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Biocatalysis in reaction mixtures with undissolved solid substrates and products

Ulijn, R.V. and De Martin, L. and Gardossi, L. and Halling, P.J. (2003) Biocatalysis in reaction mixtures with undissolved solid substrates and products. Current Organic Chemistry, 7 (13). pp. 1333-1346. ISSN 1385-2728

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Abstract

Enzymatic synthesis in reaction mixtures with mainly undissolved substrates and/or products is a synthetic strategy in which the compounds are present mostly as pure solids. It retains the main advantages of conventional enzymatic synthesis such as high regio- and stereoselectivity, absence of racemisation and reduced side-chain protection. The reaction yields are improved and the necessity to use organic solvents to shift the thermodynamic equilibrium toward synthesis is reduced by product precipitation, which makes the synthesis favourable even in water. The thermodynamics of these reaction systems have been investigated in the last few years, resulting in methods to predict the direction of a typical reaction a priori. Furthermore, studies on kinetics, enzyme concentration, pH/temperature effects, mixing and solvent selection have opened new perspectives for the understanding, modelling, optimisation and the possible large scale application of such a strategy. In this review we have tried to cover most of the literature published in the last five to ten years on biocatalysis in substrate suspensions, focusing especially on cases where the reaction products precipitate.

Item type: Article
ID code: 321
Keywords: Beta-lactam antibiotics, thermodynamically controlled synthesis, fatty-acid esters, kinetically controlled synthesis, protease-catalyzed synthesis, enzymatic peptide-synthesis, candida-antarctica lipase, low-water media, penicillin acylase, organic-solvents, Chemistry, Organic Chemistry
Subjects: Science > Chemistry
Department: Faculty of Science > Pure and Applied Chemistry
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    Depositing user: Users 16 not found.
    Date Deposited: 10 Mar 2006
    Last modified: 04 Sep 2014 12:02
    URI: http://strathprints.strath.ac.uk/id/eprint/321

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