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 |