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Acidophilic Bacterial Communities of Soil and Enrichment Cultures from Two Abandoned Mine Sites of the Korean Peninsula  

Mishra, Debaraj (Department of Microbiology & Molecular Biology, Chungnam National University)
Lee, Sun-Hee (Department of Microbiology & Molecular Biology, Chungnam National University)
Kim, Jae-Hee (Department of Microbiology & Molecular Biology, Chungnam National University)
Kim, Dong-Jin (Mineral Resources and Research Division, Korea Institute of Geoscience and Mineral Resources)
Rhee, Young-Ha (Department of Microbiology & Molecular Biology, Chungnam National University)
Publication Information
Korean Journal of Environmental Biology / v.29, no.4, 2011 , pp. 265-273 More about this Journal
Abstract
Bacterial diversity based on the denaturing gradient gel electrophoresis (DGGE) analysis of PCR-amplified 16S rRNA gene sequences was determined for soil samples from two abandoned mine sites and the corresponding enrichment cultures using soil sample as key inoculum. Sequencing analysis of DGGE bands obtained from both the soil samples matched mostly with sequences of uncultured and newly described organisms, or organisms recently associated with the acid mine drainage environment. However, the enrichment of soil samples in ferrous sulfate and elemental sulfur media yielded sequences that were consistent with well-known iron- and sulfur-oxidizing acidophilic bacteria. Analysis of enrichment cultures of soil samples from Dalsung mine revealed abundant ${\gamma}$-$Proteobacteria$, whereas that of Gubong mine sample displayed acidophilic groups of ${\gamma}$-$Proteobacteria$, ${\alpha}$-$Proteobacteria$, $Actinobacteria$ and $Firmicutes$. Chemical elemental analysis of the mine samples indicated that the Dalsung site contained more iron and sulfate along with other toxic components as compared with those of the Gubong site. Biogeochemistry was believed to be the primary control on the acidophilic bacterial group in the enrichment samples.
Keywords
acidic soil; acidophilic bacteria; bacterial community; enrichment; PCR-DGGE;
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