Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1927201 | Archives of Biochemistry and Biophysics | 2007 | 9 Pages |
Abstract
Heavy-atom isotope effects for the N-demethylation of nicotine have been determined in vivo in static-phase biosynthetically incompetent plant cell cultures of Nicotiana species. A 2H kinetic isotope effect of 0.587 and a 15N kinetic isotope effect of 1.0028 were obtained. An identical 15N kinetic isotope effect of 1.0032 was obtained for the nicotine analogue, N-methyl-2-phenylpyrrolidine. The magnitude of the 15N heavy-atom isotope effect indicates that the fission of the CN bond is not rate limiting for demethylation. The theoretical calculation of heavy-atom isotope effects for a model of the reaction pathway based on cytochrome P450 best fits the measured kinetic isotope effect to the addition of hydroxyl ion to iminium to form N-hydroxymethyl, for which the computed 2H- and 15N kinetic isotope effects are 0.689 and 1.0081, respectively. This large inverse 2H kinetic isotope effect is not compatible with the initial abstraction of the H from the methyl group playing a significant kinetic role in the overall kinetic limitation of the reaction pathway, since computed values for this step (4.54 and 0.9995, respectively) are inconsistent with the experimental data.
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Authors
Roland Molinié, Renata A. KwiecieÅ, Piotr Paneth, Wilfried Hatton, Jacques Lebreton, Richard J. Robins,