A crude enzyme preparation obtained from cell suspension cultures of Lupinus polyphyllus catalyzes the pyruvate dependent conversion of cadaverine into the tetracyclic lupin alkaloids. As the first reaction product 17-oxosparteine could be identified by gas-liquid chromatography and mass spectroscopy. In some experiments sparteine was found additionally. A participation of diamine oxidase could be ruled out. The cadaverine-pyruvate transaminating enzyme system (17-oxosparteine synthase) catalyzes the formation of 17-oxosparteine from three cadaverine units without releasing free intermediates. These results are inconsistent with the hypothetical mechanism thus far formulated for the lupin alkaloid biosynthesis. A new enzymatic model mechanism is proposed regarding both the results of the enzymatic experiments and those of the in vivo tracer studies. © 1979, Walter de Gruyter. All rights reserved.
CITATION STYLE
Wink, M., Hartmann, T., & Schiebel, H. M. (1979). A Model Mechanism for the Enzymatic Synthesis of Lupin Alkaloids. Zeitschrift Fur Naturforschung - Section C Journal of Biosciences, 34(9–10), 704–708. https://doi.org/10.1515/znc-1979-9-1009
Mendeley helps you to discover research relevant for your work.