Metabolic model

Overview

This model ams to simulate the entire pathway of the enterobactin production in our Iron-coli. It includes the synthetic sensing system, and the chemical reactions leading to the enterobactin.
This model has two goals:

• Have an idea of how long it would take to produce siderophores, from the very begining: the iron sensing
• Determine the ideal plasmid configuration

Assumptions

• The only limiting reagant in the pathway is the chorismic acid, which we consider being in excess
• The FUR is also considered in exccess
• All the enzymes (and the mRNA involved) needed are assimilted to a single variable, since they all play equivalent roles

Model Description

Variables:

• [Fe] : Iron concentration inside the bacteria
• [Fur] : FUR concentration inside the bacteria
• [FeFur] : Iron-FUR complex concentration inside the bacteria
• LacI : Number of inhibited LacI
• LacO : Number of non-inhibited LacO
• [mRNA]: mRNA (from LacO) concentration
• [Enz] : Enzyme concentration : EntA,-B,-C,-D,-E,-F

Fe, FUR and FeFUR:
The iron-FUR complex is simply formed that way:
 
We reduced this equation to:

Which is not annoying, since we just have to divide our [FeFur] by to to get the real complex concentration.
We can easily write down both the formation (v) and the dissociation (v') speed:

We chose to model the iron input in the bacteria using a linear function of the external iron concentration Ferext, the factor p being the cell-wall permeability for iron.
The FUR on the other hand, is produced by the bacteria. It's evolution can also be considered linerar, using a mean production rate Fur0.


In this model, we only track the free Fe-FUR and not those which are attached to a FUR Binding Site. As LacI is the number of inhibited LacI, we can use this number to express how much Fe-FUR does bind to a FBS per unit of time.

LacI-LacO system:
To simulate the inhibition phenomenon, we chose to use our logistic function under its differential form. Since it is the FeFUR that represses it, thhe LacI can be expressed as a logistic fuction of the FeFUR:

Ki1 is a non-dimensional parameter that repesents the inhibition power, and Kf is the fixation rate of the FeFUR on the FBS. Finally, Nbrpla1 is the number of pasmids containing the LacI.
In the same way, LacO is modeled with a logistic funtion. LacO is repressed by LacI:

Ki2 is the inhibition power and Nbrpla2 is the number of plasmimds containing LacO.
LacI and LacO are both ruled by a normal logistic function. If we were to track the number of expressed LacI/LacO, we would be using two inverted logistic fuctions to model a double inverter. The thing is, since LacI represents the number of repressed genes and LacO the number of expressed genes, the double inverter is still there, but the calculations are easier.

mRNA and Enzymes:
The [mRNA] and [Enz] equations are alike. The prodction rates are Kr for the mRNA and Kp for the enzymmes, and both variables have a negative degadation term:

Finally:

Parameters

Note that we don't have any informations about the KI1 and KI2 parameters, since they are purely artificial. We thus had to run simulations to study the effects of different sets of values on the model.

Results

High copy?
Here are 9 gaphs pointing out the relevance of different plasmid configurations. The goal of this simulation is to try answerig a biological question: "should we copy the plLacO plasmids or the LacI plasmids?"
The horizontal axes are the time (minutes) and the iron concentration (logarithmic scale). The vertical axis is the Enzyme production (mmol/L).

About the KI1/KI2:
Here are 9 other graphs with a set of different values for KI1 and KI2.

Temporal answers
This curve itegrates the chemical pathway developped here.