Literature DB >> 21701830

Molecular characterization and expression analysis of dihydroflavonol 4-reductase (DFR) gene in Saussurea medusa.

Houhua Li1, Jian Qiu, Fudong Chen, Xiaofen Lv, Chunxiang Fu, Dexiu Zhao, Xuejun Hua, Qiao Zhao.   

Abstract

Dihydroflavonol 4-reductase (DFR), which catalyzes the reduction of dihydroflavonols to leucoanthocyanins, is a key enzyme in the biosynthesis of anthocyanidins, proanthocyanidins, and other flavonoids of importance in plant development and human nutrition. This study isolated a full length cDNA encoding DFR, designated as SmDFR (GenBank Accession No. EF600682), by screening a cDNA library from a red callus line of Saussurea medusa, which is an endangered, traditional Chinese medicinal plant with high pharmacological value. SmDFR was functionally expressed in yeast (Saccharomyces cerevisiae) to confirm that SmDFR can readily reduce dihydroquercetin (DHQ) and dihydrokampferol (DHK), but it could not reduce dihydromyricetin (DHM). The deduced SmDFR structure shared extensive sequence similarity with previously characterized plant DFRs and phylogenetic analysis showed that it belonged to the plant DFR super-family. SmDFR also possessed flavanone 4-reductase (FNR) activity and can catalyze the conversion of eridictyol to luteoforol. Real-time PCR analysis showed that the expression level of SmDFR was higher in flowers compared with both leaves and roots. This work greatly enhances our knowledge of flavonoid biosynthesis in S. medusa and marks a major advance that could facilitate future genetic modification of S. medusa.

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Year:  2011        PMID: 21701830     DOI: 10.1007/s11033-011-1061-2

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  24 in total

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Authors:  Feng-Xia Li; Zhi-Ping Jin; De-Xiu Zhao; Li-Qin Cheng; Chun-Xiang Fu; Fengshan Ma
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4.  Molecular cloning, substrate specificity of the functionally expressed dihydroflavonol 4-reductases from Malus domestica and Pyrus communis cultivars and the consequences for flavonoid metabolism.

Authors:  Thilo C Fischer; Heidrun Halbwirth; Barbara Meisel; Karl Stich; Gert Forkmann
Journal:  Arch Biochem Biophys       Date:  2003-04-15       Impact factor: 4.013

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Authors:  De-Yu Xie; Lisa A Jackson; John D Cooper; Daneel Ferreira; Nancy L Paiva
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2.  Functional analysis of the dihydroflavonol 4-reductase family of Camellia sinensis: exploiting key amino acids to reconstruct reduction activity.

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3.  Transgenic Tobacco Overexpressing Tea cDNA Encoding Dihydroflavonol 4-Reductase and Anthocyanidin Reductase Induces Early Flowering and Provides Biotic Stress Tolerance.

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Review 4.  Recent advances on the development and regulation of flower color in ornamental plants.

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Journal:  Front Plant Sci       Date:  2015-04-27       Impact factor: 5.753

5.  Molecular cloning and characterization of three genes encoding dihydroflavonol-4-reductase from Ginkgo biloba in anthocyanin biosynthetic pathway.

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Journal:  PLoS One       Date:  2013-08-26       Impact factor: 3.240

6.  Dihydroflavonol 4-Reductase Genes from Freesia hybrida Play Important and Partially Overlapping Roles in the Biosynthesis of Flavonoids.

Authors:  Yueqing Li; Xingxue Liu; Xinquan Cai; Xiaotong Shan; Ruifang Gao; Song Yang; Taotao Han; Shucai Wang; Li Wang; Xiang Gao
Journal:  Front Plant Sci       Date:  2017-03-28       Impact factor: 5.753

7.  Whole-genome resequencing and transcriptomic analysis of genes regulating anthocyanin biosynthesis in black rice plants.

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8.  The interplay between miR156/SPL13 and DFR/WD40-1 regulate drought tolerance in alfalfa.

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9.  Functional characterization of Dihydroflavonol-4-reductase in anthocyanin biosynthesis of purple sweet potato underlies the direct evidence of anthocyanins function against abiotic stresses.

Authors:  Hongxia Wang; Weijuan Fan; Hong Li; Jun Yang; Jirong Huang; Peng Zhang
Journal:  PLoS One       Date:  2013-11-04       Impact factor: 3.240

10.  Rapid and comprehensive evaluation of (poly)phenolic compounds in pomegranate (Punica granatum L.) juice by UHPLC-MSn.

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