"
Team:Trieste/notebook6
From 2012.igem.org
(Difference between revisions)
(Created page with "{{Team:Trieste/head}} <html> <div id="body"> <div id="container"> <!-- start container --> </html>{{Team:Trieste/menu}}<html> <div id="content"> <!-- start conten...") |
Corsogiulia (Talk | contribs) |
||
| (12 intermediate revisions not shown) | |||
| Line 5: | Line 5: | ||
</html>{{Team:Trieste/menu}}<html> | </html>{{Team:Trieste/menu}}<html> | ||
<div id="content"> <!-- start content --> | <div id="content"> <!-- start content --> | ||
| - | <h1 id="h1_lf" class="main_tit"><div> | + | <h1 id="h1_lf" class="main_tit"><div>Week 6</div></h1> |
<h1 id="h1_rt" class="main_tit"><div>More</div></h1> | <h1 id="h1_rt" class="main_tit"><div>More</div></h1> | ||
<div id="box_main"> <!-- start box_main --> | <div id="box_main"> <!-- start box_main --> | ||
| Line 11: | Line 11: | ||
<div id="suicide" class="notebook_section"> | <div id="suicide" class="notebook_section"> | ||
<h2 class="notebook_title">Suicide System</h2> | <h2 class="notebook_title">Suicide System</h2> | ||
| - | + | Holin is defined as a Bglbrick part, that means it doesn't have the standard restriction sites. We transformed the standard Biobrick we needed to use, in Bglbrick by PCR.</br> | |
| + | </br> | ||
| + | The promoter T5CumateOperator(BBa_K875001) was cut EcoRI/SpeI, the fragment was eluted from the gel and then cloned upstream the RBS_B0034, into the pSB1A2 linearized backbone.</br> | ||
| + | |||
| + | We screened the colonies by PCR with the standard VF2 and VR primers and the positive ones were inoculated; we amplified the miniprep by PCR with particular primers with the EcoRI, BglII, BamHI and XhoI restriction sites. | ||
</div> | </div> | ||
<div id="antibody" class="notebook_section"> | <div id="antibody" class="notebook_section"> | ||
<h2 class="notebook_title">Antibody</h2> | <h2 class="notebook_title">Antibody</h2> | ||
| - | + | The sequences arrived, and both scFv versions (pelB-scFv and LPP-scFv) are correct, so we continued with our work. Afer different attempts, we finally ligated both scFv versions under T5LacO. We amplified the resulting plasmid in DH5L and introduced it into W3110 (with p-REP 4) which we will use for future analysis. | |
</div> | </div> | ||
<div id="chassis" class="notebook_section"> | <div id="chassis" class="notebook_section"> | ||
| - | <h2 class="notebook_title"> | + | <h2 class="notebook_title">Cumate-Switch Regulation</h2> |
| - | + | <u><b>CymR</b></u> | |
| + | <br/> | ||
| + | We ligate the CymR-B0015 X/P in the plasmid J61002 (treated with SAP) downstream the J23100. We proceed in many directions because the cloning of CymR-B0015 downstream J23100 was very difficult: we repeated the ligation with the same plasmid but with different treatment : | ||
| + | <br/> | ||
| + | -elution and SAP | ||
| + | <br/> | ||
| + | -elution without SAP | ||
| + | <br/> | ||
| + | -ligation without gel purification. | ||
| + | <br/> | ||
| + | We obtained some positive clones that we digest E/P for analysis. So we digested and ligated the right clones together. We obtain the double copy J23100-CymR-B0015. | ||
| + | <br/> | ||
| + | <br/> | ||
| + | <u><b>T5 PROMOTER - CUMATE OPERATOR</b></u> | ||
| + | <br/> | ||
| + | We started again from the T5 promoter-E0240. We cloned T5 promoter-E0240 downstream j23100. We obtained positive clones but they didn't work. | ||
</div> | </div> | ||
</div> | </div> | ||
| Line 30: | Line 49: | ||
<li><a href="https://2012.igem.org/Team:Trieste/notebook4">Week 4</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook4">Week 4</a></li> | ||
