A reproducible method has been developed for the Biolistic transformat
ion and regeneration of transgenic plants from embryogenic callus of r
ose (Rosa hybrida L.) cv. Glad Tidings. DNA delivery was optimized usi
ng the beta-glucuronidase (gus) gene. The distance between the stoppin
g screen and target explants and supplementation of pre- and post-bomb
ardment culture media with 0.25 M myo-inositol influenced the transfor
mation efficiency. Prior to culture on selection medium containing 250
mg 1(-1) kanamycin sulphate, embryogenic calli were bombarded, using
optimized gene delivery parameters, with a plasmid carrying the neomyc
in phosphotransferase (npt II) gene. Somatic embryo-derived kanamycin-
resistant plants were regenerated and subsequently transferred to glas
shouse conditions. Transformation was confirmed by kanamycin resistanc
e of calli and plants, NPT II ELISA assay and Southern analysis. All t
ransgenic plants were morphologically normal (true-to-type). (C) 1998
Annals of Botany Company.