ABSTRACT
Successful in vitro propagation through ex vitro rooting mechanism has been achieved in Piper
longum by nodal shoot segment cultures. Shoot tip explants were less proliferative compared to the
nodal meristems. The explants were sterilized using 0.1% HgCl2 and cultured on Murashige and Skoog
(MS) medium with various concentrations of growth regulators. MS medium supplemented with 1.0
mg/L 6-benzylaminopurine (BAP) was found suitable for bud breaking within four weeks. Kinetin
(Kin) was not reported impressive compared to BAP in culture induction response. The shoots were
multiplied and elongated on MS medium supplemented with 0.5 mg/L each of BAP and Kin and 0.1
mg/L indole-3 acetic acid (IAA), where the shoots were elongated up to 5.8 cm length. Rooting and
acclimatization was achieved by ex vitro rooting methods using 300 mg/L indole-3 butyric acid (IBA)
for 5 min, and 5.3 roots with 3.2 cm average length were observed. The rooted shoots were transferred
to the greenhouse for acclimatization. The hardened plantlets were transferred to earthen pots and
maintained in the greenhouse. Normal flowering was observed in micropropagated plants of P.
longum
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