Hydrogen peroxide is required for poly(phenolic) domain formation during wound-induced suberization

被引:69
作者
Razem, FA [1 ]
Bernards, MA [1 ]
机构
[1] Univ Western Ontario, Dept Plant Sci, London, ON N6A 5B7, Canada
关键词
Solanum tuberosum; Derivatization Followed by Reductive Cleavage (DFRC); diphenyleneiodonium; hydrogen peroxide; hydroxycinnamic acids; NADPH-dependent oxidase; poly(phenolic) domain; soluble phenolics; thioglycolic acid; wall-bound phenolics; wound-induced suberization;
D O I
10.1021/jf0110248
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The requirement for hydrogen peroxide (H2O2) during suberization was demonstrated ill wound-induced potato tubers by monitoring the extent of phenolic polymerization after the inhibition of H2O2 production using diphenyleneiodonium (DIPI). In DIPI-treated tissues the extent of phenolic polymerization in suberized tissues, measured using DFRC (Derivatization Followed by Reductive Cleavage) and thioglycolic acid analyses, was greatly reduced relative to untreated controls. Concomitantly, a large quantity of new soluble phenolics accumulated in the DPI-treated tissue some of which were not present in the controls. We suggest that the inhibition of H2O2 production prevented these phenolics from being oxidized by cell wall peroxidases. As a result, these phenolics were left unpolymerized and accumulated in the tissue. Several of the soluble phenolics were identified as hydroxycinnamic acid derivatives. From the data presented, it was concluded that H2O2 is required for the polymerization step in the formation of the poly(phenolic) domain of suberized potato tubers.
引用
收藏
页码:1009 / 1015
页数:7
相关论文
共 32 条
[21]   Glyceryl-acyl and aryl-acyl dimers in Pseudotsuga menziesii bark suberin [J].
Graça, J ;
Pereira, H .
HOLZFORSCHUNG, 1999, 53 (04) :397-402
[22]   rbohA a rice homologue of the mammalian gp91phox respiratory burst oxidase gene [J].
Groom, QJ ;
Torres, MA ;
FordhamSkelton, AP ;
HammondKosack, KE ;
Robinson, NJ ;
Jones, JDG .
PLANT JOURNAL, 1996, 10 (03) :515-522
[23]   BIO-POLYESTER MEMBRANES OF PLANTS - CUTIN AND SUBERIN [J].
KOLATTUKUDY, PE .
SCIENCE, 1980, 208 (4447) :990-1000
[24]   The oxidative burst in plant disease resistance [J].
Lamb, C ;
Dixon, RA .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1997, 48 :251-275
[25]  
Lewis NG., 1999, COMPREHENSIVE NATURA, P617
[26]   Derivatization followed by reductive cleavage (DFRC method), a new method for lignin analysis: Protocol for analysis of DFRC monomers [J].
Lu, FC ;
Ralph, J .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1997, 45 (07) :2590-2592
[27]   Differential deposition of suberin phenolic and aliphatic domains and their roles in resistance to infection during potato tuber (Solanum tuberosum L.) wound-healing [J].
Lulai, EC ;
Corsini, DL .
PHYSIOLOGICAL AND MOLECULAR PLANT PATHOLOGY, 1998, 53 (04) :209-222
[28]   Glycerol is a suberin monomer. New experimental evidence for an old hypothesis [J].
Moire, L ;
Schmutz, A ;
Buchala, A ;
Stark, RE ;
Ryser, U .
PLANT PHYSIOLOGY, 1999, 119 (03) :1137-1146
[29]   Ether-linked ferulic acid amides in natural and wound periderms of potato tuber [J].
Negrel, J ;
Pollet, B ;
Lapierre, C .
PHYTOCHEMISTRY, 1996, 43 (06) :1195-1199
[30]   Generation of superoxide anion and localization of CuZn-superoxide dismutase in the vascular tissue of spinach hypocotyls: Their association with lignification [J].
Ogawa, K ;
Kanematsu, S ;
Asada, K .
PLANT AND CELL PHYSIOLOGY, 1997, 38 (10) :1118-1126