Effects of sugar metabolism on NaCl stress in rice

Paper Details

Research Paper 01/07/2013
Views (748)
current_issue_feature_image
publication_file

Effects of sugar metabolism on NaCl stress in rice

Saeed Vazan, Sepideh Torabi
Int. J. Biosci. 3(7), 8-14, July 2013.
Copyright Statement: Copyright 2013; The Author(s).
License: CC BY-NC 4.0

Abstract

Tow rice genotypes, salt-tolerant FL478 and salt sensitive IR29 from the IRRI (International Rice Research Institute) were used in this study. For the greenhouse trial, rice plants were grown in a hydroponic culture at ABRII (Agricultural Biotechnology Research Institute of Iran). The average greenhouse temperature and humidity over the growth season was 28 ºC and 57%, respectively. A complete randomized design was used, with 4 replicates for each treatment. All samples were collected for metabolite measurements at IPK (Leibniz Institute of Plant Genetics and Crop Plant Research-Germany). Mean comparisons indicated that Na+ accumulation was more in blade of IR29 in salinity condition which showed that this genotype was not able to salt exclusion. The salt stress caused to reduce glucose in root of salt sensitive genotype (IR29) but in Fl478 it increased in salt stress. Glucose can play an important role as an osmotic solution in mitigation of salt effects in tolerant genotype. Fructose variations and its partitioning over the plant organs were similar to glucose in every genotype at stress and control condition. Total sucrose content in above ground organs was too more than root. Sucrose content in stress and control conditions were similar in IR478. It could be related to more tolerance of this genotype but this variation in IR29 was more accelerate. Starch content didn’t have significant difference in blade and root in control and stress conditions. Its content was very low in different organs and was less than glucose, fructose and sucrose content.

Bohnert HJ, Jensen RG. 1996. Strategies for engineering water-stress tolerance in plants. Trends in Biotechnology 14, 89-97. http://dx.doi.org/10.1016/0167-7799(96)80929-2

Chen Z, Newman I, Zhou M, Mendham N, Zhang G, Shabala S. 2005. Screening plants for salt tolerance by measuring K+ flux: a case study for barley. Plant, cell & environment 28, 1230-1246. http://dx.doi.org/10.1111/j.1365-3040.2005.01364.x

Chen Z, Zhou M, Newman IA, Mendham NJ, Zhang G, Shabala S. 2007. Potassium and sodium relations in salinised barley tissues as a basis of differential salt tolerance. Functional Plant Biology 34, 150-162. http://dx.doi.org/10.1071/FP06237

Epstein E, Norlyn JD, Rush DW, Kingsbury RW, Kelley DB, Cunningham GA, Wrona AF. 1980.  Saline  culture  of  crops:  a  genetic  approach. Science 210, 399. http://dx.doi.org/10.1126/science.210.4468.399

Flowers TJ, Yeo AR. 1995. Breeding for Salinity Resistance in Crop Plants: Where Next? Aust J Plant Physiol 22, 875–884. http://dx.doi.org/10.1071/PP9950875

Frommer WB, Ludewig U, Rentsch D. 1999. Taking transgenic plants with a pinch of salt. Science 285, 1222. http://dx.doi.org/10.1126/science.285.5431.1222

Greenway H, Munns R. 1980. Mechanisms of salt tolerance in nonhalophytes. Annu Rev Plant Physiol 31,149–190. http://dx.doi.org/10.1146/annurev.pp.31.060180.001 053

Grover A, Pental D. 2003. Breeding objectives and requirements for producing transgenic for the major field crops of India. Curr Sci 84, 310–320.

Hajirezaei MR, Takahata Y, Trethewey RN, Willmitzer L, Sonnewald U. 2000. Impact of elevated cytosolic and apoplastic invertase activity on carbon metabolism during potato tuber development. J Exp Bot. 51, 439-445. http://dx.doi.org/10.1093/jexbot/51.suppl_1.439

Hanson AD, Hitz WD. 1982 Metabolic responses of mesophytes to plant water deficits. Annual Review of Plant Physiology 33, 163-203. http://dx.doi.org/10.1146/annurev.p.33.060182.0011 15

Hasegawa PM, Bressan RA, Zhu JK, Bohnert HJ. 2000. Plant cellular and molecular responses to high salinity. Annual Review of Plant Physiology and Plant Molecular Biology 51, 463-499. http://dx.doi.org/10.1146/annurev.arplant.51.1.463

Minhas D, Grover A. 1999. Transcript levels of genes encoding various glycolytic and fermentation enzymes change in response to abiotic stress. Plant Science 146, 41–51. http://dx.doi.org/10.1016/S0168-9452(99)00092-8

Poljakoff-Mayber A. 1982. Biochemical and physiological responses of higher plants to salinity stress. Biosaline Research: A Look to the Future. Plenum Press, New York, 245-269.

