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 AbstractIdentification of a Novel Moth Sex Pheromone Component from Chilecomadia valdiviana    Next AbstractEffect of the type of wood used for ageing on the volatile composition of Pedro Ximenez sweet wine »

PLoS One


Title:"Linoleic acid and stearic acid are biosynthetic precursors of (7Z,10Z)-7,10-hexadecadienal, the major component of the sex pheromone of Chilecomadia valdiviana (Lepidoptera: Cossidae)"
Author(s):Herrera H; Barros-Parada W; Bergmann J;
Address:"Instituto de Quimica, Facultad de Ciencias, Pontificia Universidad Catolica de Valparaiso, Valparaiso, Chile. Nucleo de Quimica y Bioquimica, Facultad de Estudios Interdisciplinarios, Universidad Mayor, Santiago, Chile. Escuela de Agronomia, Facultad de Ciencias Agronomicas y de los Alimentos, Pontificia Universidad Catolica de Valparaiso, Quillota, Chile"
Journal Title:PLoS One
Year:2019
Volume:20190423
Issue:4
Page Number:e0215769 -
DOI: 10.1371/journal.pone.0215769
ISSN/ISBN:1932-6203 (Electronic) 1932-6203 (Linking)
Abstract:"The main pheromone compound of Chilecomadia valdiviana (Lepidoptera: Cossidae) has been recently identified as (7Z,10Z)-7,10-hexadecadienal. The biosynthesis of this pheromone compound showing attributes of both Type I and Type II lepidopteran pheromones was studied by the topical application of isotope-labeled fatty acids to the pheromone gland and subsequent analysis of the gland contents (pheromone compounds and fatty acyl compounds) by gas chromatography-mass spectrometry. The deuterium label of D11-linoleic acid was incorporated into the pheromone compound and its putative acyl precursor (7Z,10Z)-7,10-hexadecadienoate, demonstrating that the pheromone compound is biosynthesized from linoleic acid by chain-shortening and further functional group transformation. Furthermore, the deuterium label of D3-stearic acid was also incorporated into the pheromone compound, which indicates that the pheromone can be synthesized de novo by C. valdiviana, as is the case for Type I lepidopteran pheromone compounds"
Keywords:Alkadienes/*metabolism Animals Female Linoleic Acid/*metabolism Moths/*metabolism Scent Glands/metabolism Sex Attractants/*biosynthesis Stearic Acids/*metabolism;
Notes:"MedlineHerrera, Heidy Barros-Parada, Wilson Bergmann, Jan eng Research Support, Non-U.S. Gov't 2019/04/24 PLoS One. 2019 Apr 23; 14(4):e0215769. doi: 10.1371/journal.pone.0215769. eCollection 2019"

 
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 27-12-2024