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1.
Mol Biol Rep ; 39(3): 2991-9, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-21701830

RESUMEN

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.


Asunto(s)
Oxidorreductasas de Alcohol/genética , Oxidorreductasas de Alcohol/metabolismo , Especies en Peligro de Extinción , Filogenia , Saussurea/enzimología , Oxidorreductasas de Alcohol/química , Secuencia de Bases , Cromatografía Líquida de Alta Presión , Biología Computacional , Cartilla de ADN/genética , ADN Complementario/genética , Escherichia coli , Flavonoides/metabolismo , Flavonoles/metabolismo , Flores/metabolismo , Perfilación de la Expresión Génica , Espectrometría de Masas , Datos de Secuencia Molecular , Estructura Molecular , Quercetina/análogos & derivados , Quercetina/metabolismo , Reacción en Cadena en Tiempo Real de la Polimerasa , Saccharomyces cerevisiae , Análisis de Secuencia de ADN
2.
Plant Cell Rep ; 29(12): 1325-37, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-20842365

RESUMEN

Snow lotus is commonly used as a medicinal plant and has great pharmacological value. To protect these endangered plants, in vitro propagation and cell cultures have been established in order to meet the growing market demand. The phenolic composition, antioxidant activities, total phenolic content (TPC) and total flavonoid content (TFC) from three most commonly used species, in vitro propagated lines and the cell cultures were investigated to qualify their pharmacological value. Quantitative analysis showed that the phenolics varied greatly among different species and the same species at different habitats. From this it can be inferred that the phenolics were influenced by genetic background and the environmental conditions. Significant correlations were observed between the antioxidant activity and several phenolics/TPC/TFC, suggesting that the phenolics are a major contributor of the antioxidant activity and are important for quality evaluation of snow lotus. Based on the abundance of phenolics, TPC, TFC and antioxidant activity, the order of the quality for wild species would be Saussurea involucrata > Saussurea medusa > Saussurea gossypiphora. For S. medusa, its quality judged by origin would be Shigatse > Lhasa > Nagqu. For in vitro propagated plants, the matured plants could be a reliable substitute for wild plants, and the dynamics of phenolics is critical for quality control of this monocarpic species. We provide the first report of quality comparison between the wild plants and the cell cultures. The advantages of developing cell cultures as alternatives for plants collected from the wild are discussed.


Asunto(s)
Antioxidantes/aislamiento & purificación , Saussurea/química , Antioxidantes/química , Antioxidantes/farmacología , Línea Celular , Cromatografía Liquida , Fenoles/química , Fenoles/aislamiento & purificación , Fenoles/farmacología , Espectrofotometría Ultravioleta
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