Microbial diversity in lake sediments detected by PCR-DGGE

ZHAO Xinqing, YANG Liuyan, CHEN Can, XIAO Lin, JIANG Lijuan, MA Zhe, ZHU Haowei, YU Zhenyang, YIN Daqiang

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Front. Biol. ›› 2008, Vol. 3 ›› Issue (3) : 293-299. DOI: 10.1007/s11515-008-0044-8

Microbial diversity in lake sediments detected by PCR-DGGE

  • ZHAO Xinqing, YANG Liuyan, CHEN Can, XIAO Lin, JIANG Lijuan, MA Zhe, ZHU Haowei, YU Zhenyang, YIN Daqiang
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Abstract

In this study, PCR-denaturing gradient gel electrophoresis (DGGE) was applied to analyze the microbial communities in lake sediments from Lake Xuanwu, Lake Mochou in Nanjing and Lake Taihu in Wuxi. Sediment samples from seven locations in three lakes were collected and their genomic DNAs were extracted. The DNA yields of the sediments of Lake Xuanwu and Lake Mochou were high (10 ?g/g), while that of sediments in Lake Taihu was relatively low. After DNA purification, the 16S rDNA genes (V3 to V5 region) were amplified and the amplified DNA fragments were separated by parallel DGGE. The DGGE profiles showed that there were five common bands in all the lake sediment samples indicating that there were similarities among the populations of microorganisms in all the lake sediments. The DGGE profiles of Lake Xuanwu and Lake Mochou were similar and about 20 types of microorganisms were identified in the sediment samples of both lakes. These results suggest that the sediment samples of these two city lakes (Xuanwu, Mochou) have similar microbial communities. However, the DGGE profiles of sediment samples in Lake Taihu were significantly different from these two lakes. Furthermore, the DGGE profiles of sediment samples in different locations in Lake Taihu were also different, suggesting that the microbial communities in Lake Taihu are more diversified than those in Lake Xuanwu and Lake Mochou. The differences in microbial diversity may be caused by the different environmental conditions, such as redox potential, pH, and the concentrations of organic matters. Seven major bands of 16S rDNA genes fragments from the DGGE profiles of sediment samples were further re-amplified and sequenced. The results of sequencing analysis indicate that five sequences shared 99%–100% homology with known sequences (Bacillus and Brevibacillus, uncultured bacteria), while the other two sequences shared 93%–96% homology with known sequences (Acinetobacter, and Bacillus). The study shows that the PCR-DGGE technique combined with sequence analysis is a feasible and efficient method for the determination of microbial communities in sediment samples.

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ZHAO Xinqing, YANG Liuyan, CHEN Can, XIAO Lin, JIANG Lijuan, MA Zhe, ZHU Haowei, YU Zhenyang, YIN Daqiang. Microbial diversity in lake sediments detected by PCR-DGGE. Front. Biol., 2008, 3(3): 293‒299 https://doi.org/10.1007/s11515-008-0044-8

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