1.Introduction

   To understand, predict and ultimately control the behavior of our engineered microbial group effect, we have developed dynamic model of the system, based on transerential equations which describe and integrate the individual processes. This model involves several entities going from the molecular level (genes, RNAs, proteins, and metabolites) up to the cellular and population levels, distinct intracellular and extracellular compartments, and a wide range of biological and physical processes (transcription, translation, signalling, growth, transusion, etc). Here we can show the concentrate of DspB and Enterobactin produced by our engineered bacteria and the biofilm and rust removing time through calculating.

2.Observations

  Naturally, when there is a certain amount of HSL in the environment, HSL complex with afeR proteins and bind to afeR promoter which regulate positively the genes downstream (as shown on the Figure 1) and on that our sensing system relies to produce DspB and enterobactin.

3.Goals

  Our goal of this model is to create a generic quorum sensing model so that:

  • We can determine the effect of afeR promoter and predict the production of DspB and enterobactin.

   We can predict hao long our engineered bacteria would take to remove the biofilm and rust.

4.Materials and Methods

4.1 HSL Transfer

  HSL is produced by iron bacterias and realeased into the water environment. So the first step of our sensing is HSL transfering into our engineered E.coli from the water. And a passive transusion model is used for this process that the transfer rate of HSL can be described as this:

  • K_HSL,W-C : transfer coefficient through the membrane (s−1)

   We can predict hao long our engineered bacteria would take to remove the biofilm and rust.