期刊
BIOTECHNOLOGY AND BIOENGINEERING
卷 113, 期 11, 页码 2342-2349出版社
WILEY
DOI: 10.1002/bit.26011
关键词
flow microreactor; silica-binding module; immobilization; glass; microfluidics; enzymatic oxidation
Exploiting enzymes for chemical synthesis in flow microreactors necessitates their reuse for multiple rounds of conversion. To achieve this goal, immobilizing the enzymes on microchannel walls is a promising approach, but practical methods for it are lacking. Using fusion to a silica-binding module to engineer enzyme adsorption to glass surfaces, we show convenient immobilization of D-amino acid oxidase on borosilicate microchannel plates. In confocal laser scanning microscopy, channel walls appeared uniformly coated with target protein. The immobilized enzyme activity was in the range expected for monolayer coverage of the plain surface with oxidase (2.37 x 10(-5) nmol/mm(2)). Surface attachment of the enzyme was completely stable under flow. The operational half-life of the immobilized oxidase (25 degrees C, pH 8.0; soluble catalase added) was 40 h. Enzymatic oxidation of D-Met into alpha-keto-gamma-(methylthio) butyric acid was characterized in single-pass and recycle reactor configurations, employing in-line measurement of dissolved O-2, and off-line determination of the keto-acid product. Reaction-diffusion time-scale analysis for different flow conditions showed that the heterogeneously catalyzed reaction was always slower than diffusion of O-2 to the solid surface (Da(Pi) <= 0.3). Potential of the microreactor for intensifying O-2-dependent biotransformations restricted by mass transfer in conventional reactors is thus revealed. (C) 2016 Wiley Periodicals, Inc.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据