Literature DB >> 27642253

Single-Step Purification of Ovalbumin from Egg White Using Aqueous Biphasic Systems.

Matheus M Pereira1, Rafaela A P Cruz1, Mafalda R Almeida1, Álvaro S Lima2, João A P Coutinho1, Mara G Freire1.   

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 25ºC 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 almost 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.

Entities:  

Keywords:  Aqueous Two Phase; Downstream Processing; Egg White; Ovalbumin; Protein Recovery; Separation

Year:  2016        PMID: 27642253      PMCID: PMC5026300          DOI: 10.1016/j.procbio.2016.03.002

Source DB:  PubMed          Journal:  Process Biochem        ISSN: 1359-5113            Impact factor:   3.757


  23 in total

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Authors:  Dileep A Omana; Jiapei Wang; Jianping Wu
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6.  Two-step chromatographic procedure for the purification of hen egg white ovomucin, lysozyme, ovotransferrin and ovalbumin and characterization of purified proteins.

Authors:  A C Awadé; S Moreau; D Mollé; G Brulé; J L Maubois
Journal:  J Chromatogr A       Date:  1994-08-19       Impact factor: 4.759

7.  Thermodynamic study of forces involved in bovine serum albumin and ovalbumin partitioning in aqueous two-phase systems.

Authors:  B Nerli; M Espariz; G Picó
Journal:  Biotechnol Bioeng       Date:  2001-02-20       Impact factor: 4.530

8.  Modulation of protein aggregation by polyethylene glycol conjugation: GCSF as a case study.

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9.  Insight into the interactions that control the phase behaviour of new aqueous biphasic systems composed of polyethylene glycol polymers and ionic liquids.

Authors:  Mara G Freire; Jorge F B Pereira; María Francisco; Héctor Rodríguez; Luís Paulo N Rebelo; Robin D Rogers; João A P Coutinho
Journal:  Chemistry       Date:  2012-01-03       Impact factor: 5.236

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5.  Non-toxic Polymeric Dots with the Strong Protein-Driven Enhancement of One- and Two-Photon Excited Emission for Sensitive and Non-destructive Albumin Sensing.

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Review 6.  Functional Properties and Extraction Techniques of Chicken Egg White Proteins.

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  6 in total

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