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. 2014 May 22;53(23):3738–3746. doi: 10.1021/bi5000838

Table 1. Monomer Stability of Purified AcrB Constructs and Their Activities in the BW25113ΔacrB Strain.

  MIC (μg/mL)
   
protein Ery Nov R6G TPP EtBr accumulation rate (s–1) transition point ([SDS]/[DDM])
no AcrBa 2.5 5 5 5 (1.4 ± 0.4) × 10–1  
AcrB 80 160 320 640 (8.9 ± 5.0) × 10–3 1.6 ± 0.1
AcrBL886G 80 160 320 640 (1.1 ± 0.4) × 10–2 1.5 ± 0.1
AcrBE893G 80 160 320 640 (7.6 ± 3.0) × 10–3 1.5 ± 0.1
AcrBW895G 80 160 320 640 (1.0 ± 0.5) × 10–2 1.5 ± 0.1
AcrBL886G/E893G 40 40 320 40 (4.9 ± 0.6) × 10–2 1.4 ± 0.1
AcrBE893G/W895G 40 40 320 40 (2.3 ± 0.3) × 10–2 1.5 ± 0.1
AcrBL886G/E893G/W895G 20 10 160 20 (8.3 ± 0.8) × 10–2 1.5 ± 0.1
AcrBC493A/C887A 80 160 320 640    
AcrBW13C/C493A/C887A 80 160 320 640    
a

BW25113ΔacrB transformed with the empty vector pQE70 was used as the negative control for the activity assay.