Abstract

An efficient in vitro propagation protocol was developed for the production of bioactive compounds from shoot cultures of Aronia melanocarpa (Michx.) Elliott. Nodal explants obtained from mature field-grown plants of A. melanocarpa were cultured on Murashige and Skoog (MS) medium supplemented with 0.25, 0.5, 1.0 or 2.0mgl−1 thidiazuron (TDZ) alone or in combination with 0.1 or 0.5mgl−1 α-naphthaleneacetic acid (NAA) for shoot multiplication. Among the various concentrations of TDZ studied, the maximum frequency of shoot multiplication (85.2%), mean number of (10.4) shoots per explant and mean shoot length (3.2cm) were obtained on MS medium fortified with 0.5mgl−1 TDZ. The culture medium containing TDZ with low concentration of NAA produced more shoots than with high NAA concentration. The highest frequency of shoot multiplication (98.9%), mean number of (19.8) shoots per explant and mean shoot length (3.8cm) were obtained on MS medium fortified with 0.5mgl−1 TDZ and 0.1mgl−1 NAA. Hyperhydric shoots were observed on MS medium fortified with 2.0mgl−1 TDZ and 0.1mgl−1 NAA. The highest frequency of rooted shoots (100%), mean number of (10.6) roots per shoot and mean root length (5.4cm) were obtained on 1/2 MS medium fortified with 1.0mgl−1 IBA after 30 days of culture. The in vitro-developed plantlets were successfully acclimatized in the greenhouse with 100% survival. The highest contents of carotenoids, α-tocopherol and fatty acids were found in leaves collected from greenhouse-grown in vitro plants followed by normal and hyperhydric leaves obtained from in vitro-regenerated shoots. All-E-lutein was the most abundant carotenoid (65.1–191.4μgg−1 fresh weight) in A. melanocarpa leaf samples. Linolenic acid was the most abundant fatty acid in A. melanocarpa leaf samples tested, comprising 45.91–50.04% of total fatty acid.

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