Suspension culture cells of barley (Hordeum vulgare L. cv Pokko) were
stably transformed with two separate plasmids containing genes coding
for neomycin phosphotransferase II and beta-glucuronidase, respectivel
y. Transformed cultures were selected with the antibiotic Geneticin(R)
. Enzymatic activity was tested in the Geneticin(R) resistant cultures
, and in 96 % of them neomycin phosphotransferase could be detected. T
he non-selected marker, detected as beta-glucuronidase activity, was e
xpressed in 40 % of the resistant cultures. Stable transformation was
confirmed with Southern blot hybridization.