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Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani

Fungi are one of the most prolific sources of microbial secondary metabolites. The production of new metabolites can be achieved using multiple fermentation conditions and by adding small-molecule effectors, including epigenetic modifiers. In the framework of our Natural Product screening programme...

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Autores principales: González-Menéndez, Victor, Crespo, Gloria, Toro, Clara, Martín, Jesús, de Pedro, Nuria, Tormo, Jose R, Genilloud, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835440/
https://www.ncbi.nlm.nih.gov/pubmed/31546616
http://dx.doi.org/10.3390/metabo9100197
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author González-Menéndez, Victor
Crespo, Gloria
Toro, Clara
Martín, Jesús
de Pedro, Nuria
Tormo, Jose R
Genilloud, Olga
author_facet González-Menéndez, Victor
Crespo, Gloria
Toro, Clara
Martín, Jesús
de Pedro, Nuria
Tormo, Jose R
Genilloud, Olga
author_sort González-Menéndez, Victor
collection PubMed
description Fungi are one of the most prolific sources of microbial secondary metabolites. The production of new metabolites can be achieved using multiple fermentation conditions and by adding small-molecule effectors, including epigenetic modifiers. In the framework of our Natural Product screening programme targeting the discovery of new antimicrobial compounds, we applied multiple fermentation conditions and adsorptive polymeric resins on a large collection of fungal endophytes, to increase and stimulate their fungal secondary metabolite production. During this work the endophytic fungus Dimorphosporicola tragani CF-090383 showed antimicrobial activity only when grown in presence of adsorptive polymeric resins. In addition, seven epigenetic modifiers were added to fermentations of this endophytic fungus, in an attempt to activate its cryptic pathways as well as to analyse the metabolites produced under these conditions. D. tragani was seen to produce three different mycotoxin dendrodolides when the epigenetic modifiers 5-azacytidine and valproic acid were added to the fermentations, and these compounds were further characterized. However, the fungus produced the fatty acid synthesis inhibitor cerulenin, a molecule not previously described to be produced by this fungal species, only when cultivated in presence of the XAD-16 resin. We have found that the addition of XAD-16 resin resulted in four-fold higher titers in the production of cerulenin when compared to the best production conditions described in literature for the original fungal producer strain, Cephalosporium caerulens KF-140 (=Sarocladium oryzae), in a zeolite-based fermentation, used as an ammonium ion-trapping agent. The production of cerulenin by this strain of D. tragani, represents an alternative source for the improved production of cerulenin with better yields.
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spelling pubmed-68354402019-11-25 Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani González-Menéndez, Victor Crespo, Gloria Toro, Clara Martín, Jesús de Pedro, Nuria Tormo, Jose R Genilloud, Olga Metabolites Article Fungi are one of the most prolific sources of microbial secondary metabolites. The production of new metabolites can be achieved using multiple fermentation conditions and by adding small-molecule effectors, including epigenetic modifiers. In the framework of our Natural Product screening programme targeting the discovery of new antimicrobial compounds, we applied multiple fermentation conditions and adsorptive polymeric resins on a large collection of fungal endophytes, to increase and stimulate their fungal secondary metabolite production. During this work the endophytic fungus Dimorphosporicola tragani CF-090383 showed antimicrobial activity only when grown in presence of adsorptive polymeric resins. In addition, seven epigenetic modifiers were added to fermentations of this endophytic fungus, in an attempt to activate its cryptic pathways as well as to analyse the metabolites produced under these conditions. D. tragani was seen to produce three different mycotoxin dendrodolides when the epigenetic modifiers 5-azacytidine and valproic acid were added to the fermentations, and these compounds were further characterized. However, the fungus produced the fatty acid synthesis inhibitor cerulenin, a molecule not previously described to be produced by this fungal species, only when cultivated in presence of the XAD-16 resin. We have found that the addition of XAD-16 resin resulted in four-fold higher titers in the production of cerulenin when compared to the best production conditions described in literature for the original fungal producer strain, Cephalosporium caerulens KF-140 (=Sarocladium oryzae), in a zeolite-based fermentation, used as an ammonium ion-trapping agent. The production of cerulenin by this strain of D. tragani, represents an alternative source for the improved production of cerulenin with better yields. MDPI 2019-09-21 /pmc/articles/PMC6835440/ /pubmed/31546616 http://dx.doi.org/10.3390/metabo9100197 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
González-Menéndez, Victor
Crespo, Gloria
Toro, Clara
Martín, Jesús
de Pedro, Nuria
Tormo, Jose R
Genilloud, Olga
Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title_full Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title_fullStr Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title_full_unstemmed Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title_short Extending the Metabolite Diversity of the Endophyte Dimorphosporicola tragani
title_sort extending the metabolite diversity of the endophyte dimorphosporicola tragani
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835440/
https://www.ncbi.nlm.nih.gov/pubmed/31546616
http://dx.doi.org/10.3390/metabo9100197
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