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 AbstractThe GTP hydrolysis defect of the Saccharomyces cerevisiae mutant G-protein Gpa1(G50V)    Next AbstractAnalysis of rainbow trout Oncorhynchus mykiss epidermal mucus and evaluation of semiochemical activity for polar filament discharge in Myxobolus cerebralis actinospores »

Plant Physiol


Title:"Nicotiana attenuata SIPK, WIPK, NPR1, and fatty acid-amino acid conjugates participate in the induction of jasmonic acid biosynthesis by affecting early enzymatic steps in the pathway"
Author(s):Kallenbach M; Alagna F; Baldwin IT; Bonaventure G;
Address:"Max Planck Institute for Chemical Ecology, Department of Molecular Ecology, Jena 07745, Germany"
Journal Title:Plant Physiol
Year:2010
Volume:20091106
Issue:1
Page Number:96 - 106
DOI: 10.1104/pp.109.149013
ISSN/ISBN:1532-2548 (Electronic) 0032-0889 (Print) 0032-0889 (Linking)
Abstract:"Wounding and herbivore attack elicit the rapid (within minutes) accumulation of jasmonic acid (JA) that results from the activation of previously synthesized biosynthetic enzymes. Recently, several regulatory factors that affect JA production have been identified; however, how these regulators affect JA biosynthesis remains at present unknown. Here we demonstrate that Nicotiana attenuata salicylate-induced protein kinase (SIPK), wound-induced protein kinase (WIPK), nonexpressor of PR-1 (NPR1), and the insect elicitor N-linolenoyl-glutamate [corrected] (18:3-Glu) participate in mechanisms affecting early enzymatic steps of the JA biosynthesis pathway. Plants silenced in the expression of SIPK and NPR1 were affected in the initial accumulation of 13-hydroperoxy-linolenic acid (13-OOH-18:3) after wounding and 18:3-Glu elicitation by mechanisms independent of changes in 13-lipoxygenase activity. Moreover, 18:3-Glu elicited an enhanced and rapid accumulation of 13-OOH-18:3 that depended partially on SIPK and NPR1 but was independent of increased 13-lipoxygenase activity. Together, the results suggested that substrate supply for JA production was altered by 18:3-Glu elicitation and SIPK- and NPR1-mediated mechanisms. Consistent with a regulation at the level of substrate supply, we demonstrated by virus-induced gene silencing that a wound-repressed plastidial glycerolipase (NaGLA1) plays an essential role in the induction of de novo JA biosynthesis. In contrast to SIPK and NPR1, mechanisms mediated by WIPK did not affect the production of 13-OOH-18:3 but were critical to control the conversion of this precursor into 12-oxo-phytodienoic acid. These differences could be partially accounted for by reduced allene oxide synthase activity in WIPK-silenced plants"
Keywords:"Amino Acids/chemistry/*metabolism Cyclopentanes/*metabolism Fatty Acids/chemistry/genetics/*metabolism Gene Expression Regulation, Plant/physiology Gene Silencing Lipase/genetics/metabolism Oxylipins/*metabolism Plant Leaves/genetics/metabolism Plant Prot;"
Notes:"MedlineKallenbach, Mario Alagna, Fiammetta Baldwin, Ian Thomas Bonaventure, Gustavo eng Research Support, Non-U.S. Gov't 2009/11/10 Plant Physiol. 2010 Jan; 152(1):96-106. doi: 10.1104/pp.109.149013. Epub 2009 Nov 6"

 
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