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Biosynthesis of Cyanogenic Glycosides in Butterflies and Moths: Incorporation of Valine and Isoleucine into Linamarin and Lotaustralin by Zygaena and Heliconius Species (Lepidoptera)
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1983
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BiologyBiosynthesisBiotransformationBiochemistryHeliconius SpeciesAmino AcidNatural SciencesSecondary MetaboliteNatural Product BiosynthesisPhytochemistryIntact UnitsCyanogenic Glycosides
Abstract C -13 NMR data for linamarin and lotaustralin, obtained after feeding of either Zygaena Jilipendulae or Heliconius melpomone (Lepidoptera) with C-13 enriched valine and isoleucine respectively, indicate that intact units of amino acid with loss of the carboxyl group are incorporated during the biosynthesis of these cyanogenic glycosides.