Jump to: Page Content, Section Navigation, Site Navigation, Site Search, Account Information, or Site Tools.
|
|
Articles
Aldehyde Pheromones in Lepidoptera: Evidence for an Acetate Ester Precursor in Choristoneura fumiferana
1 Department of Biochemistry, McGill University, Montreal, H3G 1Y6 Canada
Labeling studies of the eastern spruce budworm in vivo indicate that trans-11-tetradecenyl acetate is synthesized specifically in the pheromone-producing gland and is degraded in concert with pheromone release; hence it may be a precursor to the trans-11-tetradecenal pheromone. Radioactivity from exogenously added labeled fatty acids did not appear to be directly incorporated into the ester, suggesting that de novo biosynthesis from acetate is the major route of ester biosynthesis. Conversion of the acetate ester to alcohol and aldehyde functional groups may be the principal method of regulating pheromone specificity between species of Choristoneura. Accepted on July 11, 1984
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
|
Science. ISSN 0036-8075 (print), 1095-9203 (online)