Sipos Rita, Székely Anna, Révész Sára, Márialigeti Károly
Department of Microbiology, Eötvös Loránd University, Budapest, Hungary.
Methods Mol Biol. 2010;599:37-58. doi: 10.1007/978-1-60761-439-5_3.
Each step of a molecular environmental microbiology study is prone to errors, though the qualitative and quantitative biases of PCR amplification could result in the most serious biases. One has to be aware of this fact, and well-characterized PCR biases have to be avoided by using target-optimized PCR protocols. The most important tasks are primer and thermal profile optimization. We have shown that primer mismatches, even in the case of universal primers, can cause almost complete missing of common taxa from clone libraries, for example. Similarly high annealing temperatures can drastically distort community composition of the sample in the PCR product. Strategies of primer selection and PCR thermal profile design are discussed in detail.
分子环境微生物学研究的每一步都容易出错,尽管PCR扩增的定性和定量偏差可能导致最严重的偏差。必须意识到这一事实,并且通过使用针对目标优化的PCR方案来避免特征明确的PCR偏差。最重要的任务是引物和热循环参数的优化。例如,我们已经表明,即使是通用引物,引物错配也可能导致克隆文库中常见分类群几乎完全缺失。同样,高退火温度会极大地扭曲PCR产物中样品的群落组成。本文将详细讨论引物选择策略和PCR热循环参数设计。