Durner J, Klessig D F
Waksman Institute, Rutgers, State University of New Jersey, Piscataway 08855, USA.
Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11312-6. doi: 10.1073/pnas.92.24.11312.
In recent years, it has become apparent that salicylic acid (SA) plays an important role in plant defense responses to pathogen attack. Previous studies have suggested that one of SA's mechanisms of action is the inhibition of catalase, resulting in elevated levels of H2O2, which activate defense-related genes. Here we demonstrate that SA also inhibits ascorbate peroxoidase (APX), the other key enzyme for scavenging H2O2. The synthetic inducer of defense responses, 2,6-dichloroisonicotinic acid (INA), was also found to be an effective inhibitor of APX. In the presence of 750 microM ascorbic acid (AsA), substrate-dependent IC50 values of 78 microM and 95 microM were obtained for SA and INA, respectively. Furthermore, the ability of SA analogues to block APX activity correlated with their ability to induce defense-related genes in tobacco and enhance resistance to tobacco mosaic virus. Inhibition of APX by SA appears to be reversible, thus differing from the time-dependent, irreversible inactivation by suicide substrates such as p-aminophenol. In contrast to APX, the guaiacol-utilizing peroxidases, which participate in the synthesis and crosslinking of cell wall components as part of the defense response, are not inhibited by SA or INA. The inhibition of both catalase and APX, but not guaiacol peroxidases, supports the hypothesis that SA-induced defense responses are mediated, in part, through elevated H2O2 levels or coupled perturbations of the cellular redox state.
近年来,水杨酸(SA)在植物对病原体攻击的防御反应中发挥重要作用已变得显而易见。先前的研究表明,SA的作用机制之一是抑制过氧化氢酶,导致过氧化氢(H2O2)水平升高,从而激活与防御相关的基因。在此我们证明,SA还抑制抗坏血酸过氧化物酶(APX),这是另一种清除H2O2的关键酶。防御反应的合成诱导剂2,6-二氯异烟酸(INA)也被发现是APX的有效抑制剂。在存在750微摩尔抗坏血酸(AsA)的情况下,SA和INA的底物依赖性半数抑制浓度(IC50)值分别为78微摩尔和95微摩尔。此外,SA类似物阻断APX活性的能力与其在烟草中诱导防御相关基因以及增强对烟草花叶病毒抗性的能力相关。SA对APX的抑制作用似乎是可逆的,因此不同于对氨基酚等自杀底物的时间依赖性、不可逆失活。与APX不同,参与细胞壁成分合成和交联作为防御反应一部分的利用愈创木酚的过氧化物酶不受SA或INA的抑制。过氧化氢酶和APX均被抑制,而愈创木酚过氧化物酶未被抑制,这支持了SA诱导的防御反应部分通过升高的H2O2水平或细胞氧化还原状态的相关扰动介导的假说。