dc.description.abstract |
The study was undertaken with a view to establish a protocol for in vitro
culture and plant regeneration from shoot tip explants of banana cv.
Amritasagar and Sabri. This experiment was setup at Proshika Tissue Culture
Centre Trust (PTCCT) laboratory, Manikgonj during the period from April to
November, 2008. In the present study, BAP (0.0, 1.0, 2.0, 3.0, 4.0, 5.0, 6.0 and
7.0 mg/I) and ISA (0.0. 1.0, 2.0, 3.0, 4.0 and 5.0 mg/I) have been used in
different concentrations on MS medium to assess the influence on in vitro
shoot regeneration and subsequent root formation. Explants were sterilized by
0.1% I-lgCl2 for 14 minutes and cent percent shoot tip explants were found free
from contamination after 10 days of sterilization and inoculation. Explants of
Anritasagar and Sabri turned brown, light green, green and dark green in
colour after ID days of inoculation but after 20 days all became dark green at
all concentrations of BAP except control in Amritasagar and control and 1.0
mg/I in Sabri. The response of single shoot lbniiation in Amritasagar was the
highest (50%) followed by Sabri (300/4) at 5.0 mg/I BAP within 10-15 days.
Among the concentrations of BAP, 5.0 mg/I showed the best shoot
proliferation and the lowest was at 1.0 mg/I. No response was observed at
control. Shoot proliferation rate of Amritasagar was better than that of Sabri.
The eultivar Amritasagar and Sabri produced 3.50 shoots/explant and 2.00
shoots/explant, respectively at 5.0 mg/I BAP at 30 DAI. Amritasagar also
produced longer shoot (2.64 cm) compared to Sabri (2.16 cm) at 5.0 mg/I BAP
at 30 DAI. Among the concentrations of iSA, 3.0 mg/I proved to be the best for
root induction. Amritasagar showed superior performance (4.10 roots/plantict)
for root induction over Sabri (3.63 roots/plantlet) at 3.0 mg/I IBA at 30 DAI.
The survival of the plantlets of both eultivars tinder cx vitro condition was
more than 82% and all of them resumed growth in the field. |
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