Browse > Article
http://dx.doi.org/10.5333/KGFS.2014.34.4.262

Proteomic Response of Alfalfa Subjected to Aluminum (Al) Stress at Low pH Soil  

Rahman, Md. Atikur (Division of Applied Life Sciences (BK21Plus), IALS, PMBBRC, Gyeongsang National University)
Kim, Yong-Goo (Division of Applied Life Sciences (BK21Plus), IALS, PMBBRC, Gyeongsang National University)
Lee, Byung-Hyun (Division of Applied Life Sciences (BK21Plus), IALS, PMBBRC, Gyeongsang National University)
Publication Information
Journal of The Korean Society of Grassland and Forage Science / v.34, no.4, 2014 , pp. 262-268 More about this Journal
Abstract
In order to reveal the aluminum (Al) stress tolerance mechanisms in alfalfa plant at low pH soil, a proteomic approach has been conducted. Alfalfa plants were exposed to Al stress for 5 days. The plant growth and total chlorophyll content are greatly affected by Al stress. The malondialdehyde (MDA) and $H_2O_2$ contents were increased in a low amount but free proline and soluble sugar contents, and the DPPH-radical scavenging activity were highly increased. These results indicate that antioxidant activity (DPPH activity) and osmoprotectants (proline and sugar) may involve in ROS ($H_2O_2$) homeostasis under Al stress. In proteomic analysis, over 500 protein spots were detected by 2-dimentional gel electrophoresis analysis. Total 17 Al stress-induced proteins were identified, of which 8 protein spots were up-regulated and 9 were down-regulated. The differential expression patterns of protein spots were selected and analyzed by the peptide mass fingerprinting (PMF) using MALDI-TOF MS analysis. Three protein spots corresponding to Rubisco were significantly down-regulated whereas peroxiredoxin and glutamine synthetase were up-regulated in response to Al stress. The different regulation patterns of identified proteins were involved in energy metabolism and antioxidant / ROS detoxification during Al stress in alfalfa. Taken together, these results provide new insight to understand the molecular mechanisms of alfalfa plant in terms of Al stress tolerance.
Keywords
Alfalfa; Aluminum stress; Proteome;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Lichtenthaler, H.K. 1987. Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes. In: Lester Packer R.D (ed) Methods in Enzymology, vol. Volume 148, Academic Press, pp. 350-382.
2 Manzano-Leon, N., Delgado-Coello, B., Guaderrama-Diaz, M. and Mas-Oliva, J. 2006. ${\beta}$-adaptin: Key molecule for microglial scavenger receptor function under oxidative stress. Biochemical and Biophysical Research Communications. 351:588-594.   DOI
3 Lin, C.C. and Kao, C.H. 2001. Abscisic acid induced changes in cell wall peroxidase activity and hydrogen peroxide level in roots of rice seedlings. Plant Science. 160: 323-329.   DOI   ScienceOn
4 Liu, P., Yang, Y.S., Xu, G., Guo, S., Zheng, X. and Wang, M. 2006. Physiological responses of four herbaceous plants to aluminum stress in South China. Frontiers of Biology in China 1:295-302.   DOI
5 Lowry, O.H., Rosebrough, N.J., Farr, A.L. and Randall, R.J. 1951. Protein measurement with the folinphenol reagent. Journal of Biological Chemistry. 193:265-275.
6 Narasimhamoorthy, B., Blancaflor, E.B., Bouton, J.H., Payton, M.E. and Sledge, M.K. 2007. A comparison of hydroponics, soil, and root staining methods for evaluation of aluminum tolerance in Medicago truncatula (Barrel Medic) germplasm. Crop Science. 47: 321-328.   DOI
7 Nunes-Nesi, A., Brito, D.S., Inostroza-Blancheteau, C., Fernie, A.R. and Araujo W.L. 2014. The complex role of mitochondrial metabolism in plant aluminum resistance. Trends in Plant Science. 19:399-407.   DOI
8 Pietrini, F., Iannelli, M.A., Pasqualini. S. and Massacci, A. 2003. Interaction of cadmium with glutathione and photosynthesis in developing leaves and chloroplasts of Phragmites australis (Cav.) Trin. ex Steudel. Plant physiology. 133:829-837.   DOI
9 Dwivedi, R.S., Breiman, A. and Herman, E.M. 2003. Differential distribution of the cognate and heat-stress-induced isoforms of high Mr cis-trans prolyl peptidyl isomerase (FKBP) in the cytoplasm and nucleoplasm. Journal of Experimental Botany 54:2679-2689.   DOI
10 Fukui, K., Wakamatsu, T., Agari, Y., Masui, R. and Kuramitsu, S. 2011. Inactivation of the DNA repair genes mutS, mutL or the anti-recombination gene mutS2 leads to activation of vitamin B1 biosynthesis genes. PLoS One 6:e19053.   DOI
11 Haider, S.I., Kang, W., Ghulam, J. and Guo-ping, Z. 2007. Interactions of cadmium and aluminum toxicity in their effect on growth and physiological parameters in soybean. Journal of Zhejiang University Science B. 8:181-188.   DOI
12 Hansen, J. and Moller, I.B. 1975. Percolation of starch and soluble carbohydrates from plant tissue for quantitative determination with anthrone. Anal Biochemistry : 87-94.
