TABLE 4.
DNA primers used for PCR and DNA sequencing reactions
Usea | Gene | 5′ primer | 3′ primer | DNA sequenceb | Used for PCRc | Used for sequencingd |
---|---|---|---|---|---|---|
Entire gene | hisC | + | 5′ ATCAGGCGCTGCAGGAGTTTGAGG 3′ | + | + | |
+ | 5′ GACCGGCGAGCAATATTGTATCTTTCA 3′ | + | + | |||
Internal | hisC | + | 5′ CAAACACGGTTACTGCTGC 3′ | + | ||
+ | 5′ AAGGCATACGGTCTGGCAG 3′ | + | ||||
Entire gene | metB | + | 5′ AACTGCAGAAACGGGGAAATAATGGAGGTG 3′ | + | + | |
+ | 5′ CGGGATCCGGTGCCCTGTCAAAAAGACTTG 3′ | + | + | |||
Internal | metB | + | 5′ TGCGCCGATCGAGCATTTGG 3′ | + | ||
+ | 5′ CATGATTTCCTTGAGCTCTTCCCA 3′ | + | ||||
Entire gene | leuC | + | 5′ ACGCGTCGACAATACAATTTCTAATGTGTGACAG 3′ | + | + | |
+ | 5′ ACGCGTCGACATCCGATTTAATACGGGTGCTTTCC 3′ | + | + | |||
Internal | leuC | + | 5′ CAGTGTGGATCAAGGGATTGTC 3′ | + | ||
+ | 5′ ACGATGGATGAACGAATGACTG 3′ | + | ||||
+ | 5′ TTGAAGACATTAAAGTGGAGCAC 3′ | + |
Entire gene, primers used for sequencing of the entire genes used for stationary-phase mutagenesis assay; Internal, primers used for internal sequencing of the gene.
Bold sequences are not part of the coding region of the gene but were used for cloning purposes.
Primers used in PCRs to amplify the genes, as described in Materials and Methods.
Primers used for sequencing as described in Materials and Methods.