Transgenic plants of Gladiolus were produced following particle bombar
dment of cormel slices. Plant cells were cotransformed with the gene f
or phosphinothricin acetyltransferase under control of the cauliflower
mosaic virus 35S promoter and the uidA gene coding for beta-glucuroni
dase (GUS) under control of the actin promoter isolated from rice. The
optimum concentration for the first selection of transformed plants w
as 8 mg/l phosphinothricin which resulted in 14% of the bombarded corm
el slices regenerating plants that were transformed as confirmed by po
lymerase chain reaction amplification. Polymerase chain reaction ampli
fication, Southern hybridization and histochemical staining for GUS ge
ne expression on plants after two selective screenings with phosphinot
hricin indicated that regenerated plants were transformed. Histochemic
al staining for GUS gene expression showed that the actin promoter res
ulted in GUS gene expression primarily in callus cells and root merist
ems. Leaves were typically chimeric for GUS gene expression.