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Functional characterization of triterpene synthases in Cibotium barometz

Cibotium barometz (Linn.) J. Sm., a tree fern in the Dicksoniaceae family, is an economically important industrial exported plant in China and widely used in Traditional Chinese Medicine. C. barometz produces a range of bioactive triterpenes and their metabolites. However, the biosynthetic pathway o...

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Autores principales: Ji, Zhongju, Fan, Baolian, Chen, Yidu, Yue, Jingyang, Chen, Jiabo, Zhang, Rongrong, Tong, Yi, Liu, Zhongqiu, Liang, Jincai, Duan, Lixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320381/
https://www.ncbi.nlm.nih.gov/pubmed/37416896
http://dx.doi.org/10.1016/j.synbio.2023.06.005
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author Ji, Zhongju
Fan, Baolian
Chen, Yidu
Yue, Jingyang
Chen, Jiabo
Zhang, Rongrong
Tong, Yi
Liu, Zhongqiu
Liang, Jincai
Duan, Lixin
author_facet Ji, Zhongju
Fan, Baolian
Chen, Yidu
Yue, Jingyang
Chen, Jiabo
Zhang, Rongrong
Tong, Yi
Liu, Zhongqiu
Liang, Jincai
Duan, Lixin
author_sort Ji, Zhongju
collection PubMed
description Cibotium barometz (Linn.) J. Sm., a tree fern in the Dicksoniaceae family, is an economically important industrial exported plant in China and widely used in Traditional Chinese Medicine. C. barometz produces a range of bioactive triterpenes and their metabolites. However, the biosynthetic pathway of triterpenes in C. barometz remains unknown. To clarify the origin of diverse triterpenes in C. barometz, we conducted de novo transcriptome sequencing and analysis of C. barometz rhizomes and leaves to identify the candidate genes involved in C. barometz triterpene biosynthesis. Three C. barometz triterpene synthases (CbTSs) candidate genes were obtained. All of them were highly expressed in C. barometz rhizomes, consisting of the accumulation pattern of triterpenes in C. barometz. To characterize the function of these CbTSs, we constructed a squalene- and oxidosqualene-overproducing yeast chassis by overexpressing all the enzymes in the MVA pathway under the control of GAL-regulated promoter and disrupted the GAL80 gene in Saccharomyces cerevisiae simultaneously. Heterologous expressing CbTS1, CbTS2, and CbTS3 in engineering yeast strain produced cycloartenol, dammaradiene, and diploptene, respectively. Phylogenetic analysis revealed that CbTS1 belongs to oxidosqualene cyclase, while CbTS2 and CbTS3 belong to squalene cyclase. These results decipher enzymatic mechanisms underlying the origin of diverse triterpene in C. barometz.
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spelling pubmed-103203812023-07-06 Functional characterization of triterpene synthases in Cibotium barometz Ji, Zhongju Fan, Baolian Chen, Yidu Yue, Jingyang Chen, Jiabo Zhang, Rongrong Tong, Yi Liu, Zhongqiu Liang, Jincai Duan, Lixin Synth Syst Biotechnol Original Research Article Cibotium barometz (Linn.) J. Sm., a tree fern in the Dicksoniaceae family, is an economically important industrial exported plant in China and widely used in Traditional Chinese Medicine. C. barometz produces a range of bioactive triterpenes and their metabolites. However, the biosynthetic pathway of triterpenes in C. barometz remains unknown. To clarify the origin of diverse triterpenes in C. barometz, we conducted de novo transcriptome sequencing and analysis of C. barometz rhizomes and leaves to identify the candidate genes involved in C. barometz triterpene biosynthesis. Three C. barometz triterpene synthases (CbTSs) candidate genes were obtained. All of them were highly expressed in C. barometz rhizomes, consisting of the accumulation pattern of triterpenes in C. barometz. To characterize the function of these CbTSs, we constructed a squalene- and oxidosqualene-overproducing yeast chassis by overexpressing all the enzymes in the MVA pathway under the control of GAL-regulated promoter and disrupted the GAL80 gene in Saccharomyces cerevisiae simultaneously. Heterologous expressing CbTS1, CbTS2, and CbTS3 in engineering yeast strain produced cycloartenol, dammaradiene, and diploptene, respectively. Phylogenetic analysis revealed that CbTS1 belongs to oxidosqualene cyclase, while CbTS2 and CbTS3 belong to squalene cyclase. These results decipher enzymatic mechanisms underlying the origin of diverse triterpene in C. barometz. KeAi Publishing 2023-06-25 /pmc/articles/PMC10320381/ /pubmed/37416896 http://dx.doi.org/10.1016/j.synbio.2023.06.005 Text en © 2023 The Authors https://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 Research Article
Ji, Zhongju
Fan, Baolian
Chen, Yidu
Yue, Jingyang
Chen, Jiabo
Zhang, Rongrong
Tong, Yi
Liu, Zhongqiu
Liang, Jincai
Duan, Lixin
Functional characterization of triterpene synthases in Cibotium barometz
title Functional characterization of triterpene synthases in Cibotium barometz
title_full Functional characterization of triterpene synthases in Cibotium barometz
title_fullStr Functional characterization of triterpene synthases in Cibotium barometz
title_full_unstemmed Functional characterization of triterpene synthases in Cibotium barometz
title_short Functional characterization of triterpene synthases in Cibotium barometz
title_sort functional characterization of triterpene synthases in cibotium barometz
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320381/
https://www.ncbi.nlm.nih.gov/pubmed/37416896
http://dx.doi.org/10.1016/j.synbio.2023.06.005
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