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Overexpression of the GbF3'H1 Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic Populus.

Identifieur interne : 000232 ( Main/Exploration ); précédent : 000231; suivant : 000233

Overexpression of the GbF3'H1 Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic Populus.

Auteurs : Yaqiong Wu [République populaire de Chine, Canada] ; Tongli Wang [Canada] ; Yue Xin [République populaire de Chine] ; Guibin Wang [République populaire de Chine] ; Li-An Xu [République populaire de Chine]

Source :

RBID : pubmed:31910001

Descripteurs français

English descriptors

Abstract

Ginkgo biloba L. leaves are a flavonoid resource for the pharmaceutical industry. The flavonoid 3'-hydroxylase (F3'H) is a key enzyme in the flavonoid biosynthesis pathway. However, the role of F3'H in flavonoid biosynthesis and metabolism is unclear. In this study, we characterized and functionally analyzed the ginkgo F3'H gene GbF3'H1 that encodes a protein of 520 amino acids. Expression profiling showed that GbF3'H1 was highly expressed in the leaves of ginkgo in September. Subcellular localization showed that GbF3'H1 occurred predominately in the cytoplasm. Transgenic poplars overexpressing GbF3'H1 had more red pigmentation in leaves than did wild-type (WT) plants. Furthermore, the concentrations of epigallocatechin, gallocatechin, and catechin in the downstream products synthesized by flavonoids were significantly higher in the transgenic plants than in the WT plants. These results indicate that the overexpression of GbF3'H1 enhances flavonoid production in transgenic plants and provides new insights into flavonoid biosynthesis and metabolism.

