Abstract
Introduction. The significant reduction of orchards in recent decades is associated with the impact of unfavorable abiotic factors and the spread of bacterial pathogens, leading to a considerable decline in pear cultivar diversity. The rapid introduction of resistant cultivars and rootstocks into commercial horticulture is constrained by the limited availability of high-quality planting material. Methods. This study presents the results of clonal micropropagation of the seedling pear rootstock Pyrus pyraster and clonal rootstocks OHxF230 and OHxF69 . An optimal explant sterilization protocol ensuring high survival during the establishment of aseptic culture was developed. The effects of different concentrations of nitrogen salts (NH₄NO₃ and KNO₃) and plant growth regulators (BAP, IBA, GA₃) on shoot proliferation were evaluated. Results. Sterilization of Pyrus pyraster explants with 0.2 % HgCl₂ for 4 min resulted in the highest shoot regeneration rate (78.57 %), whereas shorter exposure increased contamination levels. The highest multiplication efficiency was achieved on a medium containing 75 % of the standard nitrate salt concentration supplemented with 0.8 mg L⁻¹ BAP, 0.5 mg L⁻¹ GA₃, and 0.1 mg L⁻¹ IBA. In contrast, a higher BAP concentration (1.8 mg L⁻¹) combined with reduced nitrogen levels decreased proliferation efficiency, particularly in Pyrus pyraster. However, a relatively high multiplication coefficient (2.67 ± 1.15) was observed for OHxF230 . Conclusions. The results demonstrate the potential to optimize in vitro culture conditions to enhance the efficiency of pear rootstock micropropagation and can be applied to the development of biotechnological propagation protocols.
01 Introduction
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02 References
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