Skip to main content
. 2011 Nov;55(11):5143–5149. doi: 10.1128/AAC.05045-11

Table 3.

Kinetic parameters and inhibition profile of SMB-1a

Substrate or chelating agent Km (μM) kcat (s−1) kcat/Km (M−1·s−1) Relative kcat/Kmd IC50 (μM)
Ampicillin 102 247 2.4 × 106 100
Piperacillin 380 68 1.8 × 105 7.5
Cephalothin 15 28 1.9 × 106 79
Cefuroxime 22 30 1.4 × 106 58
Cefotaxime 35 31 8.9 × 105 37
Ceftazidime 57 4.4 7.7 × 104 3.2
Cefepime 747 2.7 3.6 × 103 0.15
Cefoxitin 26 39 1.5 × 106 63
Aztreonam NHb NDc ND ND
Imipenem 133 518 3.9 × 106 163
Meropenem 144 604 4.2 × 106 175
Dipicolinic acid 2.2
1,10-o-Phenanthroline 156
EDTA 14
a

Standard deviations for each parameter were below 10%.

b

NH, no measurable hydrolysis detected with 1 μM enzyme.

c

ND, not determined.

d

Relative kcat/Km value was expressed compared to that of ampicillin, which was assigned 100.