4.5 Article

Purification of recombinant phenylalanine dehydrogenase by partitioning in aqueous two-phase systems

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ELSEVIER
DOI: 10.1016/j.jchromb.2007.04.049

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aqueous two-phase systems (ATPS); ammonium sulfate; phenylalanine dehydrogenase (PheDH); partition; purification; PEG-6000

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This study presents the partitioning and purification of recombinant Bacillus badius phenylalanine dehydrogenase (PheDH) in aqueous two-phase systems (ATPS) composed of polyethylene glycol 6000 (PEG-6000) and ammonium sulfate. A single-step operation of ATPS was developed for extraction and purification of recombinant PheDH from E. coli BL21 (DE3). The influence of system parameters including; PEG molecular weight and concentration, pH, (NH4)(2)SO4 concentration and NaCl salt addition on enzyme partitioning were investigated. The best optimal system for the partitioning and purification of PheDH was 8.5% (w/w) PEG-6000, 17.5% (w/w) (NH4)(2)SO4 and 13% (w/w) NaCl at pH 8.0. The partition coefficient, recovery, yield, purification factor and specific activity values were of 92.57, 141%, 95.85%, 474.3 and 10424.97 U/mg, respectively. Also the K-m values for L-phenylalanine and NAD(+) in oxidative deamination were 0.020 and 0. 13 mM, respectively. Our data suggested that this ATPS could be an economical and attractive technology for large-scale purification of recombinant PheDH. (C) 2007 Elsevier B.V. All rights reserved.

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