Abstract
AbstractA gas chromatographic‐mass spectrometric method using [2,2‐2H2]fatty acids has been developed to trace the biosynthesis ofcis‐vaccenic (cis‐11‐octadecenoic) acid in higher plants. The deuterated fatty acids and other unlabeled fatty acids in the biosynthetic reaction mixture were converted into bis(methylthio) derivatives and analyzed by mass chromatography. The principle of this method was based on the shift of key fragment ions (containing two deuterium atoms) due to the cleavage between the methylthio‐substituted carbons. The labeled compounds were detected by the m/z values which shifted 2 mass units from those of the corresponding unlabeled compounds and estimated by a calibration curve based on the peak areas of the key fragment ions. For metabolic experiments, a homogenate fraction was prepared from the pulp part of maturing kaki (Diospyros kaki) fruit and incubated with ammonium [2,2‐2H2]palmitoleate (cis‐9‐hexadecenoate) or [2,2‐2H2]palmitoleoyl‐CoA. The incubation resulted in the formation of detectable amounts of isotopically‐labeledcis‐vaccenic acid containing two deuterium atoms at the carbon chain between the double bond and the carboxyl group. This experimental evidence proved thatcis‐vaccenic acid was formed from palmitoleic acid by chain elongation.
Published Version
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