In collaboration with Scientific Association of Iranian Medicinal Plants

Document Type : Research Paper

Authors

1 Biology department, Faculty of Science, Shahid Beheshti University

2 Institute of Medicinal Plants, Shahid Beheshti University

Abstract

In this research investigation on parthenolide production and antioxidant defence in callus culture and micropropagated plantlets of feverfew (Tanacetum parthenium (L.) Sch. Bip. Family: Asteraceae) wounding, abscisic acid (ABA) and salicylic acid (SA) treatments were done.
For this purpose, seeds were cultured on MS/4 medium with the whole vitamins, and shoot explants of seedlings, with shoot tip and without shoot tip and also, were cultured on MS medium supplemented with NAA (0.54µM) and BAP (4.44µM). The growth of plantlets was computed as dry weight.
For biochemical investigations, shoot tip explants were cut from two months old plantlets and treated with ABA, SA and wounding (leaves discarded) for 10 hours in MS liquid medium. Parthenolide content was measured by HPLC. Antioxidant defense was evaluated as qualitative peroxidase activity.
Callus tissues were obtained from leaf explants of seedlings, in MS medium supplemented with NAA (2mg.L-1) and BAP (0.5mg.L-1). One month old calli were transferred to liquid medium with ABA, SA and DMSO treatments. After one weak, parthenolide content and peroxidase activity were measured as above. Parthenolide content of control plantlets in this investigation was 0.00863±0.00283, but SA + Wounding treatment in plantlets showed the less parthenolide content and the maximum dry weight. Parthenolide production in treatments was decreased as the growth increased. In callus tissues, parthenolide content was not different significantly between treatments, and approximately half of the plantlets. Qualitative variation in antioxidant defense was shown by electrophoretic patterns and we had an extra band in wounding treatment in micropropagated plantlets. Anionic bands were stronger than cationic bands. Electrophoretic bands had no difference in callus tissues.

Keywords

 - Aljancic, I., Vajs, V., Bulatovic, V., Menkovic,N. and Milosavljevic, S., 2001. Parthenolide from the aerial parts of Tanacetum parthenium. Biochemical Systematic and Ecology, 29: 655-657.
- Andrew, C.A. and Robert, F., 1997. Two distinct sources of elicited Reactive Oxygen Species in tobacco epidermal cells. Plant Cell, 9: 1559-1572.
- Brown, A. M. G., Lowe, K. C., Davey, M. R. and Power, J. B., 1996. Feverfew (Tanacetum parthenium): tissue culture and parthenolide synthesis. Plant Science 116: 223-232.
- Cheong, Y. H., Chang, H.-S., Gupta, R., Wang, X., Zhu, T. and Luan, Sh., 2002. Transcriptional Profiling Reveals Novel Interactions between Wounding, Pathogen, Abiotic stress and HormonalResponses in Arabidopsis. Plant Physiology, 129: 661-677.
- Dermarderosian, A., 2001. A Guid to Popular Natural Products. Facts & Comparisons. Wolters Kluwer Company. pp. 90-92.
- Fiebich, B. L., Lieb, K., Engels, S. and Heinrich, M., 2002. Inhibition of LPS-induced P42/44 MAPkinase activation and iNOS/NO synthesis by parthenolide in rat primary microglial cells, Journal of Neoroimmunology, 132: 18-24.
- Handro, W., Mello, C.M., Manzano, M. A. and Floh, E. I. S., 1997. Enhancement of stem elongation and flower bud regeneration by salicylic acid. R. Bras. Fisiol. Veg, 9: 139-142.
- Janda, T., Szalai, G., Tari, I. and Páldi, E., 1999. Hydroponic treatment with salicylic acid decreases the effects of chilling injury in maize (Zea mays L.) plants. Planta, 208: 175-180.
- Kang, G., Wang, Ch., Sun, G. and Wang, Zh., 2003. Salicylic acid changes activities of H2O2-metabolizing enzymes and increases the chilling tolerance of banana seedlings. Environmental and Experimental Botany 50: 9-15.
- Kemper, K. J., 1999. Feverfew (Tanacetumparthenium). WWW.mcp.edu/herbal/default.htm. and WWW.childrenshospital.org/holistic
- Korori, S.A., 1989. Gel Electrophoretische and spectraphotomet rishe unteruchungen zum ein slussder temperature jvs struktur and okapivitat der amylase and peroxidase isoenzyme verschicdener bsymarten. Ph.D. Thesis, University Sur Boden kalture Win.
- Kurina Sanz, M., Hernandez, X. E. and Tom, C. E., 2000. Enhancement of tessaric acid production in Tessaria absinthioides cell suspension cultures. Plant Cell Report, 19: 821-824.
- Lamb, C. and Dixon, R. A., 1997. The oxidative burst in plant disease resistance. Anna. Rev. Plant Physil. Plant Mol. Biol., 48: 251-275.
- Merkouropoulos, G., Barnett, D. C. and Shirsat, A. H., 1999. The Arabidopsis extensin gene is developmentally regulated, is induced by wounding, methyl jasmonate, abscisic acid, and codes for a protein with unusual motifs. Planta, 208: 212-219.
- Pruitt, P., 2003. Outline for a Comprehensive Theory of Plant Hormones. WWW.pruittfamily.com/paul/plants.
- Scheel, D. and Wasternack, C., 2002. Plant Signal Transduction. OxfordUniversity Press. 320p.
- Smallwood, M. F., Calvert, C. M. and Bowles, D. J., 1999. Plant Responses to Environmental Stress. BIOS Scientific Publishers, Oxford. 224p.
- Stojakowska, A. and Kisiel, W., 1997. Production of parthenolide in organ cultures of feverfew. Plant Cell, Tissue and Organ Culture, 47: 159-162.
- Taiz, L. and Zeiger, E., 2002. Plant Physiology. Sinauer., 690p.
- Walker, T. S., Bais, H. P. and Vivanco, J. M., 2002. Jasmonic acid-induced hypericin production in cell suspention cultures of Hypericum perforatum L. (st. John’s wort). Phytochemistry, 60: 289-293.
- Weber, H., 2002. Fatty acid derived signals in plants. TRENDS in Plant Science, 7: 217-224.