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首页> 外文期刊>Plant Biosystems >Novel antibiotics regeneration and genetic transformation with RsMYB1 gene of recalcitrant chrysanthemum cv. Shinma
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Novel antibiotics regeneration and genetic transformation with RsMYB1 gene of recalcitrant chrysanthemum cv. Shinma

机译:具有克兰普拉氏菊花CV的RSMYB1基因的新型抗生素再生和遗传转化。 谢麦

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摘要

This research was conducted to develop genetic transformation of the recalcitrant chrysanthemum cv. Shinma by application of appropriate antibiotics and selective agents. Clavamox had the least inhibitory effect on shoot regeneration compared to timentin, carbenicillin, and cefotaxime. Clavamox, at a concentration of 125mgL(-1), was found to be the most suitable for shoot regeneration and production of quality shoots, suppressing the growth of Agrobacterium in explants infected with strains GV3101 or C58C1 for 3 and 4weeks, respectively. The concentration of phosphinothricin (PPT) was found to be 1.0mgL(-1) for screening of putative transgenic shoots. Moreover, transgenic chrysanthemums were obtained by culturing explants co-cultivated with A. tumefaciens strain GV3101 harboring an anthocyanin regulatory gene RsMYB1 isolated from radish (Raphanus sativus), which was placed under the control of cauliflower mosaic virus promoter (CaMV) 35S and petal-specific promoter InMYB1 isolated from the morning glory (Ipomoea nil), on shoot regeneration medium supplemented with recommended concentration of antibiotic and selective agent. Flow cytometry analysis revealed that there was no variation in ploidy level between transgenic plants and donor plants (non-transformants). To our knowledge, this is the first report of the use of Clavamox and MYB transcription factor for genetic transformation of this chrysanthemum.
机译:进行该研究以发展克里族菊花CV的遗传转化。 Shinma通过应用适当的抗生素和选择性剂。与所在因,碳皮尼林和头孢噻肟相比,Clavamox对芽再生的抑制作用是最少的抑制作用。发现浓度为125mg1(-1)的Clavamox是最适合于芽再生和质量芽的产生,抑制分别感染菌株Gvv3101或C58C1的外植体的农杆菌生长3和4周。发现膦素(PPT)的浓度为1.0mg1(-1),用于筛位推定的转基因芽。此外,通过培养与含有萝卜(Raphanus Sativus)分离的花青素调节基因RSMYB1培养的培养植物的培养植体进行转基因菊花,得到了萝卜(Raphanus Sativus)的rousthocyanin调节基因RSMyB1,该roudyaincaination基因rsmyb1置于花椰菜马赛克病毒启动子(CAMV)35s和Paver-的控制下特异性启动子INMYB1从早晨的辉煌(IPOMOEA NIL)中分离,用​​于补充有推荐的抗生素和选择性药剂的芽再生培养基。流式细胞术分析表明,转基因植物和供体植物(非转化体)之间没有倍率水平的变化。据我们所知,这是第一次使用Clavamox和MyB转录因子的遗传转化使用该菊花的报告。

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