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Agrobacterium - mediated transformation of paulownia (Paulownia fortunei)

机译:农杆菌介导的泡桐转化(泡桐)

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Genetically transformed calli of paulownia (Paulownia fortunei) were generated at high frequency after co-cultivation of petiole segments with Agrobacterium tumefaciens strain LBA4404 that harbored a binary vector (pBI121) which included genes for GUS and NPT II. The effects of acetosyringone, carbon sources and pH on (he transformation of paulownia were examined. The presence of acetosyringone in the co-cultivation medium enhanced the induction efficiency of kanamycin- resistant calli. Sucrose wasmost suitable carbon source in the medium. The pH of the medium had no significant effect on the efficiency at pH 5 to 8. Successful transformation was confirmed by histochemical analysis of GUS activity in kanamycin-resistant calli, and by the detectionof NPT II gene in the genome. Kanamycin-resistant calli induced from petiole segments had the ability of regeneration, however, the frequency of regeneration of shoot was very low.
机译:与根癌农杆菌菌株LBA4404共培养叶柄片段后,高频率产生了泡桐遗传转化的愈伤组织(Paulownia fortunei),该菌株带有二元载体(pBI121),该载体包含GUS和NPT II基因。研究了乙酰丁香酮,碳源和pH对泡桐转化的影响。共培养培养基中乙酰丁香酮的存在增强了卡那霉素抗性愈伤组织的诱导效率。蔗糖是培养基中最合适的碳源。该培养基在pH 5至8时对效率没有明显影响。通过对卡那霉素抗性愈伤组织中GUS活性的组织化学分析以及基因组中NPT II基因的检测,证实了成功的转化。具有再生能力,但是芽的再生频率非常低。

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