Involvement of superoxide generation in salicylic acid-induced stomatal closure in Vicia faba

被引:137
|
作者
Mori, IC
Pinontoan, R
Kawano, T
Muto, S [1 ]
机构
[1] Nagoya Univ, Biosci Ctr, Chikusa Ku, Nagoya, Aichi 4648601, Japan
[2] Nagoya Univ, Grad Sch Bioagr Sci, Chikusa Ku, Nagoya, Aichi 4648601, Japan
基金
日本学术振兴会;
关键词
peroxidase; salicylic acid; stomatal closure; superoxide anion; Vicia faba;
D O I
10.1093/pcp/pce176
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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(radical anion)). The SA-induced generation of chemiluminescence was suppressed by O-2(radical anion)-specific scavengers superoxide dismutase (SOD) and 4,5-dihydroxy-1,3-benzenedisulfonic acid (Tiron). These results suggest that O-2(radical anion) 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(radical anion) 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.
引用
收藏
页码:1383 / 1388
页数:6
相关论文
共 50 条
  • [41] Nitric oxide, actin reorganization and vacuoles change are involved in PEG 6000-induced stomatal closure in Vicia faba
    Huang, Ai-Xia
    She, Xiao-Ping
    Cao, Bin
    Zhang, Bei
    Mu, Juan
    Zhang, Shao-Jie
    PHYSIOLOGIA PLANTARUM, 2009, 136 (01) : 45 - 56
  • [42] Inhibition of dark-induced stomatal closure by fusicoccin involves a removal of hydrogen peroxide in guard cells of Vicia faba
    She, Xiao-Ping
    Huang, Ai-Xia
    Li, Jin
    Han, Xi-Zhu
    PHYSIOLOGIA PLANTARUM, 2010, 140 (03) : 258 - 268
  • [43] Hydrogen sulfide may function downstream of hydrogen peroxide in salt stress-induced stomatal closure in Vicia faba
    Ma, Yinli
    Zhang, Wei
    Niu, Jiao
    Ren, Yu
    Zhang, Fan
    FUNCTIONAL PLANT BIOLOGY, 2019, 46 (02) : 136 - 145
  • [44] Gels and gelled emulsions prepared by acid-induced gelation of mixtures of faba bean (Vicia faba) protein concentrate and λ-carrageenan
    Dille, Morten J.
    Knutsen, Svein H.
    Draget, Kurt I.
    APPLIED FOOD RESEARCH, 2022, 2 (02):
  • [45] PHOSPHATIDIC ACID-INDUCED SUPEROXIDE GENERATION IN ELECTROPERMEABILIZED HUMAN NEUTROPHILS
    TAMURA, M
    OGATA, K
    TAKESHITA, M
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 305 (02) : 477 - 482
  • [46] Protein tyrosine phosphatases mediate the signaling pathway of stomatal closure of Vicia faba L.
    Shi, WL
    Liu, X
    Jia, WS
    Zhang, SQ
    JOURNAL OF INTEGRATIVE PLANT BIOLOGY, 2005, 47 (03) : 319 - 326
  • [47] EFFECT OF ABSCISIC-ACID PRETREATMENTS ON STOMATAL REOPENING IN VICIA-FABA
    WARDLE, K
    DOBBS, EB
    SHORT, KC
    PHYSIOLOGIA PLANTARUM, 1982, 56 (03) : 312 - 316
  • [48] The involvement of a P38-like MAP kinase in ABA-induced and H2O2-mediated stomatal closure in Vicia faba L
    Jiang, Jing
    Wang, Pengtao
    An, Guoyong
    Wang, Pengcheng
    Song, Chun-Peng
    PLANT CELL REPORTS, 2008, 27 (02) : 377 - 385
  • [49] Hydrogen Sulfide May Function Downstream of Nitric Oxide in Ethylene-Induced Stomatal Closure in Vicia faba L.
    LIU Jing
    HOU Zhi-hui
    LIU Guo-hua
    HOU Li-xia
    LIU Xin
    JournalofIntegrativeAgriculture, 2012, 11 (10) : 1644 - 1653
  • [50] Inhibition of darkness-induced stomatal closure by ethylene involves a removal of hydrogen peroxide from guard cells of Vicia faba
    Song, X. G.
    She, X. P.
    Wang, J.
    RUSSIAN JOURNAL OF PLANT PHYSIOLOGY, 2012, 59 (03) : 372 - 380