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 Abstract"Caste-specific expression patterns of immune response and chemosensory related genes in the leaf-cutting ant, Atta vollenweideri"    Next AbstractA novel bacterial sulfur oxidation pathway provides a new link between the cycles of organic and inorganic sulfur compounds »

Plant Physiol


Title:Differential induction of plant volatile biosynthesis in the lima bean by early and late intermediates of the octadecanoid-signaling pathway
Author(s):Koch T; Krumm T; Jung V; Engelberth J; Boland W;
Address:"Max Planck Institute for Chemical Ecology, Tatzendpromenade 1a, 07745 Jena, Germany"
Journal Title:Plant Physiol
Year:1999
Volume:121
Issue:1
Page Number:153 - 162
DOI: 10.1104/pp.121.1.153
ISSN/ISBN:0032-0889 (Print) 1532-2548 (Electronic) 0032-0889 (Linking)
Abstract:"Plants are able to respond to herbivore damage with de novo biosynthesis of an herbivore-characteristic blend of volatiles. The signal transduction initiating volatile biosynthesis may involve the activation of the octadecanoid pathway, as exemplified by the transient increase of endogenous jasmonic acid (JA) in leaves of lima bean (Phaseolus lunatus) after treatment with the macromolecular elicitor cellulysin. Within this pathway lima bean possesses at least two different biologically active signals that trigger different biosynthetic activities. Early intermediates of the pathway, especially 12-oxo-phytodienoic acid (PDA), are able to induce the biosynthesis of the diterpenoid-derived 4,8, 12-trimethyltrideca-1,3,7,11-tetraene. High concentrations of PDA result in more complex patterns of additional volatiles. JA, the last compound in the sequence, lacks the ability to induce diterpenoid-derived compounds, but is highly effective at triggering the biosynthesis of other volatiles. The phytotoxin coronatine and amino acid conjugates of linolenic acid (e.g. linolenoyl-L-glutamine) mimic the action of PDA, but coronatine does not increase the level of endogenous JA. The structural analog of coronatine, the isoleucine conjugate of 1-oxo-indanoyl-4-carboxylic acid, effectively mimics the action of JA, but does not increase the level of endogenous JA. The differential induction of volatiles resembles previous findings on signal transduction in mechanically stimulated tendrils of Bryonia dioica"
Keywords:"Amino Acids/metabolism/pharmacology Cellulase/pharmacology Cucurbitaceae Cyclopentanes/antagonists & inhibitors/metabolism/pharmacology Fabaceae/drug effects/*metabolism Fatty Acids, Unsaturated/antagonists & inhibitors/metabolism/pharmacology Indenes/pha;"
Notes:"MedlineKoch, T Krumm, T Jung, V Engelberth, J Boland, W eng Comparative Study Research Support, Non-U.S. Gov't 1999/09/11 Plant Physiol. 1999 Sep; 121(1):153-62. doi: 10.1104/pp.121.1.153"

 
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 22-11-2024