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A roadmap to engineering antiviral natural products synthesis in microbes

Natural products continue to be the inspirations for us to discover and acquire new drugs. The seemingly unstoppable viruses have kept records high to threaten human health and well-being. The diversity and complexity of natural products (NPs) offer remarkable efficacy and specificity to target vira...

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Detalles Bibliográficos
Autores principales: Ma, Jingbo, Gu, Yang, Xu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419324/
https://www.ncbi.nlm.nih.gov/pubmed/32795662
http://dx.doi.org/10.1016/j.copbio.2020.07.008
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author Ma, Jingbo
Gu, Yang
Xu, Peng
author_facet Ma, Jingbo
Gu, Yang
Xu, Peng
author_sort Ma, Jingbo
collection PubMed
description Natural products continue to be the inspirations for us to discover and acquire new drugs. The seemingly unstoppable viruses have kept records high to threaten human health and well-being. The diversity and complexity of natural products (NPs) offer remarkable efficacy and specificity to target viral infection steps and serve as excellent source for antiviral agents. The discovery and production of antiviral NPs remain challenging due to low abundance in their native hosts. Reconstruction of NP biosynthetic pathways in microbes is a promising solution to overcome this limitation. In this review, we surveyed 23 most prominent NPs (from more than 200 antiviral NP candidates) with distinct antiviral mode of actions and summarized the recent metabolic engineering effort to produce these compounds in various microbial hosts. We envision that the scalable and low-cost production of novel antiviral NPs, enabled by metabolic engineering, may light the hope to control and eradicate the deadliest viruses that plague our society and humanity.
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spelling pubmed-74193242020-08-12 A roadmap to engineering antiviral natural products synthesis in microbes Ma, Jingbo Gu, Yang Xu, Peng Curr Opin Biotechnol Article Natural products continue to be the inspirations for us to discover and acquire new drugs. The seemingly unstoppable viruses have kept records high to threaten human health and well-being. The diversity and complexity of natural products (NPs) offer remarkable efficacy and specificity to target viral infection steps and serve as excellent source for antiviral agents. The discovery and production of antiviral NPs remain challenging due to low abundance in their native hosts. Reconstruction of NP biosynthetic pathways in microbes is a promising solution to overcome this limitation. In this review, we surveyed 23 most prominent NPs (from more than 200 antiviral NP candidates) with distinct antiviral mode of actions and summarized the recent metabolic engineering effort to produce these compounds in various microbial hosts. We envision that the scalable and low-cost production of novel antiviral NPs, enabled by metabolic engineering, may light the hope to control and eradicate the deadliest viruses that plague our society and humanity. Elsevier 2020-12 /pmc/articles/PMC7419324/ /pubmed/32795662 http://dx.doi.org/10.1016/j.copbio.2020.07.008 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ma, Jingbo
Gu, Yang
Xu, Peng
A roadmap to engineering antiviral natural products synthesis in microbes
title A roadmap to engineering antiviral natural products synthesis in microbes
title_full A roadmap to engineering antiviral natural products synthesis in microbes
title_fullStr A roadmap to engineering antiviral natural products synthesis in microbes
title_full_unstemmed A roadmap to engineering antiviral natural products synthesis in microbes
title_short A roadmap to engineering antiviral natural products synthesis in microbes
title_sort roadmap to engineering antiviral natural products synthesis in microbes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7419324/
https://www.ncbi.nlm.nih.gov/pubmed/32795662
http://dx.doi.org/10.1016/j.copbio.2020.07.008
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