Mori I C, Pinontoan R, Kawano T, Muto S
Nagoya University Bioscience Center, Chikusa-ku, Nagoya, 464-8601 Japan.
Plant Cell Physiol. 2001 Dec;42(12):1383-8. doi: 10.1093/pcp/pce176.
Salicylic acid (SA), the known mediator of systemic acquired resistance, induced stomatal closure of Vicia faba L. Application of SA to the epidermal peels evoked an elevation of chemiluminescence of Cripridina lucigenin-derived chemiluminescent reagent (CLA) which is sensitive to superoxide anion (O(2)(.-)). The SA-induced generation of chemiluminescence was suppressed by O(2)(.-)-specific scavengers superoxide dismutase (SOD) and 4,5-dihydroxy-1,3-benzenedisulfonic acid (Tiron). These results suggest that O(2)(.-) was generated in epidermal peels by SA-treatment. A peroxidase inhibitor salicylhydroxamic acid (SHAM) inhibited guaiacol peroxidase activity and suppressed the SA-induced CLA chemiluminescence in the epidermal peels, suggesting that O(2)(.-) generation occurred by the peroxidase-catalyzed reaction as proposed for SA-treated tobacco cell suspension culture [Kawano et al. (1998) Plant Cell Physiol. 39: 721]. SOD, Tiron or SHAM suppressed the SA-induced stomatal closure. Moreover, application of superoxide-generating system also induced stomatal closure. These results support the concept of involvement of reactive oxygen species in signal transduction in SA-induced stomatal closure.
水杨酸(SA)是已知的系统获得性抗性介质,可诱导蚕豆气孔关闭。将SA施加于表皮组织可引起对超氧阴离子(O(2)(.-))敏感的光泽精衍生化学发光试剂(CLA)的化学发光增强。SA诱导的化学发光产生受到超氧阴离子特异性清除剂超氧化物歧化酶(SOD)和4,5-二羟基-1,3-苯二磺酸(Tiron)的抑制。这些结果表明,SA处理可在表皮组织中产生活性氧(O(2)(.-))。过氧化物酶抑制剂水杨羟肟酸(SHAM)抑制了愈创木酚过氧化物酶活性,并抑制了SA诱导的表皮组织CLA化学发光,这表明正如SA处理的烟草细胞悬浮培养所提出的那样,O(2)(.-)的产生是由过氧化物酶催化的反应引起的[Kawano等人(1998年)《植物细胞生理学》39:721]。SOD、Tiron或SHAM抑制了SA诱导的气孔关闭。此外,超氧产生系统的应用也诱导了气孔关闭。这些结果支持了活性氧参与SA诱导气孔关闭信号转导的概念。