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. 2018 Apr 9;8:5685. doi: 10.1038/s41598-018-24134-3

Figure 3.

Figure 3

Contribution of surface displayed PbrR to enhanced adsorption of lead(II) in vitro. (A) Accumulation of lead(II) by cells surface-displayed Lpp-OmpA-PbrR. The adsorption assay was performed in 25 mmol/L HEPES pH 7.0 containing 150 μmol/L lead acetate at 25 °C for 12 h. (B) Lead(II) adsorption capacity of cells surface-displayed Lpp-OmpA-PbrR in different concentrations of lead solution. The assay was performed in 25 mmol/L HEPES pH 7.0 containing 50 or 300 μmol/L lead acetate at 25 °C for just 1 h. (C) Effect of pH value on lead ion adsorption by cells surface-displayed Lpp-OmpA-PbrR. The assay was performed in 25 mmol/L acetate pH 3.0 or 25 mmol/L HEPES pH 7.0 containing 150 μmol/L lead acetate at 25 °C for 1 h. (D) Selective adsorption of lead and other metal elements by cells surface-displayed Lpp-OmpA-PbrR. The assay was performed in 25 mmol/L HEPES pH 7.0 containing 50 μmol/L Pb2+, Ca2+, Mg2+, Fe2+, Zn2+ and Cu2+ at 25 °C for 1 h. The data shown represent the mean values of three independently experiments. *A significant difference (t test, P < 0.001) between E. coli surface-displayed Lpp-OmpA-PbrR and E. coli surface-displayed Lpp-OmpA.