Skip to main content
. 2001 May;67(5):2371–2374. doi: 10.1128/AEM.67.5.2371-2374.2001

FIG. 1.

FIG. 1

DGGE profiles of the 16S rDNA fragments of the stock culture amplified with universal bacterial PCR primers (lane B1) and with methanogen-specific primers (lane M1) and of the BES culture amplified with universal bacterial primers (lane B2). No PCR products were obtained from the BES culture using methanogen-specific primers (lane M2).