期刊
JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC
卷 134, 期 -, 页码 302-309出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molcatb.2016.10.017
关键词
Hydrogen peroxide; Catalase; Immobilization; Porous solid support; Superoxygenation; Oxygen sensing; Oxygen gradients; Process intensification
资金
- Austrian Science Fund (FWF) [W 901] Funding Source: researchfish
Besides merely destroying H2O2, an important use of the catalase reaction, H2O2 -> 1/2 O-2 + H2O, is to supply O-2 to oxygenation reactions. Due to convenient spatiotemporal control over O2 release, oxygenation from H2O2 is useful in particular for enzymatic reactions confined to solid supports. Because commercial catalases are difficult to immobilize, we have developed a one-step procedure of purification and immobilization of Bordetella pertussis catalase, recornbinantly produced in Escherichia coli. Fusion of the catalase to a positively charged binding module enabled effective immobilization of the chimeric enzyme on anionic support (Relisorb SP 400), giving a controllable activity loading of between 5000 and 100,000 unitsig support. Use of the immobilized catalase in combination with H2O2 feeding provided O-2 to the reaction of glucose oxidase in solution for a range of volumetric conversion rates (0.2-1.5 mM/min). Using optical sensing to measure the O-2 concentration in the liquid but also in the solid phase, we showed that internal superoxygenation of the support was made possible under these conditions, resulting in an inverted (that is, negative) O-2 concentration gradient between the bulk and the particle and allowing the internal O-2 concentration to exceed by up to 4-fold the limit of atmospheric-pressure air saturation in solution. By tailored immobilization of B. pertussis catalase, therefore, an efficient biocatalytic system for hydrogen peroxide conversion in porous solid support was developed. This could find application for bubble-free oxygenation of O-2-dependent enzymes co-immobilized with the catalase whereby enhanced internal availability of O-2 would contribute to biocatalytic reaction intensification. (C) 2016 Elsevier B.V. All rights reserved.
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