Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractMicroarray analysis of Arabidopsis plants in response to allelochemical L-DOPA    Next AbstractComplex phenotype of mice homozygous for a null mutation in the Sp4 transcription factor gene »

J Chem Ecol


Title:"Biosynthesis of (3Z,6Z,9Z)-3,6,9-octadecatriene: the main component of the pheromone blend of Erannis bajaria"
Author(s):Goller S; Szocs G; Francke W; Schulz S;
Address:"Institut fur Organische Chemie, Technische Universitat Braunschweig, Hagenring 30, 38106 Braunschweig, Germany"
Journal Title:J Chem Ecol
Year:2007
Volume:20070704
Issue:8
Page Number:1505 - 1509
DOI: 10.1007/s10886-007-9324-z
ISSN/ISBN:0098-0331 (Print) 0098-0331 (Linking)
Abstract:"The hydrocarbons (3Z,6Z,9Z)-3,6,9-octadecatriene (3Z,6Z,9Z-18:H) and (3Z,6Z,9Z)-3,6,9-nonadecatriene (3Z,6Z,9Z-19:H) constitute the pheromone of the winter moth, Erannis bajaria. These compounds belong to a large group of lepidopteran pheromones which consist of unsaturated hydrocarbons and their corresponding oxygenated derivatives. The biosynthesis of such hydrocarbons with an odd number of carbons in the chain is well understood. In contrast, knowledge about the biosynthesis of even numbered derivatives is lacking. We investigated the biosynthesis of 3Z,6Z,9Z-18:H by applying deuterium-labeled precursors to females of E. bajaria followed by gas chromatography-mass spectrometry analysis of extracts of the pheromone gland. A mixture of deuterium-labeled [17,17,18,18-(2)H(4)]-3Z,6Z,9Z-18:H and the unlabeled 3Z,6Z,9Z-18:H was obtained after topical application and injection of (10Z,13Z,16Z)-[2,2,3,3-(2)H(4)]-10,13,16-nonadecatrienoic acid ([2,2,3,3-(2)H(4)]-10Z,13Z,16Z-19:acid) or (11Z,14Z,17Z)-[3,3,4,4-(2)H(4)]-11,14,17-icosatrienoic acid ([3,3,4,4-(2)H(4)]-11Z,14Z,17Z-20:acid). These results are consistent with a biosynthetic pathway that starts with alpha-linolenic acid (9Z,12Z,15Z-18:acid). Chain elongation leads to 11Z,14Z,17Z-20:acid, which is shortened by alpha-oxidation as the key step to yield 10Z,13Z,16Z-19:acid. This acid can be finally reduced to an aldehyde and decarbonylated or decarboxylated to furnish the pheromone component 3Z,6Z,9Z-18:H. A similar transformation of 11Z,14Z,17Z-20:acid yields the second pheromone component, 3Z,6Z,9Z-19:H"
Keywords:Alkenes/*metabolism Animals Gas Chromatography-Mass Spectrometry Moths/*metabolism Pheromones/*metabolism;
Notes:"MedlineGoller, Stephan Szocs, Gabor Francke, Wittko Schulz, Stefan eng 2007/07/05 J Chem Ecol. 2007 Aug; 33(8):1505-9. doi: 10.1007/s10886-007-9324-z. Epub 2007 Jul 4"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 21-09-2024