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. 2014 May;58(5):2754–2762. doi: 10.1128/AAC.02565-13

TABLE 1.

Sequences of the oligonucleotides used in this study

Oligonucleotide Sequence/position Used in:
dnaK-F 12,136GACCGAATTCATAGTGGAGACG12,157a PCR amplification of the dnaK gene
dnaK-R 14,113CCCGTGTCAGTATAATTACCC14,093 PCR amplification of the dnaK gene
sbmA-del-F 395,804CGGTCATGCGGTTAATACACAG395,825 PCR amplification of the sbmA gene
sbmA-del-R 397,168CCTGACTACTACACCCCGCTAA397,147 PCR amplification of the sbmA gene
DB-F 390,900GCGTTGACCGAATCTACTGGGT390,921 Mapping of the deletion boundaries in E. coli C600 mutants
DB-R 397,995CACCTTTCTCTAACTGACGGCG397,974 Mapping of the deletion boundaries in E. coli C600 mutants
DB-R1 397,410GGTCAATCTCTTGCCAGGCGAT397,389 Mapping of the deletion boundaries in E. coli C600 mutants
sbmA-pET22-F GCATCACATATGTTTAAGTCTTTTTTCCAb Cloning of sbmA in E. coli C600 mutants Mut2 to Mut4
sbmA-pET22-R ACATGCGAGCTCGCTCAAGGTATGGGGc Cloning of sbmA in E. coli C600 mutants Mut2 to Mut4
T7 forward CCCGCGAAATTAATACGACTCACTA Sequencing of sbmA-complemented and resistant mutants
T7 reverse GCTAGTTATTGCTCAGCGG Sequencing of sbmA-complemented and resistant mutants
a

Numbers indicate nucleotide positions with reference to the published genome of E. coli K-12 substrain W3110 (NCBI accession number NC_007779.1).

b

The NdeI restriction site is underlined.

c

The SacI restriction site is underlined.