Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-7649
Main Title: Studies on the Biosynthesis of γ–Decalactone in Sporobolomyces odorus
Author(s): Albrecht, Wolfgang
Tressl, Roland
Type: Article
Language Code: en
Abstract: Incubation of racemic ethyl [2,2-2H2]-(E)-3,4-epoxydecanoate and the corresponding acid with intact cells of Sporobolomyces odorus led to the formation of deuterium labeled γ-decalaetone. The detection of labeled 2-decen-4-olide and 4-oxodecanoic acid made it possi­ble to propose the biogenetic sequence leading to γ-decalactone. The determination of the en­ antiomeric ratio of the lactone revealed an unspecific metabolism of the precursor. In contrast to the (E)-isomer, after administration of ethyl [5,6-2H2]-(Z)-3,4-epoxydeeanoate no transfor­mation could be detected. These results indicate that (E)-3,4-epoxydecanoic acid, formed from (E)-3-decenoyl-CoA , an intermediate of the β-oxidation of linoleic acid, is the genuine precur­sor in the biosynthesis of γ-decalactone.
URI: https://depositonce.tu-berlin.de//handle/11303/8503
http://dx.doi.org/10.14279/depositonce-7649
Issue Date: 1990
Date Available: 10-Nov-2018
DDC Class: 570 Biowissenschaften; Biologie
Subject(s): Sporobolomyces odorus
biosynthesis
License: https://creativecommons.org/licenses/by-nc-nd/3.0/
Journal Title: Zeitschrift für Naturforschung C
Publisher: De Gruyter
Publisher Place: Berlin
Volume: 45
Issue: 3-4
Publisher DOI: 10.1515/znc-1990-3-411
Page Start: 207
Page End: 216
EISSN: 1865-7125
ISSN: 0939-5075
Appears in Collections:Inst. Biotechnologie » Publications

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