Team:INSA Toulouse/contenu/lab practice/results/general inducer

From 2013.igem.org

(Difference between revisions)
Line 160: Line 160:
   <h2 class="title2">Result</h2>
   <h2 class="title2">Result</h2>
-
<p class="texte">We didn't managed to get the contruction under a strong promoter but we suceeded to obtain the previous assembly with a weak promoter (BBa_J23116) : <br>
+
<p class="texte">We didn't managed to get the contruction under a strong promoter but we suceeded to obtain the previous assembly with a weak promoter (BBa_J23116). The part is available here: <a href="http://parts.igem.org/Part:BBa_K1132022" "target="_blank">BBa_K1132022</a>.  <br>
   <br><img src="https://static.igem.org/mediawiki/2013/d/d4/General_inducer_notebook_-_680px.png" /><br><br>
   <br><img src="https://static.igem.org/mediawiki/2013/d/d4/General_inducer_notebook_-_680px.png" /><br><br>
After 18 hours, clones containing this assembly (BBa_J23116-TetR-pTet-RFP) show a leaky basal expression of mRFP. We suppose that the promoter was too weak to express TetR in large quantity.
After 18 hours, clones containing this assembly (BBa_J23116-TetR-pTet-RFP) show a leaky basal expression of mRFP. We suppose that the promoter was too weak to express TetR in large quantity.

Revision as of 23:58, 4 October 2013

logo


Results - General Inducer Characterization

Objective

Characterize the general inducer system using the couple TetR-pTet without and with aTc. Reminder: TetR is an inducer that binds to pTet promoter and thus, represses expression the downstream system. Supply of tetracycline or its analog aTc (anhydrotetracycline) is known to bind to tetR and invert the operation (inhibits expression of mRFP in this case).

Conception

A constitutive promoter is bind to tetR and then is assembled to pTet-rbs-RFP-term (Bba_I13521).

Result

We didn't managed to get the contruction under a strong promoter but we suceeded to obtain the previous assembly with a weak promoter (BBa_J23116). The part is available here: BBa_K1132022.



After 18 hours, clones containing this assembly (BBa_J23116-TetR-pTet-RFP) show a leaky basal expression of mRFP. We suppose that the promoter was too weak to express TetR in large quantity.

Besides, an experience was done to analyze the effect of the aTc inducer. Result show a visible induction of the red fluorescent protein expression by addition of aTC (60 ng/mL).

Discussion

Assembly of a stronger promoter could improve the system and lock the response to an ON/OFF response.