Coronalon:: a powerful tool in plant stress physiology

被引:81
作者
Schüler, G
Mithöfer, A
Baldwin, IT
Berger, S
Ebel, J
Santos, JG
Herrmann, G
Hölscher, D
Kramell, R
Kutchan, TM
Maucher, H
Schneider, B
Stenzel, I
Wasternack, C
Boland, W
机构
[1] Max Planck Inst Chem Okol, D-07745 Jena, Germany
[2] Inst Biochem Pflanzen, D-06120 Halle An Der Saale, Germany
[3] Univ Munich, Dept Biol 1, D-80638 Munich, Germany
关键词
coronalon; indanoyl isoleucine conjugate; octadecanoid; plant stress response;
D O I
10.1016/S0014-5793(04)00239-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Coronalon, a synthetic 6-ethyl indanoyl isoleucine conjugate, has been designed as a highly active mimic of octa-decanoid phytohormones that are involved in insect and disease resistance. The spectrum of biological activities that is affected by coronalon was investigated in nine different plant systems specifically responding to jasmonates and/or 12-oxo-phytodienoic acid. In all bioassays analyzed, coronalon demonstrated a general strong activity at low micromolar concentrations. The results obtained showed the induction of (i) defense-related secondary metabolite accumulation in both cell cultures and plant tissues, (ii) specific abiotic and biotic stress-related gene expression, and (iii) root growth retardation. The general activity of coronalon in the induction of plant stress responses together with its simple and efficient synthesis suggests that this compound might serve as a valuable tool in the examination of various aspects in plant stress physiology. Moreover, coronalon might become employed in agriculture to elicit plant resistance against various aggressors. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 39 条
[1]   CONSTRAINTS ON AN INDUCED DEFENSE - THE ROLE OF LEAF-AREA [J].
BALDWIN, IT ;
SCHMELZ, EA .
OECOLOGIA, 1994, 97 (03) :424-430
[2]   Quantification, correlations and manipulations of wound-induced changes in jasmonic acid and nicotine in Nicotiana sylvestris [J].
Baldwin, IT ;
Zhang, ZP ;
Diab, N ;
Ohnmeiss, TE ;
McCloud, ES ;
Lynds, GY ;
Schmelz, EA .
PLANTA, 1997, 201 (04) :397-404
[3]   Two methyl jasmonate-insensitive mutants show altered expression of AtVsp in response to methyl jasmonate and wounding [J].
Berger, S ;
Bell, E ;
Mullet, JE .
PLANT PHYSIOLOGY, 1996, 111 (02) :525-531
[4]   A phytoalexin from roots of Musa acuminata var Pisang sipulu [J].
Binks, RH ;
Greenham, JR ;
Luis, JG ;
Gowen, SR .
PHYTOCHEMISTRY, 1997, 45 (01) :47-49
[5]   Impact of phyto-oxylipins in plant defense [J].
Blée, E .
TRENDS IN PLANT SCIENCE, 2002, 7 (07) :315-321
[6]   JASMONIC ACID AND CORONATIN INDUCE ODOR PRODUCTION IN PLANTS [J].
BOLAND, W ;
HOPKE, J ;
DONATH, J ;
NUSKE, J ;
BUBLITZ, F .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1995, 34 (15) :1600-1602
[7]   Biosynthesis and action of jasmonates in plants [J].
Creelman, RA ;
Mullet, JE .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1997, 48 :355-381
[8]  
Ebel J, 1998, BIOESSAYS, V20, P569, DOI 10.1002/(SICI)1521-1878(199807)20:7&lt
[9]  
569::AID-BIES8&gt
[10]  
3.0.CO