DOI: 10.1021/acs.jafc.9b07008
PubMed: 31910001


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic
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'
<i>H1</i>
Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic
<i>Populus</i>
.</title>
<author>
<name sortKey="Wu, Yaqiong" sort="Wu, Yaqiong" uniqKey="Wu Y" first="Yaqiong" last="Wu">Yaqiong Wu</name>
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<country xml:lang="fr">République populaire de Chine</country>
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<name sortKey="Wang, Tongli" sort="Wang, Tongli" uniqKey="Wang T" first="Tongli" last="Wang">Tongli Wang</name>
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<nlm:affiliation>Department of Forest and Conservation Sciences, Faculty of Forestry , The University of British Columbia , Vancouver V6T 1Z4 , Canada.</nlm:affiliation>
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<wicri:regionArea>Department of Forest and Conservation Sciences, Faculty of Forestry , The University of British Columbia , Vancouver V6T 1Z4 </wicri:regionArea>
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<name sortKey="Xin, Yue" sort="Xin, Yue" uniqKey="Xin Y" first="Yue" last="Xin">Yue Xin</name>
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<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Co-Innovation Center for Sustainable Forestry in Southern China , Nanjing Forestry University , 159 Longpan Road , Nanjing 210037 </wicri:regionArea>
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<term>Catechin (analogs & derivatives)</term>
<term>Catechin (biosynthesis)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Ginkgo biloba (genetics)</term>
<term>Plant Leaves (genetics)</term>
<term>Plant Leaves (metabolism)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Plants, Genetically Modified (metabolism)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Catéchine (analogues et dérivés)</term>
<term>Catéchine (biosynthèse)</term>
<term>Feuilles de plante (génétique)</term>
<term>Feuilles de plante (métabolisme)</term>
<term>Ginkgo biloba (génétique)</term>
<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Végétaux génétiquement modifiés (génétique)</term>
<term>Végétaux génétiquement modifiés (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en">
<term>Catechin</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Catechin</term>
</keywords>
<keywords scheme="MESH" qualifier="analogues et dérivés" xml:lang="fr">
<term>Catéchine</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Catéchine</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Ginkgo biloba</term>
<term>Plant Leaves</term>
<term>Plant Proteins</term>
<term>Plants, Genetically Modified</term>
<term>Populus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Feuilles de plante</term>
<term>Ginkgo biloba</term>
<term>Populus</term>
<term>Protéines végétales</term>
<term>Végétaux génétiquement modifiés</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Plant Leaves</term>
<term>Plant Proteins</term>
<term>Plants, Genetically Modified</term>
<term>Populus</term>
</keywords>
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<term>Feuilles de plante</term>
<term>Populus</term>
<term>Protéines végétales</term>
<term>Végétaux génétiquement modifiés</term>
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<keywords scheme="MESH" xml:lang="en">
<term>Gene Expression Regulation, Plant</term>
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<front>
<div type="abstract" xml:lang="en">
<i>Ginkgo biloba</i>
L. leaves are a flavonoid resource for the pharmaceutical industry. The flavonoid 3'-hydroxylase (
<i>F3'H</i>
) is a key enzyme in the flavonoid biosynthesis pathway. However, the role of
<i>F3'H</i>
in flavonoid biosynthesis and metabolism is unclear. In this study, we characterized and functionally analyzed the ginkgo
<i>F3</i>
'
<i>H</i>
gene
<i>GbF3</i>
'
<i>H1</i>
that encodes a protein of 520 amino acids. Expression profiling showed that
<i>GbF3</i>
'
<i>H1</i>
was highly expressed in the leaves of ginkgo in September. Subcellular localization showed that
<i>GbF3</i>
'
<i>H1</i>
occurred predominately in the cytoplasm. Transgenic poplars overexpressing
<i>GbF3</i>
'
<i>H1</i>
had more red pigmentation in leaves than did wild-type (WT) plants. Furthermore, the concentrations of epigallocatechin, gallocatechin, and catechin in the downstream products synthesized by flavonoids were significantly higher in the transgenic plants than in the WT plants. These results indicate that the overexpression of
<i>GbF3</i>
'
<i>H1</i>
enhances flavonoid production in transgenic plants and provides new insights into flavonoid biosynthesis and metabolism.</div>
</front>
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</Journal>
<ArticleTitle>Overexpression of the
<i>GbF3</i>
'
<i>H1</i>
Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic
<i>Populus</i>
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<AbstractText>
<i>Ginkgo biloba</i>
L. leaves are a flavonoid resource for the pharmaceutical industry. The flavonoid 3'-hydroxylase (
<i>F3'H</i>
) is a key enzyme in the flavonoid biosynthesis pathway. However, the role of
<i>F3'H</i>
in flavonoid biosynthesis and metabolism is unclear. In this study, we characterized and functionally analyzed the ginkgo
<i>F3</i>
'
<i>H</i>
gene
<i>GbF3</i>
'
<i>H1</i>
that encodes a protein of 520 amino acids. Expression profiling showed that
<i>GbF3</i>
'
<i>H1</i>
was highly expressed in the leaves of ginkgo in September. Subcellular localization showed that
<i>GbF3</i>
'
<i>H1</i>
occurred predominately in the cytoplasm. Transgenic poplars overexpressing
<i>GbF3</i>
'
<i>H1</i>
had more red pigmentation in leaves than did wild-type (WT) plants. Furthermore, the concentrations of epigallocatechin, gallocatechin, and catechin in the downstream products synthesized by flavonoids were significantly higher in the transgenic plants than in the WT plants. These results indicate that the overexpression of
<i>GbF3</i>
'
<i>H1</i>
enhances flavonoid production in transgenic plants and provides new insights into flavonoid biosynthesis and metabolism.</AbstractText>
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<AffiliationInfo>
<Affiliation>Department of Forest and Conservation Sciences, Faculty of Forestry , The University of British Columbia , Vancouver V6T 1Z4 , Canada.</Affiliation>
</AffiliationInfo>
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<LastName>Xu</LastName>
<ForeName>Li-An</ForeName>
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<Affiliation>Co-Innovation Center for Sustainable Forestry in Southern China , Nanjing Forestry University , 159 Longpan Road , Nanjing 210037 , China.</Affiliation>
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<MeshHeading>
<DescriptorName UI="D002392" MajorTopicYN="N">Catechin</DescriptorName>
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<QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName>
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<MeshHeading>
<DescriptorName UI="D018515" MajorTopicYN="N">Plant Leaves</DescriptorName>
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<MeshHeading>
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</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
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<Keyword MajorTopicYN="N">flavonoid</Keyword>
<Keyword MajorTopicYN="N">gene function</Keyword>
<Keyword MajorTopicYN="N">metabolite</Keyword>
<Keyword MajorTopicYN="N">transgenic plant</Keyword>
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<country name="Canada">
<noRegion>
<name sortKey="Wu, Yaqiong" sort="Wu, Yaqiong" uniqKey="Wu Y" first="Yaqiong" last="Wu">Yaqiong Wu</name>
</noRegion>
<name sortKey="Wang, Tongli" sort="Wang, Tongli" uniqKey="Wang T" first="Tongli" last="Wang">Tongli Wang</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/PoplarV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000232 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000232 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Bois
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   |flux=    Main
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   |clé=     pubmed:31910001
   |texte=   Overexpression of the GbF3'H1 Gene Enhanced the Epigallocatechin, Gallocatechin, and Catechin Contents in Transgenic Populus.
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Pour générer des pages wiki

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Data generation: Wed Nov 18 12:07:19 2020. Site generation: Wed Nov 18 12:16:31 2020