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Abstract
Aim: The aim of this
experiment was to optimize a procedure for in-vitro micro-propagation of
Miniature Rose cv. Ice Fairy (Rosa hybrida L.) utilizing the nodal
segments as an explant.
Methodology: The impact of
cytokinins and gibberellins was investigated under in-vitro conditions.
Different levels of BAP (6- Benzylaminopurine) (1, 1.5, 2, 2.5 mg l-1),
focusing on the developmental stages of explant whereas GA3
(Gibberellic acid) was employed for shoot elongation and flowering. Activated
charcoal (1 g l-1) was added into the medium to inhibit phenolic
oxidation.
Results: The highest shoot
initiation was found in treatment T4 (94 %) with culture survival
rate of 86 % when Murashige and Skoog (MS) medium was supplemented with 2.5
mg l-1 BAP and 1 g l-1 activated charcoal. The highest
number of elongated shoots were noted in the medium containing 2.5 mg l-1
BAP and 1 mg l-1 GA3. It was observed that MS media
supplemented with BAP was successful for shooting as well as rooting. In-vitro
plantlets with 5 to 6 roots, each measuring 4-5 cm in length were carefully
removed and transplanted into sterilized glass jars. The jars had a mixture
of sand, coco-peat and soil in 1:1:2 (v/v) ratio, which was moistened with 30
% of MS basal liquid medium.
Interpretation: These findings
may therefore contribute towards the commercial micropropagation of miniature
roses.
Key
words:
6-Benzylaminopurine, In-vitro propagation, Miniature rose, MS media,
Phenolic oxidation
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