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. 2008 Dec 8;53(2):696–702. doi: 10.1128/AAC.00652-07

TABLE 1.

Primer sequences used for PCR amplification and sequencing

Gene Primer Sequence (5′ to 3′) Annealing temp (°C) Reference
16S rRNAa pA AGAGTTTGATCCTGGCTCAG 62 11
pH AAGGAGGTGATCCAGCCGCA
sul1 sul1bF CTTCGATGAGAGCCGGCGGC 63 29
sul1bR GCAAGGCGGAAACCCGCGCC
sul2 sul2F TCGTCAACATAACCTCGGACAG 60 V. Enne
sul2R GTTGCGTTTGATACCGGCAC
sul3 sul3F GAGCAAGATTTTTGGAATCG 51 18
sul3R CATCTGCAGCTAACCTAGGGCTTTGGA
intI1 intA ACAGGGCAAGCTTAGTAAAGCC 67 22
intB CTCGCTAGAACTTTTGGAAA
intI2 int2F CACGGATATGCGACAAAAAGGT 58.5 32
int2R GTAGCAAACGAGTGACGAAATG
qacE KazamF1 GGGAATTCGCCCTACACAACAAATTGGGAGA 50 14
KazamR1 TACTCGAGTTAGTGGGCACTTGCTTTGG
qacEΔ1 KazamF2 GGGAATTCGCCCTACACAACAAATTGGGAGA 60 14
KazamR2 GCTGCAGCTGCGGTACCACTGCCACAA
a

16S rRNA gene sequence from bp 8 to 1522.