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Abstract
Aim: To develop a
systematic and robust in vitro multiplication method for production of guava
rootstock.
Methodology:
Nodal segments and shoot tip explants were sourced from in vitro and poly
house raised seedlings. These explants were inoculated in Murashige and Skoog
(MS) basal media supplemented with different concentrations and combinations
of growth regulators for establishment, shoot proliferation and root
induction.
Results: The supplementation
of basal MS media with 6-Benzylaminopurine (BAP) (2.0 mg l-1) +
Kinetin (0.5 mg l-1) facilitated the successful establishment of
explants sourced from in vitro raised guava seedlings, resulting in higher
establishment rates for nodal segments (62.67 %). Optimal shoot proliferation
(55.70 %) and shoot length (2.78 cm) was achieved by incorporating BAP (2.0
mg l-1) + gibberellic acid (GA3) (0.5 mg l-1)
into the MS media whereas 1-Naphthaleneacetic acid (NAA) at a concentration
of 0.5 mg l-1 resulted in the highest levels of root induction
(54.63%) and number of roots per shoot (2.94).
Interpretation: Successful in vitro
regeneration of guava plants was attained by adding 2.0 mg l-1 of
BAP and 0.5 mg l-1 of GA3 to the MS medium for highest
shoot proliferation with NAA @ 0.5 mg l-1 for the optimum rooting
of plantlets. The rooted plants were effectively acclimatized using a mixture
of cocopeat, vermiculite and perlite (2:1:1) as a growing medium.
Key
words:
Micropropagation, Psidium guajava, Plant growth regulators, Tissue
culture
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