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. 2012 Aug;50(8):2688–2694. doi: 10.1128/JCM.00728-12

Table 2.

Primers used for amplification and sequencing, PCR annealing temperatures, and the region used for phylogenetic analysis

Gene Primer Nucleotide sequence (5′–3′) Amplicon size (bp) Annealing temp (°C) Region used for MLSA (bp)a
atpD atpD-35F CCGTGGTGGATATTCAGT 491 50 85–480
atpD-522R CTTGGCGATGTTGTTGAT
icd icd-685F CTGGTSCACAAGGGCAACAT 532 55 832–1167
icd-1216R ACACCTGVGTSGCVCCTTC
recA recA-64F TCGCAGATCGAAAAGCAGTT 549 50 133–591
recA-615R CATGCGGATCTGGTTGATGAAG
rpoB rpoB-903F GCTGGCCAAGAACATCGT 586 50 958–1470
rpoB-1488R GTGCGGCATYAGGTTTTC
tyrB tyrB-391F CCSAGCTGGGAAAACCAYCG 477 58 454–843
tyrB-867R CGGGTTGSAGTAGWTGGYG
16S rRNA 16f27 AGAGTTTGATCMTGGCTCAG 1495 55 89–1397
16r1492 TACGGYTACCTTGTTACGACTT
16f357 ACTCCTACGGGAGGCAGCAG
a

Position relative to A. xylosoxidans A8 genomic sequence.