Single-step purification of ovalbumin from egg white using aqueous biphasic systems. Issue 6 (June 2016)

• Record Type: Journal Article
• Authors: Pereira, Matheus M.; Cruz, Rafaela A.P.; Almeida, Mafalda R.; Lima, Álvaro S.; Coutinho, João A.P.; Freire, Mara G.
• Is Part Of: Process biochemistry. Volume 51:Issue 6(2016:Jun.)
• Page Start: 781
• Page End: 791
• Publication Date: 2016-06
• Subjects: Ovalbumin -- Protein recovery -- Separation -- Aqueous two phase -- Downstream processing -- Egg white; Biochemical engineering -- Periodicals; Biotechnology -- Periodicals; Biochemistry -- periodicals; Biotechnology -- periodicals; Chemical Engineering -- periodicals; Génie biochimique -- Périodiques; Biotechnologie -- Périodiques; Biochemical engineering; Biotechnology; Periodicals; 660.63
• DOI: 10.1016/j.procbio.2016.03.002
• Languages: English
• ISSNs: 1359-5113

Abstract

Graphical abstract: Highlights: ABS composed of PEG and potassium citrate/citric acid were investigated. Ovalbumin preferentially migrates to the PEG-rich phase. Extraction efficiencies up to 98.9% were attained using commercial and pure ovalbumin. The isolation of pure ovalbumin with a recovery yield of 65% was attained in a single-step. Abstract: The ability of aqueous biphasic systems (ABS) composed of polyethylene glycols of different molecular weights (PEG 400, 600 and 1000) and buffered aqueous solutions of potassium citrate/citric acid (pH 5.0–8.0) to selectively extract ovalbumin from egg white was here investigated. Phase diagrams, tie-lines and tie-line lengths were determined at 25 °C and the partitioning of ovalbumin in these systems was then evaluated. Aiming at optimizing the selective extraction of ovalbumin in the studied ABS, factors such as pH, PEG molecular weight and amount of the phase-forming components were initially investigated with pure commercial ovalbumin. In all ABS, it was observed a preferential partitioning of ovalbumin to the polymer-rich phase, with extraction efficiencies higher than 90%. The best ABS were then applied in the purification of ovalbumin from the real egg white matrix. In order to ascertain on the ovalbumin purity and yield, sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and size exclusion high performance liquid chromatography (SE-HPLC) analyses were conducted, confirming that the isolation/purification of ovalbumin from egg white was completely achieved in a single-step with a recovery yield of 65%. The results obtained show that polymer-salt-based ABS allow the selective extraction of ovalbumin from egg white with a simpler approach and better performance than previously reported. Finally, it is shown that ovalbumin can be completely recovered from the PEG-rich phase by an induced precipitation using an inexpensive and sustainable separation platform which can be easily applied on an industrial scale.