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首页> 外文期刊>In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association >Improved Agrobacterium tumefaciens-mediated transformation of soybean [Glycine max (L.) Merr.] following optimization of culture conditions and mechanical techniques
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Improved Agrobacterium tumefaciens-mediated transformation of soybean [Glycine max (L.) Merr.] following optimization of culture conditions and mechanical techniques

机译:改进了肿瘤术造介型大豆介导的转化[甘氨酸MAX(L.)Merr。]培养条件优化和机械技术

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摘要

In the present study, Agrobacterium tumefaciens-mediated transformation of Glycine max (L.) Merr. (soybean) cv. DS-9712 using half-seed explants was optimized for eight different parameters, including seed imbibition, medium pH, infection mode (sonication and vacuum infiltration), co-cultivation conditions, concentrations of supplementary compounds, and selection. Using this improved protocol, maximum transformation of 14% and regeneration efficiencies of 45% were achieved by using explants prepared from mature seeds imbibed for 36 h, infected with A. tumefaciens strain EHA105 at an optical density (OD600) of 0.8, suspended in pH 5.4 medium containing 0.2 mM acetosyringone and 450 mg L-1 L-cysteine, followed by sonication for 10 s, vacuum infiltration for 2 min, and co-cultivated for 3 d on 35 mg L-1 kanamycin-containing medium. Independent transgenic lines were confirmed to be transgenic after -glucuronidase histochemical assays, polymerase chain reaction, and southern hybridization analysis. The protocol developed in the present study showed high regeneration efficiency within a relatively short time of 76 d. This rapid and efficient protocol might overcome some hurdles associated with the genetic manipulation of soybean.
机译:在本研究中,土壤杆菌癌症介导的甘氨酸Max(L.)Merr的转化。 (大豆)CV。 DS-9712针对八种不同参数进行了优化的DS-9712,包括种子吸收,培养基,感染模式(超声处理和真空浸润),共培养条件,补充化合物的浓度和选择。使用这种改进的协议,通过使用从吸收36小时的成熟种子制备的外植体在光密度(OD600)中悬浮在pH下的光密度(OD600)中,通过使用从成熟的种子制备的外植体实现14%和再生效率为45%的最大转化。 5.4含有0.2mM乙酰苯乙烯的培养基和450mg L-1 L-半胱氨酸,然后超声处理10 s,真空浸润2分钟,并在含35mg L-1卡那霉素的培养基上共培养3d。确认独立的转基因系在葡糖酶组织化学测定,聚合酶链反应和Southern杂交分析后是转基因的。本研究中开发的方案在76天的相对较短的时间内显示出高的再生效率。这种快速高效的协议可能会克服与大豆遗传操作相关的一些障碍。

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