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. 2018 Oct 31:6:529.
doi: 10.3389/fchem.2018.00529. eCollection 2018.

Purification of the Recombinant Green Fluorescent Protein Using Aqueous Two-Phase System Composed of Recyclable CO2-Based Alkyl Carbamate Ionic Liquid

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Purification of the Recombinant Green Fluorescent Protein Using Aqueous Two-Phase System Composed of Recyclable CO2-Based Alkyl Carbamate Ionic Liquid

Cher Pin Song et al. Front Chem. .

Abstract

The formation of aqueous two-phase system (ATPS) with the environmentally friendly and recyclable ionic liquid has been gaining popularity in the field of protein separation. In this study, the ATPSs comprising N,N-dimethylammonium N',N'-dimethylcarbamate (DIMCARB) and thermo-responsive poly(propylene) glycol (PPG) were applied for the recovery of recombinant green fluorescent protein (GFP) derived from Escherichia coli. The partition behavior of GFP in the PPG + DIMCARB + water system was investigated systematically by varying the molecular weight of PPG and the total composition of ATPS. Overall, GFP was found to be preferentially partitioned to the hydrophilic DIMCARB-rich phase. An ATPS composed of 42% (w/w) PPG 1000 and 4.4% (w/w) DIMCARB gave the optimum performance in terms of GFP selectivity (1,237) and yield (98.8%). The optimal system was also successfully scaled up by 50 times without compromising the purification performance. The bottom phase containing GFP was subjected to rotary evaporation of DIMCARB. The stability of GFP was not affected by the distillation of DIMCARB, and the DIMCARB was successfully recycled in three successive rounds of GFP purification. The potential of PPG + DIMCARB + water system as a sustainable protein purification tool is promising.

Keywords: aqueous two-phase system; dialkyl carbamate; green fluorescent protein; poly(propylene glycol); purification; recycling.

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Figures

Figure 1
Figure 1
Percentage relative concentration of GFP incubated in 50 mM Tris-HCl buffer at different pH for 60 min at 25°C.
Figure 2
Figure 2
Percentage relative concentration of GFP incubated in 50 mM Tris-HCl buffer at pH 8 for 60 min at different temperature.
Figure 3
Figure 3
Photos of PPG 400/700/1000 + DIMCARB + water systems showing the partitioning of GFP between phases.
Figure 4
Figure 4
Characterization of DIMCARB. (A) FT-IR spectra of the pure DIMCARB and the DIMCARB recovered from distillation; (B) 13C NMR spectra of the pure DIMCARB; (C) 13C NMR spectra of the DIMCARB recovered from distillation.
Figure 5
Figure 5
Schematic diagram of the recycling ATPSs for three successive rounds of GFP purification.
Figure 6
Figure 6
SDS-PAGE analysis. Lane M, protein marker; Lane C, crude feedstock; Lane P, GFP standard; Lanes T15 and B15, the top phase and bottom phase of the optimized ATPS (sample number 15, as stated in Table 1), respectively; Lane S, distilled bottom phase of 100-g ATPS; Lane D, distillate obtained from the recovery of DIMCARB.

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