"
Team:INSA Toulouse/contenu/lab practice/results/polT7
From 2013.igem.org
Mesnageclem (Talk | contribs) |
|||
| Line 151: | Line 151: | ||
<div class="maincontent" style="width: 720px; margin: 25px 0 25px 0; float: right;"> | <div class="maincontent" style="width: 720px; margin: 25px 0 25px 0; float: right;"> | ||
| - | <h1 class="title1">Results - T7 Polymerase | + | <h1 class="title1">Results - T7 Polymerase characterization</h1> |
<h2 class="title2">Objective</h2> | <h2 class="title2">Objective</h2> | ||
| Line 159: | Line 159: | ||
<p class="texte">The following constructions were designed:<br><br> | <p class="texte">The following constructions were designed:<br><br> | ||
<img src="https://static.igem.org/mediawiki/2013/0/07/Result_polT7_1.jpg" class="imgcenter" /><br><br> | <img src="https://static.igem.org/mediawiki/2013/0/07/Result_polT7_1.jpg" class="imgcenter" /><br><br> | ||
| - | + | The coding sequence of T7 polymerase was extracted from the genome of <i>E. coli</i> BL21-DE3. Further cloning steps were necessary to add a promoter, a rbs and a terminator. The expected functioning is: | |
| - | - Production | + | - Production of RFP if T7 polymerase is present (red colonies) |
- Absence of RFP if T7 polymerase is absent (white colonies)</p> | - Absence of RFP if T7 polymerase is absent (white colonies)</p> | ||
<h2 class="title2">Result</h2> | <h2 class="title2">Result</h2> | ||
| - | <p class="texte"> | + | <p class="texte">The addition of a promoter and a rbs to the T7 polymerase gene was successful. However, we did not have time to go further and add the terminator to the construct. Nevertheless, a new biobrick pT7-RFP was created! |
| - | Nevertheless, a new biobrick pT7-RFP was created! | + | |
| - | Following is the electrophoresis gel showing that we obtained a fragment of expected length (829 bp) by restriction EcoRI/PstI:<br><br> | + | Following is the electrophoresis gel showing that we obtained a fragment of expected length (829 bp) by restriction with EcoRI/PstI:<br><br> |
<img src="https://static.igem.org/mediawiki/2013/f/f9/Result_polT7_2.jpg" class="imgcenter" /><br><br> | <img src="https://static.igem.org/mediawiki/2013/f/f9/Result_polT7_2.jpg" class="imgcenter" /><br><br> | ||
| - | + | Verifications of the validity of the constructions were performed with visual inspection of the colours of the colonies. The pT7-RFP plasmid was transformed into competent BL21-DE3. Plates were supplemented or not with IPTG. White colonies were obtained on the Petri dishes with no IPTG and red colonies on the Petri dishes containing IPTG. <br><br> | |
| - | White colonies | + | |
<img src="https://static.igem.org/mediawiki/2013/4/43/Result_polT7_3.jpg" class="imgcenter" /><br> | <img src="https://static.igem.org/mediawiki/2013/4/43/Result_polT7_3.jpg" class="imgcenter" /><br> | ||
<img src="https://static.igem.org/mediawiki/2013/3/3e/Result_polT7_4.jpg" class="imgcenter" /></p> | <img src="https://static.igem.org/mediawiki/2013/3/3e/Result_polT7_4.jpg" class="imgcenter" /></p> | ||
| - | <h2 class="title2"> | + | <h2 class="title2">Discussion</h2> |
| - | <p class="texte">The biobrick behave as expected. It was submitted to the registry | + | <p class="texte">The biobrick behave as expected. It was submitted to the registry as <a href=" http://parts.igem.org/Part:BBa_K1132045" target="_blank"> BBa_K1132045</a>.</p> |
Revision as of 07:28, 4 October 2013
Results - T7 Polymerase characterization
Objective
Characterize the activity of T7 polymerase with an RFP reporter under a T7 promoter. Reminder: T7 polymerase is necessary in our system to activate the two T7 promoters in the AND1 and AND2 gate.
Conception
The following constructions were designed:
The coding sequence of T7 polymerase was extracted from the genome of E. coli BL21-DE3. Further cloning steps were necessary to add a promoter, a rbs and a terminator. The expected functioning is:
- Production of RFP if T7 polymerase is present (red colonies)
- Absence of RFP if T7 polymerase is absent (white colonies)
Result
The addition of a promoter and a rbs to the T7 polymerase gene was successful. However, we did not have time to go further and add the terminator to the construct. Nevertheless, a new biobrick pT7-RFP was created!
Following is the electrophoresis gel showing that we obtained a fragment of expected length (829 bp) by restriction with EcoRI/PstI:
Verifications of the validity of the constructions were performed with visual inspection of the colours of the colonies. The pT7-RFP plasmid was transformed into competent BL21-DE3. Plates were supplemented or not with IPTG. White colonies were obtained on the Petri dishes with no IPTG and red colonies on the Petri dishes containing IPTG.
Discussion
The biobrick behave as expected. It was submitted to the registry as BBa_K1132045.
