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. 2005 Jun;71(6):2925–2933. doi: 10.1128/AEM.71.6.2925-2933.2005

TABLE 2.

PCR primers used in this study

Primera Sequence (5′ to 3′)b Positionc Specificity Reference(s)
B341f CCTACGGGIGGCIGCA 341-357 Bacteria 46
U515f GTGYCAGCMGCCGCGGTAA 515-533 Universal 46
U533rd TTACCGCGGCKGCTGRCAC 515-533 Universal 46
U1492r GGYTACCTTGTTACGACTT 1492-1510 Universal 11
GAM660rd AATTCCACTTCCCTCTAC 660-674 Sulfur-oxidizing bacteria and some other bacteria in Thiotrichales 32
SRB385mfd CCTGACGCAGCRACGCC 385-401 Sulfate-reducing bacteria in δ-Proteobacteria and some other bacteria (e.g., Clostridium spp.) 1, 29
U926rd CCGTCAATTCMTTTRAGTTT 907-926 Universal 2
Dv687rd TCTACGGATTTCACTCCT 687-704 Desulfovibrio spp. 10
Sval428fd GTAAAATCCTGTCAGATGG 428-446 Desulfotalea spp. and Desulfofustis spp. 35
DSS658rd TCCACTTCCCTCTCCCAT 658-685 Desulfosarcina spp. and Desulfofaba spp. 26
T7W TAATACGACTCACTATAGGGC pGEM-T vector 45
SP6W ATTTAGGTGACACTATAGAATACTC pGEM-T vector 45
a

f, forward PCR primer; r, reverse PCR primer.

b

According to International Union of Biochemistry codes for bases. I, inosine.

c

Corresponding to the numbering in the sequence of the 16S rRNA gene of E. coli.

d

These primers were used for qcPCR.