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 AbstractDetailed chemical analysis of regional-scale air pollution in western Portugal using an adapted version of MCM v3.1    Next Abstract"Design and Synthesis of Fluorophore-Tagged Disparlure Enantiomers to Study Pheromone Enantiomer Discrimination in the Pheromone-Binding Proteins from the Gypsy Moth, Lymantria dispar" »

Biochemistry


Title:Cryptoregiochemistry of the delta11-myristoyl-CoA desaturase involved in the biosynthesis of Spodoptera littoralis sex pheromone
Author(s):Pinilla A; Camps F; Fabrias G;
Address:"Department of Biological Organic Chemistry, IIQAB-CSIC, Barcelona, Spain"
Journal Title:Biochemistry
Year:1999
Volume:38
Issue:46
Page Number:15272 - 15277
DOI: 10.1021/bi990972n
ISSN/ISBN:0006-2960 (Print) 0006-2960 (Linking)
Abstract:"Many moth species biosynthesize their sex pheromones by the action of unique desaturases. These membrane-bound family of enzymes are especially interesting, since some of them produce (E)-unsaturated fatty acids either exclusively or along with the (Z)-isomer. In this article we present the first mechanistic study on one of these enzymes, namely, the Delta11-myristoyl-CoA desaturase of the moth Spodoptera littoralis. Intermolecular primary isotope effect determinations were performed in competition experiments. The unusual use of odd-number fatty acids, tridecanoic acid and deuterium-labeled tridecanoic acid, in these experiments showed the existence of a large isotope effect for the carbon-hydrogen bond cleavage at C11, but no isotope discrimination occurred in the removal of C12-H. The results of the competitive experiments are consistent with the hypothesis that this Delta11-desaturase involves a first slow, isotope-sensitive C11-H bond cleavage, with probable formation of an unstable intermediate, followed by a second fast C12-H bond removal. We suggest that a single enzyme may be responsible for the formation of both (Z)- and (E)-11-tetradecenoic acids by accommodating both gauche and anti conformers of the substrate, respectively. It is also possible that two mechanistically identical discrete enzymes are involved in each desaturation. In this case, the geometry of the resulting double bond would result from the different conformation adopted by the acyl substrate at each enzyme active site"
Keywords:Animals Deuterium/chemistry Fatty Acid Desaturases/*chemistry/metabolism Female Gas Chromatography-Mass Spectrometry Molecular Conformation Myristic Acid/*chemistry/metabolism Sex Attractants/*biosynthesis/chemistry/metabolism Spodoptera/*enzymology Stere;
Notes:"MedlinePinilla, A Camps, F Fabrias, G eng Research Support, Non-U.S. Gov't 1999/11/24 Biochemistry. 1999 Nov 16; 38(46):15272-7. doi: 10.1021/bi990972n"

 
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