Critical assessment of E. coli genome-scale metabolic model with high-throughput mutant fitness data
Bernstein, D. B.; Akkas, B.; Price, M. N.; Arkin, A. P.
Show abstract
The E. coli genome-scale metabolic model (GEM) is a gold standard for the simulation of cellular metabolism. Experimental validation of model predictions is essential to pinpoint model uncertainty and ensure continued development of accurate models. Here we assessed the accuracy of the E. coli GEM using published mutant fitness data for the growth of gene knockout mutants across thousands of genes and 25 different carbon sources. We explored the progress of the E. coli GEM versions over time and further investigated errors in the latest version of the model (iML1515). We observed that model size is increasing while prediction accuracy is decreasing. We identified several adjustments that improve model accuracy - the addition of vitamins/cofactors and re-assignment of reaction reversibility and isoenzyme gene to reaction mapping. Furthermore, we applied a machine learning approach which identified hydrogen ion exchange and central metabolism branch points as important determinants of model accuracy. Continued integration of experimental data to validate GEMs will improve predictive modeling of the mapping from genotype to metabolic phenotype in E. coli and beyond. Synopsis O_FIG_DISPLAY_L [Figure 1] M_FIG_DISPLAY C_FIG_DISPLAY E. coli genome-scale metabolic model flux balance analysis (FBA) prediction accuracy was quantified with published experimental data assaying gene knockout mutant growth across different carbon sources. Insights into model development trends and sources of inaccuracy were revealed. O_LIModel representational power (size) has been increasing over time, while accuracy has been decreasing. C_LIO_LIAdding vitamins/cofactors to the model environment and re-assigning reaction reversibility and isoenzyme gene-to-reaction mapping improves correspondence between model predictions and experimental data. C_LIO_LIMachine learning reveals hydrogen ion exchange and central metabolism branch points as important features in the determination of model accuracy. C_LI
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Quantifying cumulative phenotypic and genomic evidence for procedural generation of metabolic network reconstructions 96%
- Computation of condition-dependent proteome allocation reveals variability in the macro and micro nutrient requirements for growth 94%
- Flux-based hierarchical organization of Escherichia coli’s metabolic network 94%
Similar papers in this journal
- A computational toolbox to investigate the metabolic potential and resource allocation in fission yeast 96%
- Reconstruction and analysis of thermodynamically-constrained models reveal metabolic responses of a deep-sea bacterium to temperature perturbations 94%
- AMiGA: software for automated Analysis of Microbial Growth Assays 93%
Similar papers in this journal
Similar papers in this journal
Similar papers in this journal
- High-throughput protein characterization by complementation using DNA barcoded fragment libraries 93%
- Regulatory kinase genetic interaction profiles differ between environmental conditions and cellular states 93%
- Analysis of proteome adaptation reveals a key role of the bacterial envelope in starvation survival 93%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.