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Team:INSA Toulouse/contenu/lab practice/results/general inducer
From 2013.igem.org
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<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). | + | <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> |
<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 ( | + | 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. |
<br><br> | <br><br> | ||
| - | 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 | + | 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).<br> |
<br><img src="https://static.igem.org/mediawiki/2013/e/e1/Induct_gen_pfaible.png" /></p> | <br><img src="https://static.igem.org/mediawiki/2013/e/e1/Induct_gen_pfaible.png" /></p> | ||
<h2 class="title2">Discussion</h2> | <h2 class="title2">Discussion</h2> | ||
| - | <p class="texte">Assembly of a stronger promoter could improve the system and lock the response to an ON/OFF response.</p> | + | <p class="texte">The construction with the weak promoter is available here: <a href="http://parts.igem.org/Part:BBa_K1132022" "target="_blank">BBa_K1132022</a>. Assembly of a stronger promoter could improve the system and lock the response to an ON/OFF response. An intermediate construction was assembled without any promoter and is ready to be cloned to a strong promoter: <a href="http://parts.igem.org/Part:BBa_K1132021" "target="_blank">BBa_K1132021</a>.</p> |
</div> | </div> | ||
Revision as of 00:13, 5 October 2013
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).
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
The construction with the weak promoter is available here: BBa_K1132022. Assembly of a stronger promoter could improve the system and lock the response to an ON/OFF response. An intermediate construction was assembled without any promoter and is ready to be cloned to a strong promoter: BBa_K1132021.
