Efecto de dos citoquininas, acido ascorbico y sacarosa en la obtencion de plantas in vitro de Sorghum bicolor para la formacion de callos

The current work aimed to obtain in vitro shoots by direct organogenesis from sorghum variety CIAP 2E-95, for the formation of calluses with embryogenic structures. Mature seeds were collected from plants grown under controlled conditions, which were disinfected and were placed in a germination medi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Revista Colombiana de biotecnologia 2012-07, Vol.14 (2), p.101
Hauptverfasser: Silvio de Jesús Martínez Medina, Rafael Gómez Kosky, Laisyn Posada Pérez, Raúl Barbón Rodríguez, Maira Acosta Suárez, Maritza Reyes Vega, Martha Pérez Benitez, Damaris Torres Rodíguez, Mileidys Pons Corona, Mariana La O Cardenas
Format: Artikel
Sprache:eng ; spa
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The current work aimed to obtain in vitro shoots by direct organogenesis from sorghum variety CIAP 2E-95, for the formation of calluses with embryogenic structures. Mature seeds were collected from plants grown under controlled conditions, which were disinfected and were placed in a germination medium with MS salts, myo-inositol 100 mg L-1, 3% sucrose, pH 5.7, phytagel 2.5 g L-1. Different concentrations of 6-benzylaminopurine (6-BAP) and kinetin were studied for shoot multiplication. Using 6 - BAP 0.22 mg L-1 in the multiplication culture mediumincreased the number of shoots per explant, showing phenolic oxidation. Adding 50 mg L-1 of ascorbic acid to the culture medium resisted phenolic oxidation and the number of sprouts (5.0), height and number of leaves increased significantly. Quality in vitro buds for callus formation were obtained stimulating the thickening by using MS salts, without growth regulators, ascorbic acid 50 mg L-1, phytagel 2.5 g L-1and pH 5.7 and 40 g L-1 of sucrose. The largest diameter of shoots, height, number of leaves and roots of in vitro plants, was achieved after 21 days of cultured in MS salts with 40 g L-1 sucrose. Calluses formation with embryogenic structures from the central cylinder of curled leaves of the nearest segment to the base of thickened shoots was achieved after 45 days of culture. Segments from the central cylinder of the curled leaves are a safe source for the formation of embryogenic calli.
ISSN:0123-3475
1909-8758