13 Houde, M. and Diallo, A.O. 2008. Identification of genes and pathways associated with aluminum stress and tolerance using transcriptome profiling of wheat near-isogenic lines. BMC Genomics. 9:1-13.   DOI
14 Hurkman, W.J. and Tanaka, C.K. 1986. Solubilization of plant membrane proteins for analysis by two dimensional gel electrophoresis. Plant Physiology. 81:802-806.   DOI   ScienceOn
15 Wilkins, M.R., Sanchez, J.C., Gooley, A.A., Appel, R.D., Humphery-Smith, I., Hochstrasser, D.F. and Williams, K.L. 1996. Progress with proteome projects: why all proteins expressed by a genome should be identified and how to do it. Biotechnology and Genetic Engineering Reviews. 13:19-50.   DOI   ScienceOn
16 Sharma, A.D. and Singh, P. 2003. Comparative studies on droughtinduced changes in peptidyl prolyl cis-trans isomerase activity in drought-tolerant and susceptible cultivars of Sorghum bicolor. Current Science. 84:911-918.
17 Vidigal, P., Carvalho, R., Amancio, S. and Carvalho, L. 2013. Peroxiredoxins are involved in two independent signalling pathways in the abiotic stress protection in Vitis vinifera. Biologia Plantarum. 57:675-683.   DOI
18 Weger, H.G. and Turpin, D.H. 1989. Mitochondrial respiration can support NO(3) and NO(2) reduction during photosynthesis : Interactions between photosynthesis, respiration, and N assimilation in the N-limited green alga Selenastrum minutum. Plant Physiology. 89: 409-415.   DOI
19 Zhang, Y., Xu, W., Li, Z., Deng, X.W., Wu, W. and Xue, Y. 2008. F-box protein DOR functions as a novel inhibitory factor for abscisic acid-induced stomatal closure under drought stress in Arabidopsis. Plant Physiology. 148(4): 2121-2133.   DOI   ScienceOn
20 Zheng, L., Lan, P., Shen, R.F. and Li, W.F. 2014. Proteomics of aluminum tolerance in plants. Proteomics. 14:566-578.   DOI
21 Duressa, D., Soliman, K., Taylor, R. and Senwo, Z. 2011. Proteomic analysis of soybean roots under aluminum stress. International Journal of Plant Genomics. 2011:1-12.
22 Kang, H.-M. and Saltveit, M.E. 2001. Antioxidant Enzymes and DPPH-radical scavenging activity in chilled and heat-shocked rice (Oryza sativa L.) seedlings radicles. Journal of Agricultural and Food Chemistry. 50:513-518.
23 Kochian, L.V., Hoekenga, O.A. and Pineros, M.A. 2004. How do crop plants tolerate acid soils? Mechanisms of aluminum tolerance and phosphorous efficiency. Annual Review of Plant Biology. 55:459-493.   DOI
24 Lee, D.G., Ahsan, N., Lee, S.H., Kang, K.Y., Bahk, J.D., Lee, I.J. and Lee, B.H. 2007. A proteomic approach in analyzing heatresponsive proteins in rice leaves. Proteomics. 7:369-3383.
25 Ezzine, M. and Ghorbel, M.H. 2006. Physiological and biochemical responses resulting from nitrite accumulation in tomato (Lycopersicon esculentum Mill. cv. Ibiza F1). Journal of Plant Physiology. 163:1032-1039.   DOI
26 Bates, L.S., Waldren, R.P. and Teare, I.D. 1973. Rapid determination of free proline for water-stress studies. Plant and Soil. 39: 205-207.   DOI   ScienceOn
27 Sha Valli Khan, P.S., Nagamallaiah, G.V., Dhanunjay Rao, M., Sergeant, K. and Hausman, J.F. 2014. Abiotic stress tolerance in plants Insights from proteomics. In: Emerging Technologies and Management of Crop Stress Tolerance A Sustainable Approach, Academic Press, USA, 2: pp.41-45.