Organogénesis indirecta en fresa (Fragaria x ananassa Duch.) usando dos tipos de explantes
DOI:
https://doi.org/10.57188/manglar.2026.022Keywords:
Callo, micropropagación, regeneración, reguladores de crecimientoAbstract
La propagación in vitro es importante por generar producción masiva de plantas homogéneas, libres de enfermedades y de gran calidad. El objetivo fue desarrollar un protocolo de organogénesis indirecta en fresa. Se usó dos explantes: hojas cotiledonares e hipocótilo. En desinfección se usaron tres concentraciones de hipoclorito de sodio (0,9; 1,1 y 1,3 %); en inducción a callos, se utilizó el medio basal MS con 2,4 D (0,2 mg. L-1 y 1 mg. L-1) y BAP (0,1 mg. L-1) o TDZ (1 mg. L-1); y, en regeneración de brotes, el medio basal MS con BAP (2 mg. L-1), TDZ (0,5 mg. L-1) y 2,4 D (0,2 mg. L-1) o ANA (0,2 mg. L-1). El diseño estadístico fue factorial 2x3 Completamente al azar. Los resultados, en hojas cotiledonares e hipocótilo, indicaron que el NaClO al 1,3% fue el más apropiado en desinfección, mientras que, el medio para inducir mayor porcentaje de callos fue con 0,2 mg. L-1 2,4 D y 1 mg. L-1 TDZ. Los mayores porcentajes de regeneración de brotes en hojas cotiledonares e hipocótilo fueron con los tratamientos de 2,4D y ANA respectivamente. El protocolo obtenido se constituye en un instrumento de valor para futuras investigaciones.
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Copyright (c) 2026 Gabriela Alexandra García-Carrasco, Arturo Adolfo Arbulú-Zuazo, Henry Robles-Cueva, Humberto Rivera-Calle, Luis Conrado Guzmán-Farfán

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