Malaysian Applied Biology Journal

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41-1-3

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Malays. Appl. Biol. 41(1): 23–28

ANTIOXIDANTS ACTIVITY IN PINEAPPLE CV. N36 CULTURE UNDER ALUMINIUM STRESS

AZIZ, A.* and NURHALIM, M.S.

Department of Biological Sciences, Faculty Science and Technology University,
Malaysia Terengganu Kuala Terengganu, Terengganu, 21030 Malaysia.
*Email: This e-mail address is being protected from spambots. You need JavaScript enabled to view it ; Phone: 609-6684165; Fax: 6096684167

ABSTRACT

Aluminium is an important stress factor for plants in acidic environments. In the present study, the effect of aluminium-stress on the oxidative enzymes and antioxidant activities in pineapple cv. N36 plantlets was investigated. The plantlets were cultured in MS medium containing 100 µM Al (pH 4.0) for 30 days. Results showed that fresh and dry weight, ascorbic acid content and catalase (CAT) enzyme activity were not significantly (p>0.05) affected by Al-stress. Al did significantly (p<0.05) reduce the alpha-tocopherol content (2.76 mg/fwt.) and guaiacol peroxidase (GPX) enzyme activity (3.39 units/mg protein), and increased the enzyme ascorbate peroxidase (APX) activity (7.16 units/mg protein). These results indicated that long-term Al-stress did change antioxidant substances content and oxidative enzymes activities in the leaves of pineapple cv. N36 plantlets.


ABSTRAK

Aluminium merupakan faktor tekanan utama bagi tumbuhan di kawasan berasid. Dalam kajian ini, kesan tekanan-aluminum ke atas enzim oksidatif dan aktiviti aktioksidan dalam Ananas cv. N36 telah dikaji. Anak benih telah dikultur dalam medium MS mengandungi 100 µM Al (pH 4.0) selama 30 hari. Keputusan menunjukkan berat basah dan kering, kandungan asid askorbik dan aktiviti enzim katalase (CAT) tidak dipengaruhi (p>0.05) oleh tekanan Al. Al memberi kesan yang bererti (p<0.05) terhadap penurunan kandungan tokoferol (2.76 mg/berat basah) dan aktiviti enzim guaikol peroksidase (GPX) (3.39 unit/mg protein), dan peningkatan aktiviti enzim askorbat peroksidase (APX) (7.16 unit/mg protein). Keputusan ini menunjukkan tekanan jangka panjang Al telah mengubah kandungan sebatian antioksidan dan aktiviti enzim oksidatif dalam daun-daun anak pokok Ananas cv. N36.

Key words: catalase, peroxidase, ascorbate peroxidase, carotenoids, ascorbic acid, alpha-tocopherol

REFERRENCES

Agrawal, R. & Patwardhan, M.V. 1993. Production of peroxidase enzymes by callus cultures of Citrus aurantifolia S. Journal Science Food Agriculture 61: 377-378.

Azmat, R. & Hasan, S. 2008. Photochemistry of light harvesting pigments and some biochemical changes under aluminium stress. Pakistan Journal Botany 2008; 40(2): 779-784,

Boscolo, P.R.S., Menossi, M. & Jorge, R.A. 2003. Aluminium-induced oxidative stress in maize. Phytochemistry 62: 181-189.

Bradford, M. 1976. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochemistry 72: 248–254.

Claiborne, A. 1985. Catalase activity. In Greenwald, R.A. (ed.), Handbook of Methods of Oxygen Radical Research. CRC Press, Boca Raton, FL, pp. 283-284.

Darkó, E., Ambrusa, H., Stefanovits-Bányai, E., Fodor, J., Bakos, F. & Barnabás, B. 2004. Aluminium toxicity, Al tolerance and oxidative stress in an Al-sensitive wheat genotype and in Al-tolerant lines developed by in vitro microspore selection. Plant Science 166: 583- 591.

Ghanati, F., Morita, A. & Yokota, H. 2005. Effects of aluminum on the growth of tea plant and activation of antioxidant system. Plant and Soil 276: 133-141

Gill, S.S. & Tuteja, N. 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry 48: 909-930.

Ishikawa, S. & Wagatsuma, T. 1998. Plasma membrane permeability of root-tip cells following temporary exposure to Al ions is a rapid measure of Al tolerance among plant species. Plant Cell Physiology 39(5): 516-525.

Jagota, S.K. & Dani, H.M. 1982. A new colorimetric technique for the estimation of vitamin C using Folin phenol reagent. Analytical Biochemistry 127: 178-182.

Kanno, C. & Yamauchi, K. 1977. Application of a new iron reagent, 3-(2-pyridyl)-5,6- diphenyl- 1,2,4- triazine, to spectrophotometric deter- mination of tocopherol. Agricultural Biological Chemistry 41(3): 593-596.

Lichtenthaler, H.K. 1987. Chlorophylls and carotenoids: Pigments of photosynthetic biomembranes. In: (eds.) Packer I, Dauce R. Methods in Enzymology. Academic Press, New York. 148: Pp. 350-382.

Matsumoto, H. 2000. Cell biology of aluminium toxicity tolerance in higher plants. International Review of Cytology 200: 1-46.

Mittler, R. 2002. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science 7(9): 405-410.

Munne-Bosch, S. 2005. The role of tocopherol in plant stress tolerance. Journal of Plant Physiology 162: 743-748.

Murashige, T. & Skoog, F. 1962. A Revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiologia Plantarum 15: 473- 497.

Radic, S., Babic, M., Skobic, D., Roje, V. & Pevalek- Kozlina, B. 2010. Ecotoxicological effects of aluminum and zinc on growth and antioxidants in Lemna minor L. Ecotoxicology and Environmental Safety 73: 336-342.

Sairam, R.K., Shukla, D.S. & Sayena, D.C. 1998. Stress-induced injury and antioxidant enzymes in relation to drought tolerance in wheat genotypes. Biology Plantarum. 40: 357-364.

Sharma, P. & Dubey, R.S. 2007. Involvement of oxidative stress and role of antioxidative defence system in growing rice seedlings exposed to toxic concentrations of aluminium. Plant Cell Reports 26(11): 2027-2038.

Yamamoto, Y., Kobayashi, Y., Devi, S.R., Rikiishi, S. & Matsumoto, H. 2002. Aluminium toxicity is associated with mitochondrial dysfunction and the production of reactive oxygen species in plant cells. Plant Physiology 128(1): 63-72.
 

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