Agrobacterium-Mediated Transformation of Cry8db Gene in Vietnam Sweet Potato Cultivar
1. Institute of Biotechnology, Vietnam Academy of Science and Technology, 18-Hoang Quoc Viet, Cau Giay, Ha Noi 10000, Vietnam
2. College of Science, Thai Nguyen University, Tan Thinh, Thai Nguyen 23000, Vietnam
3. University of Science and Technology of Ha Noi, 18-Hoang Quoc Viet, Cau Giay, Ha Noi 10000, Vietnam
Received: May 29, 2015 / Accepted: June 22, 2015 / Published: June 30, 2015.
The C58cv strain carrying a pBI121 backbone which contained cry8Db delta-endotoxin gene regulated under 35S CaMV promoter, and the selection marker gene, neomycin phosphotransferase (nptII) gene, was subjected for plant transformation. Callus induced from shoot tips and leaf explants were inoculated and cocultured with A. tumefaciens. The selection occurred during callus producing and plant regenerating steps. A total of 201 transgenic putative plant lines were produced, and 21 transgenic lines were positively confirmed by PCR and finalized by Southern blot. Four putative transgenic lines confirming a single copy of the cry8Db gene were transferred into soil pots in greenhouse. Biological activity evaluation for the insecticidal capacity of these transgenic lines under controlled conditions showed that the level of infestation by sweet potato weevils (Cylas formicarius) in untransformed plants was higher than that of transgenic lines.
Key words: Sweet potato, Agrobacterium tumefaciens, plant transformation, cry8Db, sweet potato weevil resistance, cylas formicarius.
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