Bioactive secondary metabolites with multiple activities from a fungal endophyte. Issue 1 (19th December 2016)
- Record Type:
- Journal Article
- Title:
- Bioactive secondary metabolites with multiple activities from a fungal endophyte. Issue 1 (19th December 2016)
- Main Title:
- Bioactive secondary metabolites with multiple activities from a fungal endophyte
- Authors:
- Bogner, Catherine W.
Kamdem, Ramsay S.T.
Sichtermann, Gisela
Matthäus, Christian
Hölscher, Dirk
Popp, Jürgen
Proksch, Peter
Grundler, Florian M.W.
Schouten, Alexander - Abstract:
- Summary: 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 LC50 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. Abstract : GA text‐Biochemical and biological analysis of constituents produced by an endophyte can lead to the discovery of individual compounds with a dual protective role in plant‐pathogen interactions, i.e., directly, by intoxicating a plant pathogen on the one hand and, indirectly, by inducing an increase in plant vigor and triggering plant defenses against a pathogen on the other. This supports the discovery of new nematocides that are environmentally more sound and, from theSummary: 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 LC50 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. Abstract : GA text‐Biochemical and biological analysis of constituents produced by an endophyte can lead to the discovery of individual compounds with a dual protective role in plant‐pathogen interactions, i.e., directly, by intoxicating a plant pathogen on the one hand and, indirectly, by inducing an increase in plant vigor and triggering plant defenses against a pathogen on the other. This supports the discovery of new nematocides that are environmentally more sound and, from the perspective of resistance development, potentially more robust than those that are currently available on the market. … (more)
- Is Part Of:
- Microbial biotechnology. Volume 10:Issue 1(2017:Jan.)
- Journal:
- Microbial biotechnology
- Issue:
- Volume 10:Issue 1(2017:Jan.)
- Issue Display:
- Volume 10, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 10
- Issue:
- 1
- Issue Sort Value:
- 2017-0010-0001-0000
- Page Start:
- 175
- Page End:
- 188
- Publication Date:
- 2016-12-19
- Subjects:
- Microbial biotechnology -- Periodicals
Biotechnology
Microbiology
660.62 - Journal URLs:
- http://ejournals.ebsco.com/direct.asp?JournalID=714890 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1751-7915 ↗
http://www.blackwellpublishing.com/mbt_enhanced/aims.asp ↗
http://www3.interscience.wiley.com/journal/118902527/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1751-7915.12467 ↗
- Languages:
- English
- ISSNs:
- 1751-7915
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5756.911050
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 592.xml