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. 2009 May 29;191(15):4934–4942. doi: 10.1128/JB.01831-08

TABLE 2.

Oligonucleotide primers used in this study

Primer Purpose Sequence Reference
PUC18KNcoIF Amplification of apha-3 cassette and attachment of NcoI tails 5′-CATGCCATGGTGACTAAACTAGGAGGAATAAATGGCTAAAATGAGA-3′ This study
PUC18KNcoIR Amplification of apha-3 cassette and attachment of NcoI tails 5′-CATGCCATGGTCATTATTCCCTCCAGGTACTAAAACAATTCATC-3′ This study
Agg1F Primer internal to hra1; used to verify mutant 5′-ATTGCGGTTTCAGCGCTTGC-3′ This study
Agg1R Primer internal to hra1; used to verify mutant 5′-AGATAGCGATAGCTGAGGTC-3′ This study
Hra1upF Upstream of hra1 but absent from hra1 deletion construct pSB1; used for primary cloning of the gene and to verify mutant 5′-GCAAATCACAACCTTCCTGA-3′ This study
Hra1dnR Downstream of hra1 and present in hra1 deletion construct pSB1; used for primary cloning of gene and to verify mutant 5′-CTTCGGAGTGGATGTATCTG-3′ This study
AA432F Amplifies portion of aggregative plasmid gene aatA; used to verify mutant 5′-CTGGCGAAAGACTGTATCAT-3′ 8
AA432R Amplifies portion of aggregative plasmid gene aatA; used to verify mutant 5′-CAATGTATAGAAATCCGCTGTT-3′ 8