Benzothiadiazole, an inducer of plant defenses, inhibits catalase and ascorbate peroxidase

被引:98
作者
Wendehenne, D
Durner, J
Chen, ZX
Klessig, DF
机构
[1] Rutgers State Univ, Waksman Inst, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Dept Mol Biol & Biochem, Piscataway, NJ 08854 USA
[3] Univ Idaho, Dept Microbiol Mol Biol & Biochem, Moscow, ID 83844 USA
基金
美国国家科学基金会;
关键词
Nicotiana tabacum; Solanaceae; benzothiadiazole; salicylic acid; catalase; ascorbate peroxidase; defense genes;
D O I
10.1016/S0031-9422(97)00604-3
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
Benzothiadiazole (BTH) is a recently described synthetic inducer of plant defenses. Molecular and genetic studies have suggested that it acts as a functional analogue of the endogenous defense signalling molecule salicylic acid (SA). Here we demonstrate that BTH inhibits catalase and ascorbate peroxidase, two potential targets through which SA has been proposed to act. BTH was found to be a considerably better inhibitor of catalase than SA. This is consistent with its greater potency for inducing the expression of defense-related genes, such as the acidic PR-I, PR-2 and PR-3 genes. In addition, induction of PR-I gene expression by either BTH or SA was suppressed by antioxidants. These results suggest that changes in H2O2 levels or the cellular redox status may be involved in the BTH/SA-mediated activation of certain defense responses. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:651 / 657
页数:7
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