Transient and stable expression of foreign genes has been achieved in
sweet potato using the particle bombardment system of gene delivery. C
allus and root isolates of two genotypes (Jewel and TIS-70357) with po
sitive signs of transformation have been recovered. Tungsten microcarr
iers coated with plasmid DNA (pBI221 containing the gusA gene) were ac
celerated at high velocity using a biolistic device into sweet potato
target tissues. Histochemical examination of bombarded leaf and petiol
e explants revealed that most had cells expressing the gusA gene. When
explants were cultured, calli and roots developed in most bombarded t
issues. Similar results but with a lower frequency of transformation w
ere observed when the plasmid pBI121 (with gusA and antibiotic resista
nce nptII genes) was employed and bombarded explants cultured on an an
tibiotic selection medium. Subcultured roots and calli were positive f
or gusA expression when tested even after one year of in vitro culture
, and thus the expression of the foreign gene is fairly stable. The pa
rticle bombardment approach of gene delivery appears to have a potenti
al for generating transgenic sweet potatoes with useful agronomic trai
ts.