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 AbstractReference samples guide variable selection for correlation of wine sensory and volatile profiling data    Next AbstractProduction of a Mating Inhibitor by Ustilago hordei »

Biochemistry


Title:Synthesis and biological activity of fluorescent yeast pheromones
Author(s):Sherrill C; Khouri O; Zeman S; Roise D;
Address:"Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla 92093-0506"
Journal Title:Biochemistry
Year:1995
Volume:34
Issue:11
Page Number:3553 - 3560
DOI: 10.1021/bi00011a009
ISSN/ISBN:0006-2960 (Print) 0006-2960 (Linking)
Abstract:"The mating pheromones of Saccharomyces cerevisiae and derivatives of these pheromones have been synthesized and tested for biological activity in a solution-phase assay. The effects of native alpha-factor and a-factor on the growth of target cells in these assays were identical. A derivative of alpha-factor in which the amino terminus was modified with the fluorescent probe, 6-amino-N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)hexanoyl, was only slightly less active than the unmodified pheromone. Derivatives of a-factor that contain various alkyl groups in place of the farnesyl moiety of the native pheromone were also synthesized and tested for biological activity. A derivative in which the farnesyl moiety is substituted with an unbranched decyl group exhibited activity identical to that of the natural pheromone, whereas a derivative that contains an unbranched pentyl group exhibited significantly lower biological activity than native a-factor. The derivatives of a-factor have in addition been modified to incorporate 6-amino-N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) at the terminus of the alkyl chains. A derivative with the probe attached to a decyl chain displayed activity similar to that of the native pheromone, whereas the same modification on a pentyl chain produced a derivative with very low activity. The fluorescence spectra of the modified alpha-factor and a-factors were measured in methanol, aqueous solution, and aqueous solution containing phospholipid vesicles. The fluorescence of the probes depends on the environment of the pheromones and can be used to monitor the association of the pheromones with the lipid bilayer"
Keywords:"Amino Acid Sequence Cell Cycle/drug effects Fluorescent Dyes/chemistry Mating Factor Molecular Sequence Data Peptides/*chemical synthesis/pharmacology Pheromones/*chemical synthesis/pharmacology Saccharomyces cerevisiae/*chemistry/cytology Spectrometry, F;"
Notes:"MedlineSherrill, C Khouri, O Zeman, S Roise, D eng NCRR BRTP 01614/RR/NCRR NIH HHS/ NCRR BRTP 04112/RR/NCRR NIH HHS/ T32 GM07313/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 1995/03/21 Biochemistry. 1995 Mar 21; 34(11):3553-60. doi: 10.1021/bi00011a009"

 
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 26-12-2024