Immobilisation and characterisation of biocatalytic co-factor recycling enzymes, glucose dehydrogenase and NADH oxidase, on aldehyde functional ReSyn™ polymer microspheres

被引:24
作者
Twala, Busisiwe V. [1 ]
Sewell, B. Trevor [2 ]
Jordaan, Justin [1 ]
机构
[1] CSIR Biosci, Mol Biomat, ZA-0091 Brummeria, South Africa
[2] Univ Cape Town, Dept Clin Lab Sci, Inst Infect Dis & Mol Med, Observatory, South Africa
关键词
Immobilisation; Dehydrogenase; Oxidase; ReSyn (TM); Stability; Biocatalysis; STABILIZATION; REGENERATION; STABILITY; ACID; SUPPORTS; LIPASE;
D O I
10.1016/j.enzmictec.2012.03.003
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
The use of enzymes in industrial applications is limited by their instability, cost and difficulty in their recovery and re-use. Immobilisation is a technique which has been shown to alleviate these limitations in biocatalysis. Here we describe the immobilisation of two biocatalytically relevant co-factor recycling enzymes, glucose dehydrogenase (GDH) and NADH oxidase (NOD) on aldehyde functional ReSyn (TM) polymer microspheres with varying functional group densities. The successful immobilisation of the enzymes on this new high capacity microsphere technology resulted in the maintenance of activity of similar to 40% for GDH and a maximum of 15.4% for NOD. The microsphere variant with highest functional group density of similar to 3500 mu mol g(-1) displayed the highest specific activity for the immobilisation of both enzymes at 33.22 U mg(-1) and 6.75 U mg(-1) for GDH and NOD with respective loading capacities of 51% (0.51 mg mg(-1)) and 129% (1.29 mg mg(-1)). The immobilised GDH further displayed improved activity in the acidic pH range. Both enzymes displayed improved pH and thermal stability with the most pronounced thermal stability for GDH displayed on ReSyn (TM) A during temperature incubation at 65 degrees C with a 13.59 fold increase, and NOD with a 2.25-fold improvement at 45 degrees C on the same microsphere variant. An important finding is the suitability of the microspheres for stabilisation of the multimeric protein GDH. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:331 / 336
页数:6
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