Team:Warsaw/results

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lacI/cI bistable switch

Control of cell invasion and further operation of our system - the BacInVader is done by two bistable switches. The first one controls expression of invasion genes.

Design

The structure of this switch is shown below:


The most important components of the switch are repressor proteins cI (denoted here as cIts, see explanation below) and lacI. The whole device is composed of two main parts:

LacI under control of 'cI lam' promoter


and

cI under control of Plac promoter


How it works?

Because cI is repressor of 'cI lam' promoter and lacI is repressor of Plac promoter (denoted here as 'LacI') there are only two mutually exclusive states of the switch:

  • Plac promoter is active which leads to cI expression. CI binds to 'cI lam' promoter and represses it so no genes under this promoter are expressed.
  • 'cI lam' promoter is active which leads to LacI expression. LacI binds to Plac promoter and represses it.

According to this, state of the switch should be stable in time until some external stimulus is applied.

How to switch its state?

To set the state of the switch 0,1mM IPTG and high temperature (42oC) are used.

  • After addition of 0,1mM IPTG LacI gets inactivated and transcription from Plac starts. cI is expressed which leads to repression of 'cI lam' promoter.
  • Heating the bacteria in 42oC inactivates CI protein and starts expression from 'cI lam' promoter.

Experimental results

To test if our assumptions are correct we have assembled switch testing device . In this device we have connected GFP with Plac dependent part of the switch and mRFP with 'cI lam' dependent part. After transformation of the complete construct at 30oC random distribution of green and red colonies was observed. It was expected because we haven't used temperature nor IPTG to set the initial state of the switch.

termosensitive version of lambda cI protein

selection of strains compatible with switch