Plotka Magdalena, Wozniak Mateusz, Kaczorowski Tadeusz
Laboratory of Extremophiles Biology, Department of Microbiology, University of Gdansk, Gdansk, Poland.
PLoS One. 2017 Jan 13;12(1):e0169846. doi: 10.1371/journal.pone.0169846. eCollection 2017.
Bacteria can be considered as biological nanofactories that manufacture a cornucopia of bioproducts most notably recombinant proteins. As such, they must perfectly match with appropriate plasmid vectors to ensure successful overexpression of target genes. Among many parameters that correlate positively with protein productivity plasmid copy number plays pivotal role. Therefore, development of new and more accurate methods to assess this critical parameter will result in optimization of expression of plasmid-encoded genes. In this study, we present a simple and highly accurate method for quantifying plasmid copy number utilizing an EvaGreen single colour, droplet digital PCR. We demonstrate the effectiveness of this method by examining the copy number of the pBR322 vector within Escherichia coli DH5α cells. The obtained results were successfully validated by real-time PCR. However, we observed a strong dependency of the plasmid copy number on the method chosen for isolation of the total DNA. We found that application of silica-membrane-based columns for DNA purification or DNA isolation with use of bead-beating, a mechanical cell disruption lead to determination of an average of 20.5 or 7.3 plasmid copies per chromosome, respectively. We found that recovery of the chromosomal DNA from purification columns was less efficient than plasmid DNA (46.5 ± 1.9% and 87.4 ± 5.5%, respectively) which may lead to observed differences in plasmid copy number. Besides, the plasmid copy number variations dependent on DNA template isolation method, we found that droplet digital PCR is a very convenient method for measuring bacterial plasmid content. Careful determination of plasmid copy number is essential for better understanding and optimization of recombinant proteins production process. Droplet digital PCR is a very precise method that allows performing thousands of individual PCR reactions in a single tube. The ddPCR does not depend on running standard curves and is a straightforward and reliable method to quantify the plasmid copy number. Therefore we believe that the ddPCR designed in this study will be widely used for any plasmid copy number calculation in the future.
细菌可被视为生物纳米工厂,能制造大量生物制品,最显著的是重组蛋白。因此,它们必须与合适的质粒载体完美匹配,以确保目标基因的成功过表达。在众多与蛋白质生产力呈正相关的参数中,质粒拷贝数起着关键作用。因此,开发新的、更准确的方法来评估这一关键参数将有助于优化质粒编码基因的表达。在本研究中,我们提出了一种利用EvaGreen单色液滴数字PCR定量质粒拷贝数的简单且高度准确的方法。我们通过检测大肠杆菌DH5α细胞内pBR322载体的拷贝数来证明该方法的有效性。所得结果通过实时PCR成功验证。然而,我们观察到质粒拷贝数强烈依赖于用于分离总DNA的方法。我们发现,使用基于硅胶膜的柱子纯化DNA或使用珠磨法(一种机械细胞破碎方法)分离DNA,分别导致每条染色体平均测定出20.5个或7.3个质粒拷贝。我们发现从纯化柱中回收染色体DNA的效率低于质粒DNA(分别为46.5±1.9%和87.4±5.5%),这可能导致观察到的质粒拷贝数差异。此外,除了质粒拷贝数因DNA模板分离方法而异外,我们发现液滴数字PCR是一种测量细菌质粒含量的非常方便的方法。仔细测定质粒拷贝数对于更好地理解和优化重组蛋白生产过程至关重要。液滴数字PCR是一种非常精确的方法,允许在单个管中进行数千次单独的PCR反应。数字PCR不依赖于绘制标准曲线,是一种直接且可靠的定量质粒拷贝数的方法。因此,我们相信本研究中设计的数字PCR未来将广泛用于任何质粒拷贝数的计算。