Overview

In our inital model, we chose a 5 cm long cylindrical channel with a radius of 1 mm (or equivalently 2 mm diameter). This channel is connected to a reservoir filled with medium and the toxic molecule. For the purpose of modeling the diffusion and degradation of the toxic molecule in the channel, we assumed that the reservoir has constant toxic molecule concentration (or equivalently has infinite size).

In our system, we degrade a toxic substance diffusing from a reservoir into a block of e. Coli cells immobilized in agarose in order to generate a toxic substance gradient. The two substances we consider in our model are acetaldehyde and xylene. In our first microfluidics model we conducted a feasibility study and thus only investigated acetaldehyde degradation.

Diffusion

First of all, we have to model diffusion of Acetaldehyde from the reservoir to the closed end of the microfluidics channel. The relevant partial differential equation is the one for isotropic diffusion, i.e. diffusion that is uniform in all directions:

For the relevant diffusion parameter, D_AcAl, see the microfludics model section on the parameters page.

Degradation

Cell Density

In order to able to determine how much Acetaldehyde our smoColi cells are able to degrade, we first need to determine the cell density of the immobilized cells in agarose. For this calculation, we assume we have a cell culture with OD₆₀₀ with which we fill the channel. Parameter-wise, to determine the relative cell density in the channel voume, we need to know:

• the mean cell density in [cells/volume] at OD₆₀₀=1, cd_{OD600, undiluted}, and
• the mean cell volume of a single cell, V_eColi.

A parameter we can choose suitably is the dilution of the cells in agarose, c_Dilution. Then we can calculate the relative cell density in the smoColi-agarose-filled microfluidics channel:

Enzymatic Degradation

Now that we know what the cell concentration in the channel is, we can model the degradation of the toxic molecule by the cell culture in agarose. This process, together with diffusion of more toxic molecules from the reservoir, will finally generate the toxic molecule gradient.

In our enzymatic degradation model, we assume diffusion into the cells is fast compared to the degradation process. The degradation process then is modeled using Michaelis-Menten enzyme reaction kinetics:

The constants are the usual ones for Michaelis-Menten-type reactions:

• v_max,AcAl is the maximum reaction rate, i.e. the rate the toxic molecule degradation reaction occurs with at saturation point, and
• K_M,AcAl is the Michaelis Menten constant, i.e. the Acetaldehyde concentration at which the reaction rate is half of v_max,AcAl

Estimation of v_max,AcAl

For the degradation of acetaldehyde we only had direct literature values for K_M,AcAl, but not for v_max,AcAl. However, we did find values for the specific activity K_cat,AcAl of acetaldehyde dehydrogenase in e. Coli, which we used to estimate v_max,AcAl with the following equation:

Here, [E]^T is the total enzyme concentration of acetaldehyde dehydrogenase. This value we derived from the concentration of acetaldehyde dehydrogenase in cell extract, which we in turn calculated by estimating the number of acetaldehyde dehydrogenase enyzmes n_ADH in a single e. Coli cell.

The number of acetaldehyde dehydrogenase enzymes n_ADH in a single e. Coli cell was estimated from diluted cell-free extract with dilution ratio dil_Extract and diluted concentration of [ADH]_Extract.

Model

Now that we have values for all of the parameters, we can finally combine both the partial differential equation for diffusion and the local ordinary differential equation for reaction into the spatiotemporal reaction-diffusion (or in our case, degradation-diffusion) system:

Simulation

To see if we can indeed create an acetaldehyde gradient, we first solved for the gradient steady state in the channel. We chose an acetaldehyde concentration of 100 mg/l for the reservior in these simulations.

Steady State

First, we simulated the steady state of the acetaldehyde gradient in channels with different diameters. Our

Simulation for 100 mg/l of acetaldehyde, standard channel width

Simulation for 100 mg/l of acetaldehyde, 0.1x standard channel diameter (200μm)

Simulation for 100 mg/l of acetaldehyde, 3x standard channel diameter (6mm)

We can see that the diameter does not influence the mean dynamics of the acetaldehyde gradient (observant readers will notice that the concentration at the end of the channel is not exactly the same - this effect is a result of numerical imprecision). We note that there may be stochastic behavior for very thin channels, since there will be only very few cells. For the channel diameter we chose, a mean field approximation should be sufficient though, as the amount of cells involved in the degradation is sufficiently high.

Dynamics

We were also interested in finding out the time scale which is needed to create the gradient. Therefore we also analyzed the dynamics in a spatiotemporal reaction (degradation) - diffusion simulation.