Abstract
Through genetic engineering it is possible to introduce targeted genetic changes and hereby engineer the metabolism of microbial cells with the objective to obtain desirable phenotypes. However, owing to the complexity of metabolic networks, both in terms of structure and regulation, it is often difficult to predict the effects of genetic modifications on the resulting phenotype. Recently genome-scale metabolic models have been compiled for several different microorganisms where structural and stoichiometric complexity is inherently accounted for. New algorithms are being developed by using genome-scale metabolic models that enable identification of gene knockout strategies for obtaining improved phenotypes. However, the problem of finding optimal gene deletion strategy is combinatorial and consequently the computational time increases exponentially with the size of the problem, and it is therefore interesting to develop new faster algorithms. In this study we report an evolutionary programming based method to rapidly identify gene deletion strategies for optimization of a desired phenotypic objective function. We illustrate the proposed method for two important design parameters in industrial fermentations, one linear and other non-linear, by using a genome-scale model of the yeast Saccharomyces cerevisiae. Potential metabolic engineering targets for improved production of succinic acid, glycerol and vanillin are identified and underlying flux changes for the predicted mutants are discussed. We show that evolutionary programming enables solving large gene knockout problems in relatively short computational time. The proposed algorithm also allows the optimization of non-linear objective functions or incorporation of non-linear constraints and additionally provides a family of close to optimal solutions. The identified metabolic engineering strategies suggest that non-intuitive genetic modifications span several different pathways and may be necessary for solving challenging metabolic engineering problems.
MeSH Terms
Algorithms
Benzaldehydes/chemistry
Computational Biology/methods
Computer Simulation
Escherichia coli/metabolism
Evolution, Molecular
Gene Expression Regulation
Genetic Engineering
Genome, Fungal
Glycerol/metabolism
Models, Biological
Models, Genetic
Phenotype
Protein Engineering/methods
Protein Interaction Mapping
Saccharomyces cerevisiae/genetics,metabolism
Software
Succinic Acid/metabolism
Chemicals
Benzaldehydes
Succinic Acid
vanillin
Glycerol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Patil Kiran Raosaheb
Center for Microbial Biotechnology, BioCentrum-DTU, Building 223, Technical University of Denmark, DK-2800 Kgs, Lyngby, Denmark.
[email protected]
Rocha Isabel
Förster Jochen
Nielsen Jens
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