JXB Advance Access published online on November 7, 2005
Journal of Experimental Botany, doi:10.1093/jxb/eri312
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Department of Plant Biology and Forest Genetics, Swedish University of Agricultural Sciences, Box 7080, SE 750 07 Uppsala, Sweden
* To whom correspondence should be addressed. In this study, the uptake of Na+ into the cytosol of rice (Oryza sativa L. cvs Pokkali and BRRI Dhan29) protoplasts was measured using the acetoxy methyl ester of the fluorescent sodium-binding benzofuran isopthalate, SBFI-AM, and fluorescence microscopy. By means of inhibitor analyses the mechanisms for uptake and sequestration of Na+ in the salt-sensitive indica rice cv. BRRI Dhan29 and in the salt-tolerant indica rice cv. Pokkali were detected. Less Na+ was taken up into the cytosol of Pokkali than into BRRI Dhan29. The results indicate that K+-selective channels do not contribute to the Na+ uptake in Pokkali, whereas they are the major pathways for Na+ uptake in BRRI Dhan29 along with non-selective cation channels. However, non-selective cation channels seem to be the main pathways for Na+ uptake in Pokkali. Protoplasts from Pokkali leaves took up Na+ only transiently in the presence of extracellular Na+ at 5-100 mM. Therefore, it is likely that the protoplasts have a mechanism for fast extrusion of Na+ out of the cytoplasm. Experiments with protoplasts pretreated with NH4NO3 and NH4VO3 suggest that the salt-tolerant Pokkali extrudes Na+ mainly into the vacuole. After cultivation of both cultivars in the presence of 10 or 50 mM NaCl for 72 h, the isolated protoplasts from Pokkali took up less Na+ than the control protoplasts. The results suggest that the salt-tolerance in Pokkali depends on reduced uptake through K+-selective channels and a fast extrusion of Na+ into the vacuoles.
Received May 10, 2005
Accepted September 15, 2005
RESEARCH PAPER
Uptake of sodium in protoplasts of salt-sensitive and salt-tolerant cultivars of rice, Oryza sativa L. determined by the fluorescent dye SBFI
Sylvia Lindberg, E-mail: Sylvia.Lindberg{at}vbsg.slu.se
![]()
Abstract ![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
P. Senadheera, R. K. Singh, and F. J. M. Maathuis Differentially expressed membrane transporters in rice roots may contribute to cultivar dependent salt tolerance J. Exp. Bot., July 1, 2009; 60(9): 2553 - 2563. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Szczerba, D. T. Britto, S. A. Ali, K. D. Balkos, and H. J. Kronzucker NH4+-stimulated and -inhibited components of K+ transport in rice (Oryza sativa L.) J. Exp. Bot., September 1, 2008; 59(12): 3415 - 3423. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. J. Kronzucker, M. W. Szczerba, L. M. Schulze, and D. T. Britto Non-reciprocal interactions between K+ and Na+ ions in barley (Hordeum vulgare L.) J. Exp. Bot., July 1, 2008; 59(10): 2793 - 2801. [Abstract] [Full Text] [PDF] |
||||
![]() |
Md. A. Kader, T. Seidel, D. Golldack, and S. Lindberg Expressions of OsHKT1, OsHKT2, and OsVHA are differentially regulated under NaCl stress in salt-sensitive and salt-tolerant rice (Oryza sativa L.) cultivars J. Exp. Bot., December 1, 2006; 57(15): 4257 - 4268. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Szczerba, D. T. Britto, and H. J. Kronzucker Rapid, Futile K+ Cycling and Pool-Size Dynamics Define Low-Affinity Potassium Transport in Barley Plant Physiology, August 1, 2006; 141(4): 1494 - 1507. [Abstract] [Full Text] [PDF] |
||||

