Establishment of a shoot proliferation protocol for banana (abb group) cv. ‘pisang awak’ via temporary immersion system

• Published in: Journal of plant nutrition Vol. 36; no. 4; pp. 529 - 538
• Main Authors: Hui, Au Vun, Bhatt, Arvind, Sreeramanan, S, Keng, Chan Lai
• Format: Journal Article
• Language: English
• Published: Philadelphia, NJ Taylor & Francis Group 01.01.2013; Taylor & Francis; Taylor & Francis Ltd
• Subjects: Agronomy. Soil science and plant productions; bananas; benzyladenine; Biological and medical sciences; Economic plant physiology; explants; Fundamental and applied biological sciences. Psychology; inoculum; Metabolism; Metabolism. Physicochemical requirements; Musa spp; Nutrition. Photosynthesis. Respiration. Metabolism; Pisang Awak; Plant physiology and development; shoot proliferation; shoots; sucrose; temporary immersion system; vitrification; Monocotyledones; Protocols; Tropical crop; Climacteric; Musaceae; shoot proliferation; Immersion; Proliferation; System; Banana; Musa spp; Musa; Tropical fruit; Fruit crop; Plant nutrition; Angiospermae; Spermatophyta; Pisang Awak; temporary immersion system
• ISSN: 1532-4087; 0190-4167; 1532-4087
• DOI: 10.1080/01904167.2012.748068

□ Initial study of evaluating the factors affecting shoot proliferation of ‘Pisang Awak’ using temporary immersion system was carried out using four half shoots in each experimental unit as explants and repeated with four to seven experimental units for each factor. The inoculum size finally used for shoot proliferation was eight half-shoots for each experimental unit (250 mL culture flask) in MS liquid medium supplemented with 5.0 mg L⁻¹ benzyladenine (BA) and 30 g L⁻¹ sucrose, the shoot proliferation medium and an average of 4.9 ± 0.3 shoots was produced from each half-shoot explant after five weeks of culture. The final protocol for shoot proliferation using the temporary immersion system was established by inoculating eight half-shoot explants into the shoot proliferation medium adjusted to pH 5.7 with the inoculated shoots immersed once a day in the medium for 10 minutes. The cultures were incubated under continuous light for enhancement of shoot proliferation without vitrification.