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Updated: Jul 13, 2026

High-Throughput Metabolic Profiling for Model Refinements of Microalgae
Published on: December 4, 2021
WILDkCAT: extract, retrieve, and predict enzyme turnover numbers of constraint-based metabolic models
Hugues Escoffier1, Carole Linster2, Thomas Sauter1
1Department of Health, Medicine and Life Sciences (DHML), University of Luxembourg, Esch-sur-Alzette L-4362, Luxembourg.
Summary:
Accurate enzyme turnover numbers are essential for building enzyme-constrained genome-scale metabolic models. However, collecting and curating these parameters remains a major bottleneck. Indeed, kcat values are scattered across multiple databases, reported under varying experimental conditions, and often missing for many enzymes. To address this challenge, we present WILDkCAT, a Python-based pipeline that enables the retrieval of kcat values from wild-type enzyme measured under user-specified pH and temperature ranges for a given metabolic model. The application to Escherichia coli (iML1515) and Homo sapiens (Human-GEM) models demonstrated the ability of WILDkCAT to retrieve substantial kcat coverage and its applicability across diverse genome-scale models.
Availability And Implementation:
WILDkCAT is available at https://github.com/sysbiolux/WILDkCAT and from PyPI. WILDkCAT works on all major operating systems and computer architectures. The documentation is available at https://sysbiolux.github.io/WILDkCAT.
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