To develop a less genotype-dependent maize-transformation procedure, w
e used 10-month-old Type I callus as target tissue for microprojectile
bombardment. Twelve transgenic callus lines were obtained from two of
the three anther-culture-derived callus cultures representing differe
nt gentic backgrounds. Multiple fertile transgenic plants (T-0) were r
egenerated from each transgenic callus line. Transgenic leaves treated
with the herbicide Basta showed no symptoms, indicating that one of t
he two introduced genes, bai, was functionally expressing. Data from D
NA hybridization analysis confirmed that the introduced genes (bar and
uidA) were integrated into the plant genome and that all lines derive
d from independent transformation events. Transmission of the introduc
ed genes and the functional expression of bar in T-1 progeny was also
confirmed. Germination of T-1 immature embryos in the presence of bial
aphos was used as a screen for functional expression of bar; however,
leaf painting of T-1 plants proved a more accurate predictor of bar ex
pression in plants. This study suggests that maize Type I callus can b
e transformed efficiently through microprojectile bombardment and that
fertile transgenic plants can be recovered. This system should facili
tate the direct introduction of agronomically important genes into com
mercial genotypes.