Abstract

Among the sex pheromone components of the turnip moth, Agrotis segetum, (Z)-5-decenyl acetate, (Z)-7-dodecenyl acetate and (Z)-9-tetradecenyl acetate are biosynthetically derived from palmitic acid by Δ11-desaturation, chain-shortening, reduction and acetylation. Females of a Zimbabwean population produce the three components in a 78:20:2 ratio, while Swedish females produce the three components in a 12:59:29 ratio. We found that the titers of primary pheromone precursors, such as 16:Acyl and Z11-16:Acyl, did not differ significantly between the two populations. However, the amounts of intermediate precursors Z5-10:Acyl, Z7-12:Acyl and Z9-14:Acyl were significantly higher in the Swedish female extracts. There was no obvious correlation between the ratios of pheromone precursors and the ratios of pheromone components. By application of D 3-16:COOH, D 9-Z11-16:COOH, D 9-Z9-14:COOH and D 9-Z7-12:COOH to the female pheromone glands, we found that Zimbabwean females produced more labelled D 9-Z5-10:OAc than Swedish females. In contrast, in Swedish females, the labelled precursors were mainly converted to D 9-Z9-14:OAc and D 9-Z7-12:OAc, rather than to D 9-Z5-10:OAc. Moreover, the conversion rate of D 9-Z5-10:COOH to D 9-Z5-10:OAc, was significantly higher in Zimbabwean females than in Swedish females. Our results indicate that differences in chain shortening and/or the preferential reduction of acids with different chain lengths may lead to the production of different ratios. Brain-SOG homogenates from the two populations increased the pheromone production of decapitated females of both populations, but did not change the pheromone ratios of the two populations.

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