Da. Guo et al., PHYTOSTEROL BIOSYNTHESIS - ISOTOPE EFFECTS ASSOCIATED WITH BIOMETHYLATION FORMATION TO 24-ALKENE STEROL ISOMERS, Tetrahedron letters, 37(38), 1996, pp. 6823-6826
Changes in 24-alkene sterol product distribution resulting from deuter
ium substitution on the coenzyme methyl group of AdoMet and on the ste
rol acceptor molecule at C-23 and C-24 were used to determine kinetic
isotope effects for the terminating deprotonations involved in sterol
biomethylation catalyzed by (S)-adenosyl-L-methionine-Delta(24)-sterol
methyl transferase (SMT) enzyme. By this method 24(28)-methylene cycl
oartanol and cyclosadol were shown to be synthesized by two different
SMT enzymes. Copyright (C) 1996 Published by Elsevier Science Ltd