Faculty of Humanities and Sciences

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    Facile synthesis of silver/iron-TiO2 nanoparticles for sterilization of Nodal explants of Dracaena sanderiana Sander ex Mast. cvs ‘Gold’ and ‘Victory’ and growth regulator effects on in vitro growth
    (OICC Press, 2025-02-08) Seneviratne, K.L; Peiris, S. E.; Peiris, C. N; Shashikala, R. P. A; Jayasinghe, S; Kottegoda, N
    This study investigates the application of silver/iron-titanate (Ag/Fe-TiO2) nanoparticles (NPs) as a sterilizing agent for in vitro cultures of Dracaena sanderiana cultivars ‘Gold’ and ‘Victory’. The motivation behind this research is to find an effective sterilization method that does not harm plant growth. The Ag/Fe-TiO2 NPs, activated by visible light, exhibit catalytic properties that eliminate harmful microbes such as Escherichia coli, Staphylococcus aureus, and Fusarium spp. The main findings indicate that the combination of Benzyl Amino Purine (BAP) at 1.5 mg/L and Indole Acetic Acid (IAA) at 0.01 mg/L significantly enhances shoot number and length in both cultivars. The use of 200 mg/L Ag/Fe-TiO2 NPs achieved 90% contamination-free cultures in the first cycle, with a slight decrease to 80% in the second cycle and 70% in the third cycle. Importantly, the treatment not only sterilizes but also promotes plant growth, suggesting that Ag/Fe-TiO2 NPs could be a sustainable solution for in vitro plant mass production. © 2025 The Author(s)
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    A Successful Surface Sterilization Technique for in vitro Establishment of Dracaena sanderiana Sander ex Mast. Nodal Explants
    (Faculty of Humanities and Sciences,SLIIT, 2021-09-25) Seneviratne, K. L; Malwattage, G; Weerakkody, G. K; Peiris, S. E; Peiris, C. N
    Dracaena sanderiana Sander ex Mast. is the number one cut foliage exported from Sri Lanka and it is also a popular potted plant. In order to promote dracaena cultivation, micropropagation techniques can be employed to produce high quality large number of clones as planting materials. However, severe microbial contaminations in the in vitro establishment stage mitigate the micropropagation application on this species. Therefore, this study was undertaken with the objective of using silver nitrate (AgNO3) to eliminate surface adhered microorganisms to obtain high amount of contamination free cultures at the in vitro establishment stage. Investigations also carried out to explore reusability of AgNO3 after the first wash in surface sterilization. Apical parts of about 8 cm of D. sanderiana cv ‘White’ were used in this study. Silver nitrate solution in 200 mg/L and Clorox™ in 10% concentrations were used for the surface sterilization of the nodal explants. Results revealed that 200 mg/L AgNO3 produced 90% and 10% Clorox produced 20% contamination free cultures after 8 weeks of establishment in vitro. Also, in the experiment of investigation of reusability of AgNO3 it was observed that the second and third washings of AgNO3 produced 80 and 70% non-contaminated cultures, respectively. Results of this study suggest that AgNO3 is a highly effective low-cost non-toxic material which can be used in surface sterilization of D. sanderiana nodal explants. With this promising results it can be suggested that 200 mg/L AgNO3 solution can be considered to replace toxic heavy metals such as mercuric chloride frequently used in Micropropagation.