Literature DB >> 14755564

Salt-activation of nonhydrolase enzymes for use in organic solvents.

John A Morgan1, Douglas S Clark.   

Abstract

Enzymatic reactions are important for the synthesis of chiral molecules. One factor limiting synthetic applications of enzymes is the poor aqueous solubility of numerous substrates. To overcome this limitation, enzymes can be used directly in organic solvents; however, in nonaqueous media enzymes usually exhibit only a fraction of their aqueous-level activity. Salt-activation, a technique previously demonstrated to substantially increase the transesterification activity of hydrolytic enzymes in organic solvents, was applied to horse liver alcohol dehydrogenase, soybean peroxidase, galactose oxidase, and xanthine oxidase, which are oxidoreductase and oxygenase enzymes. Assays of the lyophilized enzyme preparations demonstrated that the presence of salt protected enzymes from irreversible inactivation. In organic solvents, there were significant increases in activity for the salt-activated enzymes compared to nonsalt-activated controls for every enzyme tested. The increased enzymatic activity in organic solvents was shown to result from a combination of protection against inactivation during the freeze-drying process and other as-yet undetermined factors. Copyright 2004 Wiley Periodicals, Inc.

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Year:  2004        PMID: 14755564     DOI: 10.1002/bit.10895

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  2 in total

1.  Reflections on charge state distributions, protein structure, and the mystical mechanism of electrospray ionization.

Authors:  Omar M Hamdy; Ryan R Julian
Journal:  J Am Soc Mass Spectrom       Date:  2011-11-11       Impact factor: 3.109

2.  Hydrogen/deuterium exchange study of subtilisin Carlsberg during prolonged exposure to organic solvents.

Authors:  Ezio Fasoli; Amaris Ferrer; Gabriel L Barletta
Journal:  Biotechnol Bioeng       Date:  2009-03-01       Impact factor: 4.530

  2 in total

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