Effect of Plant Growth Regulators on Different Explants and Explant Size of Yellow Everlasting (Helichrysum pallasii Sprengel Ledeb.) Under in vitro Conditions
Abstract views: 184 / PDF downloads: 117
DOI:
https://doi.org/10.5281/zenodo.10874612Keywords:
Explant size, Helichrysum, immortal flower, source of explant, tissue cultureAbstract
In this study, different explants (leaf, stem and root) and explant size (0.5, 1, 1.5 and 2 cm) of yellow everlasting, Helichrysum pallasii (Sprengel) Ledeb., cultured under in vitro conditions including kinetin, 2,4-D, TDZ and zeatin concentrations. Concentrations of 0.5 mgl−1 kinetin + 0.5 mgl−1 2,4-Dichlorophenoxyacetic acid (2,4-D) and 1mgl−1 kinetin (KIN) + 1 mgl−1 2,4-D were used for callus induction. Concentrations of 1 mgl−1 thidiazuron (TDZ) and 1 mgl−1 thidiazuron (TDZ) + 0.1 mgl−1 zeatin (ZEA) were used for inducing shoot regeneration. MS medium without any plant grow regulators was preferred as control group. Rooting medium was preferred 1 mgl−1 NAA. In callus regeneration, highest regeneration rates were found as respectively 86.6%, 53.3% and 35.5% from root, stem and leaf explants with 1 cm explant length while the lowest rate (4.4%) found in control group from leaf explant with 2 cm explant length. It was obtained from the medium containing the highest shoot regeneration and from root (24.6%), stem (20.6%) and leaf (16%) explants with an explant length of 1 cm. Similarly, rooting rate from leaf, root and stem explants were found as respectively 43.8%, 32.3% and 21.9% with the 1 cm explant length obtained from 1 mgl−1 TDZ + 0.1 mgl−1 ZEA medium. In conclusion, 1 cm of explant length produced the highest regeneration rate in all source of explants. Also, 1 mgl−1 TDZ combined with 0.1 mgl−1 ZEA were more effective than 1 mgl−1 TDZ treatment alone in shoot regeneration.
References
Balandrin, M.F., Klocke, J.A., 1988. Medicinal, aromatic, and industrial materials from plants. In Medicinal and aromatic plants I. Berlin, Heidelberg: Springer Berlin Heidelberg.
Boissier, P.E., 1875. Flora Orientalis, 3. Geneve, Basel, Lyon.
Clasquin, S., Henry, M., 2002. Micropropagation d'Helichrysum arenarium (L.) Moench. Acta Botanica Gallica, 149(2): 189-195.
Davis, P.H., 1970. Flora of Turkey and the East Aegean Islands. Edinburgh University Press, 3.
Davis, P.H., Mill, R.R., Tan, K., 1988. Flora of Turkey and the East Aegean Islands. Edinburgh University Press.
Dimitrova, N., Nacheva, L., 2018. Micropropagation of Helichrysum italicum (ROTH) G. Don – a medicinal plant with ornamental value. Journal of BioScience and Biotechnology, 7(2): 97-101.
Fowler, M.W., 1985. Problems in commercial exploitation of plant tissue cultures, In: K.H. Neumann, W. Barz, E. Reinhardt (Eds.), Primary and Secondary Metabolism of Plant Cell Cultures, Springer, Berlin, pp. 362-378.
Giovannini, A., Amoretti, M., Savona, M., Di Guardo, A., Ruffoni, B., 2001. Tissue culture in Helichrysum spp. I International Symposium on Acclimatization and Establishment of Micropropagated Plants, pp. 339-342.
Kieran, P.M., MacLoughlin, P.F., Malone, D.M., 1997. Plant suspension cultures: some engineering considerations. Journal of Biotechnology, 59: 39-52.
Morone-Fortunato, I., Montemurro, C., Ruta, C., Perrini, R., Sabetta, W., Blanco, A., Lorusso, E., Avato, P., 2010. Essential oils, genetic relationships and in vitro establishment of Helichrysum italicum (Roth) G. Don ssp. italicum from wild Mediterranean germplasm. Industrial Crops and Products, 32(3): 639-649.
Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bio assays with tobacco tissue cultures. Physiologia Plantarum, 15(3): 473-497.
Perrini, R., Morone-Fortunato, I., Lorusso, E., Avato, P., 2009b. Glands, essential oils and in vitro establishment of Helichrysum italicum (Roth) G. Don ssp. italicum. Industrial Crops and Products, 29: 395-403.
Phillipson, J.D., 1990. Plants as source of valuable products. In: B.V. Charlwood, M.J.C. Rhodes (Eds.). Secondary Products From Plant Tissue Culture, Oxford: Clarendon Press, pp. 1-21.
Rao, S.R., Ravishankar, G.A., 2002. Plant cell cultures: chemical factories of secondary metabolites. Biotechnology Advances, 20: 101-153.
Raquel Pretto, F., Romanato Santarém, E., 2000. Callus formation and plant regeneration from Hypericum perforatum leaves. Plant Cell, Tissue and Organ Culture, 62: 107-113.
Sajc, L., Grubisic, D., Vunjak-Novakovic, G., 2000. Bioreactors for plant engineering: An outlook for further research. Biochemical Engineering Journal, 4: 89-99.
Shuler, M.L., 1981. Production of secondary metabolites from plant tissue culture-problems and prospects. Annals of the New York Academy of Sciences, 369: 65-79.
Yurteri, E., Seyis, F., Küplemez, H., 2021. The essential oil components of Helichrysum pallasii flowers. Turkish Journal of Agriculture-Food Science and Technology, 9: 2591-2593.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 ISPEC Journal of Agricultural Sciences
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.