Abstract

Ensemble Modeling (EM) is a recently developed method for metabolic modeling, particularly for utilizing the effect of enzyme tuning data on the production of a specific compound to refine the model. This approach is used here to investigate the production of aromatic products in Escherichia coli. Instead of using dynamic metabolite data to fit a model, the EM approach uses phenotypic data (effects of enzyme overexpression or knockouts on the steady state production rate) to screen possible models. These data are routinely generated during strain design. An ensemble of models is constructed that all reach the same steady state and are based on the same mechanistic framework at the elementary reaction level. The behavior of the models spans the kinetics allowable by thermodynamics. Then by using existing data from the literature for the overexpression of genes coding for transketolase (Tkt), transaldolase (Tal), and phosphoenolpyruvate synthase (Pps) to screen the ensemble, we arrive at a set of models that properly describes the known enzyme overexpression phenotypes. This subset of models becomes more predictive as additional data are used to refine the models. The final ensemble of models demonstrates the characteristic of the cell that Tkt is the first rate controlling step, and correctly predicts that only after Tkt is overexpressed does an increase in Pps increase the production rate of aromatics. This work demonstrates that EM is able to capture the result of enzyme overexpression on aromatic producing bacteria by successfully utilizing routinely generated enzyme tuning data to guide model learning.

Highlights

  • The manipulation of the enzymatic reactions which make up metabolic networks is at the heart of metabolic engineering

  • Rather than attempting to construct a traditional kinetic model that matches dynamic metabolite concentration data and facing the issue of kinetic parameter identification, we focused on utilizing enzyme overexpression phenotype data, which are plentiful and relatively straightforward to acquire, to screen models

  • The Ensemble Modeling (EM) approach is used to construct an ensemble of models for four different flux distributions, which are screened using enzyme overexpression data from the literature

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Summary

Introduction

The manipulation of the enzymatic reactions which make up metabolic networks is at the heart of metabolic engineering. Kinetic parameters are determined in order to best fit the time-dependent metabolite concentration data obtained from experiment, using a wide variety of kinetic rate expressions. These types of data are rare and are not commonly generated in a typical strain improvement process. Enzyme overexpressions or knockouts are commonly used in strain development, and the effects of enzyme expression tuning on product formation or substrate consumption are the typical readouts To our knowledge, such data are difficult to incorporate into modeling, when the results are semi-quantitative, since the fold-changes of enzyme overexpression are rarely measured

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