Green fluorescent protein extraction and LPS removal from Escherichia coli fermentation medium using aqueous two-phase micellar system

• Published in: Separation and purification technology 2011-10, Vol.81 (3), p.339-346
• Main Authors: Lopes, André M., Magalhães, Pérola O., Mazzola, Priscila G., Rangel-Yagui, Carlota O., de Carvalho, João C.M., Penna, Thereza C.V., Pessoa, Adalberto
• Format: Article
• Language: English
• Subjects: Applied sciences; Biological and medical sciences; Biotechnology; Chemical engineering; Endotoxins; Escherichia; Exact sciences and technology; Fundamental and applied biological sciences. Psychology; Green fluorescent protein; Liquid-liquid extraction; LPS removal; Methods. Procedures. Technologies; Others; Protein purification; Triton X-114; Various methods and equipments
• ISSN: 1383-5866; 1873-3794
• DOI: 10.1016/j.seppur.2011.07.043

► ATPMS are an interesting alternative for GFPuv extraction and LPS removal. ► ATPMS technology proved to be effective in GFPuv recovery. ► GFPuv is recovered into the micelle-poor phase, due to excluded-volume interactions. ► Triton X-114 can be applied for removal of higher LPS concentrations. ► ATPMS can be exploited as the first step for purification in biotechnology processes. The viability of large-scale industrial production of recombinant biomolecules of pharmaceutical interest significantly depends on the separation and purification techniques used. In biotechnology, endotoxin (LPS) removal from recombinant proteins is a critical and challenging step in the preparation of injectable therapeutics, since endotoxin is a natural component of bacterial expression systems widely used to manufacture therapeutic proteins. This work aimed to study the use of aqueous two-phase micellar systems (ATPMS) from preparations containing recombinant proteins of pharmaceutical interest, such as green fluorescent protein (GFPuv), which works as a biological indicator. The GFPuv extraction and LPS removal were evaluated in ATPMS, partition assays were carried out using pure GFPuv and cell lysate from Escherichia coli. The ATPMS technology proved to be effective in GFPuv recovery, preferentially into the micelle-poor phase ( K GFPuv > 1), and LPS removal into the micelle-rich phase (% REM LPS > 98%). GFPuv was partitioned preferentially into the micelle-poor phase due to excluded-volume interactions in the micelle-rich phase. Therefore, this system can be exploited as the first step for purification in biotechnology processes for removal of higher LPS concentrations.