4.7 Article

In Vitro Propagation of Pyracantha angustifolia (Franch.) CK Schneid.

Journal

HORTICULTURAE
Volume 8, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/horticulturae8100964

Keywords

culture medium; micropropagation; ornamental trees and shrubs; plant growth regulators

Categories

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This study presents an efficient in vitro propagation method for narrow-leaf firethorn, using different hormones and culture media for axillary shoot multiplication and root induction.
Narrow-leaf firethorn or pyracantha (Pyracantha angustifolia (Franch.) C.K. Schneid.), from the family Rosaceae, is a species of large and thorny evergreen shrub. In this study, a procedure is presented for efficient axillary shoot multiplication and root induction in P. angustifolia using Murashige and Skoog (MS), woody plant (WPM), and Linsmaier and Skoog (LS) culture media supplanted with 6-benzylaminopurine (BAP) and indole-3-butyric acid (IBA). The disinfection of the axillary buds was performed with a 70.23% success rate on a basal MS medium augmented with 0.5 mg center dot L-1 gibberellic acid (GA(3)). Uniform and axenic explants were then cultured on MS, WPM, and LS media enriched with different concentrations of BAP, 0.3 mg center dot L-1 GA(3), and 0.1 mg center dot L-1 IBA. The highest multiplication coefficient (2.389) was obtained for the MS medium supplemented with 2.5 mg center dot L-1 BAP. After one month, newly formed micro-shoots were transferred to rooting media (MS, WPM, and LS) containing different concentrations of IBA, together with a constant concentration of 0.1 mg center dot L-1 BAP. The micro-shoots were kept in the dark for one week and then cultured in a 16/8 h light/dark regime. The MS medium supplemented with 1 mg center dot L-1 IBA was the most effective in stimulating rooting (88.76% of micro-shoots). The highest number of roots (3.5 per micro-shoot) was produced in the MS medium enriched with 1.5 mg center dot L-1 IBA. The rooted plantlets were transferred into pots filled with perlite and peat moss in a 2:1 proportion and acclimatized to ambient greenhouse conditions, with a resultant mean 92.84% survival rate. Thus, this protocol can be successfully applied for the in vitro mass propagation of P. angustifolia.

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