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In vitro propagation of Leptocarpha rivularis,a native medicinal plant
Authors:Dorta  Fernando  Polanco  Victor  Ramírez  Ingrid  Seeger  Michael  Madrid  Alejandro  Montenegro  Iván
Affiliation:1.Centro de Biotecnología “Dr. Daniel Alkalay Lowitt”, Universidad Técnica Federico Santa María, Avda. España 1680, 2390123, Valparaíso, Chile
;2.Centro de Genómica y Bioinformática, Facultad de Ciencias, Universidad Mayor, Camino la Pirámide 5750, 8580000, Santiago, Chile
;3.Laboratorio de Microbiología Molecular y Biotecnología Ambiental. Departamento de Química, Universidad Técnica Federico Santa María, Avda. España 1680, 2390123, Valparaíso, Chile
;4.Laboratorio de Productos Naturales y Síntesis Orgánica (LPNSO), Departamento de Química, Facultad de Ciencias Naturales y Exactas, Universidad de Playa Ancha, Avda. Leopoldo Carvallo 270, Playa Ancha, 2340000, Valparaíso, Chile
;5.Escuela de Obstetricia y Puericultura, Facultad de medicina, Universidad de Valparaíso, Angamos 655, Reñaca, 2520000, Viña del Mar, Chile
;
Abstract:

Leptocarpha rivularis, commonly known as “palo negro”, is a species of the Astereaceae family, endemic in the forests of Southern Chile. The extracts of this plant have medicinal properties attributable to its secondary metabolites, mainly identified as flavonoids and terpenes. Among them, leptocarpine has gained importance as a powerful anticarcinogen. The aim of this study was the in vitro establishment of L. rivularis to develop future alternatives to obtain biomass for medicinal purposes. Young shoots obtained from plants in growth chambers were treated with Captan™ (2.5% (w/v)), subjected to disinfection method with ethanol, commercial chlorine, and antioxidants and tested in different Murashige & Skoog based media to establish in vitro culture. The most effective growth was observed with half strength Murashige & Skoog medium supplemented with 20 g L−1 sucrose and 3.2 g L−1 gelrite (MGS medium) with 95% survival at 30-d and shooting reaching 82% of the explants when Plant Preservative Mixture™ is added to the medium. The addition of 1 mg L−1 of indole-3-butyric acid to the MSG medium was necessary for inducing roots and obtaining well-rooted plants that were acclimatized and successfully established in the greenhouse. Our study represents the first report describing the in vitro culture of L. rivularis, allowing the sustainable use of this plant.

Keywords:
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