Dry entrapment of enzymes by epoxy or polyester resins hardened on different solid supports

被引:9
作者
Barig, Susann [1 ]
Funke, Andreas [1 ]
Merseburg, Andrea [1 ]
Schnitzlein, Klaus [2 ]
Stahmann, K. -Peter [1 ]
机构
[1] Brandenburg Univ Technol Cottbus Senftenberg, Fak 6, D-01958 Senftenberg, Germany
[2] Brandenburg Univ Technol Cottbus Senftenberg, Fak 4, D-03046 Cottbus, Germany
关键词
Immobilization; Epoxy resin; Polyester resin; Thermomyces lanuginosus lipase; Ashbya gossypii threonine aldolase; Cross linked enzyme aggregates; THREONINE ALDOLASE; WHOLE CELLS; IMMOBILIZATION; LIPASE; STABILIZATION; PURIFICATION; BIOCATALYSTS; HYDROLYSIS; ADSORPTION; GLYCINE;
D O I
10.1016/j.enzmictec.2014.03.013
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
Embedding of enzymes was performed with epoxy or polyester resin by mixing in a dried enzyme preparation before polymerization was started. This fast and low-cost immobilization method produced enzymatically active layers on different solid supports. As model enzymes the well-characterized Thermomyces lanuginosus lipase and a new threonine aldolase from Ashbya gossypii were used. It was shown that T. lanuginosus lipase recombinantly expressed in Aspergillus oryzae is a monomeric enzyme with a molecular mass of 34 kDa, while A. gossypii threonine aldolase expressed in Escherichia coli is a pyridoxa1-5'-phosphate binding homotetramer with a mass of 180 kDa. The enzymes were used freeze dried, in four different preparations: freely diffusing, adsorbed on octyl sepharose, as well as cross-linked enzyme aggregates or as suspensions in organic solvent. They were mixed with standard two-component resins and prepared as layers on solid supports made of different materials e.g. metal, glass, polyester. Polymerization led to encapsulated enzyme preparations showing activities comparable to literature values. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 55
页数:9
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