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 AbstractDifferentiation of algal chemoreceptors. A comparative receptor study with two seaweed pairs: Cutleria multifida/Syringoderma phinneyi and Desmarestia aculeata/Ectocarpus siliculosus (Phacophyceae)    Next Abstract"The chemistry of gamete attraction: chemical structures, biosynthesis, and (a)biotic degradation of algal pheromones" »

Eur J Biochem


Title:Biosynthesis of algal pheromones. A model study with the composite Senecio isatideus
Author(s):Boland W; Mertes K;
Address:
Journal Title:Eur J Biochem
Year:1985
Volume:147
Issue:1
Page Number:83 - 91
DOI: 10.1111/j.1432-1033.1985.tb08722.x
ISSN/ISBN:0014-2956 (Print) 0014-2956 (Linking)
Abstract:"Several cyclic and alicyclic C11 hydrocarbons have been shown to act as gamete releasing and/or attracting pheromones during sexual reproduction of brown algae (Phaeophyceae). The same compounds are also found in the essential oils of various plants, of which the occurrence of the cycloheptadiene-pheromone ectocarpene in Senecio isatideus (Compositae) is noteworthy. Administration of [3H]dodeca-3,6,9-trienoic acid to cuttings of this plant leads to incorporation of radioactivity into ectocarpene. Double-bond-deuterated nona-3,6-dienoic acid is converted to fucoserratene, the pheromone of several Fucales, which is certainly not present among the hydrocarbons of Senecio. This proves that the pool of medium-chain, multiply unsaturated fatty acids includes precursors of all types of highly unsaturated hydrocarbons. Appropriately labelled (deuterium markers) fatty acid homologues were synthesized and applied to Senecio plantlets to unravel the mechanistic aspects. The results strongly suggest radical initiation of the pheromone biosynthesis by abstraction of a single hydrogen from a 1,4-pentadienyl segment of the fatty acid followed by oxidation to the corresponding cation. This causes fragmentation of the reactive intermediate into an olefine and carbon dioxide by neighbouring-group participation of the flanking double bonds. A tentative biosynthetic scheme is deduced from the experimental results which also sets the stereochemistry of the algal pheromones into a uniform mechanistic concept"
Keywords:"Animals Chemical Phenomena Chemistry Chromatography, Gas Cycloheptanes/biosynthesis Deuterium Eukaryota/*metabolism Fatty Acids/metabolism Hydrocarbons/analysis Lipid Metabolism Mass Spectrometry Phaeophyta/*metabolism Pheromones/*biosynthesis *Plants, To;"
Notes:"MedlineBoland, W Mertes, K eng Research Support, Non-U.S. Gov't England 1985/02/15 Eur J Biochem. 1985 Feb 15; 147(1):83-91. doi: 10.1111/j.1432-1033.1985.tb08722.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 16-11-2024