Aqueous Biphasic Systems Composed of Cholinium Chloride and Polymers as Effective Platforms for the Purification of Recombinant Green Fluorescent Protein

• Published in: ACS sustainable chemistry & engineering Vol. 6; no. 7; pp. 9383 - 9393
• Main Authors: dos Santos, Nathalia V, Martins, Margarida, Santos-Ebinuma, Valéria C, Ventura, Sónia P. M, Coutinho, João A. P, Valentini, Sandro R, Pereira, Jorge F. B
• Format: Journal Article
• Language: English
• Published: American Chemical Society 02.07.2018
• Subjects: Aqueous biphasic systems; Purification; Integrated downstream process; Cholinium chloride; Green fluorescent protein
• ISSN: 2168-0485; 2168-0485
• DOI: 10.1021/acssuschemeng.8b01730

Green fluorescent protein (GFP) has excellent properties as a biosensor and biomarker; however, its widespread use is limited by its purification costs. Alternative low-cost purification techniques can overcome this issue. The aim of this work was to evaluate aqueous biphasic systems (ABS) composed of cholinium chloride ([Ch]­Cl) and different polymers as effective platforms to recover GFP from cell lysate of recombinant Escherichia coli BL21. All systems completely extracted GFP from cell lysate (>99%) into the polymeric- or [Ch]­Cl-rich phases. In general, [Ch]­Cl-based ABS allowed a good purification capacity (GFP 80–100% pure), with the best results (approximately 100% pure GFP) achieved with a polypropylene glycol (PPG)-400/[Ch]Cl ABS in a single-step extraction or in a two-step extraction (back-extraction) by the integration of a polyethylene glycol (PEG)/sodium polyacrylate+[Ch]­Cl ABS with a following stage using a PEG/[Ch]­Cl-based ABS. Additionally, to demonstrate the potential of the PPG-400/[Ch]Cl ABS in downstream processing, solvent recycling and GFP polishing were carried out using ultrafiltration. Finally, the capacity of the PPG-400/[Ch]Cl ABS to extract other fluorescent proteins was also confirmed. The results clearly demonstrated that the PPG-400/[Ch]Cl ABS can be applied in downstream processing for the purification of proteins, not only enhancing purification yields but also providing simpler, quicker, cost-effective, and biocompatible processes.