both UDP-Glc and UDP-Gal are used as sugar donors, with UDP-Glc beinng preferred. The highest catalytic activity is observed toward gallic acid among the C6-C1 substrates and toward p-coumaric acid among the C6-C3 substrates
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expressed as a recombinant fusion protein in Escherichia coli. Wide variety of secondary metabolites. Expression of UGT71C1 in transgenic Arabidopsis is driven by the constitutive cauliflower mosaic virus 35 S (CaMV35S) promoter. Nine independent transgenic lines. The level of expression of UGT71C1 is enhanced considerably in several lines, leading to a higher level of the corresponding enzyme activity and a higher level of caffeoyl-3-O-glucoside
development of a high-throughput assay for screening recombinant UDP-glucose-dependent glycosyltransferases and analysis of the activity with xenobiotics 2,4,5-trichlorophenol, 4-nitrophenol, 2-chloro-4-trifluoromethylphenol, 1-naphthol, triclosan and expression profiling of UDP-glucose-dependent glycosyltransferases following treatment with the herbicide safener fenclorim
Employment of high-performance liquid chromatography for the determination of uridine-5'-diphosphoglucose:phenol-beta-D-glucosyltransferase activity in vitro by use of partially purified enzyme from plants Beta vulgaris ssp. rapacea var. altissima Döll