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Biosynthesis of gallotannins. Enzymatic conversion of 1,6-digalloylglucose to 1,2,6-trigalloylglucose
Authors:Klaus Denzel  Gerhard Schilling  Georg G Gross
Institution:(1) Abteilung Allgemeine Botanik, Universität Ulm, Oberer Eselsberg, D-7900 Ulm, Federal Republic of Germany;(2) Organisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 270, D-6900 Heidelberg, Federal Republic of Germany
Abstract:Cell-free extracts from Rhus typhina L. (staghorn sumach) leaves were found to catalyze the transfer of the galloyl moiety of beta-glucogallin (1-O-galloyl-beta-D-glucose) to 1,6-di-O-galloyl-beta-D-glucose, resulting in the specific formation of 1,2,6-tri-O-galloyl-beta-D-glucose, an intermediate of gallotannin biosynthesis. The reaction product was unequivocally identified by co-chromatography with authentic references using reversed-phase high-performance liquid chromatography and by 1H-nuclear-magnetic-resonance spectroscopy.Abbreviations HPLC high-performance liquid chromatography - NMR nuclear magnetic resonance
Keywords:1  6-Di-O-galloyl-beta-D-glucose" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-D-glucose  Gallotannin biosynthesis  beta-Glucogallin" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-Glucogallin  Leaf (gallotannin synthesis)  1  2  6-Tri-O-galloyl-beta-D-glucose" target="_blank">gif" alt="beta" align="MIDDLE" BORDER="0">-D-glucose  Rhus
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