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Flux model

Introduction

In this part of our modeling work we focus on genome scale analysis of the enterobactin production pathway. A major concern about our system is its non-orthogonality with the natural metabolic network of the cells : E. coli already possesses the genes for producing enterobactins. Therefore we wanted to assess the possible interactions between our system and the bacterial metabolism.

Observations

This model stems from the following observations :

• Enterobactin production pathway is a metabolic process;
• Any of the involved metabolites may limit the rate of the reactions.

The Figure 1 presents the biochemical pathway for producing the enterobactin compound in E. coli.

As can be seen in the Figure 1 the pathway is 4 steps long and composed of six different enzymes. Hence there exists 4 possible metabolites which concentration may be limiting :

• Chorismate
• Isochorismate
• 2,3-dihydroxy-2,3-dihydrobenzoate
• 2,3-dihydroxybenzoat

Goals

We highlighted two main kind of interactions between the bacteria and our system :

1. The synthetic system interacts with the bacterial metabolism. Leading to a depletion of the metabolites involved in the pathway for the other (possibly essential) metabolic reactions of the cell.
2. The other way round, the metabolic reactions could prevent our synthetic system to work as expected by limiting the quantity of the involved metabolites available.

From these assumptions we formulated the following questions :

• Is the metabolic model of E. coli able to provide any information about the possible interactions between our system and the metabolism?
• Is the concentration of any metabolite limiting ?
• In the latter case, what is the quantity of precursor that should be added in the medium?

Materials and Methods

Model

We used the metabolic model E. coli iJR904 downloaded from the BiGG model database[1]. We chose this model because it contains all the metabolites involved in the enterobactin production pathway.

This model contains 4037 reactions and 625 metabolites but lacks the enterobactin synthase (the last reaction of the enterobactin production pathway). We thus extended the model by adding three new reactions :

Name	Formula
ENTSYNTH	6 ATP + 3 2,3-DIHYDROXYBENZOATE + 3 L-SERINE => ENTEROBACTIN + 6 AMP + 6 DIPHOSPHATE
ENTOUT	=> -1 ENTEROBACTIN
CHORIN	=> +1 CHORISMATE

The last two reactions are respectively output flux of ENTOUT and intput flux of CHORIN that are artificial reactions used to measure and interact with our system. The modified E. coli iJR904 model containing these two new reactions can be found in the download section at the bottom of the page.

Network Reduction

As an analysis of the whole network is too complex, we focused our analysis on the subnetwork presented in Figure 2. We considered the CHORISMIC ACID (hereafter called CHORISMATE) as the first step of the anterobactin production pathway. This is justified by the fact that chorismate can be bought from any compound supplier (for example sigma).

We also found that it would also be possible to by the 2-3-DIHYDROXYBENZOATE compound from the same provider. This compound may be very interesting to test our constructions later as the last precursor of the pathway. For the same reason, and because it does participate in any other reaction in the used model, this compound has no interest in our metabolic modeling.

Figure 2:

The considered subnetwork of metabolic reactions of E. coli. Red arrows are reaction consuming compounds used in the ENTEROBACTIN production pathway. Arrows : reactions, circles : enzymes.

Flux Balance Analysis

The metabolic model of E. Coli is represented as a stoichiometry matrix S representing the metabolic network. Our modified version has the size 4039 (reactions) * 625 (compounds). The unknown is the flux distribution vector v, a 4039-vector representing the flow of matter (mmol/gDW/h) going through each reactions.

The Flux Balance Analysis method[2] is about finding this flux repartition vector v given an objective function to optimize (usually the growth rate) and a set of constraints of fluxes.

Assumptions of the model

The Two assumptions at the heart of the method are the following :

1. steady state: The fluxes are considered to have attained a static equilibrium value and do not change through time.
2. No enzyme saturation: The enzymes are supposed to be not saturated, the number of enzymes is always greater than the number of the corresponding reactions happening.

Formalism

The FBA method use a representation of the metabolic reaction network in the form of a stoichiometry matrix S where :

• Each row corresponds to a reaction R_i
• Each column corresponds to a metabolite C_j

The definition of S is :

The FBA problem is then formulated as a maximisation problem under some constraints :

where :

• v is the vector of unknown reaction fluxes
• c is a vector of constants defining the objective function
• S is the stoichiometry matrix
• lowerbound and upperbound are vector of constraints (minimal and maximal flux values for each reactions)

The values for the lower and upper bounds on the flux of each reactions are either deduced from experiments or put to a very high value when unknown (most of the time) :

Tunning these boundaries allows to represent different experimental conditions, for example reducing an upper bound to a low value may represent a loss of reaction flux due to the scarcity of a certain compound.

Such optimization is then realized through a linear programming algorithm finding an approximated solution of the real optimal flux distribution (the distribution maximizing the objective function).

Software used

To perform the simulations we decided to use the cobrapy software[3] in conjunction with the GLPK (GNU Linear Progamming Kit) linear programming solver.

All the simulations of model modifications were made through python scripts, available at the end of the document.

Results

The results are presented on the two following pages:

1. Metabolic Interactions on this page.
2. The effects of supplying chorismate on this page.

Conclusion

The metabolic models presented in this sections have been used to answer the general questions we had about our system.

First, we wanted to know if adding new synthetic constructs would perturb the metabolism of E. coli. This was answered by a first model plotting a modified objective function optimizing both ENTEROBACTIN production and growth rate. The model showed that the enterobactin pathway perturbs the CHORISMATE MUTASE and DEOXYCHORISMATE SYNTHASE reactions.

In two other models, we showed that the CHORISMATE MUTASE AND DEOXYCHORISMATE SYNTHASE were very crucial for the bacteria, as a reduction of their maximal upper flux lead to a direct (linear) decrease of the growth rate function. Resulting in the extreme case with a nul growth rate for a nul flux.

Finally, we analysed how we could find a workaround to this problem by adding some CHORISMATE to the medium. This situation was represented in a third model with a CHORISMATE input flux that we plotted against the modified objective function. This model clearly showed that the ENTEROBACTIN flux attained a maximal stable region for any value of the objective function starting from 17 mmol/gDW/h of CHORISMATE. Finally, the dynamic of the model is very smoother as more CHORISMATE is added, showing that this addition could paliate the effects of the addition of the ENTEROBACTIN pathway.

In the end, this FBA model shows that it is possible to paliate the effect of our construction on the metabolism of E. coli by adding some CHORISMATE to the medium. This justifies the other models developed that did the assumption that no metabolite was limiting.

Models and Scripts

Metabolic Models

The two metabolic models used are :

1. Wild-Type E. coli iJR904
2. ENTOUT(enterobactin outflux) + ENTSYNTH(enterobactin synthase) E. coli iJR904

These models can be found in this tarball.

Scripts

The scripts used to generates the curves on this page can be found on this archive. They are Python scripts with distinct names corresponding to the simulation they represent.

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