GbFLSa overexpression negatively regulates proanthocyanin biosynthesis

Flavonoids are important secondary metabolites with extensive pharmacological functions. Ginkgo biloba L. (ginkgo) has attracted extensive attention because of its high flavonoid medicinal value. However, little is understood about ginkgo flavonol biosynthesis. Herein, we cloned the full-length ging...

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Main Authors: Jing Guo, Yaqiong Wu, Tongli Wang, Yue Xin, Guibin Wang, Qi Zhou, Li-An Xu
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-02-01
Series:Frontiers in Plant Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fpls.2023.1093656/full
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author Jing Guo
Yaqiong Wu
Yaqiong Wu
Yaqiong Wu
Tongli Wang
Yue Xin
Guibin Wang
Qi Zhou
Qi Zhou
Li-An Xu
author_facet Jing Guo
Yaqiong Wu
Yaqiong Wu
Yaqiong Wu
Tongli Wang
Yue Xin
Guibin Wang
Qi Zhou
Qi Zhou
Li-An Xu
author_sort Jing Guo
collection DOAJ
description Flavonoids are important secondary metabolites with extensive pharmacological functions. Ginkgo biloba L. (ginkgo) has attracted extensive attention because of its high flavonoid medicinal value. However, little is understood about ginkgo flavonol biosynthesis. Herein, we cloned the full-length gingko GbFLSa gene (1314 bp), which encodes a 363 amino acid protein that has a typical 2-oxoglutarate (2OG)-Fe(II) oxygenase region. Recombinant GbFLSa protein with a molecular mass of 41 kDa was expressed in Escherichia coli BL21(DE3). The protein was localized to the cytoplasm. Moreover, proanthocyanins, including catechin, epicatechin, epigallocatechin and gallocatechin, were significantly less abundant in transgenic poplar than in nontransgenic (CK) plants. In addition, dihydroflavonol 4-reductase, anthocyanidin synthase and leucoanthocyanidin reductase expression levels were significantly lower than those of their CK counterparts. GbFLSa thus encodes a functional protein that might negatively regulate proanthocyanin biosynthesis. This study helps elucidate the role of GbFLSa in plant metabolism and the potential molecular mechanism of flavonoid biosynthesis.
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spelling doaj.art-9d0d93ea16784f7392493836257d263e2023-02-15T09:46:59ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2023-02-011410.3389/fpls.2023.10936561093656GbFLSa overexpression negatively regulates proanthocyanin biosynthesisJing Guo0Yaqiong Wu1Yaqiong Wu2Yaqiong Wu3Tongli Wang4Yue Xin5Guibin Wang6Qi Zhou7Qi Zhou8Li-An Xu9Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaInstitute of Botany, Jiangsu Province and Chinese Academy of Sciences, Nanjing, ChinaDepartment of Forest and Conservation Sciences, Faculty of Forestry, University of British Columbia, Vancouver, BC, CanadaDepartment of Forest and Conservation Sciences, Faculty of Forestry, University of British Columbia, Vancouver, BC, CanadaCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaForest Breeding Institute, Zhejiang Academy of Forestry, Hangzhou, ChinaCo-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing, ChinaFlavonoids are important secondary metabolites with extensive pharmacological functions. Ginkgo biloba L. (ginkgo) has attracted extensive attention because of its high flavonoid medicinal value. However, little is understood about ginkgo flavonol biosynthesis. Herein, we cloned the full-length gingko GbFLSa gene (1314 bp), which encodes a 363 amino acid protein that has a typical 2-oxoglutarate (2OG)-Fe(II) oxygenase region. Recombinant GbFLSa protein with a molecular mass of 41 kDa was expressed in Escherichia coli BL21(DE3). The protein was localized to the cytoplasm. Moreover, proanthocyanins, including catechin, epicatechin, epigallocatechin and gallocatechin, were significantly less abundant in transgenic poplar than in nontransgenic (CK) plants. In addition, dihydroflavonol 4-reductase, anthocyanidin synthase and leucoanthocyanidin reductase expression levels were significantly lower than those of their CK counterparts. GbFLSa thus encodes a functional protein that might negatively regulate proanthocyanin biosynthesis. This study helps elucidate the role of GbFLSa in plant metabolism and the potential molecular mechanism of flavonoid biosynthesis.https://www.frontiersin.org/articles/10.3389/fpls.2023.1093656/fullflavonol synthasegene expressionflavonoid biosynthesistransgenic poplarmetabolite
spellingShingle Jing Guo
Yaqiong Wu
Yaqiong Wu
Yaqiong Wu
Tongli Wang
Yue Xin
Guibin Wang
Qi Zhou
Qi Zhou
Li-An Xu
GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
Frontiers in Plant Science
flavonol synthase
gene expression
flavonoid biosynthesis
transgenic poplar
metabolite
title GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
title_full GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
title_fullStr GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
title_full_unstemmed GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
title_short GbFLSa overexpression negatively regulates proanthocyanin biosynthesis
title_sort gbflsa overexpression negatively regulates proanthocyanin biosynthesis
topic flavonol synthase
gene expression
flavonoid biosynthesis
transgenic poplar
metabolite
url https://www.frontiersin.org/articles/10.3389/fpls.2023.1093656/full
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