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Aqueous Two‐Phase Systems Containing Urea: Influence on Phase Separation and Stabilization of Protein Conformation by Phase Components
Author(s) -
Rämsch Christian,
Kleinelanghorst Lutz B.,
Knieps Esther A.,
Thömmes Jörg,
Kula MariaRegina
Publication year - 1999
Publication title -
biotechnology progress
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.572
H-Index - 129
eISSN - 1520-6033
pISSN - 8756-7938
DOI - 10.1021/bp990030+
Subject(s) - urea , chemistry , peg ratio , aqueous solution , ethylene glycol , chromatography , urease , phase (matter) , partition coefficient , lysozyme , aqueous two phase system , biochemistry , organic chemistry , finance , economics
During recombinant Escherichia coli fermentation with high expression levels, inclusion bodies are often formed. Aqueous two‐phase systems have been used in the presence of urea for the initial recovery steps. To investigate phase behavior of such systems we determined phase diagrams of poly(ethylene glycol) (PEG) /sodium sulfate/urea/water and PEg/dextran T‐500 (DEX) /urea/phosphate buffer/water at different concentrations of urea and different molecular weight of PEG. PEg/Na 2 SO 4 aqueous two‐phase systems could be obtained including up to 30% w/w urea at 25 °C and PEg/dextran T‐500 up to 35% w/w urea. The binodial was displaced toward higher concentrations with increasing urea concentrations. The partition coefficient of urea was near unity. An unstable mutant of T4‐lysozyme with an amino acid replacement in the core (V149T) was used to analyze the effect of phase components on the conformation of the enzyme. We showed that partitioning of tryptophan was not dependent on the concentration of urea in the phase system.
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