Main Article Content
Somatic embryogenesis and plant regeneration of recalcitrant cottons (Gossypium hirsutum)
Abstract
Many restrictive factors still remain in cotton tissue culture such as long duration, unpredictability and a high degree of genotype dependence. The main objective of this study was to develop a protocol
allowing consistent somatic embryogenesis and plant regeneration from five recalcitrant cotton cultivars. Our results showed that the best medium for calli induction is MSB (MS medium + vitamine B5) supplemented with indolebutyric acid (IBA, 0.1 mg.l-1), kinetin (KIN, 0.1 mg.l-1) and 2,4- dichlorophenoxyacetic acid (2,4-D, 0.1 mg.l-1). Embryogenic calli of all the five genotypes used were successfully from MSB medium supplemented with IBA (0.3 mg.l-1) and KIN (0.05 mg.l-1). Somatic embryos and transformation of somatic embryos into plants were successfully induced on MSB medium supplemented with ½×NH4NO3 (825 mg.l-1), 2×KNO3 (3800 mg.l-1), glutamine (2.0 g/l) and asparagines (0.5 g/l). The protocol developed in this study for cotton plant regeneration could be shortened to 4 - 5 months. Furthermore, the firstly-obtained regenerated plants of above five cultivars will broaden the range of genotypes for in vitro manipulation for cotton improvement.
allowing consistent somatic embryogenesis and plant regeneration from five recalcitrant cotton cultivars. Our results showed that the best medium for calli induction is MSB (MS medium + vitamine B5) supplemented with indolebutyric acid (IBA, 0.1 mg.l-1), kinetin (KIN, 0.1 mg.l-1) and 2,4- dichlorophenoxyacetic acid (2,4-D, 0.1 mg.l-1). Embryogenic calli of all the five genotypes used were successfully from MSB medium supplemented with IBA (0.3 mg.l-1) and KIN (0.05 mg.l-1). Somatic embryos and transformation of somatic embryos into plants were successfully induced on MSB medium supplemented with ½×NH4NO3 (825 mg.l-1), 2×KNO3 (3800 mg.l-1), glutamine (2.0 g/l) and asparagines (0.5 g/l). The protocol developed in this study for cotton plant regeneration could be shortened to 4 - 5 months. Furthermore, the firstly-obtained regenerated plants of above five cultivars will broaden the range of genotypes for in vitro manipulation for cotton improvement.