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. 2018 Jun 25;200(14):e00178-18. doi: 10.1128/JB.00178-18

TABLE 1.

Oligonucleotide primers used in this study

Primer Sequence (5′–3′)a Siteb Templatec
HP0545-5P(400-430)-KpnI gggcgaattgggtaccTTTCTTGTCTTTCAAATTTTTG KpnI H. pylori
HP0547-3P(1785-1860) TGTTTCTCCTTACTATACCTAG H. pylori
HP0547-5P(1808-1828) ataataagcggatgaATGACTAACGAAACTATTGATC H. pylori
HP0547-3P(1542-1569)-SacI caaaagctggagctcTTGGACATGGGGAACTGG SacI H. pylori
Ch-5 gaattcctgcagAAATCCTGGTGTCCCTGTTG pBC SK+
Ch-3 TCATCCGCTTATTATCACT pBC SK+
EGFP-5 GTGAGCAAGGGCGAGGAGCTGTTCACCGG pEGFP-C1
EGFP-3 ctgcaggaattcTTACTTGTACAGCTCGTCCAT pEGFP-C1
HydA-F ctaggtatagtaaggagaaacaATGTTCTACGATGAAAAAAAGACC H. pylori
HydA-R cagctcctcgcccttgctcacCGCCTTCAAAGTCAAGGGAGCAAAAC H. pylori
KapA-F ctaggtatagtaaggagaaacaATGAAACGAAGGGATTTTATTAAAAC H. pylori
KapA-Δtat-F ctaggtatagtaaggagaaacaATGACGACTACTTTAGGCGCTACAGGTGC H. pylori
KapA-R cagctcctcgcccttgctcacTGCCTGCAAAATCTGTGCTCC H. pylori
TorA-F ctaggtatagtaaggagaaacaATGAACAATAACGATCTCTTTCAGG E. coli
TorA-R ctaggtatagtaaggagaaacaCGCCGCTTGCGCCGCAGTCGCAC E. coli
a

Sequences in uppercase type are derived from the genome sequences of H. pylori 26695 (51) and E. coli (32) and vector sequences. Sequences introduced for cloning purposes (end-terminal homology with the adjacent fragment) are in lowercase type, and restriction recognition sites are underlined.

b

Restriction recognition sites.

c

Genomic DNA from H. pylori strain G27 and E. coli Top10 and plasmid DNA from pBS SK+ and pEGFP-C1 served as templates for PCR.