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Discovery and excavation of lichen bioactive natural products
Lichen natural products are a tremendous source of new bioactive chemical entities for drug discovery. The ability to survive in harsh conditions can be directly correlated with the production of some unique lichen metabolites. Despite the potential applications, these unique metabolites have been u...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149937/ https://www.ncbi.nlm.nih.gov/pubmed/37138611 http://dx.doi.org/10.3389/fmicb.2023.1177123 |
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author | Ren, Meirong Jiang, Shuhua Wang, Yanyan Pan, Xinhua Pan, Feng Wei, Xinli |
author_facet | Ren, Meirong Jiang, Shuhua Wang, Yanyan Pan, Xinhua Pan, Feng Wei, Xinli |
author_sort | Ren, Meirong |
collection | PubMed |
description | Lichen natural products are a tremendous source of new bioactive chemical entities for drug discovery. The ability to survive in harsh conditions can be directly correlated with the production of some unique lichen metabolites. Despite the potential applications, these unique metabolites have been underutilized by pharmaceutical and agrochemical industries due to their slow growth, low biomass availability, and technical challenges involved in their artificial cultivation. At the same time, DNA sequence data have revealed that the number of encoded biosynthetic gene clusters in a lichen is much higher than in natural products, and the majority of them are silent or poorly expressed. To meet these challenges, the one strain many compounds (OSMAC) strategy, as a comprehensive and powerful tool, has been developed to stimulate the activation of silent or cryptic biosynthetic gene clusters and exploit interesting lichen compounds for industrial applications. Furthermore, the development of molecular network techniques, modern bioinformatics, and genetic tools is opening up a new opportunity for the mining, modification, and production of lichen metabolites, rather than merely using traditional separation and purification techniques to obtain small amounts of chemical compounds. Heterologous expressed lichen-derived biosynthetic gene clusters in a cultivatable host offer a promising means for a sustainable supply of specialized metabolites. In this review, we summarized the known lichen bioactive metabolites and highlighted the application of OSMAC, molecular network, and genome mining-based strategies in lichen-forming fungi for the discovery of new cryptic lichen compounds. |
format | Online Article Text |
id | pubmed-10149937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101499372023-05-02 Discovery and excavation of lichen bioactive natural products Ren, Meirong Jiang, Shuhua Wang, Yanyan Pan, Xinhua Pan, Feng Wei, Xinli Front Microbiol Microbiology Lichen natural products are a tremendous source of new bioactive chemical entities for drug discovery. The ability to survive in harsh conditions can be directly correlated with the production of some unique lichen metabolites. Despite the potential applications, these unique metabolites have been underutilized by pharmaceutical and agrochemical industries due to their slow growth, low biomass availability, and technical challenges involved in their artificial cultivation. At the same time, DNA sequence data have revealed that the number of encoded biosynthetic gene clusters in a lichen is much higher than in natural products, and the majority of them are silent or poorly expressed. To meet these challenges, the one strain many compounds (OSMAC) strategy, as a comprehensive and powerful tool, has been developed to stimulate the activation of silent or cryptic biosynthetic gene clusters and exploit interesting lichen compounds for industrial applications. Furthermore, the development of molecular network techniques, modern bioinformatics, and genetic tools is opening up a new opportunity for the mining, modification, and production of lichen metabolites, rather than merely using traditional separation and purification techniques to obtain small amounts of chemical compounds. Heterologous expressed lichen-derived biosynthetic gene clusters in a cultivatable host offer a promising means for a sustainable supply of specialized metabolites. In this review, we summarized the known lichen bioactive metabolites and highlighted the application of OSMAC, molecular network, and genome mining-based strategies in lichen-forming fungi for the discovery of new cryptic lichen compounds. Frontiers Media S.A. 2023-04-17 /pmc/articles/PMC10149937/ /pubmed/37138611 http://dx.doi.org/10.3389/fmicb.2023.1177123 Text en Copyright © 2023 Ren, Jiang, Wang, Pan, Pan and Wei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Ren, Meirong Jiang, Shuhua Wang, Yanyan Pan, Xinhua Pan, Feng Wei, Xinli Discovery and excavation of lichen bioactive natural products |
title | Discovery and excavation of lichen bioactive natural products |
title_full | Discovery and excavation of lichen bioactive natural products |
title_fullStr | Discovery and excavation of lichen bioactive natural products |
title_full_unstemmed | Discovery and excavation of lichen bioactive natural products |
title_short | Discovery and excavation of lichen bioactive natural products |
title_sort | discovery and excavation of lichen bioactive natural products |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10149937/ https://www.ncbi.nlm.nih.gov/pubmed/37138611 http://dx.doi.org/10.3389/fmicb.2023.1177123 |
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