Treatment of alfalfa cell suspension cultures with elicitor preparations from baker's yeast or from cell walls of Colletotrichum lindemuthianum resulted in a ca 200-fold induction of isoflavone O-methyltransferase (IOMT) activity. The elicited cultures contained O-methyltransferase activity against isoflavone, isoflavan and pterocarpan substrates. These activities could be separated into two distinct fractions by ion-exchange chromatography. The major IOMT activity (IOMT II) was purified to homogeneity by a combination of anion exchange chromatography, hydrophobic interaction chromatography and chromatofocussing. It is a monomeric enzyme of subunit Mr41 000 which could be photoaffinity labelled with tritiated SAM. IOMT II converted the isoflavone daidzein to its 7-O-methyl ether isoformononetin, with Kmvalues of 20, μM for daidzein and 150 μM for SAM and a pH optimum of 8.5. Both IOMT II and the less abundant IOMT species (IOMT I) exhibited greatest activity with 6,7,4′-trihydroxyisoflavone as methyl acceptor. IOMT I, but not IOMT II, also catalysed the A-ring methylation of the pterocarpan phytoalexin medicarpin. Isoflavone 4′-OMT activity, which is believed necessary for the formation of the B-ring methoxy substituent of medicarpin, was present at very low activity in extracts from the cultures and was only weakly induced by elicitor. © 1991.
Edwards, R., & Dixon, R. A. (1991). Isoflavone O-methyltransferase activities in elicitor-treated cell suspension cultures of Medicago sativa. Phytochemistry, 30(8), 2597–2606. https://doi.org/10.1016/0031-9422(91)85107-B