ArticleBMC systems biology2011
Steady-state global optimization of metabolic non-linear dynamic models through recasting into power-law canonical models.
Article in BMC systems biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 24 citations in OpenAlex.
- Article
- Optimal control of agent-based models via surrogate modeling.PLoS computational biology · 2025Article
- A Review of Dynamic Modeling Approaches and Their Application in Computational Strain Optimization for Metabolic Engineering.Frontiers in microbiology · 2018Review
- Tailored parameter optimization methods for ordinary differential equation models with steady-state constraints.BMC systems biology · 2016Article
- k-OptForce: integrating kinetics with flux balance analysis for strain design.PLoS computational biology · 2014Article
- Metabolomics and systems pharmacology: why and how to model the human metabolic network for drug discovery.Drug discovery today · 2014Review
- Fuzzy optimization for detecting enzyme targets of human uric acid metabolism.Bioinformatics (Oxford, England) · 2013Article
- Identification of regulatory structure and kinetic parameters of biochemical networks via mixed-integer dynamic optimization.BMC systems biology · 2013Article
- Deterministic global optimization algorithm based on outer approximation for the parameter estimation of nonlinear dynamic biological systems.BMC bioinformatics · 2012Article
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Authors and funding
6 authors at 3 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundDesign of newly engineered microbial strains for biotechnological purposes would greatly benefit from the development of realistic mathematical models for the processes to be optimized. Such models can then be analyzed and, with the development and application of appropriate optimization techniques, one could identify the modifications that need to be made to the organism in order to achieve the desired biotechnological goal. As appropriate models to perform such an analysis are necessarily non-linear and typically non-convex, finding their global optimum is a challenging task. Canonical modeling techniques, such as Generalized Mass Action (GMA) models based on the power-law formalism, offer a possible solution to this problem because they have a mathematical structure that enables the development of specific algorithms for global optimization.
resultsBased on the GMA canonical representation, we have developed in previous works a highly efficient optimization algorithm and a set of related strategies for understanding the evolution of adaptive responses in cellular metabolism. Here, we explore the possibility of recasting kinetic non-linear models into an equivalent GMA model, so that global optimization on the recast GMA model can be performed. With this technique, optimization is greatly facilitated and the results are transposable to the original non-linear problem. This procedure is straightforward for a particular class of non-linear models known as Saturable and Cooperative (SC) models that extend the power-law formalism to deal with saturation and cooperativity.
conclusionsOur results show that recasting non-linear kinetic models into GMA models is indeed an appropriate strategy that helps overcoming some of the numerical difficulties that arise during the global optimization task.
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