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 AbstractMating pheromone-induced alteration of cell surface proteins in the heterobasidiomycetous yeast Tremella mesenterica    Next Abstract"Involvement of protein sulfhydryls in the trigger reaction of rhodotorucine A, a farnesyl peptide mating pheromone of Rhodosporidium toruloides" »

Eur J Biochem


Title:"Biosynthesis and secretion of tremerogen A-10, a polyisoprenyl peptide mating pheromone of Tremella mesenterica"
Author(s):Miyakawa T; Tabata M; Tsuchiya E; Fukui S;
Address:
Journal Title:Eur J Biochem
Year:1985
Volume:147
Issue:3
Page Number:489 - 493
DOI: 10.1111/j.0014-2956.1985.00489.x
ISSN/ISBN:0014-2956 (Print) 0014-2956 (Linking)
Abstract:"The biosynthetic pathway of tremerogen A-10, a polyisoprenyl peptide mating pheromone produced by mating type AB cells of the heterobasidiomycetous yeast Tremella mesenterica, was investigated by immunological techniques with antibody specific to the peptide moiety of the pheromone. Using the biological assay and the radioimmunoassay of the pheromone and its related substances, it was suggested that the peptide is synthesized near the end of logarithmic phase of growth with a temporary accumulation of precursors in the cell. The precursors initially appeared in membrane-bound form and were subsequently converted to soluble forms prior to the secretion. The pheromone acquired its biological activity during the secretion. In the presence of tunicamycin or compactin, pheromone production was blocked with accumulation of membrane-bound precursors. Monensin, however, blocked pheromone production with accumulation of soluble precursors. The molecular species which accumulated in the presence of the antibiotics were analyzed by immunoprecipitation followed by sodium dodecyl sulfate/urea/polyacrylamide gel electrophoresis. In the absence of the inhibitors, membrane-bound precursors with molecular masses of 28 kDa, 12 kDa, 7.8 kDa and 2.8 kDa were found. The precursors which accumulated in the presence of tunicamycin and compactin were the 12-kDa and 28-kDa species, respectively. The results suggested that membrane-bound very high-molecular-mass precursors were initially formed and their extensive modifications, including glycosylation, farnesylation and proteolytic digestion, occur in the membrane. Based on these data, a biosynthetic and secretory pathway was postulated"
Keywords:"Animals Anti-Bacterial Agents/pharmacology Antibody Specificity Basidiomycota/*metabolism Chemical Phenomena Chemical Precipitation Chemistry Electrophoresis, Polyacrylamide Gel Immunochemistry Mating Factor *Peptide Biosynthesis Peptides/metabolism Phero;"
Notes:"MedlineMiyakawa, T Tabata, M Tsuchiya, E Fukui, S eng Research Support, Non-U.S. Gov't England 1985/03/15 Eur J Biochem. 1985 Mar 15; 147(3):489-93. doi: 10.1111/j.0014-2956.1985.00489.x"

 
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 19-12-2024