At low water activity alpha-chymotrypsin is more active in an ionic liquid than in non-ionic organic solvents

M Eckstein, M Sesing, U Kragl, Patrick Adlercreutz

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The kinetics of the alpha-chymotrypsin catalysed transesterification of N-acetyl-l-phenylalanine ethyl ester with 1-butanol and the competing hydrolysis were evaluated at fixed water activity in two ionic liquids and two non-ionic organic solvents. In most respects the four solvents behaved similarly. However, at a water activity of 0.33, higher catalytic activity was observed in the ionic liquid, 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide, than in the other solvents, and at a(w)=0.11 catalysis was only observed in this solvent.
    Original languageEnglish
    Pages (from-to)867-872
    JournalBiotechnology Letters
    Volume24
    Issue number11
    DOIs
    Publication statusPublished - 2002

    Subject classification (UKÄ)

    • Industrial Biotechnology

    Free keywords

    • water activity
    • alpha-chymotrypsin
    • ionic liquids

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