In vitro multiplication of clonal apple rootstock MM111
DOI:
https://doi.org/10.24154/jhs.v20i2.2902Keywords:
Apple, clonal rootstock, in vitro, MM111Abstract
The present investigation was carried out in five stages with an aim to establish the rapid and most economically viable methodology to facilitate in vitro propagation of clonal rootstock MM111 of apple using shoot tip and nodal segment as explants (0.5 to 0.75 cm). For culture establishment, MS medium was used either alone or in combination with 1.0 to 3.0 mg/L BAP and 1.0 to 3.0 mg/L GA3. Rooting medium involved half-strength MS medium with 0.5 to 2.0 mg/L NAA and 0.5 to 2.0 mg/L IBA along with 0.2% activated charcoal. The highest culture establishment (61.11 and 77.66%) in minimum days (32.20 and 25.40) was recorded with MS + 1.0 mg/L BAP + 1.0 mg/L GA3 for shoot tip and nodal segment explants, respectively. Maximum number of shoots (2.43 and 5.43) and shoot length (3.21 and 3.47 cm) were recorded using MS + 1.0 mg/L BAP + 1.0 mg/L GA3 with an addition of 0.2% NAA. The media composition involving half-strength MS + 1.0 mg/L NAA produced the highest rooted cultures (66.67%) in fewest days (13.00) amongst all the media compositions. Furthermore, the maximum survival rate (76.67%) of in vitro raised plantlets was observed with soil + sand + vermiculite + FYM (1:1:1:1, v/v/v/v).
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