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Original scientific paper

https://doi.org/10.15255/CABEQ.2025.2459

Addressing Sensitivity and Non-Uniqueness in the Determination of Enzyme Kinetic Parameters

M. Lakner ; Independent Scholar
I. Plazl orcid id orcid.org/0000-0002-5247-1387 ; Faculty of Chemistry and Chemical Technology, University of Ljubljana, Ljubljana, Slovenia


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Abstract

Accurate determination of enzyme kinetic parameters is critical for model-based design and intensification of biocatalytic processes, particularly in microscale systems. While Michaelis-Menten kinetics provides a foundational framework, its extension to reversible, multi-substrate, and inhibited reactions introduces significant challenges in parameter estimation-most notably, parameter sensitivity and non-uniqueness.
This study systematically investigates these challenges across three case studies of increasing complexity: (i) mono-substrate Michaelis-Menten kinetics, (ii) reversible enzymatic reactions with four parameters, and (iii) a six-parameter reversible mono-substrate kinetic model with substrate and product inhibition. In the first two cases, we show that vastly different parameter sets can yield nearly indistinguishable model fits to experimental data, exposing the limitations of classical graphical and nonlinear regression methods.
In the mono-substrate case based on real experimental data, two parameter sets differing by nearly two orders of magnitude produce virtually identical model outputs, demonstrating practical non-uniqueness even for simple kinetic models.
For the six-parameter inhibited system, a theoretical and numerical analysis reveals intrinsic non-uniqueness of the parameter estimation problem, characterized by an infinite family of parameter vectors yielding identical solutions. These results demonstrate that parameter non-uniqueness is not merely a consequence of experimental noise, but a structural property of complex kinetic models, emphasizing the need for more robust and structurally informed modeling approaches in biocatalysis.







This work is licensed under a Creative Commons Attribution 4.0 International License.

Keywords

enzyme kinetics; kinetic parameter estimation; parameter non-uniqueness

Hrčak ID:

344462

URI

https://hrcak.srce.hr/344462

Publication date:

12.2.2026.

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