Received: 16-08-2023
Accepted: 05-01-2024
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Study on In vitroPropagation of Purple petunia (Petunia hybrida Hort.)
Keywords
Activated charcoal, BA, Petunia hybrida Hort., tissue culture
Abstract
Purple petunia (Petunia hybrida Hort.), belonging to the Solanacea family, is a popular and high - value potted ornamental plant on the flower market. Therefore, in vitro propagation research of Purple petunia has been carried out in order to produce large numbers of genetically uniform and pathogen-free plantlets to meet market demand. All experiments were arranged in a randomized complete design (RCD) with three replicates. The results showed that Murashige and Skoog (MS) solid medium supplemented with 0.3 mg/l BA was the most suitable medium for shoot regeneration and multiplication of Purple petunia, with a high multiplication rate (19.78 shoots/explant), and a shoot height of 2.36cm after 6 weeks of culture. The most suitable medium for Purple petunia shoot nursing was MS solid medium supplemented with 40 g/l sucrose, producinglarge and green shoot and leaves. The results also showed that the suitable medium for the rooting stage and acclimatization was MS solid medium supplemented with 0.1 g/l activated charcoal (AC), resulting in the root formation rate of 100%; 12.83 roots/plantlet; 2.28 cm in root length with white, long and big roots. After 2 weeks of acclimatization in the net house, plantlets derived from MS solid rooting medium supplemented with 0.1 g/l AC had a survival rate of 100% with 6.47cm in plant height and 15.07 leaves/plant.
References
Aguilar M.L., Espadas F., Maust B. & Sáenz L. (2009). Endogenous cytokinin contentin coconut palms affected by lethal yellowing. Journal of Plant Pathology. 91(1): 141-146.
Belinda M., Maureen R.H. & Frederick M.A. (1980). Effect of charcoal and hormones on anther culture 1980 of Petunia and Nicotiana. Zeitschrift fur pflanzenphysiologie. 102(2): 109-116.
Borkird C. & Sink K.C. (1983). Medium components for shoot cultures of chlorophyll-deficient mutants of Petunia inflata. Plant Cell Reports. 2: 1-4.
Bùi Thị Cúc, Đồng Huy Giới & Bùi Thị Thu Hương (2017). Nhân nhanh in vitro cây Dạ yến thảo hoa hồng sọc tím (Petuniahybrida L.). Tạp chí Khoa học và Công nghệ Lâm nghiệp. 10: 3-10.
Farooq I., Qadri Z.A., Rather Z.A., Nazki I.T., Banday N., Rafiq S., Masoodi K.Z., Noureldeen A. & Mansoor S. (2021). Optimization of an improved, efficient and rapid in vitromicropropagation protocol for Petunia hybridaVilm. cv. ‘‘Bravo”. Saudi Journal of Biological Sciences. 28: 3701-3709.
Izhar S. & Zelcer A. (1984). Cell, tissue, and organ culture in Petunia. In: Sink, K.C. (eds) Petunia. Monographs on Theoretical and Applied Genetics. Vol 9. Springer, Berlin, Heidelberg. doi.org/10.1007/978-3-662-02387-7_9.
Gago J., Martinez-Nunez L., Landin M., Flexas J. & Gallego P.P. (2014). Modeling the effects of light and sucrose on in vitropropagated plants: a multiscale system analysis using artificial intelligence technology. PLoS One. 9 (1): 1-11.
Muller B., Pantin F., Ge´nard M., Turc O., Freixes S., Piques M. &Gibon Y. (2011). Water deficitsuncouple growth from photosynthesis, increase C content, and modify therelationships between C and growth in sink organs. J Exp Bot. 62: 1715-1729.
Murashige T. & Skoog F. (1962). A revised medium for rapid growth and bio assays with Tobacco tissue cultures. Plant Physiology. 15: 473-497.
Natalija B., AuSra B. & Vaida J. (2015). In vitro regeneration from leaf explants of Petunia hybrrida L.Propagation of Ornamental plants. 15(2): 47-52.
Nguyễn Tiến Long, Lã Thị Thu Hằng, Trần Thị Triêu Hà, Dương Thanh Thủy & Lê Như Cương (2021). Nghiên cứu tạo nguồn vật liệu khởi đầu trong nhân giống in vitrocây hoa Dạ yến thảo (Petunia hybridaL.). Khoa học Nông nghiệp. 63(7): 53-56.
Phạm Hoàng Hộ (2000). Cây cỏ Việt Nam(Tập 2). Nhà xuất bản Trẻ. tr. 769.
Sakakibara H. (2006). Cytokinins: activity, biosynthesis, and translocation. Annu Rev Plant Biol. 57: 431-449.
Sara E.G. & Naglaa M.E. (2015). In vitropreliminary study on Petunia hybridabreeding under sodium chloride stress conditions. Middle East Journal of Agriculture Research. 4(4): 867-872.
Thomas & Dennis T. (2008). The role of activated charcoal in plant tissue culture”, Biotechnol. Adva. 26: 618-631.
Yong J.W.H., Ge L., Yan F. Ng & Tan S.N. (2009). The chemical composition and biological properties of coconut (Cocos nuciferaL.) water. Molecules. 14: 5144-5164.