Team:Grenoble/Biology/AND gate

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<h1>A new characterization of the paraBAD promoter</h1>
<h1>A new characterization of the paraBAD promoter</h1>
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In order to characterize the paraBAD promoter we used a transcriptional fusion of the promoter and gfpmut2 from Alon on pUA66 in BW25113 &delta;cyaA.<br/>
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In order to characterize the paraBAD promoter we used a transcriptional fusion of the promoter and gfpmut2 from Alon on pUA66 in BW25113 &Delta;cyaA.<br/>
We followed the fluorescent expression of the GFP versus different concentrations of arabinose AND cAMP over time. We made this experiment in different growth media:<br/>
We followed the fluorescent expression of the GFP versus different concentrations of arabinose AND cAMP over time. We made this experiment in different growth media:<br/>

Revision as of 00:49, 27 September 2012

iGEM Grenoble 2012

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paraBAD

In order to develop our device we needed a biological AND gate. We found a promoter which can be activated by 2 molecules : CRP-cAMP complex and the AraC protein. The paraBAD promoter has two states; in absence of L-arabinose the paraBAD promoter is repressed by AraC, whereas the the paraC promoter is activated (unless an excess of AraC is present) [Schemes].







In presence of L-arabinose and the CRP-cAMP complex, the promoter is activated thus enabling the transcription of the downstream elements.







This AND gate provides a filter to biological noise. Check out our main results page to for the AND gate characterization.

Cyclic Adenosine Monophosphate

In order to make our AND work we need to produce cyclic Adenosine Monophosphate (cAMP). cAMP is produce by adenyl cyclase (encoded by the cyaA gene). It is an enzyme which catalyses the conversion of ATP to 3’,5’-cAMP. In Escherichia coli, cAMP is involved in carbon catabolite repression [1] and binds to the cAMP receptor protein (CRP). The corresponding complex (CRP-cAMP) is a transcriptional factor controlling the expression of more than 220 operons [2]. It has been known for a long time that E. coli actively exports cAMP into the growth medium [3][4].

Gene transcription

The transcription of the cyaA gene and the crp gene is negatively regulated by CRP-cAMP [5] [6].
The translation of adenylate cyclase mRNA is ineffective as to prevent excessive synthesis of adenylate cyclase. This can be attributed to the fact that overproduction of cAMP is lethal to Escherichia coli possibly due to an accumulation of methylglyoxal [7] [8]. As we want to use paraBAD like an AND Gate and because high a concentration of cAMP is lethal for E. Coli we make our device in a BW25113 ΔcyaA.

A new characterization of the paraBAD promoter

In order to characterize the paraBAD promoter we used a transcriptional fusion of the promoter and gfpmut2 from Alon on pUA66 in BW25113 ΔcyaA.
We followed the fluorescent expression of the GFP versus different concentrations of arabinose AND cAMP over time. We made this experiment in different growth media:
  • M9 complement with 0.03% of glucose and 0.03% of acetate
  • M9 complement with 0.1% of glycerol
  • M9 complement with 0.1% of acetate

(Protocol) Those different media did not affect bacterial growth (Figure1) In a first place, we tested the robustness of the AND gate (Figure 2) As you can see on this figure even after few hours there is no fluorescent expression if one activator is absent.

Now for our system we studied the half-expression of GFP versus the cAMP concentration at 1.6% of arabinose. (Figure 3) As you can see in the two first media we have the half expression of GFP at 0.4mM of cAMP whereas in the third medium its concentration is: 0.8mM. We want a sensitive detector, therefore the third medium conditions are not optimum.
One of ours imperative is: a fast response. Consequently, we need to know the time it takes to reach the half expression (Figure 4). In this figure we can see that GFP expression is faster in the medium with glycerol.

References

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