Team:Tsinghua-A/fluid model

Discription
Fluid model
I Introduction
    The system we designed involves many kinds of relationships between populations and individuals. To help us understand these relationships better, we designed models to describe how the amount of E.coli and substance change with time.
    Concretely, to consider population interactions in a fluid environment, we designed a fluid model based on ODE. The system we considered here has no substance exchange except for some gas, which is, however, not considered in our model.
    What's more, we can use this model to help us design our experiment. (See more details at Improved gene circuit and Regulation of killing ability)
    Furthermore, we found that it will be much easier to consider the effects of some factors (Like the initial number of each populations) on population interactions if we can visualize it. Therefore, we designed our game---Fluid E.coli War based on our fluid model to satisfy our needs. What's more, the game can also help us realize educational purpose of our project and make public know more about synthetic biology! (Exhibition at National Museum)
    Our game is made on the structure of html5. The small video below is Fluid E.coli War.
    See more details on Fluid E.coli War.

II Gene circuit of six characters
Note: Here for simplicity, we hypothesize that this gene circuit is orthogonal.

III ODE, explanation and parameter resource
Note:
1. Subscript 1 indicate warrior I, subscript 2 indicate farmer I, subscript 3 indicate beggar I, subscript 4 indicate warrior I, subscript 5 indicate farmer II, subscript 6 indicate beggar II.
2. Volume of medium (Vsys) here is 0.005L. Volume of E.coli(Vcell) is 1μm3

Detailed ODEs are shown below:
1. Amount of population (cell/medium):
2. Concentration of sucrose inside medium:S(sucrose/medium)1 medium=0.005L
3. Concentration of invertase inside medium:Inv(invertase/medium)
4. Concentration of glucose + fructose inside medium: glu.(glucose/medium) 1 medium=0.005L
5. Carrying capacity:Kn
6. Concentration of 3OC6HSL molecule inside cell:C6n. (C6/cell)
7. Concentration of 3OC12HSL molecule inside cell:C12n. (C12/cell)
8. Concentration of 3OC6HSL molecule inside medium: C6e (C6/L)
9. Concentration of 3OC12HSLinside medium C12e(C12/L)
10. Concentration of lacI inside cell:lacIn.lacI/cell
11.Concentration of CmR inside cell:CmRn. CmR/cell
12.Concentration of LuxI inside warrior I. LuxI (LuxI/cell)
13.Concentration of LasI inside warrior II. LasI (LasI/cell)
14. Concentration of chloramphenicol inside cell: Cm. (Cm/cell)
15.Concentration of chloramphenicol inside medium:Cme (Cm/L)

IV Results
    We extract part of this complete model and adapt it to our experiment results so that we can know how to design our experiment.
Concretely, we use our model to help us do things below:
(1)Design warriors that can be killed only by the warrior from the other group. See more at Improved gene circuit.
(2)Design an easy way to regulate killing ability of warriors. See more at Regulation of killing abilities.
    What is more, we use this model to design a game---Fluid E.coli War to help us consider effects of some factors (Like initial number of each populations) on population interactions and make the public more interested in synthetic biology. (See more at Fluid E.coli War)

V Discussion
Why we detect RFP intensity but not OD600 directly in simplified model used in experiment
    When we look at the model, we will find most part of the model uses hypothesis that is commonly used, like Volterra-Lotka equation or Michaelis-Menten equation, and they can be confirmed experimentally. However,some parts of it are not, like the hypothesis that the decreasing effect of chloramphenicol on population growth rate is proportional to the amount of chloramphenicol inside that character. This is not confirmed by our experiment yet. Therefore, it is still not reasonable now to detect OD600 directly in simplified model used in experiment design. What's more, using RFP intensity to detect LacI and thus killing effect is confirmed by our experiment---Killing Test and so we detect RFP intensity to indicate killing effect.

VI Reference
[1] Wolfenden R, Yuan Y. Rates of spontaneous cleavage of glucose, fructose, sucrose, and trehalose in water, and the catalytic proficiencies of invertase and trehalas[J]. Journal of the American Chemical Society, 2008, 130(24):7548.
[2] Yadira B, Alejandro V, Jesus, P. Promoter and transcription factor dynamics tune protein mean and noise strength in a quorum sensing-based feedback synthetic circuit[DB/OL]. BioRxiv, 2017(2017-2-6)[2017-6-1]. https://www.biorxiv.org/content/early/2017/02/06/106229. DOI:10.1101/106229.
[3] BioNumbers. [2017-6-1]. http://www.bionumbers.hms.harvard.edu/
[4] Chen Y, Kim J K, Hirning A J, et al. SYNTHETIC BIOLOGY. Emergent genetic oscillations in a synthetic microbial consortium[J]. Science, 2015, 349(6251):986-9.
[5] Pai A, You L. Optimal tuning of bacterial sensing potential[J]. Molecular Systems Biology, 2009, 5(1):286-286.
[6] ETH_Zurich 2014: https://2014.igem.org/Team:ETH_Zurich/modeling/whole#Alternate_Design
[7] Murray I A, Shaw W V. O-Acetyltransferases for chloramphenicol and other natural products.[J]. Antimicrobial Agents & Chemotherapy, 1997, 41(1):1.


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