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. 2015 May 14;59(6):3357–3364. doi: 10.1128/AAC.04669-14

TABLE 2.

MICs of β-lactams and specific activities of BlaA in wild-type S. oneidensis and its derivative strains

Straina MIC (μg/ml)b
Mean β-lactamase activityc ± SD
AMP CTX IPM No inducer Inducer
WT 4 0.02 0.5 12 ± 0.8 125 ± 7
ΔmrcA 128 0.08 4 258 ± 22 228 ± 21
ΔlpoA 32 0.04 2 71 ± 11 241 ± 23
ΔmrcB 4 0.02 0.5 13 ± 0.8 116 ± 7.9
ΔlpoB 4 0.02 0.5 13 ± 1.2 128 ± 13
ΔampG 128 0.08 2 29 ± 4 238 ± 5.1
ΔblaA <0.5 <0.005 <0.06 2 ± 1 0
ΔmrcA/mrcA 128 0.08 4
ΔmrcA/mrcA + Ara 32 0.04 1 44 ± 2.3 227 ± 7.1
ΔlpoA/lpoA 32 0.04 2
ΔlpoA/lpoA + Ara 8 0.02 0.5 19 ± 0.1 174 ± 17
ΔmrcA ΔblaA <0.5 <0.005 <0.06 3 ± 0.5 0
ΔlpoA ΔblaA <0.5 <0.005 <0.06 3 ± 0.8 0
ΔmrcA ΔampG 128 0.08 2 216 ± 35 236 ± 18
a

ΔmrcA/mrcA and ΔlpoA/lpoA represent the ΔmrcA and ΔlpoA strains, respectively, complemented with pHGC02 harboring a copy of the corresponding S. oneidensis genes in trans. Ara, arabinose.

b

AMP, ampicillin; CTX, cefotaxime; IPM, imipenem.

c

Nanomoles of nitrocefin hydrolyzed per minute per milligram of protein. Induction was carried out with 200 μg/ml ampicillin for 2 h. −, not tested.