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 AbstractFormaldehyde and TVOC emission behaviors according to finishing treatment with surface materials using 20 L chamber and FLEC    Next Abstract"The fission yeast GATA factor, Gaf1, modulates sexual development via direct down-regulation of ste11+ expression in response to nitrogen starvation" »

Anal Chem


Title:Development of a method to quantitate nematode pheromone for study of small-molecule metabolism in Caenorhabditis elegans
Author(s):Kim KY; Joo HJ; Kwon HW; Kim H; Hancock WS; Paik YK;
Address:"Department of Biochemistry, College of Life Sciences and Biotechnology, Yonsei Proteome Research Center, Yonsei University, Seoul, Korea"
Journal Title:Anal Chem
Year:2013
Volume:20130214
Issue:5
Page Number:2681 - 2688
DOI: 10.1021/ac4001964
ISSN/ISBN:1520-6882 (Electronic) 0003-2700 (Linking)
Abstract:"Pheromones produced by Caenorhabditis elegans are considered key regulators of development, mating, and social behaviors in this organism. Here, we present a rapid mass spectrometry-based method (PheroQu) for absolute quantitation of nematode pheromones (e.g., daumone 1, 2, and 3) both in C. elegans worm bodies (as few as 20 worms) and in liquid culture medium. Pheromones were separated by ultra performance liquid chromatography and monitored by a positive electrospray ionization detector in the multiple-reaction monitoring mode. The daf-22 mutant worms were used as surrogate matrix for calibration, and stable deuterated isotope-containing pheromone was used as internal standard for measuring changes in pheromones in N2 wild-type and other strains under different growth conditions. The worm-body pheromones were extracted by acidified acetonitrile solvent, and the secreted pheromones were extracted from culture medium with solid-phase extraction cartridges. The run time was achieved in less than 2 min. The method was validated for specificity, linearity, accuracy, precision, recovery, and stability. The assay was linear over an amount range of 2-250 fmol, and the limit of quantitation was 2 fmol amounts for daumone 1, 2, and 3 in both worm bodies and culture medium. With the PheroQu method, we were able to identify the location of pheromone biosynthesis and determine the changes in different pheromone types synthesized, according to developmental stages and aging process. This method, which is simple, rapid, sensitive, and specific, will be useful for the study of small-molecule metabolism during developmental stages of C. elegans"
Keywords:"Aging/metabolism Animals Caenorhabditis elegans/genetics/growth & development/*metabolism/physiology Chromatography, High Pressure Liquid Culture Media/metabolism Limit of Detection Mass Spectrometry/*methods Mutation Pheromones/biosynthesis/*chemistry/is;"
Notes:"MedlineKim, Kwang-Youl Joo, Hyoe-Jin Kwon, Hye-Won Kim, Heekyeong Hancock, William S Paik, Young-Ki eng Research Support, Non-U.S. Gov't 2013/01/26 Anal Chem. 2013 Mar 5; 85(5):2681-8. doi: 10.1021/ac4001964. Epub 2013 Feb 14"

 
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