Effects of sugar metabolism on NaCl stress in rice

Paper Details

Research Paper 01/07/2013
Views (792)
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

Phytochemical investigation and in vitro evaluation of cholinesterase inhibitory and antioxidant properties of Aglaonema hookerianum stems

K. M. Monirul Islam, Simin Shabnam Lopa, Joya Rani*, Md. Aslam Sheikh, Md. Golam Sadik, Int. J. Biosci. 28(6), 60-67, June 2026.

Comparative responses of rice (Oryza sativa L.) to iron toxicity, drought and salinity stress: Morphological, physiological, biochemical and molecular regulation mechanisms

Yaya Touré*, Brahima André Soumahoro, Arthur Martin Affery, Tchoa Koné, Mongomaké Koné, Int. J. Biosci. 28(6), 37-50, June 2026.

Biocontrol potential of indigenous fungal antagonists from soils naturally suppressive to Fusarium oxysporum f. sp. cubense tropical race 4

Arnel V. Somolostro*, Carolina D. Amper, Mellprie B. Marin, Darwin M. Apistar, Myrna G. Ballentes, Ailyn Q. Daniel, Int. J. Biosci. 28(6), 27-36, June 2026.

Basal stem rot of oil palm in Africa: Emerging epidemiology, pathogen diversity and future management challenges

Emmanuel Fumbuka Mabula*, Agatha Aloyce, Alfonce Leonard, Pavithravani B. Venkataramana, Int. J. Biosci. 28(6), 13-26, June 2026.

The role of aberrant glycosylation in autoimmune disease development and progression

Md. Nafis Fuad Prottoy, Sayad Md. Didarul Alam*, Int. J. Biosci. 28(6), 1-12, June 2026.

Cholinesterase inhibition and antioxidant activity of the stem bark of Abroma augusta: Correlation with phenolic and flavonoid content

K. M Monirul Islam, Tahmida Sharmin, Md. Minhaz Khan Mithun, Simin Shabnam Lopa, Joya Rani*, Md. Aslam Sheikh, Md. Golam Sadik, Int. J. Biosci. 28(5), 117-124, May 2026.

Solvents’ influence on polyphenolic compound extractions from Lippia multiflora leaves (Mold, 1949), and their antioxidant activity

Kelemin Awa Koné*, Tagouèlbè Tiho, Mariam Sanogo, Casimir Kekou, Kouassi Hervé Tani, Int. J. Biosci. 28(5), 109-116, May 2026.