Team:St Andrews/project/modelling/model 4

From 2010.igem.org

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=Theory & assumptions=
=Theory & assumptions=
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Although our previous work presented many insights into the LuxR quorum sensing system, a new model of further complexity was deemed necessary to investigate some of the subtleties of bistable behaviour.  This was accomplished by changing focus from the interactions in one cell, to the population of bacteria as a whole.  In doing this, not only were we able to reproduce the results from previous models on a population-wide scale, but our results would be empirically verifiable in the lab.
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The primary development from previous models - the change of focus from one cell to the whole culture - was implemented by making many small adjustments to the previous differential equations we used.  In addition to the biochemical reactions changing chemical concentrations, we also had a volumetric term describing the increase of volume (and subsequent decrease in concentration) as new cells were added to the colony.  This can be understood by taking the derivative of the HSL concentration:
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<math>[HSL] = (Number of molecules/Volume)</math>
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<math>d[HSL]/dt = dN/dt * (1 / V) - 1 / (V ^ 2) * N </math>
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Similar to model 3, the cell density was initially increased by a cell growth function, where the number of bacteria doubled every 20 minutes.  Having ran to a realistic maximum cell density, there was a stationary phase in the cell growth to allow steady state concentrations of chemicals to be realised.  The cell death function was then called, and the cell density was ran back to it's starting value.
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=Results=
The code on which this model is based can be found [[Team:St_Andrews/project/modelling/downloads|here]].
The code on which this model is based can be found [[Team:St_Andrews/project/modelling/downloads|here]].

Revision as of 17:04, 23 October 2010


St Andrews from East Sands

University of St Andrews iGEM 2010

Welcome!

The Saints

University of St Andrews iGEM 2010

Our first year at iGEM!

Model 4: Pseudo Multi Cell Two Dimensions

Theory & assumptions

Although our previous work presented many insights into the LuxR quorum sensing system, a new model of further complexity was deemed necessary to investigate some of the subtleties of bistable behaviour. This was accomplished by changing focus from the interactions in one cell, to the population of bacteria as a whole. In doing this, not only were we able to reproduce the results from previous models on a population-wide scale, but our results would be empirically verifiable in the lab.

The primary development from previous models - the change of focus from one cell to the whole culture - was implemented by making many small adjustments to the previous differential equations we used. In addition to the biochemical reactions changing chemical concentrations, we also had a volumetric term describing the increase of volume (and subsequent decrease in concentration) as new cells were added to the colony. This can be understood by taking the derivative of the HSL concentration:

<math>[HSL] = (Number of molecules/Volume)</math>

<math>d[HSL]/dt = dN/dt * (1 / V) - 1 / (V ^ 2) * N </math>

Similar to model 3, the cell density was initially increased by a cell growth function, where the number of bacteria doubled every 20 minutes. Having ran to a realistic maximum cell density, there was a stationary phase in the cell growth to allow steady state concentrations of chemicals to be realised. The cell death function was then called, and the cell density was ran back to it's starting value.

Results

The code on which this model is based can be found here.