Journal article
Kinetic model discrimination of penicillin G acylase thermal deactivation by non-isothermal continuous activity assay
Chemical engineering science, v 187, pp 79-86
21 Sep 2018
Abstract
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.
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Details
- Title
- Kinetic model discrimination of penicillin G acylase thermal deactivation by non-isothermal continuous activity assay
- Creators
- Matthew A. McDonald - Georgia Institute of TechnologyLukas Bromig - Georgia Institute of TechnologyMartha A. Grover - Georgia Institute of TechnologyRonald W. Rousseau - Georgia Institute of TechnologyAndreas S. Bommarius - Georgia Institute of Technology
- Publication Details
- Chemical engineering science, v 187, pp 79-86
- Publisher
- Elsevier
- Number of pages
- 8
- Grant note
- Georgia Research Alliance (Atlanta, GA, USA) Cecil J. "Pete" Silas Endowment
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Chemical and Biological Engineering
- Web of Science ID
- WOS:000436773400008
- Scopus ID
- 2-s2.0-85046691300
- Other Identifier
- 991021958009304721
InCites Highlights
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- Collaboration types
- Domestic collaboration
- International collaboration
- Web of Science research areas
- Engineering, Chemical