Nocker Andreas, Burr Mark, Camper Anne K
Center for Biofilm Engineering, Montana State University, Bozeman, MT 59717-3980, USA.
Microb Ecol. 2007 Aug;54(2):276-89. doi: 10.1007/s00248-006-9199-5. Epub 2007 Mar 8.
Microbial ecology has undergone a profound change in the last two decades with regard to methods employed for the analysis of natural communities. Emphasis has shifted from culturing to the analysis of signature molecules including molecular DNA-based approaches that rely either on direct cloning and sequencing of DNA fragments (shotgun cloning) or often rely on prior amplification of target sequences by use of the polymerase chain reaction (PCR). The pool of PCR products can again be either cloned and sequenced or can be subjected to an increasing variety of genetic profiling methods, including amplified ribosomal DNA restriction analysis, automated ribosomal intergenic spacer analysis, terminal restriction fragment length polymorphism, denaturing gradient gel electrophoresis, temperature gradient gel electrophoresis, single strand conformation polymorphism, and denaturing high-performance liquid chromatography. In this document, we present and critically compare these methods commonly used for the study of microbial diversity.
在过去二十年中,微生物生态学在用于分析自然群落的方法方面经历了深刻变革。重点已从培养转向对特征性分子的分析,包括基于分子DNA的方法,这些方法要么依赖于DNA片段的直接克隆和测序(鸟枪法克隆),要么常常依赖于利用聚合酶链反应(PCR)对目标序列进行预先扩增。PCR产物库既可以再次进行克隆和测序,也可以采用越来越多的遗传图谱分析方法,包括扩增核糖体DNA限制性分析、自动核糖体基因间隔区分析、末端限制性片段长度多态性分析、变性梯度凝胶电泳、温度梯度凝胶电泳、单链构象多态性分析以及变性高效液相色谱分析。在本文档中,我们展示并严格比较了这些常用于研究微生物多样性的方法。