Difference between revisions of "Team:Aix-Marseille/Parts"
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<li>-Cytochrome C of <i>S.oneidensis</i> (BBa_K1601000), a proteobacterium which can live in both environments with or without oxygen that suggests a cytochrome with high activity. The stop codon has been deleted to facilitate a protein fusion.</li><br/> | <li>-Cytochrome C of <i>S.oneidensis</i> (BBa_K1601000), a proteobacterium which can live in both environments with or without oxygen that suggests a cytochrome with high activity. The stop codon has been deleted to facilitate a protein fusion.</li><br/> | ||
<li>-Heme A from <i>E.coli</i> K12 (BBa_K1601002)that enables the heme overproduction</li><br/> | <li>-Heme A from <i>E.coli</i> K12 (BBa_K1601002)that enables the heme overproduction</li><br/> | ||
| − | <li>-Yeast signal CXXCH from <i>Synechocystis sp</i> responsible for the <i>S.oneidensis</i> CytC translocation into the periplasm using TAT system ( | + | <li>-Yeast signal CXXCH from <i>Synechocystis sp</i> responsible for the <i>S.oneidensis</i> CytC translocation into the periplasm using TAT system (BBa_S05319)</li><br/> |
| − | <li>-Yeast signal CXXCH from <i>Synechocystis sp</i> responsible for the <i>Synechocystis sp</i> CytC translocation into the periplasm using TAT system</li><br/> | + | <li>-Yeast signal CXXCH from <i>Synechocystis sp</i> responsible for the <i>Synechocystis sp</i> CytC translocation into the periplasm using TAT system (BBa_S05320)</li><br/> |
</ul> | </ul> | ||
</div></p></span> | </div></p></span> | ||
Revision as of 19:57, 18 September 2015
Parts
New biobricks using existing ones
We use existing biobrick to create new biobricks we needed:
- -T7 promoter with RBS (Bba_K525998) and optimized Laccase from T.Thermophilus (Bba_K863011), protein likely to be more thermostable by its origin. A tag 10xHis (Bba_K844000)is located to the end of the protein (Cterm) to enable its purification (BBa_K1601015)
- -T7 promoter with RBS and optimized Laccase from T.Thermophilus, protein likely to be more thermostable by its origin. The stop codon has been deleted to facilitate a protein fusion (BBa_S05313)
New biobricks we designed
We use sequences whiche were not present in the biobrick registry to create new biobricks we needed:
- -Cytochrome C Synechocystis sp (BBa_K1601001), a cyanobacteria that suggests a cytochrome c
- -Cytochrome C of S.oneidensis (BBa_K1601000), a proteobacterium which can live in both environments with or without oxygen that suggests a cytochrome with high activity. The stop codon has been deleted to facilitate a protein fusion.
- -Heme A from E.coli K12 (BBa_K1601002)that enables the heme overproduction
- -Yeast signal CXXCH from Synechocystis sp responsible for the S.oneidensis CytC translocation into the periplasm using TAT system (BBa_S05319)
- -Yeast signal CXXCH from Synechocystis sp responsible for the Synechocystis sp CytC translocation into the periplasm using TAT system (BBa_S05320)
Linkers we designed
We designed some linker to facilitate the meeting of the laccase and the cytochrom C
- Rigid and structured linker designed to link (or connect) Laccase T.Thermophilus and CytC S.oneidensis (BBa_K1601008)
- Rigid and structured linker designed to link (or connect) Laccase T.Thermophilus and CytC P.denitrificans (BBa_K1601011)
- Rigid and structured linker designed to link (or connect) T.Thermophilus and CytC Synechocystis sp(BBa_K1601013)
- Rigid and structured linker designed to link (or connect) Laccase E.coli and CytC P.denitrificans (BBa_K1601009)
- Rigid and structured linker designed to link (or connect) Laccase E.coli and CytC Synechocystis sp (BBa_K1601010)
- Rigid and structured linker designed to link (or connect) Laccase E.coli and CytC S.oneidensis(BBa_K1601012)
