Literature DB >> 21824621

Recombinant protein purification using gradient assisted simulated moving bed hydrophobic interaction chromatography. Part II: process design and experimental validation.

Ludmila Gueorguieva1, Sivakumar Palani, Ursula Rinas, Guhan Jayaraman, Andreas Seidel-Morgenstern.   

Abstract

In the first part of this work adsorption isotherm parameters were acquired to describe the migration of recombinant streptokinase in Butyl Sepharose columns at different salt concentrations. Based on these results, a simulated moving bed (SMB) chromatographic process was designed and realised, which exploits a two-step salt gradient and allows the continuous separation of streptokinase from contaminants present in a clarified Escherichia coli cell lysate solution. This second part describes the design of the three-zone open-loop gradient SMB process applying both equilibrium theory and an equilibrium stage model and presents results of a series of experiments aiming to obtain pure streptokinase. Moreover, the potential of the SMB process and the design approach are evaluated.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21824621     DOI: 10.1016/j.chroma.2011.07.008

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  1 in total

Review 1.  Preparative purification of recombinant proteins: current status and future trends.

Authors:  Mayank Saraswat; Luca Musante; Alessandra Ravidá; Brian Shortt; Barry Byrne; Harry Holthofer
Journal:  Biomed Res Int       Date:  2013-12-17       Impact factor: 3.411

  1 in total

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