Literature DB >> 15839479

(7R,8S)-cis-7,8-epoxy-2-methyloctadec-17-ene: a novel trace component from the sex pheromone gland of gypsy moth, Lymantria dispar.

Regine Gries1, Grigori Khaskin, Paul W Schaefer, Roger Hahn, Tadao Gotoh, Gerhard Gries.   

Abstract

Considering the vast Eurasian distribution of gypsy moth, Lymantria dispar (Lepidoptera: Lymantriidae), the many subspecies, and their presence in different lymantriid communities, we tested the hypothesis that L. dispar populations in eastern Asia employ one or more pheromone components in addition to the previously known single component pheromone (7R,8S)-cis-7,8-epoxy-2-methyloctadecane [= (+)-disparlure]. Coupled gas chromatographic-electroantennographic detection (GC-EAD) analyses of pheromone gland extracts of female L. dispar sensu lato (including both AGM and NAGM) on four GC columns (DB-5, DB-23, DB-210, and SP-1000) revealed a new trace component that eluted just before (DB-5; DB-210) or after (DB-23, SP-1000) disparlure, and elicited strong antennal responses. Isolation of this compound by high-performance liquid chromatography and hydrogenation produced disparlure, suggesting that the new component had the molecular skeleton of disparlure, with one or more double bonds. Of all possible monounsaturated cis-7,8-epoxy-2-methyloctadecenes, only cis-7,8-epoxy-2-methyloctadec-17-ene co-chromatographed with the insect-produced compound on all GC columns and elicited comparable antennal responses. In field experiments in Honshu (Japan) with enantioselectively synthesized compounds, (7R,8S)-cis-7,8-epoxy-2-methyloctadec-17-ene (7R8S-epo-2me-17-ene-18Hy) was weakly attractive to male L. dispar, but was less effective as a trap bait than (+)-disparlure, and failed to enhance attractiveness of (+)-disparlure when tested in blends. The antipode, (7S,8R)-cis-7,8-epoxy-2-methyloctadec-17-ene, was not attractive, and when added to (+)-disparlure and/or 7R8S-epo-2me-17-ene-18Hy reduced attractiveness. Thus, the biological role of 7R8S-epo-2me-17-ene-18Hy remains unclear. It may enhance pheromone attractiveness or specificity in other L. dispar populations within their vast Eurasian distribution.

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Year:  2005        PMID: 15839479     DOI: 10.1007/s10886-005-0973-5

Source DB:  PubMed          Journal:  J Chem Ecol        ISSN: 0098-0331            Impact factor:   2.626


  5 in total

1.  A GENERALIZATION OF THE RETENTION INDEX SYSTEM INCLUDING LINEAR TEMPERATURE PROGRAMMED GAS-LIQUID PARTITION CHROMATOGRAPHY.

Authors:  H VANDENDOOL; P D KRATZ
Journal:  J Chromatogr       Date:  1963-08

2.  Potent sex attractant of the gypsy moth: its isolation, identification, and synthesis.

Authors:  B A Bierl; M Beroza; C W Collier
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

3.  Reproductive character displacement in Lymantria monacha from northern Japan?

Authors:  G Gries; P W Schaefer; R Gries; J Liska; T Gotoh
Journal:  J Chem Ecol       Date:  2001-06       Impact factor: 2.626

4.  Mitochondrial DNA variation among worldwide populations of gypsy moths, Lymantria dispar.

Authors:  S M Bogdanowicz; P W Schaefer; R G Harrison
Journal:  Mol Phylogenet Evol       Date:  2000-06       Impact factor: 4.286

5.  (Z,Z)-4,7-tridecadien-(S)-2-yl acetate: sex pheromone of Douglas-fir cone gall midge, Contarinia oregonensis.

Authors:  Regine Gries; Grigori Khaskin; Gerhard Gries; Robb G Bennett; G G Skip King; Petra Morewood; Keith N Slessor; W Dean Morewood
Journal:  J Chem Ecol       Date:  2002-11       Impact factor: 2.626

  5 in total
  4 in total

1.  (7E,11E)-3,5,9,11-Tetramethyltridecadienal: Sex Pheromone of the Strepsipteran Xenos peckii.

Authors:  Michael Hrabar; Huimin Zhai; Regine Gries; Paul W Schaefer; Jason Draper; Robert Britton; Gerhard Gries
Journal:  J Chem Ecol       Date:  2015-08-14       Impact factor: 2.626

2.  Structural and functional difference of pheromone binding proteins in discriminating chemicals in the gypsy moth, Lymantria dispar.

Authors:  Yanxue Yu; Fei Ma; Yixia Cao; Junhua Zhang; Yongan Zhang; Shengnan Duan; Yadong Wei; Shuifang Zhu; Naizhong Chen
Journal:  Int J Biol Sci       Date:  2012-07-30       Impact factor: 6.580

3.  Sex pheromone components of Indian gypsy moth, Lymantria obfuscata.

Authors:  Regine Gries; Paul W Schaefer; Roger Hahn; Grigori Khaskin; Gujjandadu Ramaseshiah; Balbir Singh; Gagandeep K Hehar; Gerhard Gries
Journal:  J Chem Ecol       Date:  2007-07-20       Impact factor: 2.793

4.  Synthesis of disparlure and monachalure enantiomers from 2,3-butanediacetals.

Authors:  Adam Drop; Hubert Wojtasek; Bożena Frąckowiak-Wojtasek
Journal:  Beilstein J Org Chem       Date:  2020-04-03       Impact factor: 2.883

  4 in total

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