Protoplasts isolated from wild cotton Gossypium davidsonii were cultured in KM8P medium supplemented with different phytohormones. The most effective combination was 0.45 μM 2,4-dichlorophenoxyacetic acid, 2.68 μM α-naphthaleneacetic acid and 0.93 μM kinetin and the division percentage at the 8th day was 30.78 ± 3.04 %. The density of protoplasts at 2-10 × 105 cm-3 was suitable for protoplast division and calli formation, with a division percentage of 32.21 ± 3.64 % and a plating efficiency of 9.12 ± 2.61 % at the 40 th day. The optimal osmotic potential was achieved using 0.5 M glucose or 0.1 M glucose plus 0.5 M mannitol. Protoplasts were cultured in three ways, a double-layer culture system, with liquid over solid medium was proved to be the best way. Embryo induction was further increased by addition of 0.14 μM gibberellic acid. © 2007 Institute of Experimental Botany, ASCR.
CITATION STYLE
Yang, X., Guo, X., Zhang, X., Nie, Y., & Jin, S. (2007). Plant regeneration from Gossypium davidsonii protoplasts via somatic embryogenesis. Biologia Plantarum, 51(3), 533–537. https://doi.org/10.1007/s10535-007-0115-8
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