首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >A simple and efficient procedure to improve plant regeneration fromprotoplasts isolated from long-term cell-suspension cultures of Indicarice
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A simple and efficient procedure to improve plant regeneration fromprotoplasts isolated from long-term cell-suspension cultures of Indicarice

机译:一种简单有效的方法,可改善从Indicarice的长期细胞悬浮培养物中分离的原生质体中的植物再生

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摘要

A simple and efficient method has been developed to improve plant regeneration from protoplasts isolated from >1-yr-old cell-suspension culture of Indica rice (Oryza sativa) cv. Pusa Basmati I. A two-step regeneration procedure, involving the transfer of calluses to shoot-regeneration medium containing 1% (w/v) agarose prior tc, culture on a medium containing 0.4% (w/v) agarose, was found to improve plant regeneration. high concentrations of kinetin in the regeneration medium were also found to be beneficial. The two-step regeneration procedure, combined with a high concentration of kinetin (10.0 mg l(-1)) in the medium, significantly increased plant regeneration. By this method, even though protoplasts were isolated from over 1-yr-old cell-suspension cultures, protoplast-derived plant regeneration frequency reached 16.1%, compared with <4% regeneration frequency without such treatment. Use of a similar protocol might improve plant regeneration from other plant species, especially recalcitrant species.
机译:已经开发出一种简单有效的方法来改善从from稻(Oryza sativa)cv的> 1岁细胞悬浮培养物中分离的原生质体的植物再生。 Pusa Basmati I.发现分两步进行的再生程序:将愈伤组织转移至含有1%(w / v)琼脂糖的芽再生培养基,然后在含有0.4%(w / v)琼脂糖的培养基上进行培养。改善植物再生。还发现在再生培养基中高浓度的激动素是有益的。两步再生程序,与培养基中高浓度的激动素(10.0 mg l(-1))结合,可显着提高植物的再生能力。通过这种方法,即使从超过1岁的细胞悬浮培养物中分离出原生质体,原生质体衍生的植物再生频率也达到了16.1%,而未经这种处理的再生频率不到4%。使用类似的协议可能会改善其他植物物种(特别是顽it物种)的植物再生。

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