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Study on suitable for regeneration system of genetic transformation of Kiwifruit

机译:适合猕猴桃遗传转化再生体系的研究

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The stems of Actinidia Qinmei were taken as explants and induced callus formation after having gained the aseptic seedling in primary culture successfully, and then the calli were placed on different combinations regeneration medium. The results showed that the induction medium added 1 mg/L 6-BA and 0.1 mg/L NAA was beneficial to the callus induction in dark culture condition. The suitable regeneration medium was MS containing 2.0 mg/L 6BA, 0.1 mg/L NAA and 3% (W/V) sucrose, it could improve obviously the frequency of regenerated shoots. This method separated the callus induction from shoot regeneration and obtained more callus to optimize the regenerated medium, and also was advantageous to Kiwifruit genetic transformation.
机译:成功地在原代培养中获得无菌幼苗后,以猕猴桃秦梅的茎作为外植体并诱导愈伤组织形成,然后将愈伤组织置于不同的组合再生培养基上。结果表明,诱导培养基中加入1 mg / L的6-BA和0.1 mg / L的NAA有利于黑暗培养条件下的愈伤组织诱导。适宜的再生培养基为含有2.0 mg / L 6BA,0.1 mg / L NAA和3%(W / V)蔗糖的MS,它可以显着提高再生芽的频率。该方法从芽再生中分离出愈伤组织诱导,获得了更多的愈伤组织以优化再生培养基,并且有利于猕猴桃的遗传转化。

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