Soil microbial community analysis using denaturing gradient gel electrophoresis

被引:98
|
作者
Nakatsu, C. H. [1 ]
机构
[1] Purdue Univ, Dept Agron, W Lafayette, IN 47907 USA
关键词
D O I
10.2136/sssaj2006.0080
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
The most biological diversity on this planet is probably harbored in soils. Understanding the diversity and function of the microbiological component of soil poses great challenges that are being overcome by the application of molecular biological approaches. This review covers one of many approaches being used: separation of polymerase chain reaction (PCR) amplicons using denaturing gradient gel electrophoresis (DGGE). Extraction of nucleic acids directly from soils allows the examination of a community without the limitation posed by cultivation. Polymerase chain reaction provides a means to increase the numbers of a target for its detection on gels. Using the rRNA genes as a target for PCR provides phylogenetic information on populations comprising communities. Fingerprints produced by this method have allowed spatial and temporal comparisons of soil communities within and between locations or among treatments. Numerous samples can be compared because of the rapid high throughput nature of this method. Scientists now have the means to begin addressing complex ecological questions about the spatial, temporal, and nutritional interactions faced by microbes in the soil environment.
引用
收藏
页码:562 / 571
页数:10
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