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Triterpene saponin hemi-biosynthesis of a leaf beetle’s (<Emphasis Type="Italic">Platyphora kollari</Emphasis>) defensive secretion
Authors:Jean Ghostin  Jean-Louis Habib-Jiwan  Raoul Rozenberg  Désiré Daloze  Jacques M Pasteels  Jean-Claude Braekman
Institution:(1) Department of Organic Chemistry, CP 160/06, Faculty of Sciences, University of Brussels, 50 Av. F.D. Roosevelt, 1050 Brussels, Belgium;(2) Laboratory of Cellular and Animal Biology, CP 160/12, Faculty of Sciences, University of Brussels, 50 Av. F.D. Roosevelt, 1050 Brussels, Belgium;(3) Laboratory of Mass Spectrometry, Department of Chemistry, Catholic University of Louvain, 1 Place L. Pasteur, Louvain-la-Neuve, Belgium
Abstract:The adults of the leaf beetle Platyphora kollari (Chrysomelidae) are able to metabolise the oleanane triterpene β-amyrin (1) into the glycoside 3-O-β-d-glucopyranosyl-(1→4)-β-d-glucuronopyranosyl-hederagenin (2) that is stored in their defensive glands. The aim of this study was to test the hypothesis that oleanolic acid (3) is an intermediate in the conversion of 1 into 2 and to check whether the sequestration of pentacyclic triterpenes is selective in favour of β-amyrin (1). To this end, adults of P. kollari were fed with Ipomoea batatas leaf disks painted with a solution of 2,2,3-2H3]oleanolic acid or 2,2,3-2H3]α-amyrin and the secretion of their defensive glands analysed by HPLC–ESIMS. The data presented in this work indicated that the first step of the transformation of β-amyrin (1) into the sequestered glycoside 2 is its oxidation into oleanolic acid (3) and that this conversion is selective but not specific in favour of β-amyrin (1).
Keywords:Chrysomelidae            Platyphora kollari            Defensive secretion  Pentacyclic triterpene  Hemi-biosynthesis
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