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. 1999 Feb;43(2):307–313. doi: 10.1128/aac.43.2.307

TABLE 6.

β-Lactamase inducibility in E. cloacae 8009 and various transformants

Expt. no. and strain Phenotype Inducera β-Lactamase activityb
Inducibility and inducibility ratioc
μM/min · mg of protein Ratiod
Expt 1
E. cloacae 8009 AmpA AmpR 340 1.0 Inducible
+ 2,400 7.1 7.1
 E. coli DH10B <1 <0.003 Constitutive
+ <1 <0.003 1.0e
 E. coli DH10B/pFCX300L (TF-L) AmpA AmpR 22 0.064 Inducible
+ 210 0.64 9.6
 E. coli DH10B/pFCX300M (TF-M) AmpA AmpR 119 0.35 Inducible
+ 1,720 5.1 14.5
 E. coli DH10B/pFCX301 (TF-L7) AmpA AmpR 700 2.1 Inducible
+ 6,500 19 9.2
 E. coli DH10B/pFCX302 (TF-M4) AmpA AmpR 620 1.9 Inducible
+ 7,400 22 11.9
Expt 2
 E. cloacae 8009 AmpA AmpR 260 1.0 Inducible
+ 2,500 9.6 9.3
 E. coli DH10B/pFCX310 (TF2-2) AmpA 280 1.1 Constitutive
+ 280 1.1 1.0
 E. coli DH10B/pFCX320 (TF2-3) AmpA 350 1.3 Constitutive
+ 350 1.3 1.0
a

The inducer was imipenem-cilastatin at 0.1 μg/ml. 

b

Cefotaxime (100 μM) was used as a substrate. 

c

Induced activity/uninduced activity for each set. 

d

Activity of extract/uninduced activity of E. cloacae 8009. 

e

Nitrocefin was used as the substrate for calculation of the inducibility ratio for this strain.