Modelling

Quorum Sensing

Quorum sensing mechanism was used to form biofilm of E.coli strain Top10, BL21 and DH5α that used in labwork. We have modeled growth curve of E.coli to determine when we must move E.coli colony from inoculum flask to reaction flask that contains PET. Besides growth curve, we have modeled some coupled ODEs to model growth curve, AI-2 production that affects signaling, and biofilm formation. AI-2 production in E.coli was used as colony signal of quorum sensing until it reaches specific points and finally form biofilm that affected by its quorum sensing by AI-2 signaling. We use Hill kinetics function as our approach to model AI-2 production and biofilm formation. Based on model that we built and confirmation from wetlab team, we found inoculation time until E.coli reaches quorum sensing condition is 10 hours. Not only time that necessary for quorum sensing condition, we found from model, parameter that affect significantly to biofilm formation was specific growth rate (μ) and initial amount of bacteria that will be inoculated that insightful to wetlab team when construct their parts.

Here ODEs that we used :

Growth curve

AI-2 Production

Biofilm Formation

PETase Transcription

After we have inoculated bacteria until biofilm was formed, process that we focused is PETase production in bacterium body, or usually called transcription. The illustration of transcription of PETase is given below.

We define M(t) and C(t) as functions versus time (in further discussions will be just written as M and C). Before going to differential equations that illustrate rate of mRNA (symbolized as M) and PETase production (symbolized by C), we made several assumptions for the model:

1. No inclusion body is produced during the transcription. Consecutively, there’s also no TetR produced during the transcription.

2. Initally, there are 0.05 μM of mRNA and zero amount of PETase.

There, the differential equations of each parameter obtained through the analysis of mass balance are

We choose α_m = 0.011 μmin^-1, γ_m= 0.009 μ^-1, γ_C= 0.04 μmin^-1. Each of the differential equation is solved analytically using the MATLAB. Through the graph, we can see that at the steady state, the rate of production of PETase is 1,220 mg/(liter∙h) which attained at 600/60 = 10 h. Datum of PETase production will be used as the initial value in PET degradation.

Rate of PET Degradation with Biofilm

Based on PETase production model, we use value of PETase production to be an initial value to degrade PET. The system that we designed illustrated as below.

Based on illustration above, assumptions that we used are :

1. Biofilm is covered E. coli from effect of nutrient solution, but bottom section of E. coli is contacted with PET.

2.

Enzymatic reaction of PETase is assumed to obey two mechanisms reaction, i.e. Langmuir adsorption isotherm that applied in hydrolysis reaction that using Michaelis-Menten kinetics. One of main reason Michaelis Menten kinetics not to be applied in PET degradation mechanism by PETase is PETase hydrolysis involves heterogeneous reaction []. Based on Langmuir adsorption isotherm, we can derive mathematical expression that implemented to Michaelis Menten kinetics. Langmuir adsorption isotherm equation is :

Whereas q is quality of PET enzyme adsorption by unit quality PET, g; qm is the maximum adsorption of PET enzyme by unit quality PET, g; Ka is the adsorption dissociation constant, mL/g; Ef is the concentration of free PET enzyme in the solution, g/mL.

Rate of PET Degradation without Biofilm

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