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De novo biosynthesis of liquiritin in Saccharomyces cerevisiae

Liquiritigenin (LG), isoliquiritigenin (Iso-LG), together with their respective glycoside derivatives liquiritin (LN) and isoliquiritin (Iso-LN), are the main active flavonoids of Glycyrrhiza uralensis, which is arguably the most widely used medicinal plant with enormous demand on the market, includ...

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Autores principales: Yin, Yan, Li, Yanpeng, Jiang, Dan, Zhang, Xianan, Gao, Wei, Liu, Chunsheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7161706/
https://www.ncbi.nlm.nih.gov/pubmed/32322472
http://dx.doi.org/10.1016/j.apsb.2019.07.005
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author Yin, Yan
Li, Yanpeng
Jiang, Dan
Zhang, Xianan
Gao, Wei
Liu, Chunsheng
author_facet Yin, Yan
Li, Yanpeng
Jiang, Dan
Zhang, Xianan
Gao, Wei
Liu, Chunsheng
author_sort Yin, Yan
collection PubMed
description Liquiritigenin (LG), isoliquiritigenin (Iso-LG), together with their respective glycoside derivatives liquiritin (LN) and isoliquiritin (Iso-LN), are the main active flavonoids of Glycyrrhiza uralensis, which is arguably the most widely used medicinal plant with enormous demand on the market, including Chinese medicine prescriptions, preparations, health care products and even food. Pharmacological studies have shown that these ingredients have broad medicinal value, including anti-cancer and anti-inflammatory effects. Although the biosynthetic pathway of glycyrrhizin, a triterpenoid component from G. uralensis, has been fully analyzed, little attention has been paid to the biosynthesis of the flavonoids of this plant. To obtain the enzyme-coding genes responsible for the biosynthesis of LN, analysis and screening were carried out by combining genome and comparative transcriptome database searches of G. uralensis and homologous genes of known flavonoid biosynthesis pathways. The catalytic functions of candidate genes were determined by in vitro or in vivo characterization. This work characterized the complete biosynthetic pathway of LN and achieved the de novo biosynthesis of liquiritin in Saccharomyces cerevisiae using endogenous yeast metabolites as precursors and cofactors for the first time, which provides a possibility for the economical and sustainable production and application of G. uralensis flavonoids through synthetic biology.
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spelling pubmed-71617062020-04-22 De novo biosynthesis of liquiritin in Saccharomyces cerevisiae Yin, Yan Li, Yanpeng Jiang, Dan Zhang, Xianan Gao, Wei Liu, Chunsheng Acta Pharm Sin B Original article Liquiritigenin (LG), isoliquiritigenin (Iso-LG), together with their respective glycoside derivatives liquiritin (LN) and isoliquiritin (Iso-LN), are the main active flavonoids of Glycyrrhiza uralensis, which is arguably the most widely used medicinal plant with enormous demand on the market, including Chinese medicine prescriptions, preparations, health care products and even food. Pharmacological studies have shown that these ingredients have broad medicinal value, including anti-cancer and anti-inflammatory effects. Although the biosynthetic pathway of glycyrrhizin, a triterpenoid component from G. uralensis, has been fully analyzed, little attention has been paid to the biosynthesis of the flavonoids of this plant. To obtain the enzyme-coding genes responsible for the biosynthesis of LN, analysis and screening were carried out by combining genome and comparative transcriptome database searches of G. uralensis and homologous genes of known flavonoid biosynthesis pathways. The catalytic functions of candidate genes were determined by in vitro or in vivo characterization. This work characterized the complete biosynthetic pathway of LN and achieved the de novo biosynthesis of liquiritin in Saccharomyces cerevisiae using endogenous yeast metabolites as precursors and cofactors for the first time, which provides a possibility for the economical and sustainable production and application of G. uralensis flavonoids through synthetic biology. Elsevier 2020-04 2019-07-23 /pmc/articles/PMC7161706/ /pubmed/32322472 http://dx.doi.org/10.1016/j.apsb.2019.07.005 Text en © 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Yin, Yan
Li, Yanpeng
Jiang, Dan
Zhang, Xianan
Gao, Wei
Liu, Chunsheng
De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_full De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_fullStr De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_full_unstemmed De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_short De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_sort de novo biosynthesis of liquiritin in saccharomyces cerevisiae
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7161706/
https://www.ncbi.nlm.nih.gov/pubmed/32322472
http://dx.doi.org/10.1016/j.apsb.2019.07.005
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