Transgenic tare (Colocasia esculenta Schott) plants were obtained by high-v
elocity particle bombardment. The plasmid pREXHGUS, carrying the hygromycin
resistance gene, was used as a selection marker. Highly regenerative tare
callus was obtained from the apical meristem, and maintained in liquid cult
ure. The callus was chopped into small Fragments with a forceps, then trans
formed and selected on LS medium containing BA, NAA and hygromycin. Since t
he transformed calli obtained showed vigorous growth on LS-BN medium with 2
0 mg/L hygromycin, this concentration was considered to be suitable for the
selection of transgenic tare. The transformants were confirmed by amplific
ation of the GUS gene, and Southern hybridization. The expression of the fo
reign gene was demonstrated by the GUS activity.