<li><a href="https://2012.igem.org/Team:Trieste/notebook5">Week 5</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook5">Week 5</a></li> | ||
| - | <li><a href="https://2012.igem.org/Team:Trieste/notebook6">Week 6</a></li> | + | <li class="select" ><a href="https://2012.igem.org/Team:Trieste/notebook6">Week 6</a></li> |
<li><a href="https://2012.igem.org/Team:Trieste/notebook7">Week 7</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook7">Week 7</a></li> | ||
<li><a href="https://2012.igem.org/Team:Trieste/notebook8">Week 8</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook8">Week 8</a></li> | ||
| Line 37: | Line 56: | ||
<li><a href="https://2012.igem.org/Team:Trieste/notebook11">Week 11</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook11">Week 11</a></li> | ||
<li><a href="https://2012.igem.org/Team:Trieste/notebook12">Week 12</a></li> | <li><a href="https://2012.igem.org/Team:Trieste/notebook12">Week 12</a></li> | ||
| + | <li><a href="https://2012.igem.org/Team:Trieste/notebooklast">Post European-Jamboree</a></li> | ||
</ul> | </ul> | ||
<img src="https://static.igem.org/mediawiki/2012/b/b0/Team_trieste.jpg" alt="Team iGEM 2012" id="igem_team" /> | <img src="https://static.igem.org/mediawiki/2012/b/b0/Team_trieste.jpg" alt="Team iGEM 2012" id="igem_team" /> | ||
| Line 46: | Line 66: | ||
Follow us also: | Follow us also: | ||
<a href="https://www.facebook.com/IGEMUNITS?ref=ts" target="_blank"><img src="https://static.igem.org/mediawiki/2012/f/f4/Ico_fb.png" alt="Facebook" class="fb" /></a> | <a href="https://www.facebook.com/IGEMUNITS?ref=ts" target="_blank"><img src="https://static.igem.org/mediawiki/2012/f/f4/Ico_fb.png" alt="Facebook" class="fb" /></a> | ||
| - | <a href="https://twitter.com/ | + | <a href="https://twitter.com/iGEMTrieste" target="_blank"><img src="https://static.igem.org/mediawiki/2012/2/21/Ico_twitter.png" alt="twitter" class="tw" /></a> |
</div> | </div> | ||
</div> | </div> | ||
Latest revision as of 18:07, 26 October 2012
The Jolly JoCare
a safe probiotic platform for protein expression
Week 6
More
Suicide System
Holin is defined as a Bglbrick part, that means it doesn't have the standard restriction sites. We transformed the standard Biobrick we needed to use, in Bglbrick by PCR. The promoter T5CumateOperator(BBa_K875001) was cut EcoRI/SpeI, the fragment was eluted from the gel and then cloned upstream the RBS_B0034, into the pSB1A2 linearized backbone. We screened the colonies by PCR with the standard VF2 and VR primers and the positive ones were inoculated; we amplified the miniprep by PCR with particular primers with the EcoRI, BglII, BamHI and XhoI restriction sites.Antibody
The sequences arrived, and both scFv versions (pelB-scFv and LPP-scFv) are correct, so we continued with our work. Afer different attempts, we finally ligated both scFv versions under T5LacO. We amplified the resulting plasmid in DH5L and introduced it into W3110 (with p-REP 4) which we will use for future analysis.Cumate-Switch Regulation
CymRWe ligate the CymR-B0015 X/P in the plasmid J61002 (treated with SAP) downstream the J23100. We proceed in many directions because the cloning of CymR-B0015 downstream J23100 was very difficult: we repeated the ligation with the same plasmid but with different treatment :
-elution and SAP
-elution without SAP
-ligation without gel purification.
We obtained some positive clones that we digest E/P for analysis. So we digested and ligated the right clones together. We obtain the double copy J23100-CymR-B0015.
T5 PROMOTER - CUMATE OPERATOR
We started again from the T5 promoter-E0240. We cloned T5 promoter-E0240 downstream j23100. We obtained positive clones but they didn't work.
