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Metabolic Fluxes Using Deep Learning Based on Enzyme Variations:

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2025 Jan 8
PMID 39769154
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Abstract

Metabolic pathway modeling, essential for understanding organism metabolism, is pivotal in predicting genetic mutation effects, drug design, and biofuel development. Enhancing these modeling techniques is crucial for achieving greater prediction accuracy and reliability. However, the limited experimental data or the complexity of the pathway makes it challenging for researchers to predict phenotypes. Deep learning (DL) is known to perform better than other Machine Learning (ML) approaches if the right conditions are met (i.e., a large database and good choice of parameters). Here, we use a knowledge-based model to massively generate synthetic data and extend a small initial dataset of experimental values. The main objective is to assess if DL can perform at least as well as other ML approaches in flux prediction, using 68,950 instances. Two processing methods are used to generate DL models: cross-validation and repeated holdout evaluation. DL models predict the metabolic fluxes with high precision and slightly outperform the best-known ML approach (the Cubist model) with a lower RMSE (≤0.01) in both cases. They also outperform the PLS model (RMSE ≥ 30). This study is the first to use DL to predict the overall flux of a metabolic pathway only from variations of enzyme concentrations.

References
1.
Heckmann D, Lloyd C, Mih N, Ha Y, Zielinski D, Haiman Z . Machine learning applied to enzyme turnover numbers reveals protein structural correlates and improves metabolic models. Nat Commun. 2018; 9(1):5252. PMC: 6286351. DOI: 10.1038/s41467-018-07652-6. View

2.
Kim O, Rocha M, Maia P . A Review of Dynamic Modeling Approaches and Their Application in Computational Strain Optimization for Metabolic Engineering. Front Microbiol. 2018; 9:1690. PMC: 6079213. DOI: 10.3389/fmicb.2018.01690. View

3.
Zimmermann J, Kaleta C, Waschina S . gapseq: informed prediction of bacterial metabolic pathways and reconstruction of accurate metabolic models. Genome Biol. 2021; 22(1):81. PMC: 7949252. DOI: 10.1186/s13059-021-02295-1. View

4.
Saavedra E, Encalada R, Pineda E, Jasso-Chavez R, Moreno-Sanchez R . Glycolysis in Entamoeba histolytica. Biochemical characterization of recombinant glycolytic enzymes and flux control analysis. FEBS J. 2005; 272(7):1767-83. DOI: 10.1111/j.1742-4658.2005.04610.x. View

5.
Spearman C . The proof and measurement of association between two things. By C. Spearman, 1904. Am J Psychol. 1987; 100(3-4):441-71. View