Details

Addressing sensitivity and non-uniqueness in the determination of enzyme kinetic parameters : research data underlying the article
ID Lakner, Mitja (Author), ID Plazl, Igor (Author)

.pdfPDF - Data description, Download (87,31 KB)
MD5: 397F43B62E82BCE52E6A8151B88C9E4A
Description: README
.nbNB - Research data, Download (7,32 MB)
MD5: E4CAB18B77FA4A73E3E14F38642ABB01
Description: QABEQ
.pdfPDF - Research data, Download (1,51 MB)
MD5: E72F24229A71205F36AF1D1D95643E4F
Description: QABEQ
This document has even more files. Complete list of files is available below.

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.

Language:English
Keywords:enzyme kinetics, kinetic parameter estimation, parameter non-uniqueness
Typology:2.20 - Complete scientific database of research data
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2026
PID:20.500.12556/RUL-182932 This link opens in a new window
Data col. methods:Measurements and tests
Publication date in RUL:28.05.2026
Views:114
Downloads:49
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Secondary language

Language:Slovenian
Keywords:encimska kinetika, določevanje kinetičnih parametrov, neenoličnost parametrov

Projects

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P2-0191
Name:Kemijsko inženirstvo

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J7-50041
Name:Razvoj imobiliziranih katalizatorjev za pripravo devteriranih organskih spojin

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:J4-4562
Name:Intenzifikacija biokatalitskih procesov z uporabo evtektičnih topil v mikropretočnih sistemih za trajnostno valorizacijo odpadkov
Acronym:BioInDES

Funder:EC - European Commission
Funding programme:HE
Project number:101160108
Name:Twinning for Building Excellence and Innovative Solutions in Flow Catalysis
Acronym:FLOWCAT

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Files

Loading...

Back