Abstract
A rice chitinase gene (RCC2) multiplied in Agrobacterium strain (EHA 101), wassimultaneously introduced into single buds of in vitro grown banana cultivar, Rastali (AAB).Plasmid pBI333-EN4-RCC2 contained a hygromycin phosphotransferase gene (hptII) as theselectable marker and gusA gene as a reporter marker to identify the transformants. Single budsderived from multiple bud clumps (Mbcs), were the target explants for transformation.Transformation frequency based on hygromycin selection (25 mg L-1) was higher, although nopositive transformant was confirmed based on PCR and Southern blot analyses. Stable gusAgene expression was detectable in transformed single buds, multiple bud clumps, shoots, leavesand roots derived from hygromycin selection at 50 mg L-1 ). An assay was performed to identifythe minimum concentration of two antibiotics most effective against Agrobacterium EHA 101.Protein assay showed an increase in chitinase enzyme activity of transformed plantlets. TheAgrobacterium-mediated transformation protocol reported here is suitable for future selection ofbanana meristem tissues resistant to fungal disease.
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Sreeramanan, S., Maziah, M., & Xavier, R. (2009). A protocol for Agrobacterium-mediated transformation of banana with a rice chitinase gene. Emirates Journal of Food and Agriculture, 21(2), 18–33. https://doi.org/10.9755/ejfa.v21i2.5161
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