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 AbstractAmbient volatile organic compound (VOC) concentrations around a petrochemical complex and a petroleum refinery    Next Abstract"GPCR-Galpha protein precoupling: Interaction between Ste2p, a yeast GPCR, and Gpa1p, its Galpha protein, is formed before ligand binding via the Ste2p C-terminal domain and the Gpa1p N-terminal domain" »

Analyst


Title:In situ lipid profiling of insect pheromone glands by direct analysis in real time mass spectrometry
Author(s):Cetraro N; Yew JY;
Address:"Pacific Biosciences Research Center, School of Environment and Ocean Science Technology, University of Hawai'i at Manoa, 1993 East West Road, Honolulu, HI 96822, USA. jyew@hawaii.edu. Molecular Bioscience and Bio-Engineering, College of Tropical Agriculture and Human Resources, University of Hawai'i at Manoa, 1955 East West Road, Honolulu, HI 96822"
Journal Title:Analyst
Year:2022
Volume:20220712
Issue:14
Page Number:3276 - 3284
DOI: 10.1039/d2an00840h
ISSN/ISBN:1364-5528 (Electronic) 0003-2654 (Print) 0003-2654 (Linking)
Abstract:"Lipid pheromones play a significant role in the behavior and ecology of many insects. The characterization of pheromone structures is a significant challenge due to their low abundance and ephemeral nature. Here we present a method for the analysis of lipid molecules from single pheromone glands of Drosophila melanogaster (fruit fly) using Direct Analysis in Real Time mass spectrometry (DART MS). Our results reveal that DART MS analysis of single tissues generates reproducible, species-specific lipid profiles comprised of fatty acids, wax esters, diacylglycerides and triacylglycerides. In addition, the ion source temperature and application of a solvent wash can cause significant qualitative and quantitative changes in the mass spectral profile. Lastly, we show that untargeted chemical fingerprinting of the gland can be used to accurately categorize species according to phylogenetic subgroup or genotype. Collectively, our findings indicate that DART MS is a rapid and powerful method for characterizing a broad range of lipids in tissues with minimal preparation. The application of direct tissue DART MS will expand the 'secretome' of molecules produced by pheromone glands. In addition to its direct relevance to chemical ecology, the method could potentially be used in pharmaceutical studies for the screening and detection of tissue-specific drug metabolites"
Keywords:Animals Drosophila *Drosophila melanogaster/metabolism *Insecta/metabolism Lipids Mass Spectrometry/methods Pheromones/metabolism Phylogeny;
Notes:"MedlineCetraro, Nicolas Yew, Joanne Y eng P20 GM125508/GM/NIGMS NIH HHS/ England 2022/06/18 Analyst. 2022 Jul 12; 147(14):3276-3284. doi: 10.1039/d2an00840h"

 
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