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A simplified and efficient Agrobacterium tumefaciens electroporation method

机译:一种简便有效的根癌农杆菌电穿孔方法

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摘要

Agrobacterium tumefaciens is a widely used microbial tool in plant molecular biology to transfer DNA into plant cells and produce, e.g., stable or transient transformants or induce gene silencing. In our study, we present a simplified version of electrocompetent cell preparation that is not only time and cost efficient, but it requires minimal handling of bacterial cells. Liquid cultures are normally used to prepare competent Agrobacterium cells. To overcome the difficulties of working with liquid cultures, we propose suspending bacterial cells directly from overnight agar plate cultures. In addition, we optimized several parameters to simplify the procedure and maximize the number of transformants (e.g., Agrobacterium strains, number of washing steps, amount of required plasmid DNA, electroporation parameters, type of incubation media, or incubation time). This optimized, simple, and fast protocol has proved to be efficient enough to obtain transformed colonies with low amounts (as little as 1 ng) of plasmid DNA. In addition, it also enabled us to introduce ligated plasmids directly into Agrobacterium omitting the E. coli transformation step and accelerating the cloning procedure further.
机译:根癌农杆菌是植物分子生物学中广泛使用的微生物工具,用于将DNA转移到植物细胞中并产生例如稳定或瞬时转化体或诱导基因沉默。在我们的研究中,我们提出了一种具有电感受态的细胞制备方法的简化版本,该方法不仅省时省钱,而且对细菌细胞的处理最少。液体培养物通常用于制备感受态农杆菌细胞。为了克服使用液体培养物的困难,我们建议直接从过夜琼脂平板培养物中悬浮细菌细胞。另外,我们优化了几个参数以简化程序并最大化转化体的数量(例如农杆菌菌株,洗涤步骤数,所需质粒DNA的数量,电穿孔参数,孵育介质的类型或孵育时间)。事实证明,这种优化,简单且快速的方案足以有效地获得少量(低至1 ng)质粒DNA的转化菌落。此外,它还使我们能够将连接的质粒直接导入农杆菌中,从而省去了大肠杆菌的转化步骤,并进一步加快了克隆过程。

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