PLANT PHYSIOLOGY · 1968 · 113 citations · 4 references
Life SciencesPharmacologyToxicologyMycotoxicologyPlant BiochemistryStructure-activity RelationshipsAntifungal AgentsEnzyme InhibitionFungal BiochemistryFungal Secondary MetabolitesSterol MetabolismBioactive Fungal MetabolitesFungal Bioactive CompoundsFungal Membrane LipidsFungal ToxinsHydrolysisPlant SterolsToxic Mushroom Compounds
Removal of 1 or more sugar residues from the alpha-tomatine molecule markedly decreased its fungitoxicity. While partial hydrolysis of alpha-tomatine did not greatly affect its surfactant properties, it did destroy the ability of this alkaloid to form a complex with cholesterol. Only unprotonated alpha-tomatine was capable of binding cholesterol; the protonated form did not. Since alpha-tomatine was far more toxic at a high pH than at a low pH, this suggests that the unprotonated alkaloid is the active form and that it acts by complexing with fungal sterols.
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