Cristin-resultat-ID: 412239
Sist endret: 21. oktober 2013, 12:12
Resultat
Vitenskapelig artikkel
2003

(�)-Germacrene D receptor neurones in three species of heliothine moths: structure-activity relationships

Bidragsytere:
  • Marit Stranden
  • Ilme Liblikas
  • Wilfried A. König
  • Tor Jørgen Almaas
  • Anna-Karin Borg-Karlson og
  • Hanna Mustaparta

Tidsskrift

Journal of Comparative Physiology A. Sensory, neural, and behavioral physiology
ISSN 0340-7594
e-ISSN 1432-1351
NVI-nivå 1

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2003
Volum: 189
Hefte: 7
Sider: 563 - 577

Importkilder

Bibsys-ID: r03015863

Beskrivelse Beskrivelse

Tittel

(�)-Germacrene D receptor neurones in three species of heliothine moths: structure-activity relationships

Sammendrag

Specificity of olfactory receptor neurones plays an important role in food and host preferences of a species, and may have become conserved or changed in the evolution of polyphagy and oligophagy. We have identified a major type of plant odour receptorneurones responding to the sesquiterpene germacrene D in three species of heliothine moths, the polyphagous Heliothis virescens and Helicoverpa armigera and the oligophagous Helicoverpa assulta. The neurones respond with high sensitivity and selectivityto (–)-germacrene D, as demonstrated by screening via gas chromatography with numerous mixtures of plant volatiles. Germacrene D was present in both host and non-host plants, but only in half of the tested species. The specificity of the neuroneswas similar in the three species, as shown by the "secondary" responses to a few other sesquiterpenes. The effect of (–)-germacrene D was about ten times stronger than that of the (+)-enantiomer, which again was about ten times stronger than thatof(–)-a-ylangene. Weaker effects were obtained for (+)-ß-ylangene, (+)-a-copaene, ß-copaene and two unidentified sesquiterpenes. The structure-activity relationship shows that the important properties of (–)-germacrene D in activating theneurones are the ten-membered ring system and the three double bonds acting as electron-rich centres, in addition to the direction of the isopropyl-group responsible for the different effects of the germacrene D enantiomers.

Bidragsytere

Marit Stranden

  • Tilknyttet:
    Forfatter
    ved Institutt for biologi ved Norges teknisk-naturvitenskapelige universitet

Ilme Liblikas

  • Tilknyttet:
    Forfatter

Wilfried A. König

  • Tilknyttet:
    Forfatter

Tor Jørgen Almaas

  • Tilknyttet:
    Forfatter
    ved Institutt for biologi ved Norges teknisk-naturvitenskapelige universitet

Anna-Karin Borg-Karlson

  • Tilknyttet:
    Forfatter
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