Literature DB >> 14976232

Molecular and biochemical analysis of two cDNA clones encoding dihydroflavonol-4-reductase from Medicago truncatula.

De-Yu Xie1, Lisa A Jackson, John D Cooper, Daneel Ferreira, Nancy L Paiva.   

Abstract

Dihydroflavonol-4-reductase (DFR; EC1.1.1.219) catalyzes a key step late in the biosynthesis of anthocyanins, condensed tannins (proanthocyanidins), and other flavonoids important to plant survival and human nutrition. Two DFR cDNA clones (MtDFR1 and MtDFR2) were isolated from the model legume Medicago truncatula cv Jemalong. Both clones were functionally expressed in Escherichia coli, confirming that both encode active DFR proteins that readily reduce taxifolin (dihydroquercetin) to leucocyanidin. M. truncatula leaf anthocyanins were shown to be cyanidin-glucoside derivatives, and the seed coat proanthocyanidins are known catechin and epicatechin derivatives, all biosynthesized from leucocyanidin. Despite high amino acid similarity (79% identical), the recombinant DFR proteins exhibited differing pH and temperature profiles and differing relative substrate preferences. Although no pelargonidin derivatives were identified in M. truncatula, MtDFR1 readily reduced dihydrokaempferol, consistent with the presence of an asparagine residue at a location known to determine substrate specificity in other DFRs, whereas MtDFR2 contained an aspartate residue at the same site and was only marginally active on dihydrokaempferol. Both recombinant DFR proteins very efficiently reduced 5-deoxydihydroflavonol substrates fustin and dihydrorobinetin, substances not previously reported as constituents of M. truncatula. Transcript accumulation for both genes was highest in young seeds and flowers, consistent with accumulation of condensed tannins and leucoanthocyanidins in these tissues. MtDFR1 transcript levels in developing leaves closely paralleled leaf anthocyanin accumulation. Overexpression of MtDFR1 in transgenic tobacco (Nicotiana tabacum) resulted in visible increases in anthocyanin accumulation in flowers, whereas MtDFR2 did not. The data reveal unexpected properties and differences in two DFR proteins from a single species.

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Year:  2004        PMID: 14976232      PMCID: PMC389921          DOI: 10.1104/pp.103.030221

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  57 in total

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2.  Enzymic and nonenzymic reduction of (+)-dihydroquercetin to its 3,4,-diol.

Authors:  H A Stafford; H H Lester
Journal:  Plant Physiol       Date:  1982-09       Impact factor: 8.340

3.  Genomic sequencing.

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Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

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Authors:  H A Stafford; H H Lester
Journal:  Plant Physiol       Date:  1984-09       Impact factor: 8.340

5.  The Medicago Genome Initiative: a model legume database.

Authors:  C J Bell; R A Dixon; A D Farmer; R Flores; J Inman; R A Gonzales; M J Harrison; N L Paiva; A D Scott; J W Weller; G D May
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

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Journal:  Plant Mol Biol       Date:  1993-05       Impact factor: 4.076

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5.  Metabolic engineering of anthocyanin biosynthesis in Escherichia coli.

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

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9.  Early steps in proanthocyanidin biosynthesis in the model legume Medicago truncatula.

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10.  Developmental and Metabolic Plasticity of White-Skinned Grape Berries in Response to Botrytis cinerea during Noble Rot.

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Journal:  Plant Physiol       Date:  2015-10-08       Impact factor: 8.340

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