Hölscher, Dirk
Popp, Jürgen
Proksch, Peter
Grundler, Florian M.W.
Schouten, Alexander
Bioactive secondary metabolites with multiple activities from a fungal endophyte
title Bioactive secondary metabolites with multiple activities from a fungal endophyte
title_full Bioactive secondary metabolites with multiple activities from a fungal endophyte
title_fullStr Bioactive secondary metabolites with multiple activities from a fungal endophyte
title_full_unstemmed Bioactive secondary metabolites with multiple activities from a fungal endophyte
title_short Bioactive secondary metabolites with multiple activities from a fungal endophyte
title_sort bioactive secondary metabolites with multiple activities from a fungal endophyte
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5270730/
https://www.ncbi.nlm.nih.gov/pubmed/27990770
http://dx.doi.org/10.1111/1751-7915.12467
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