Stereoselectivity on the demethylation of nicotine piperidine homologues by Nicotania plumbaginifolia cell suspension cultures

• Published in: Phytochemistry (Oxford) Vol. 66; no. 16; pp. 1890 - 1897
• Main Authors: Bartholomeusz, T.A., Molinie, R., Roscher, A., Felpin, F.X., Gillet, Françoise, Lebreton, J., Mesnard, François, Robins, J.
• Format: Journal Article
• Language: English
• Published: Elsevier 2005
• Subjects: Chemical Sciences; Life Sciences; Demethylation; Nicotiana plumbaginifolia; R; Cell suspension culture; S)-N-Methylanabasine; S)-N-Methylanatabine; (S)-Nicotine; Chiral selectivity
• ISSN: 0031-9422
• DOI: 10.1016/j.phytochem.2005.07.012

The metabolism of (R,S)-N-methylanabasine and (R,S)-N-methylanatabine has been studied in a cell suspension culture of Nicotiana plumbaginifolia. Both substrates are effectively demethylated, anabasine or anatabine, respectively, accumulating in the medium. Similarly, there is strong stereoselectivity for the (R)-isomers of both substrates. The kinetics of metabolism of (R,S)-N-methylanabasine differ significantly from those of nicotine in that no further degradation of the initial demethylation product occurs. (R,S)-N-Methylanatabine, however, shows kinetics closer to those of nicotine, with loss of alkaloid from the system. Furthermore, (R,S)-N-methylanabasine does not diminish (S)-nicotine demethylation, indicating a lack of competition. However, the metabolism of (S)-nicotine is affected by the presence of (R,S)-N-methylanabasine. Hence, the demethylation of the piperidine homologues of nicotine is seen to be similar but not identical to that of the pyridine analogues. The implications of these different metabolic profiles in relation to the demethylation activity are discussed.