C-Glucosylflavonoid biosynthesis from 2-hydroxynaringenin by Desmodium uncinatum (Jacq.) (Fabaceae) |
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Authors: | Mary L Hamilton John C Caulfield John A Pickett Antony M Hooper |
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Institution: | aBiological Chemistry Department, Centre for Sustainable Pest and Disease Management, Rothamsted Research, Harpenden, Herts AL5 2JQ, UK |
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Abstract: | 2′,3′,5′,6′-2H4]-2-Hydroxynaringenin is synthesised and incubated with commercially available UDP-glucose and the crude protein extract from Desmoduim uncinatum leaves. The organic extract produces isotopically labelled 2′,3′,5′,6′-2H4]-vitexin and 2′,3′,5′,6′-2H4]-isovitexin. Repeating the experiment with denatured protein or replacing the 2-hydroxynaringenin with 2′,3′,5′,6′-2H4]-apigenin or 2′,3′,5′,6′-2H4]-naringenin results in no observable incorporation. 2-Hydroxynaringenin is therefore the substrate for C-glucosylflavonoid biosynthesis in D. uncinatum. |
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Keywords: | Desmodium uncinatum C-Glycosyltransferase Biosynthesis C-Glycosylflavonoid 2-Hydroxynaringenin Vitexin Isovitexin Deuterium labelling |
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