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. Author manuscript; available in PMC: 2010 Jun 5.
Published in final edited form as: J Mol Biol. 2009 Apr 21;389(2):401–412. doi: 10.1016/j.jmb.2009.04.028

Table 1.

Comparison of the minimum inhibitory concentration of ampicillin for growth of E. coli TP112 and TP132 strains containing plasmids encoding BLIP alanine-scanning mutants versus the Ki value for inhibition of TEM-1 β-lactamase by the purified BLIP derivatives. “No BLIP” refers to the E. coli strain containing the pTP123 plasmid that does not encode BLIP. “Wt BLIP” refers to the E. coli strain containing the pGR32 plasmid that encodes BLIP. The Ki data is from Zhang and Palzkill28 and the ΔΔG values are calculated from the Ki values (Materials and Methods).

Ampicillin MIC (μg/ml)
BLIP mutant E. coli TP112 E. coli TP132 Ki (nM) ΔΔG (kJ/mol)
No BLIP 256 >256 - -
Wt BLIP 1.5 4 0.5 -
E31A 8 12 2.0 3.4
S35A 1.5 4 0.5 0
F36A 24 24 40 10.8
S39A 1.5 4 0.3 −1.3
H41A 64 64 34 10.4
G48A 2 12 0.7 0.8
D49A 3 16 20 9.1
Y50A 1 4 0.01 −9.7
Y51A 1.5 4 0.5 0
Y53A 4 24 21 9.3
S71A 3 6 0.2 −2.3
E73A 1.5 6 0.4 −0.5
K74A 3 24 46 11.2
W112A 1.5 16 13 8.0
S113A 1 4 0.1 −4.0
G141A 3 8 1.8 3.18
F142A 2 16 16 8.58
Y143A 1 4 0.6 0.5
R144A 1 6 0.6 0.5
H148A 24 32 21 9.3
W150A 96 256 184 14.6
R160A 2 24 11 7.7