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. 2005 Jul;71(7):4144–4148. doi: 10.1128/AEM.71.7.4144-4148.2005

FIG. 2.

FIG. 2.

DGGE analysis of the bacterial community in the linuron-degrading enrichment culture Sp8-3. Profiles of the PCR-amplified 16S rRNA genes (lanes 1 through 6) and of the reverse-transcribed 16S rRNA (lanes 7 through 9). Lanes M show size markers. Lanes 1 through 3 correspond to 16S rRNA genes from replicates 1 through 3 extracted at day 8 (Fig. 1); lanes 4 through 6 correspond to 16S rRNA genes from replicates 1 through 3 extracted at day 15 (Fig. 1); lanes 7 through 9 correspond to reverse-transcribed 16S rRNA from replicates 1 through 3 extracted at day 15; and lane 11 represents 16S rRNA genes from the strain SRS16 isolated from Sp8-3. The DGGE bands (A to F) marked by open boxes were excised and sequenced.