Chemical structure and final steps of biosynthesis of the female sex pheromone of Gastropacha quercifolia (Lepidoptera: Lasiocampidae)

The major volatile constituents in the sex pheromone gland of females of Gastropacha quercifolia (Lepidoptera: Lasiocampidae) were identified as ( Z)-5-Dodecenal 1, ( Z)-5-dodecenol 2 and ( Z)-5-dodecenyl( Z)-5-dodecenoate 3. Synthetic samples of the first two compounds 1 and 2 were able to evoke st...

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Published inInsect biochemistry and molecular biology Vol. 23; no. 7; pp. 793 - 799
Main Authors Bestmann, H.J., Attygalle, A.B., Garbe, W., Kern, F., Martichonok, V., Schäfer, D., Vostrowsky, O., Hasenfuβ, I.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 1993
Elsevier Science
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Summary:The major volatile constituents in the sex pheromone gland of females of Gastropacha quercifolia (Lepidoptera: Lasiocampidae) were identified as ( Z)-5-Dodecenal 1, ( Z)-5-dodecenol 2 and ( Z)-5-dodecenyl( Z)-5-dodecenoate 3. Synthetic samples of the first two compounds 1 and 2 were able to evoke strong electroantennographic responses from male antennae, however, no electrophysiological activity was found for the ester 3. The final steps involved in the biosynthesis of the three compounds were investigated using deuterated biosynthesis intermediates. ( Z)-5-Dodecenoic acid 14 was established as the immediate precursor of ( Z)-5-dodecenol 2 which is subsequently converted to the ( Z)-5-dodecenal 1. Since a direct desaturation of dodecanoic acid was not observed, the introduction of the double bond appears to take place at an earlier stage of biosynthesis. No evidence was found that the ester 3 might serve as a pheromone pool from which the components 1 and 2 can be derived; on the other hand, ( Z)-5-dodecenol and ( Z)-5-dodecenoic acid served as the bioprecursors of the ester 3.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0965-1748
1879-0240
DOI:10.1016/0965-1748(93)90067-3