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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Main Authors: Yan Yin, Yanpeng Li, Dan Jiang, Xianan Zhang, Wei Gao, Chunsheng Liu
Format: Article
Language:English
Published: Elsevier 2020-04-01
Series:Acta Pharmaceutica Sinica B
Online Access:http://www.sciencedirect.com/science/article/pii/S2211383519306665
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spelling doaj-6a4e703e9fab4affb0866bcfac15b1252020-11-25T02:27:47ZengElsevierActa Pharmaceutica Sinica B2211-38352020-04-01104711721De novo biosynthesis of liquiritin in Saccharomyces cerevisiaeYan Yin0Yanpeng Li1Dan Jiang2Xianan Zhang3Wei Gao4Chunsheng Liu5School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 102488, China; School of Traditional Chinese Medicine, Capital Medical University, Beijing 100069, ChinaSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 102488, China; Pharmacy Department, Beijing Longfu Hospital, Beijing 100010, ChinaSchool of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 102488, ChinaSchool of Traditional Chinese Medicine, Capital Medical University, Beijing 100069, ChinaSchool of Traditional Chinese Medicine, Capital Medical University, Beijing 100069, China; School of Pharmaceutical Sciences, Advanced Innovation Center for Human Brain Protection, Capital Medical University, Beijing 100069, China; Corresponding authors. Tel. +86 10 83916572; fax: +86 10 83911627.School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 102488, China; Corresponding authors. Tel. +86 10 83916572; fax: +86 10 83911627.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. KEY WORDS: Glycyrrhiza uralensis, Liquiritin, Isoliquiritin, Liquiritigenin, Isoliquiritigenin, Heterologous synthesis, Saccharomyces cerevisiaehttp://www.sciencedirect.com/science/article/pii/S2211383519306665
collection DOAJ
language English
format Article
sources DOAJ
author Yan Yin
Yanpeng Li
Dan Jiang
Xianan Zhang
Wei Gao
Chunsheng Liu
spellingShingle Yan Yin
Yanpeng Li
Dan Jiang
Xianan Zhang
Wei Gao
Chunsheng Liu
De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
Acta Pharmaceutica Sinica B
author_facet Yan Yin
Yanpeng Li
Dan Jiang
Xianan Zhang
Wei Gao
Chunsheng Liu
author_sort Yan Yin
title De novo biosynthesis of liquiritin in Saccharomyces cerevisiae
title_short 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_sort de novo biosynthesis of liquiritin in saccharomyces cerevisiae
publisher Elsevier
series Acta Pharmaceutica Sinica B
issn 2211-3835
publishDate 2020-04-01
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. KEY WORDS: Glycyrrhiza uralensis, Liquiritin, Isoliquiritin, Liquiritigenin, Isoliquiritigenin, Heterologous synthesis, Saccharomyces cerevisiae
url http://www.sciencedirect.com/science/article/pii/S2211383519306665
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