Spermidine treatment to rice seedlings recovers salinity stress-induced damage of plasma membrane and PM-bound H+-ATPase in salt-tolerant and salt-sensitive rice cultivars

被引:118
作者
Roy, P [1 ]
Niyogi, K [1 ]
SenGupta, DN [1 ]
Ghosh, B [1 ]
机构
[1] Bose Inst, Dept Bot, Kolkata 700009, W Bengal, India
关键词
plasma membrane; H+-ATPase; antibody; western blot; polyamine; Oryza sativa; NaCl stress;
D O I
10.1016/j.plantsci.2004.08.014
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
Due to their polycationic nature, Spermidine (Spd(3+)) and Spermine (SPM4+) are known to interact with polyanionic compounds, e.g. negatively charged head group of phospholipid membrane components, thereby stabilizing salinity stress-induced damage of plasma membrane (PM). But to what extent polyamine-mediated restoration of activities of PM-bound enzymes occurs and differs within salt-sensitive and salt-tolerant rice cultivars is totally unknown. Therefore, PM was isolated from the roots of 3-day-old rice seedlings from two salt-tolerant (Nonabokra and Pokkali) and two salt-sensitive (M-1-48 and IR8) cultivars treated with none (control) or with NaCl (150 mM, 16 h) alone or with Spd (I mM, 16 h). Vanadium sensitive but K+ stimulated H+-ATPase activity from equal amount of PM was measured by estimating released Pi. Results showed that nine-fold higher level of H+-ATPase (100% vanadium sensitive) was detected from PM of Nonabokra roots in comparison to M-1-48 roots. Salinity stress alone to the seedlings significantly reduces the activity of PM-bound H(+-)ATPase. The activity of H+-ATPase was restored to some extent in the roots treated with NaCl stress in presence of I mM Spd. Analysis of PM-bound polyamine from untreated control roots showed only Putrescine from M-1-48 and IR8 cultivars, whereas roots of salt-tolerant plants, Nonabokra and Pokkali, have only Spermidine and Spermine. PM-bound H+-ATPase activity of control and treated plants, when measured by NADH oxidation (coupled reaction), 2.5-3.0-fold higher activity was detected from salt-tolerant cultivars. Salinity stress to the plants severely inhibits H+-ATPase activity and Spermidine co-treatment significantly recovers its activity in all four cultivars. Western Blot with equal amount of 5% SDS extracted protein from roots when analyzed by the polyclonal antibody raised against H+-ATPase (PM-bound) of Arabidopsis thaliana showed NaCl stress-induced decrease and Spermidine-induced recovery of 100 kDa polypeptide (known MW of 100 kDa H+-ATPase from rice). These results clearly demonstrate for the first time that the deficit of salt-sensitive rice cultivars, e.g. high accumulation of Na+, loss of K+ ion, salinity stress-induced sharp inhibition of PM-bound H+-ATPase activity, could be overcome by supplying Spermidine exogenously. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:583 / 591
页数:9
相关论文
共 36 条
[1]  
Ames B. N., 1966, METHOD ENZYMOL, V8, P115, DOI DOI 10.1016/0076-6879(66)08014-5
[2]   POLYAMINES IN VARIOUS RICE (ORYZA-SATIVA) GENOTYPES WITH RESPECT TO SODIUM-CHLORIDE SALINITY [J].
BASU, R ;
GHOSH, B .
PHYSIOLOGIA PLANTARUM, 1991, 82 (04) :575-581
[3]  
BESFORD RT, 1993, PLANTA, V189, P201, DOI 10.1007/BF00195077
[4]   ADAPTATIONS TO ENVIRONMENTAL STRESSES [J].
BOHNERT, HJ ;
NELSON, DE ;
JENSEN, RG .
PLANT CELL, 1995, 7 (07) :1099-1111
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   MOLECULAR RESPONSES TO WATER-DEFICIT [J].
BRAY, EA .
PLANT PHYSIOLOGY, 1993, 103 (04) :1035-1040
[7]   HOW DOES THE PLANT PLASMA-MEMBRANE H+-ATPASE PUMP PROTONS [J].
BRISKIN, DP ;
HANSON, JB .
JOURNAL OF EXPERIMENTAL BOTANY, 1992, 43 (248) :269-289
[8]  
BRISKIN DP, 1987, METHOD ENZYMOL, V148, P543
[9]   Protective role of exogenous polyamines on salinity-stressed rice (Oryza sativa) plants [J].
Chattopadhayay, MK ;
Tiwari, BS ;
Chattopadhyay, G ;
Bose, A ;
Sengupta, DN ;
Ghosh, B .
PHYSIOLOGIA PLANTARUM, 2002, 116 (02) :192-199
[10]   Expression of arginine decarboxylase in seedlings of indica rice (Oryza sativa L) cultivars as affected by salinity stress [J].
Chattopadhyay, MK ;
Gupta, S ;
Sengupta, DN ;
Ghosh, B .
PLANT MOLECULAR BIOLOGY, 1997, 34 (03) :477-483