Mikhail Baryshev, Dmitrijs Merkulov, Ivan Mironov
Institute of Microbiology and Virology, Riga Stradins University, Ratsupites Str 5, Riga, 1067, Latvia.
ELMI Ltd, A Sakharova Str 8-18, Riga, 1021, Latvia.
AMB Express. 2022 Feb 22;12(1):21. doi: 10.1186/s13568-022-01360-7.
Small-scale plasmid DNA preparation or miniprep is a fundamental technique in estimation cloning experiments and is widely used for DNA methylation analysis in epigenetic research. Current plasmid DNA minipreps use the alkali-SDS-based method in a three-solution format and require spin column-based purification steps. This procedure requires the vortexing or pipetting of pelleted bacteria by centrifugation and manual mixing of the solutions. Here, we describe a centrifuge/mixer-based instrument with the ability to perform centrifugation, vibration, and rotor oscillation in order to perform all steps of plasmid DNA isolation by device only. We found that by applying rotor oscillation-driven mixing of solutions added in the lysis and neutralization steps, homogeneous mixing was achieved within 5 s at a rotor oscillation amplitude of 45° and oscillation frequency of 400 ± 30 rpm, yielding the maximal quantity and quality of plasmid DNA. No increase in host chromosome presence purified by this approach occurs for high-copy-number plasmids compared to manually performed miniprep, and indeed, there is a significant decrease in the presence of the chromosomal fraction in low-copy-number plasmids. The supercoiled form of plasmid DNA purified at a rotor oscillation amplitude of 45° does not turn into an open circular (OC) isoform when the plasmid is stored for 1 year at plus four degrees, in contrast to the plasmid purified with rotor oscillation amplitudes of 270°, 180° and 90°. The programmed time-work-efficient protocol of plasmid miniprep installed in the device gives the extreme simplicity of plasmid minipreps speeding up and facilitating the isolation of plasmid DNAs.
小规模质粒DNA制备或小量制备是估算克隆实验中的一项基本技术,在表观遗传学研究中广泛用于DNA甲基化分析。当前的质粒DNA小量制备采用基于碱-SDS的三溶液法,且需要基于离心柱的纯化步骤。该程序需要对离心沉淀的细菌进行涡旋或移液操作,并手动混合溶液。在此,我们描述了一种基于离心机/混合器的仪器,它能够进行离心、振动和转子振荡,以便仅通过该设备执行质粒DNA分离的所有步骤。我们发现,通过在裂解和中和步骤中应用转子振荡驱动的溶液混合,在转子振荡幅度为45°、振荡频率为400±30 rpm的情况下,5秒内即可实现均匀混合,从而获得最大量和最高质量的质粒DNA。与手动进行的小量制备相比,对于高拷贝数质粒,通过这种方法纯化的宿主染色体含量没有增加,实际上,对于低拷贝数质粒,染色体组分的含量显著降低。与以270°、180°和90°的转子振荡幅度纯化的质粒相比,以45°的转子振荡幅度纯化的质粒DNA超螺旋形式在4℃储存1年后不会转变为开环(OC)异构体。该设备中安装的质粒小量制备的程序化时间高效协议极大地简化了质粒小量制备过程,加快并便于质粒DNA的分离。