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 and synthesis of a female-produced sex pheromone for the cerambycid beetle Prionus californicus    Next AbstractAnaerobic rotating disc batch reactor nutrient removal process enhanced by volatile fatty acid addition »

J Chem Ecol


Title:Determination of the relative and absolute configurations of the female-produced sex pheromone of the cerambycid beetle Prionus californicus
Author(s):Rodstein J; Millar JG; Barbour JD; McElfresh JS; Wright IM; Barbour KS; Ray AM; Hanks LM;
Address:"Department of Chemistry, University of California, Riverside, CA 92521, USA"
Journal Title:J Chem Ecol
Year:2011
Volume:20101203
Issue:1
Page Number:114 - 124
DOI: 10.1007/s10886-010-9890-3
ISSN/ISBN:1573-1561 (Electronic) 0098-0331 (Print) 0098-0331 (Linking)
Abstract:"We previously identified the basic structure of the female-produced sex attractant pheromone of the cerambycid beetle, Prionus californicus Motschulsky (Cerambycidae: Prioninae), as 3,5-dimethyldodecanoic acid. A synthesized mixture of the four stereoisomers of 3,5-dimethyldodecanoic acid was highly attractive to male beetles. Here, we describe stereoselective syntheses of three of the four possible stereoisomers, and the results of laboratory and field bioassays showing that male beetles are attracted specifically to (3R,5S)-3,5-dimethyldodecanoic acid, but not to its enantiomer, (3S,5R)-3,5-dimethyldodecanoic acid, indicating that the (3R,5S)-enantiomer is the active pheromone component. The diastereomeric (3R,5R)- and (3S,5S)-enantiomers were excluded from consideration because their gas chromatographic retention times were different from that of the insect-produced compound. The mixture of the four stereoisomers of 3,5-dimethyldodecanoic acid was as attractive to male P. californicus as the (3R,5S)-enantiomer, indicating that none of the other three stereoisomers inhibited responses to the active enantiomer. Beetles responded to as little as 10 ng and 10 mug of synthetic 3,5-dimethyldodecanoic acid in laboratory and field studies, respectively. Field studies indicated that capture rate did not increase with dosages of 3,5-dimethyldodecanoic acid greater than 100 mug. In field bioassays, males of a congeneric species, P. lecontei Lameere, were captured in southern California but not in Idaho"
Keywords:Animals Coleoptera/*chemistry Female Gas Chromatography-Mass Spectrometry Magnetic Resonance Spectroscopy Male Sex Attractants/biosynthesis/*chemistry Stereoisomerism;
Notes:"MedlineRodstein, Joshua Millar, Jocelyn G Barbour, James D McElfresh, J Steven Wright, Ian M Barbour, Karen S Ray, Ann M Hanks, Lawrence M eng Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. 2010/12/04 J Chem Ecol. 2011 Jan; 37(1):114-24. doi: 10.1007/s10886-010-9890-3. Epub 2010 Dec 3"

 
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 16-11-2024