| Literature DB >> 15083507 |
Cesar Mateo1, José M Palomo, Luuk M van Langen, Fred van Rantwijk, Roger A Sheldon.
Abstract
Cross-linked enzyme aggregates (CLEAs) were prepared from several enzymes (penicillin G acylase, hydroxynitrile lyase, alcohol dehydrogenase, and two different nitrilases) by precipitation and subsequent cross-linking using dextran polyaldehyde. In most cases, higher immobilization yields were obtained using the latter cross-linker as compared with the commonly used glutaraldehyde. Active site titration of penicillin acylase CLEAs showed that the higher activity originated from a significantly lower loss in active sites using dextran polyaldehyde as a cross-linking agent. It is proposed that macromolecular cross-linkers are too large to penetrate the protein active site and react with catalytically essential amino acid residues. Copyright 2004 Wiley Periodicals, Inc.Entities:
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Year: 2004 PMID: 15083507 DOI: 10.1002/bit.20033
Source DB: PubMed Journal: Biotechnol Bioeng ISSN: 0006-3592 Impact factor: 4.530