Sahi C, Singh A, Kumar K, Blumwald E, Grover A. 2006. Salt stress response in rice: genetics, molecular biology, and comparative genomics. Funct Integr Genomics 6, 263–284. http://dx.doi.org/10.1007/s10142-006-0032-5

Sakamoto A, Murata N. 2000. Genetic engineering of glycinebetaine synthesis in plants: current status and implications for enhancement of stress tolerance. Journal of Experimental Botany 51, 81-88. http://dx.doi.org/10.1093/jexbot/51.342.81

Sanchez-Blanco MJ, Bolarín MC, Alarcón JJ, Torrecillas A. 1991. Salinity effects on water relations  in  Lycopersicon  esculentum  and  its  wild salt-tolerant relative species L. pennellii. Physiologia Plantarum 83, 269-274. http://dx.doi.org/10.1034/j.1399-3054.1991.830210.x

Shabala S, Cuin TA. 2006. Osmoregulation versus osmoprotection: re-evaluating the role of compatible solutes. In: Teixeira da Silva J, ed. Floriculture, ornamental and plant biotechnology – advances and topical issues. Tokyo, Japan: Global Science Books, 405–416.

Shimamoto K. 1999. Molecular biology of rice, Springer-Verlag, Tokyo.

Widawsky DA, O’Toole JC. 1990. Prioritizing rice biotechnology research agenda for Eastern India. The Rockefeller Foundation, New York, USA.

Zurbriggen MD, Carrillo N, Tognetti VB, Melzer M, Peisker M, Hause B, Hajirezaei MR. 2009. Chloroplast-generated reactive oxygen species play a major role in localized cell death during the non-host interaction between tobacco and Xanthomonas campestris pv. vesicatoria. Plant J. 60,962-73. http://dx.doi.org/10.1111/j.1365-313X.2009.04010.x

Related Articles

Vegetable production systems in northern Côte d’Ivoire: Constraints, economic performance and integrated soil fertility management challenges

Marie Luce MÂ Semba Ouattara*, Jean Baptiste Gnelié Gnahoua, Kouassi Brahiman Kien, Kouamé Antoine N'Guessan, Yao Casimir Brou, Int. J. Biosci. 28(4), 41-50, April 2026.

Effect of temperature on the development of immature stages of Zeugodacus cucurbitae (Diptera: Tephritidae), Coquillett, 1899, A major watermelon pest in Senegal

Madeleine Ivonne Mendy*, Toffène Diome, Mamecor Faye, Mbacké Sembène, Int. J. Biosci. 28(4), 33-40, April 2026.

Structural characteristics of populations of Vitellaria paradoxa, Parkia biglobosa and Anacardium occidentale in rice-growing areas of the Tioroniaradougou subprefecture (Northern Côte d’Ivoire)

Dofoungo Koné*, Sibirina Soro, Seguena Fofana, Zana Silue, Doudjo Noufou Ouattara, Eboua Narcisse Wandan, Int. J. Biosci. 28(4), 23-32, April 2026.

In vitro anthelmintic efficacy of betel leaf (Piper betle) ethanolic extract against Ascaridia galli at varying concentrations

Elvin P. Dalida*, Mc Nelly V. Saraña, Zandro O. Perez, Int. J. Biosci. 28(4), 17-22, April 2026.

Perceptions, effectiveness, and credibility of artificial intelligence in healthcare among medical students and interns: A cross-sectional study

Shabeer Khan, Shafee Ur Rehman*, Naile Aleyna Dede, Mishal Tahir, Romana Hussain, Int. J. Biosci. 28(4), 8-16, April 2026.

A review on ethnomedicinal uses, phytochemical profile and pharmacological properties of Tetrastigma leucostaphylum (Dennst.) Alston ex Mabb.

P. P. Stephy, Prasobh K. Mohan, Anas Bin Firoz, S. Soosai Raj*, Int. J. Biosci. 28(4), 1-7, April 2026.