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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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. |
format | Online Article Text |
id | pubmed-5270730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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