Tissue cultures were established from newly expanded leaves and axilla
ry buds of rubber trees (Hevea brasiliensis Muell. Arg.). Calli formed
from these explants, but no regeneration occurred. Shoots were obtain
ed from axillary buds cultured on Murashige and Skoog's (MS) medium (P
hysiol. Plant. 15: 473-497, 1962) supplemented with 1.0 mg/l kinetin,
1.0 mg/l 2,4-dichlorophenoxyacetic acid (2,4-D), 20 g/l sucrose and 4
g/l Difco agar. Formation of a root similar to a tap root was induced
on MS medium supplemented with 5.0 mg/l naphthaleneacetic acid (NAA),
3.0 mg/l indolylbutyric acid (IBA), 50 g/l sucrose and 4 g/l Difco a,o
ar. Several types of explants were used in attempts to recover complet
e rubber tree plants with well-developed tap roots. Leaf explants and
axillary buds formed calli on MS basic medium with different combinati
ons of kinetin, benzylaminopurine (BAP), 2,4-D, IBA, NAA and indolylac
etic acid (IAA). The antibiotic tetracycline was also used to control
possible bacterial infections. However, no antibiotic effect was noted
. Calli formation was abundant, but no regeneration was observed when
the calli from different media was transferred to MS medium without gr
owth hormones. On this basic medium, callus cultures became necrotic a
nd died. Shoots developed from axillary buds: rooted vigorously when c
ultured on MS medium with NAA, IAA, and IBA. Based on these results, f
urther studies with commercially important clones should lead to a fea
sible micropropagation technique.