Tissue cultures were established from newly expanded leaves and axillary buds of rubber trees (Hevea brasiliensis Muell. Arg.). Calli formed from these explants, but no regeneration occurred. Shoots were obtained from axillary buds cultured on Murashige and Skoog's (MS) medium (Physiol. 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 agar. Several types of explants were used in attempts to recover complete rubber tree plants with well-developed tap roots. Leaf explants and axillary buds formed calli on MS basic medium with different combinations of kinetin, benzylaminopurine (BAP), 2,4-D, IBA, NAA and indolylacetic 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 growth hormones. On this basic medium, callus cultures became necrotic and died. Shoots developed from axillary buds, rooted vigorously when cultured on MS medium with NAA, IAA, and IBA. Based on these results, further studies with commercially important clones should lead to a feasible micropropagation technique.
Culturas de tecidos in vitro foram estabelecidas de folhas recém-expandidas e de gemas axilares de seringueira (Hevea brasiliensis Muell. Arg.). Houve formação de calos nestes explantes mas a regeneração destes calos em embrióides não ocorreu. Brotos foram obtidos de gemas axilares cultivadas no meio de cultura básico de MS (Murashige and Skoog (Physiol. Plant. 15: 473-497, 1962)), suplementado com 1,0 mg/l de cinetina, 1,0 mg/l de ácido 2,4-diclorofenoxiacético (2,4-D), 20 g/l de sacarose e 4 g/l de ágar Difco. Para o desenvolvimento do sistema radicular com raiz pivotante o meio de cultura usado foi o MS, suplementado com 5,0 mg/l de ácido naftalenoacético (NAA); 3,0 mg/l de ácido indolilbutírico (IBA); 50 g/l sacarose e 4,0 g/l ágar Difco