Internodes, leaves and tuber slices from potato (Solanum tuberosum), genoty
pe 1024-2, were subjected to particle bombardment. Transient expression was
optimized using the uidA and the luc reporter genes that encode beta -gluc
uronidase (GUS) and luciferase, respectively. Stable transformation was ach
ieved using the neomycin phosphotransferase (nptII) gene, which confers res
istance to the antibiotic kanamycin. The influence of biological parameters
(tissue type, growth period before bombardment, pre- and post-bombardment
osmoticum treatment) and physical parameters (helium pressure, tissue dista
nce) that are known to possibly affect stable transformation were investiga
ted. Putative transgenic plants, which rooted in media containing kanamycin
, were obtained from all of the tissues tested although there were large di
fferences in the efficiency: internodes (0.77 plants per bombarded explant)
, microtuber slices (0.10 plants per bombarded explant) and leaves (0.02 pl
ants per bombarded explant). Southern blot analysis of putative transgenic
plants confirmed the integration of the transgenes into plant DNA. The resu
lts indicate that an efficient particle bombardment protocol is now availab
le for both transient and stable transformation of potato internodal segmen
ts, thus contributing to an enhanced flexibility in the delivery of transge
nes to this important food crop.