Preparation and characterization of cross-linked enzyme aggregates (CLEAs) of recombinant poly-3-hydroxybutyrate depolymerase from Streptomyces exfoliatus

被引：43
作者：
Hormigo, Daniel [2 ]
Garcia-Hidalgo, Javier [1 ]
Acebal, Carmen [1 ]
de la Mata, Isabel [1 ]
Arroyo, Miguel [1 ]
机构：
[1] Univ Complutense Madrid, Dept Bioquim & Biol Mol 1, Fac Ciencias Biol, E-28040 Madrid, Spain
[2] CSIC, Ctr Invest Biol, Dept Biol Medioambiental, Madrid 28040, Spain
来源：
BIORESOURCE TECHNOLOGY | 2012年 / 115卷
关键词：
Poly-(R)-3-hydroxybutyrate; PHB depolymerase; Streptomyces exfoliatus; Cross-linked enzyme aggregates; BOVINE SERUM-ALBUMIN; MICROBIAL-DEGRADATION; PENICILLIN ACYLASE; IMMOBILIZATION; POLY(3-HYDROXYBUTYRATE); POLYHYDROXYALKANOATES; POLYESTERS; CHEMICALS; ACIDS;
D O I：
10.1016/j.biortech.2011.09.035
中图分类号：
S2 [农业工程];
学科分类号：
0828 ;
摘要：
Cross-linked enzyme aggregates of poly-3-hydroxybutyrate (PHB) depolymerase from Streptomyces exfoliatus (PhaZ(Sex)-CLEAs) have been prepared. Acetone was used as the precipitating agent, while addition of bovine serum albumin (BSA) facilitated CLEAs formation. Conditions for enzyme precipitation and cross-linking have been optimized, and confocal scanning microscopy showed a homogeneous enzyme distribution in the biocatalyst. Obtained PhaZ(Sex)-CLEAs presented an average size of 50-300 mu m, showing a high PHB depolymerase activity of 255 U/g wet biocatalyst at 40 degrees C and pH 7.0. Temperature-activity profile of PhaZ(Sex)-CLEAs at pH 8.0 showed that the highest activity for pNPB hydrolysis was achieved at 60 degrees C, whereas pH-activity profile at 40 degrees C indicated that highest activity for PHB hydrolysis was achieved at pH 7.0. Additionally, immobilized biocatalyst could be recycled at least for 20 consecutive batch reactions without loss of catalytic activity, and showed higher pH and temperature stability, and better tolerance to several organic solvents than its soluble counterpart. (C) 2011 Elsevier Ltd. All rights reserved.
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收藏
页码：177 / 182
页数：6
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