A method for long-term plant regeneration of Phaseolus coccineus L, is
described. Shoot-tips and cotyledonary nodes cultured on a Murashigc
and Skoog medium supplemented with N6-benzylaminopurine, 10 muM, and a
lpha-naphthaleneacetic acid, 1 muM, formed multiple bud-shoots. These
shoots were transferred to medium containing BAP 1 muM, NAA 0.1 muM, a
nd gibberellic acid 3 muM to promote shoot growth and further shoot mu
ltiplication. Rooting was achieved in medium with 11 muM indole-3-acet
ic acid. Rooted plants grew to maturity and were fertile. Cultures hav
e maintained their ability to regenerate plants for more than two year
s. A sample of 30 regenerated plants (R0) was tested for chromosome nu
mber, all of them being diploid; seven isozymatic systems were electro
phoretically analyzed in 82 R0 regenerated plants. No differences were
observed in their electrophoretic patterns in comparison with those s
hown by seedlings. Histological studies revealed the origin of buds fr
om calluses via organogenesis.