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. 2014 Feb 7;3(2):168–181. doi: 10.1002/mbo3.158

Table 1.

Bacterial strains, plasmids, and primers used in this study. Restriction enzymes and restriction sites in the primer sequences are underlined.

Strain, plasmid, or primer Properties/Sequence Source or reference
Strains
Campylobacter jejuni NCTC-11168 Wild-type strain Dr. Q. Zhang
 ΔmfrA Chloramphenicol resistance gene inserted in the mfrA (catr) Weingarten et al. (2009)
 C-ΔmfrA Complementation strain. Kanamycin resistant (Kanr) and catr This study
Escherichia coli DH5α Library efficiency competent cells for cloning Invitrogen
Plasmids
 pIK01 pRY108+mfrA used for constructing C-ΔmfrA This study
 pRY108 Vector used in complementation studies Dr. Q. Zhang
Primers
 C-mfrA-f ACGAGGATCCAATGCAATTTATGAATGGAG (BamHI) This study
 C-mfrA-r GTCAGGTACCACAAAT TGCAGATTGACAAG (KpnI)
mfrA-RT-f GGGCATTTAGCAGGCATTG Guccione et al. (2010)
mfrA-RT-r GACCATTTCCGCCATTATTTG
katA-RT-f CAGTAGCAGGTGAAGCAGGTG IDT1
katA-RT-r GCGGATGAAGAATGTCGGAGTG
perR-RT-f GCTACTCCGCAAAGACTATGTG IDT1
perR-RT-r AGACAGATGATTGACGAGATTG
fur-RT-f CCATTTCTTTTGGTTCAGCA IDT1
fur-RT-r GCAATCAAGGCTTGCTGTCT
rpoA-RT-f ATTACAACATCTGCTTATACG IDT1
rpoA-RT-r TCTACTATTTCTTTATTTGATTCG
1

Integrated DNA Technologies, Inc.