Abstract
/l. Genomic DNA was isolated from the en-riched culture and its inoculum (activated sludge), and used for PCR-DGGE analysis of 16S rRNA genes. Microbial compositions of the enrichment culture and the activated sludge were different, as determined by their different DGGE profiles. The difference in DGGE banding patterns suggests that environmental conditions of the enrichment culture caused a change in the microbial community com-position of the inoculated activated sludge. Dominant DGGE bands in the enrichment culture sample were affiliated with the classes
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