Transformed Vigna mungo (blackgram) calli were obtained by cocultivati
ng segments of primary leaves with Agrobacterium tumefaciens vir helpe
r strains harbouring the binary vector pGA472 having kanamycin resista
nce gene as plant transformation marker. Transformed calli were select
ed on Murashige and Skoog medium supplemented with 50 mg/l kanamycin a
nd 500 mg/l carbenicillin. Transformed calli were found to be resistan
t to kanamycin up to 900 mg/l concentration. Expression of kanamycin r
esistance gene in transformed calli was demonstrated by neomycin phosp
hotransferase assay. Stable integration of transferred DNA into V. mun
go genome was confirmed by Southern blot analysis.