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. 2008 Jun 2;52(8):2977–2979. doi: 10.1128/AAC.00175-08

TABLE 2.

Kinetic parameters of VIM-15, VIM-16, and VIM-2a

Substrate VIM-15
VIM-16
VIM-2
kcat (s−1) Relativebkcat Km (μM) kcat/Km (s−1 μM−1) Relativebkcat/Km kcat (s−1) Relativebkcat Km (μM) kcat/Km (s−1 μM−1) Relativebkcat/Km kcat (s−1) Relativebkcat Km (μM) kcat/Km (s−1 μM−1) Relativebkcat/Km
Cephaloridine 190 ± 4 100 83 ± 2 2.3 100 89 ± 2 100 1400 ± 53 0.064 100 120 ± 5 100 1400 ± 6 0.086 100
Benzylpenicillin 240 ± 3 130 25 ± 0.5 9.6 420 230 ± 24 260 450 ± 8 0.51 800 73 ± 0.4 61 150 ± 1 0.49 570
Cefepime 9.5 ± 0.1 5.0 130 ± 2 0.076 3.3 0.31 ± 0.03 0.35 210 ± 1 0.0015 2.3 0.38 ± 0.02 0.32 110 ± 6 0.0035 4.1
Ceftazidime 1.0 ± 0.04 0.53 37 ± 2 0.027 1.2 0.22 ± 0.00 0.25 150 ± 2 0.0014 2.2 0.23 ± 0.01 0.19 150 ± 6 0.0015 1.7
Cefotaxime 90 ± 7 47 13 ± 1 6.9 300 81 ± 0.2 91 240 ± 9 0.34 530 NT NT NT NT NT
Imipenem 61 ± 2 32 7.3 ± 0.5 8.4 370 45 ± 2 51 89 ± 2 0.51 800 20 ± 0.3 17 60 ± 2 0.33 380
Meropenem 6.5 ± 0.05 3.4 3.4 ± 0.5 1.9 83 8.4 ± 0.3 9.4 120 ± 5 0.070 110 2.1 ± 0.1 1.8 40 ± 2 0.053 62
Aztreonamc ≤0.031 ≤0.016 ND ND ND ≤0.11 ≤0.12 ND ND ND NT NT NT NT NT
a

NT, not tested; ND, not determined as hydrolysis was too slow to determine Km.

b

The cephaloridine value was taken as 100%.

c

Hydrolysis of aztreonam was very slow; Vmax was estimated as 2 times the maximum hydrolysis rate observed.