Adventitious shoots of sweetpotato (Ipomoea batatas L. Lam.) were prod
uced in vitro using a two-stage culture method. Petiole explants were
incubated on Murashige and Skoog (MS) medium supplemented with 2,4-dic
hlorophenoxy acetic acid (0.2 mg.liter(-1)) for 3 d, and transferred t
o MS medium with thidiazuron (0 to 0.4 mg.liter(-1)). Shoot regenerati
on was observed in most explants (78.2%) of genotype PI 318846-3 withi
n 28 days when cultured on thidiazuron at 0.2 mg liter(-1). Histologic
al studies of cultured petiole explants showed meristematic activity w
ithin cells of vascular bundles and throughout the ground tissue. Expl
ants isolated from apical leaves exhibited higher shoot regeneration f
requency than those isolated from the basal portion of the shoot. Leaf
lamina explants exhibited lower frequency of regeneration than petiol
e explants. In contrast to thidiazuron, the use of zeatin riboside, an
d kinetin resulted in a lower frequency of shoot regeneration although
more sweetpotato genotypes could be regenerated using either of these
two cytokinins. The sweetpotato plants regenerated using thidiazuron
grew vigorously and rooted easily when transferred to the greenhouse.