On the importance of the support material for enzymatic synthesis in organic media
Open Access
- 1 August 1991
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 199 (3), 609-614
- https://doi.org/10.1111/j.1432-1033.1991.tb16161.x
Abstract
Enzymes were deposited on different porous support materials and these preparations were used to catalyze reactions in organic media. Reactions were carried out at specific water activities, achieved by equilibrating both the enzyme preparation and the substrate solution at the desired water activity before mixing them and thereby starting the reactions. The reaction rates obtained at the same water activity with different supports differed greatly, indicating a direct influence of the support on the enzyme. For horse liver alcohol dehydrogenase, Celite was the best support, and the reaction rate increased with increasing water activity. In the α-chymotrypsin-catalyzed alcoholysis of N-acetyl-l-phenylalanine ethyl ester with 1-butanol, high rates were again obtained with Celite, but with this support only about one third of the ethyl ester was converted to butyl ester, the rest was hydrolyzed. With the polyamide support, Accurel PA6, alcoholysis was the dominating reaction, and by using a low water activity (0.33), hydrolysis was completely suppressed while still maintaining a high alcoholysis activity. Controlled pore glass (CPG), derivatized with either hexyl or glucosyl groups, had quite different properties as enzyme supports. For horse liver alcohol dehydrogenase, glucose-CPG was a much better support than hexyl-CPG, and in the α-chymotrypsin-catalyzed reactions, glucose-CPG favored hydrolysis, and hexyl-CPG alcoholysis, at water activities exceeding 0.8. The results are discussed considering the absorption of water on the enzymes, on the supports and the solubility of water in the reaction media; all these parameters were measured separately.Keywords
This publication has 15 references indexed in Scilit:
- High-affinity binding of water by proteins is similar in air and in organic solventsBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1990
- The control of lipase‐catalysed transesterification and esterification reaction ratesEuropean Journal of Biochemistry, 1990
- Enzymatic oxidation of ethanol in the gaseous phaseBiotechnology & Bioengineering, 1989
- Micellar enzymology: its relation to membranologyBiochimica et Biophysica Acta (BBA) - Biomembranes, 1989
- Biocatalysis in a Microaqueous Organic SolventAnnals of the New York Academy of Sciences, 1988
- On the importance of the support material for bioorganic synthesisEuropean Journal of Biochemistry, 1988
- Lipase‐catalyzed ester exchange reactions in organic media with controlled humidityBiotechnology & Bioengineering, 1987
- Application of polyethylene glycol-modified enzymes in biotechnological processes: organic solvent-soluble enzymesTrends in Biotechnology, 1986
- Water and globular proteinsTrends in Biochemical Sciences, 1983
- Thermodynamic functions of biopolymer hydration. I. Their determination by vapor pressure studies, discussed in an analysis of the primary hydration processBiopolymers, 1982