Skip to main content
. Author manuscript; available in PMC: 2009 Mar 23.
Published in final edited form as: Microbiology (Reading). 2008 Dec;154(Pt 12):3624–3638. doi: 10.1099/mic.0.2008/023382-0

Table 3.

Effect of mutated Ler proteins on LEE5 expression in EPEC strain SE796

The EPEC E2348/69-derived strain SE796 contains an in-frame deletion of ler.

Fusion plasmid Protein plasmid Glucose* Arabinose* Fold-induction
    – 19 (6) 8 (3)
pRS551     – 31 (1) 43 (2)
pKMTIR3 pBAD33 692 (19) 731 (26) 1.1
pKMTIR3 pKHLB01(Ler) 526 (13) 10 218 (185) 20
pKMTIR3 pKHB1123 (H-NS) 439 (23) 216 (12) 0.5
pKMTIR3 pFL08 752 (19) 1588 (196) 2.1
pKMTIR3 pFL09 717 (74) 1887 (334) 2.6
pKMTIR3 pKHB1527(C1) 996 (68) 1067 (41) 1.1
pKMTIR3 pKHB1163(C2) 1139 (63) 1128 (38) 1.0
pKMTIR3 pKHB1047(C4) 1015 (20) 891 (13) 0.9
pKMTIR3 pKHB1167(C5) 822 (24) 3767 (113) 4.6
*

β-Galactosidase activity derived from the pKMTIR3 5–lacZ reporter gene vector in the strain SE796 was monitored in the presence of the listed protein expression and control plasmids under repressing (0.1% glucose) and inducing (0.1% arabinose) conditions. The values are presented in Miller units and represent the mean of representative assays performed in triplicate with SDs in parentheses.

Represents the ratio of transcriptional activity in the presence of the inducer (arabinose) to that in the presence of the repressor (glucose) for the indicated strains.