Kinetic model discrimination of penicillin G acylase thermal deactivation by non-isothermal continuous activity assay

被引:18
|
作者
McDonald, Matthew A. [1 ]
Bromig, Lukas [1 ,2 ]
Grover, Martha A. [1 ]
Rousseau, Ronald W. [1 ]
Bommarius, Andreas S. [1 ]
机构
[1] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
[2] Tech Univ Munich, Fac Chem, Dept Chem Engn, Lichtenbergstr 4, D-85748 Garching, Germany
关键词
Penicillin G acylase; Enzyme deactivation modeling; Lumry-Eyring mechanism; Model discrimination; Akaike information criterion; ESCHERICHIA-COLI; STABILIZATION; TEMPERATURE; INACTIVATION; SUBSTRATE; ENZYMES;
D O I
10.1016/j.ces.2018.04.046
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A novel approach for the determination of a kinetic model of enzyme deactivation is presented incorporating time and temperature dependence into a single, continuous assay. A generic method for a non-isothermal, continuous activity assay is developed. Unique temperature profiles that enhance model discrimination with fewer experiments compared to linear temperature scans were used to differentiate kinetic models of penicillin G acylase (PGA) deactivation. Three models are examined in depth but the technique is generalizable to any kinetic deactivation model. Using the Akaike information criterion (AIC), the Lumry-Eyring model was found to best capture PGA deactivation behavior and the corresponding kinetic parameters are presented for the first time. Additionally, simulated experiments on lysozyme and TEM-1 beta-lactamase were used to develop temperature profiles that best differentiate the studied kinetic models. The results from the proposed approach were consistent with conventional, but tedious, isothermal batch experiments. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:79 / 86
页数:8
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