Abstract
The development and homogeneity of apple trees are affected by rootstocks, but the output through conventional methods is seasonal and limited by many factors. The aim of the research was to establish the fastest and most economically viable methodology to facilitate in vitro propagation of clonal apple rootstock MM106. Explants (shoot tip and nodal segment) were surface sterilized using 3.0 to 12.0% NaOCl for 10–30 min and 0.05–0.3% HgCl2 for 2–6 min. For culture establishment, MS medium was used either alone or with 1.0–3.0 mg/l BAP and 1.0–3.0 mg/l GA3. Rooting medium involved half-strength MS medium with 0.5–2.0 mg/litre NAA and 0.5–2.0 mg/l IBA along with 0.2% activated charcoal. The highest culture establishment of 47.77 and 57.77% in the minimum number of days, i.e., 32.30 and 26.33, respectively, while the number of days taken for shoot proliferation (52.40 and 46.26), number of shoots (2.40 and 4.76) and shoot length (3.19 and 3.42 cm), were recorded using the MS + 1.0 mg/l BAP + 1.0 mg/litre GA3. The media composition involving half-strength MS + 1.0 mg/litre NAA produced the highest percentage of rooted cultures (60.00) in the fewest number of days amongst all the media compositions. Furthermore, the maximum survival rate (53.33) of in vitro raised plantlets was observed with soil + sand + vermiculite + FYM (1:1:1:1 v/v/v/v) with more leaves.
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All authors are very thankful to Sher-e-Kashmir University of Agricultural Sciences and Technology of Jammu, Main Campus, Chatha (J&K) for timely support and coordination.
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M. Lal, M. Jamwal, P. Bakshi, N. Sharma, A. Jasrotia and A. Sharma declare that they have no competing interests.
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Lal, M., Jamwal, M., Bakshi, P. et al. An Improved Protocol for Rapid in Vitro Multiplication of Clonal Apple Rootstock MM106. Erwerbs-Obstbau 65, 2241–2248 (2023). https://doi.org/10.1007/s10341-023-00988-4
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DOI: https://doi.org/10.1007/s10341-023-00988-4