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Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.

Bupleurum chinense DC. is a commonly used plant in traditional Chinese medicine, and saikosaponins(SSs) are the main active oleanane-typetriterpene saponins in B. chinense. β-Amyrin synthase (β-AS) is an important enzyme in oleanane-type triterpenoid saponin synthesis, but its role in saikosaponin s...

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Autores principales: Mao, Yanping, Chen, Hua, Zhao, Jun, Li, Yuchan, Feng, Liang, Yang, Yuping, Zhang, Yiguan, Wei, Ping, Hou, Dabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer India 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483273/
https://www.ncbi.nlm.nih.gov/pubmed/36160316
http://dx.doi.org/10.1007/s13562-022-00804-2
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author Mao, Yanping
Chen, Hua
Zhao, Jun
Li, Yuchan
Feng, Liang
Yang, Yuping
Zhang, Yiguan
Wei, Ping
Hou, Dabin
author_facet Mao, Yanping
Chen, Hua
Zhao, Jun
Li, Yuchan
Feng, Liang
Yang, Yuping
Zhang, Yiguan
Wei, Ping
Hou, Dabin
author_sort Mao, Yanping
collection PubMed
description Bupleurum chinense DC. is a commonly used plant in traditional Chinese medicine, and saikosaponins(SSs) are the main active oleanane-typetriterpene saponins in B. chinense. β-Amyrin synthase (β-AS) is an important enzyme in oleanane-type triterpenoid saponin synthesis, but its role in saikosaponin synthesis has rarely been studied. Here, the putative β-AS gene BcBAS1(Accession No.ON890382) selected according to metabolomic and transcriptomic analyses was cloned and functionally characterized by heterologous expression in Escherichia coli and Pichia pastoris, and its subcellular localization and expression patterns were examined. The molecular weight of the BcBAS1 recombinant protein was approximately 87 kDa, and this protein could catalyse the production of β-amyrin, the precursor of SSs. Furthermore, BcBAS1 was located in the cytosol, and relative expression in four tissues of the four genotypes was positively correlated with SSa and SSd contents. Our results indicate that BcBAS1 is a β-AS gene and may play an important role in saikosaponin biosynthesis and regulation. This study sheds light on the role of β-AS genes in the synthesis of SSs and provides insights for the metabolic engineering of SSs.
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spelling pubmed-94832732022-09-19 Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC. Mao, Yanping Chen, Hua Zhao, Jun Li, Yuchan Feng, Liang Yang, Yuping Zhang, Yiguan Wei, Ping Hou, Dabin J Plant Biochem Biotechnol Original Article Bupleurum chinense DC. is a commonly used plant in traditional Chinese medicine, and saikosaponins(SSs) are the main active oleanane-typetriterpene saponins in B. chinense. β-Amyrin synthase (β-AS) is an important enzyme in oleanane-type triterpenoid saponin synthesis, but its role in saikosaponin synthesis has rarely been studied. Here, the putative β-AS gene BcBAS1(Accession No.ON890382) selected according to metabolomic and transcriptomic analyses was cloned and functionally characterized by heterologous expression in Escherichia coli and Pichia pastoris, and its subcellular localization and expression patterns were examined. The molecular weight of the BcBAS1 recombinant protein was approximately 87 kDa, and this protein could catalyse the production of β-amyrin, the precursor of SSs. Furthermore, BcBAS1 was located in the cytosol, and relative expression in four tissues of the four genotypes was positively correlated with SSa and SSd contents. Our results indicate that BcBAS1 is a β-AS gene and may play an important role in saikosaponin biosynthesis and regulation. This study sheds light on the role of β-AS genes in the synthesis of SSs and provides insights for the metabolic engineering of SSs. Springer India 2022-09-16 2023 /pmc/articles/PMC9483273/ /pubmed/36160316 http://dx.doi.org/10.1007/s13562-022-00804-2 Text en © The Author(s), under exclusive licence to Society for Plant Biochemistry and Biotechnology 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Mao, Yanping
Chen, Hua
Zhao, Jun
Li, Yuchan
Feng, Liang
Yang, Yuping
Zhang, Yiguan
Wei, Ping
Hou, Dabin
Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title_full Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title_fullStr Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title_full_unstemmed Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title_short Molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in Bupleurum chinense DC.
title_sort molecular cloning, functional characterization and expression of the β-amyrin synthase gene involved in saikosaponin biosynthesis in bupleurum chinense dc.
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483273/
https://www.ncbi.nlm.nih.gov/pubmed/36160316
http://dx.doi.org/10.1007/s13562-022-00804-2
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