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   <subfield code="a">Plant regeneration from Gossypium davidsonii protoplasts via somatic embryogenesis</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[X. Yang, X. Guo, X. Zhang, Y. Nie, S. Jin]</subfield>
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   <subfield code="a">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 40th 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.</subfield>
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   <subfield code="a">Institute of Experimental Botany, ASCR, 2007</subfield>
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   <subfield code="a">CPW : cell and protoplast washing solution (Frearson et al. 1973)</subfield>
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   <subfield code="a">FDA : fluorescein diacetate</subfield>
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   <subfield code="a">GA3 : gibberellic acid</subfield>
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   <subfield code="a">IBA : indole-3-butyric acid</subfield>
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   <subfield code="a">Kn : kinetin</subfield>
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   <subfield code="a">MES : 2-(N-morpholino)ethane sulfonic acid</subfield>
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   <subfield code="a">MSB : MS medium (Murashige and Skoog 1962) and B5 (Gamborg et al. 1968) vitamins</subfield>
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