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Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation

Actinomycetes and filamentous fungi produce a wide range of bioactive compounds, with applications as antimicrobials, anticancer agents or agrochemicals. Their genomes contain a far larger number of gene clusters for natural products than originally anticipated, and novel approaches are required to...

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Autores principales: Wu, Changsheng, Zacchetti, Boris, Ram, Arthur F.J., van Wezel, Gilles P., Claessen, Dennis, Hae Choi, Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455117/
https://www.ncbi.nlm.nih.gov/pubmed/26040782
http://dx.doi.org/10.1038/srep10868
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author Wu, Changsheng
Zacchetti, Boris
Ram, Arthur F.J.
van Wezel, Gilles P.
Claessen, Dennis
Hae Choi, Young
author_facet Wu, Changsheng
Zacchetti, Boris
Ram, Arthur F.J.
van Wezel, Gilles P.
Claessen, Dennis
Hae Choi, Young
author_sort Wu, Changsheng
collection PubMed
description Actinomycetes and filamentous fungi produce a wide range of bioactive compounds, with applications as antimicrobials, anticancer agents or agrochemicals. Their genomes contain a far larger number of gene clusters for natural products than originally anticipated, and novel approaches are required to exploit this potential reservoir of new drugs. Here, we show that co-cultivation of the filamentous model microbes Streptomyces coelicolor and Aspergillus niger has a major impact on their secondary metabolism. NMR-based metabolomics combined with multivariate data analysis revealed several compounds that correlated specifically to co-cultures, including the cyclic dipeptide cyclo(Phe-Phe) and 2-hydroxyphenylacetic acid, both of which were produced by A. niger in response to S. coelicolor. Furthermore, biotransformation studies with o-coumaric acid and caffeic acid resulted in the production of the novel compounds (E)-2-(3-hydroxyprop-1-en-1-yl)-phenol and (2E,4E)-3-(2-carboxy-1-hydroxyethyl)-2,4-hexadienedioxic acid, respectively. This highlights the utility of microbial co-cultivation combined with NMR-based metabolomics as an efficient pipeline for the discovery of novel natural products.
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spelling pubmed-44551172015-06-10 Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation Wu, Changsheng Zacchetti, Boris Ram, Arthur F.J. van Wezel, Gilles P. Claessen, Dennis Hae Choi, Young Sci Rep Article Actinomycetes and filamentous fungi produce a wide range of bioactive compounds, with applications as antimicrobials, anticancer agents or agrochemicals. Their genomes contain a far larger number of gene clusters for natural products than originally anticipated, and novel approaches are required to exploit this potential reservoir of new drugs. Here, we show that co-cultivation of the filamentous model microbes Streptomyces coelicolor and Aspergillus niger has a major impact on their secondary metabolism. NMR-based metabolomics combined with multivariate data analysis revealed several compounds that correlated specifically to co-cultures, including the cyclic dipeptide cyclo(Phe-Phe) and 2-hydroxyphenylacetic acid, both of which were produced by A. niger in response to S. coelicolor. Furthermore, biotransformation studies with o-coumaric acid and caffeic acid resulted in the production of the novel compounds (E)-2-(3-hydroxyprop-1-en-1-yl)-phenol and (2E,4E)-3-(2-carboxy-1-hydroxyethyl)-2,4-hexadienedioxic acid, respectively. This highlights the utility of microbial co-cultivation combined with NMR-based metabolomics as an efficient pipeline for the discovery of novel natural products. Nature Publishing Group 2015-06-04 /pmc/articles/PMC4455117/ /pubmed/26040782 http://dx.doi.org/10.1038/srep10868 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wu, Changsheng
Zacchetti, Boris
Ram, Arthur F.J.
van Wezel, Gilles P.
Claessen, Dennis
Hae Choi, Young
Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title_full Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title_fullStr Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title_full_unstemmed Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title_short Expanding the chemical space for natural products by Aspergillus-Streptomyces co-cultivation and biotransformation
title_sort expanding the chemical space for natural products by aspergillus-streptomyces co-cultivation and biotransformation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455117/
https://www.ncbi.nlm.nih.gov/pubmed/26040782
http://dx.doi.org/10.1038/srep10868
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