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  • olfaction  (2)
  • Springer  (2)
  • eLife Sciences Publications
  • 1
    ISSN: 1573-1561
    Keywords: Trogoderma species ; trogodermal ; enantiomers ; chiral center ; geometric isomers ; methyl branching ; (Z)- or (E)-14-methyl-8-hexadecenal ; dermestid beetles ; Coleoptera ; Dermestidae ; pheromone ; chemoreception ; olfaction ; (Z)-hexadecenal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Responses to enantiomers of (Z)- and (E)-trogodermal (14-methyl-8-hexadecenal) suggest that fourTrogoderma species utilize the (R)-(−) configuration at C-14. Removal of the C-14 methyl branch decreased the response. These results demonstrate the high specificity associated with the configuration at a chiral center, or the methyl branch, distant in terms of numbers of bonds from a functional group.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1561
    Keywords: Boll weevil ; olfaction ; receptor cell ; Anthonomus grandis ; Coleoptera ; Curculionidae ; enantiomer ; grandisol ; chirality ; electroantennogram ; aggregation pheromone ; neurobiology ; structure-activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electrophysiological recordings from antennal olfactory receptors and field behavioral experiments showed both male and female boll weevils,Anthonomus grandis Boh. (Coleoptera: Curculionidae), to respond specifically to (+)-grandisol, an enantiomer of compound I of the boll weevil aggregation pheromone. Single-cell recordings revealed antennal olfactory neurons in both male and female weevils keyed to (+)-grandisol. Electroantennograms in response to serial dilutions of the grandisol enaniiomers showed a threshold 100 to 1000 times lower for (+)-grandisol relative to its antipode. In field behavioral experiments, both sexes were significantly more attracted to (+)-grandisol in combination with the three other pheromone components than the combination with (−)-grandisol. When (−)-grandisol was placed with the (+)-enantiomer at equal dosages, a slight although statistically insignificant inhibition occurred. Subsequent field tests showed that the low level of attraction exhibited by (−)-grandisol in combination with the other three pheromone components could be attributed to the other three components alone. These results are in contrast with an earlier study, which found (−)-grandisol to be as attractive as the (+)-enantiomer.
    Type of Medium: Electronic Resource
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