Team:ETH Zurich/Modeling
From 2013.igem.org
Line 21: | Line 21: | ||
To explain how the concentration of AHL changes over time, we have to consider the influence of two processes: local chemical reactions and diffusion which causes the molecule to spread out over the agar plate. | To explain how the concentration of AHL changes over time, we have to consider the influence of two processes: local chemical reactions and diffusion which causes the molecule to spread out over the agar plate. | ||
- | [[File:Rxn_Diff_AHL.png|500px|right|thumb|''General partial differential equation for AHL reaction-diffusion. D(AHL(x,y,t),x,y) is the diffusive term, R(AHL(x,y,t)) is the reaction term'']] | + | [[File:Rxn_Diff_AHL.png|500px|right|thumb|''Figure 1: General partial differential equation for AHL reaction-diffusion. D(AHL(x,y,t),x,y) is the diffusive term, R(AHL(x,y,t)) is the reaction term'']] |
- | [[File:Diff_AHL.png|500px|right|thumb|''General partial differential equation for AHL reaction-diffusion. D(AHL(x,y,t),x,y) is the diffusive term, R(AHL(x,y,t)) is the reaction term'']] | + | [[File:Diff_AHL.png|500px|right|thumb|''Figure 2: General partial differential equation for AHL reaction-diffusion. D(AHL(x,y,t),x,y) is the diffusive term, R(AHL(x,y,t)) is the reaction term'']] |
The change of the species concentrations in time is given by non-linear ordinary differential equations (ODEs), most of which follow Hill kinetics. The parameters we used in the model are derived from literature. In our model we consider that signalling molecules degrade at the same rate whether they are cytoplasmic or not. | The change of the species concentrations in time is given by non-linear ordinary differential equations (ODEs), most of which follow Hill kinetics. The parameters we used in the model are derived from literature. In our model we consider that signalling molecules degrade at the same rate whether they are cytoplasmic or not. | ||
<br> | <br> | ||
Line 30: | Line 30: | ||
<b>Mine Cells</b> | <b>Mine Cells</b> | ||
- | [[File:eqnSender.png|500px|right|thumb|''Figure | + | [[File:eqnSender.png|500px|right|thumb|''Figure 3: Differential equations of the mine cells'']] |
The Mine Cells lead to the synthesis the signalling molecule, by constitutive expression of ''luxI'' gene. To reveal the nature of the cells, a coloured-substrate reaction is triggered upon addition of ''5-Bromo-4-chloro-3-indoxyl-N-acetyl-beta-D-glucosaminide''; given that the glycoside hydrolase ''NagZ'' is expressed constitutively. <br><br> The ODEs for the states involved in the sender module are given below: | The Mine Cells lead to the synthesis the signalling molecule, by constitutive expression of ''luxI'' gene. To reveal the nature of the cells, a coloured-substrate reaction is triggered upon addition of ''5-Bromo-4-chloro-3-indoxyl-N-acetyl-beta-D-glucosaminide''; given that the glycoside hydrolase ''NagZ'' is expressed constitutively. <br><br> The ODEs for the states involved in the sender module are given below: | ||
<br clear="all"/> | <br clear="all"/> | ||
Line 36: | Line 36: | ||
<b>Biosensors</b> | <b>Biosensors</b> | ||
- | [[File:eqnBiosensor.png|500px|right|thumb|''Figure | + | [[File:eqnBiosensor.png|500px|right|thumb|''Figure 4: Differential equations of the receiver cells'']] |
Our Biosensor cells are engineered to respond differently to high and medium concentrations of AHL. This cells are capable of discriminate between the presence of 1 or 2 mine cells around them in the immediate vicinity. To accomplish this task, the enzymes involved in the coloured-substrate reaction are sensitive to different concentrations of the dimer LuxR-AHL (denoted as R). | Our Biosensor cells are engineered to respond differently to high and medium concentrations of AHL. This cells are capable of discriminate between the presence of 1 or 2 mine cells around them in the immediate vicinity. To accomplish this task, the enzymes involved in the coloured-substrate reaction are sensitive to different concentrations of the dimer LuxR-AHL (denoted as R). | ||
<br clear="all"/> | <br clear="all"/> | ||
<hr> | <hr> |
Revision as of 12:05, 22 August 2013
The digital bacterial-based minesweeper
To explain how the concentration of AHL changes over time, we have to consider the influence of two processes: local chemical reactions and diffusion which causes the molecule to spread out over the agar plate.
The change of the species concentrations in time is given by non-linear ordinary differential equations (ODEs), most of which follow Hill kinetics. The parameters we used in the model are derived from literature. In our model we consider that signalling molecules degrade at the same rate whether they are cytoplasmic or not.
Mine Cells
The Mine Cells lead to the synthesis the signalling molecule, by constitutive expression of luxI gene. To reveal the nature of the cells, a coloured-substrate reaction is triggered upon addition of 5-Bromo-4-chloro-3-indoxyl-N-acetyl-beta-D-glucosaminide; given that the glycoside hydrolase NagZ is expressed constitutively.
The ODEs for the states involved in the sender module are given below:
Biosensors
Our Biosensor cells are engineered to respond differently to high and medium concentrations of AHL. This cells are capable of discriminate between the presence of 1 or 2 mine cells around them in the immediate vicinity. To accomplish this task, the enzymes involved in the coloured-substrate reaction are sensitive to different concentrations of the dimer LuxR-AHL (denoted as R).