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Team:Grenoble/Biology/Notebook/June/week 26
From 2012.igem.org
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<body id="Biology"> | <body id="Biology"> | ||
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<section> | <section> | ||
| - | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June"> | + | <h1>June</h1> |
| - | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_24"> | + | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June">Week 23</a> • |
| - | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_25"> | + | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_24">Week 24</a> • |
| - | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_26"> | + | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_25">Week 25</a> • |
| - | < | + | <a href="https://2012.igem.org/Team:Grenoble/Biology/Notebook/June/week_26">Week 26</a> |
| + | </section> | ||
<br/> | <br/> | ||
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<h1> Week 26: June 25<span class="exposant">th</span> to July 01<span class="exposant">st</span> </h1> | <h1> Week 26: June 25<span class="exposant">th</span> to July 01<span class="exposant">st</span> </h1> | ||
<p>For the detection module, we decided to work on a modified membrane receptor. It consists of two merged E. coli membrane receptors. The extracellular part is the extracellular part of Tap, a dipeptide membrane receptor. The cytoplasmic part is the cytoplasmic part of the EnvZ receptor, which has the ability to activate OmpR (by phosphorilation) which is a transcription factor. | <p>For the detection module, we decided to work on a modified membrane receptor. It consists of two merged E. coli membrane receptors. The extracellular part is the extracellular part of Tap, a dipeptide membrane receptor. The cytoplasmic part is the cytoplasmic part of the EnvZ receptor, which has the ability to activate OmpR (by phosphorilation) which is a transcription factor. | ||
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It will be a proof of concept for a bigger system which is a complete pathogene detection module : | It will be a proof of concept for a bigger system which is a complete pathogene detection module : | ||
| - | <center><img src="https://static.igem.org/mediawiki/2012/5/54/Receptor_2.jpg" alt="receptor_2"/></center> | + | <center><img src="https://static.igem.org/mediawiki/2012/5/54/Receptor_2.jpg" alt="receptor_2"/></center></section> |
| - | + | <section> | |
<h2>1<span class="exposant">st</span> network : with amplifier 1 (RsmA-rsmY)</h2> | <h2>1<span class="exposant">st</span> network : with amplifier 1 (RsmA-rsmY)</h2> | ||
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<h3>Amplifier 1 : RsmA-rsmY system characterisation: (3 final plasmids)</h3> | <h3>Amplifier 1 : RsmA-rsmY system characterisation: (3 final plasmids)</h3> | ||
<h4>Plasmid Mapping</h4> | <h4>Plasmid Mapping</h4> | ||
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rsmY (iGEM Grenoble 2011) => final length ≃ 170bp<br/> | rsmY (iGEM Grenoble 2011) => final length ≃ 170bp<br/> | ||
fha1 (iGEM Grenoble 2011) => final length ≃ 80bp<br/> | fha1 (iGEM Grenoble 2011) => final length ≃ 80bp<br/> | ||
| - | < | + | </section> |
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| - | < | + | <section> |
<h2>2<span class="exposant">nd</span> network : with amplifier 2 (cAMP-CRP)</h2> | <h2>2<span class="exposant">nd</span> network : with amplifier 2 (cAMP-CRP)</h2> | ||
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<h3>Amplifier 2: cAMP-CRP system (first construction): (1 final plasmid)</h3> | <h3>Amplifier 2: cAMP-CRP system (first construction): (1 final plasmid)</h3> | ||
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pSB4K5 plasmid => final length ≃ 2400bp | pSB4K5 plasmid => final length ≃ 2400bp | ||
<h4>New parts</h4> | <h4>New parts</h4> | ||
| - | pAra/Bad_RBS_GFP ( | + | pAra/Bad_RBS_GFP (Alon collection) => final length ≃ 1300bp <br/> |
| - | RBS_Cya (E. coli chromosom) => final length ≃ 2600bp | + | RBS_Cya (E. coli chromosom) => final length ≃ 2600bp |
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</section> | </section> | ||
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</body> | </body> | ||
</html> | </html> | ||
{{:Team:Grenoble/script}} | {{:Team:Grenoble/script}} | ||
{{:Team:Grenoble/menu}} | {{:Team:Grenoble/menu}} | ||
Latest revision as of 14:07, 22 August 2012
June
Week 23 • Week 24 • Week 25 • Week 26Week 26: June 25th to July 01st
For the detection module, we decided to work on a modified membrane receptor. It consists of two merged E. coli membrane receptors. The extracellular part is the extracellular part of Tap, a dipeptide membrane receptor. The cytoplasmic part is the cytoplasmic part of the EnvZ receptor, which has the ability to activate OmpR (by phosphorilation) which is a transcription factor.
It will be a proof of concept for a bigger system which is a complete pathogene detection module :
1st network : with amplifier 1 (RsmA-rsmY)
Amplifier 1 : RsmA-rsmY system characterisation: (3 final plasmids)
Plasmid Mapping
On a pSB4K5 plasmid, we wanted to put the construction: pLAC_fha1_eCFP
Biobricks involved
pLAC_RBS (BBa_I13601) => final length ≃ 90bppLAC (BBa_I13601) => final length ≃ 90bp
eCFP (BBa_E0422 or BBa_E0022) => final length ≃ 800bp
plasmid pSB4K5 => final length ≃ 2400bp
plasmid pSB3C5 => final length ≃ 2400bp
plasmid pSB1A3 => final length ≃ 2400bp
New parts
RsmA (iGEM Grenoble 2011) => final length ≃ 200bprsmY (iGEM Grenoble 2011) => final length ≃ 170bp
fha1 (iGEM Grenoble 2011) => final length ≃ 80bp
2nd network : with amplifier 2 (cAMP-CRP)
Amplifier 2: cAMP-CRP system (first construction): (1 final plasmid)
Plasmid Mapping
On the pSB4K5 plasmid, we wanted to put the construction: pAra/Bad_RBS_GFP_RBS_Cya
Biobricks involved
pSB4K5 plasmid => final length ≃ 2400bpNew parts
pAra/Bad_RBS_GFP (Alon collection) => final length ≃ 1300bpRBS_Cya (E. coli chromosom) => final length ≃ 2600bp
