A new, mild cross-linking methodology to prepare cross-linked enzyme aggregates

被引:239
作者
Mateo, C [1 ]
Palomo, JM [1 ]
van Langen, LM [1 ]
van Rantwijk, F [1 ]
Sheldon, RA [1 ]
机构
[1] Delft Univ Technol, Lab Biocatalysis & Organ Chem, NL-2628 BL Delft, Netherlands
关键词
cross-linked enzyme aggregates (CLEAs); nitrilase; oxynitrilase; alcohol dehydrogenase; penicillin G acylase; dextran; cross-linker;
D O I
10.1002/bit.20033
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:273 / 276
页数:4
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