Home LiteratureArticle Details
PMID: 16375763 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

Evolutionary programming as a platform for in silico metabolic engineering.

BMC bioinformatics ·Vol. 6 ·2005-12-23 ·Pages 308

Patil KR, Rocha I, Förster J, Nielsen J

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
References (28)
28 references, click to expand
  1. Integrating high-throughput and computational data elucidates bacterial networks.
    Nature. 2004 May 6;429(6987):92-6 PMID: 15129285
  2. Use of genome-scale microbial models for metabolic engineering.
    Curr Opin Biotechnol. 2004 Feb;15(1):64-9 PMID: 15102469
  3. Combinatorial complexity of pathway analysis in metabolic networks.
    Mol Biol Rep. 2002;29(1-2):233-6 PMID: 12241063
  4. Energy balance for analysis of complex metabolic networks.
    Biophys J. 2002 Jul;83(1):79-86 PMID: 12080101
  5. In silico predictions of Escherichia coli metabolic capabilities are consistent with experimental data.
    Nat Biotechnol. 2001 Feb;19(2):125-30 PMID: 11175725
  6. Genome-scale microbial in silico models: the constraints-based approach.
    Trends Biotechnol. 2003 Apr;21(4):162-9 PMID: 12679064
  7. Advances in flux balance analysis.
    Curr Opin Biotechnol. 2003 Oct;14(5):491-6 PMID: 14580578
  8. Uncovering transcriptional regulation of metabolism by using metabolic network topology.
    Proc Natl Acad Sci U S A. 2005 Feb 22;102(8):2685-9 PMID: 15710883
  9. A functional genomics approach using metabolomics and in silico pathway analysis.
    Biotechnol Bioeng. 2002 Sep 30;79(7):703-12 PMID: 12209793
  10. Analysis of optimality in natural and perturbed metabolic networks.
    Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15112-7 PMID: 12415116
  11. A general definition of metabolic pathways useful for systematic organization and analysis of complex metabolic networks.
    Nat Biotechnol. 2000 Mar;18(3):326-32 PMID: 10700151
  12. Theory for the systemic definition of metabolic pathways and their use in interpreting metabolic function from a pathway-oriented perspective.
    J Theor Biol. 2000 Apr 7;203(3):229-48 PMID: 10716907
  13. Regulatory on/off minimization of metabolic flux changes after genetic perturbations.
    Proc Natl Acad Sci U S A. 2005 May 24;102(21):7695-700 PMID: 15897462
  14. Metabolic engineering.
    Appl Microbiol Biotechnol. 2001 Apr;55(3):263-83 PMID: 11341306
  15. Optknock: a bilevel programming framework for identifying gene knockout strategies for microbial strain optimization.
    Biotechnol Bioeng. 2003 Dec 20;84(6):647-57 PMID: 14595777
  16. Escherichia coli K-12 undergoes adaptive evolution to achieve in silico predicted optimal growth.
    Nature. 2002 Nov 14;420(6912):186-9 PMID: 12432395
  17. Saccharomyces cerevisiae phenotypes can be predicted by using constraint-based analysis of a genome-scale reconstructed metabolic network.
    Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13134-9 PMID: 14578455
  18. Description and interpretation of adaptive evolution of Escherichia coli K-12 MG1655 by using a genome-scale in silico metabolic model.
    J Bacteriol. 2003 Nov;185(21):6400-8 PMID: 14563875
  19. Exploiting biological complexity for strain improvement through systems biology.
    Nat Biotechnol. 2004 Oct;22(10):1261-7 PMID: 15470466
  20. METATOOL: for studying metabolic networks.
    Bioinformatics. 1999 Mar;15(3):251-7 PMID: 10222413
  21. Optimization-based framework for inferring and testing hypothesized metabolic objective functions.
    Biotechnol Bioeng. 2003 Jun 20;82(6):670-7 PMID: 12673766
  22. Fat synthesis in adipose tissue. An examination of stoichiometric constraints.
    Biochem J. 1986 Sep 15;238(3):781-6 PMID: 3800960
  23. Glycerol production by microbial fermentation: a review.
    Biotechnol Adv. 2001 Jun;19(3):201-23 PMID: 14538083
  24. Genome-scale reconstruction of the Saccharomyces cerevisiae metabolic network.
    Genome Res. 2003 Feb;13(2):244-53 PMID: 12566402
  25. Integrated genomic and proteomic analyses of a systematically perturbed metabolic network.
    Science. 2001 May 4;292(5518):929-34 PMID: 11340206
  26. In vivo analysis of the mechanisms for oxidation of cytosolic NADH by Saccharomyces cerevisiae mitochondria.
    J Bacteriol. 2000 May;182(10):2823-30 PMID: 10781551
  27. OptStrain: a computational framework for redesign of microbial production systems.
    Genome Res. 2004 Nov;14(11):2367-76 PMID: 15520298
  28. Whole-cell simulation: a grand challenge of the 21st century.
    Trends Biotechnol. 2001 Jun;19(6):205-10 PMID: 11356281
Article Info
Journal
BMC bioinformatics
Abbr.
BMC Bioinformatics
ISSN
1471-2105
Published
2005-12-23
Epub
2005-00-23
Pages
308
Language
English
Region
England
NLM ID
100965194
PMCID
PMC1327682
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]