Affiliation:
1. Institut für Lebensmittelchemie der Universität Karlsruhe und Institut für Chemisch-technische Analyse und chemische Lebensmitteltechnologie der TU München, Weihenstephan
Abstract
Banana slices metabolize 8-14C-octanoic acid via β-oxidation to ketones, alcohols, and fatty acids depending on the climacteric state of the fruits. Simultaneously, esterification of the octanoic acid and its reduction to octanol take place. The latter was found as alkyl component in various esters.
As the typical banana-aroma component cis-hepten- (4) -ol- (2) was found. The position of the double bond was determined by treatment with osmium tetroxide, sililation of the resulting hydroxycompound, and mass spectrometric fragmentation.
Strawberries have a similar composition of the aroma but cis-hepten- (4) -ol- (2) was not formed.
The occurence of 14C-labelled oenanth- and valeric acid is explained by α-oxidation.
Cited by
16 articles.
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