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Team:EPF Lausanne/Project parts
From 2010.igem.org
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First the legend: | First the legend: | ||
| - | *Ori = Origin of replication for Asaia and E. | + | *Ori = Origin of replication for Asaia and ''E. coli'' |
*S = Strong Promoter | *S = Strong Promoter | ||
*W = Weak Promoter | *W = Weak Promoter | ||
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We made basic parts to build the complexest one. | We made basic parts to build the complexest one. | ||
| - | [http://partsregistry.org/Part:BBa_K320000 *C3 + Ori] We made this plasmid because we needed an origin of replication that works in Asaia. After experiences we conclued that it also work with E. | + | [http://partsregistry.org/Part:BBa_K320000 *C3 + Ori] We made this plasmid because we needed an origin of replication that works in Asaia. After experiences we conclued that it also work with ''E. coli''. |
[http://partsregistry.org/Part:BBa_K320001 *C3 + Immu] The immunotoxine is the main part of the project, we obtain it by syntetisation. For a better unerstanding, go [https://2010.igem.org/Team:EPF_Lausanne/Project_immuno there]. | [http://partsregistry.org/Part:BBa_K320001 *C3 + Immu] The immunotoxine is the main part of the project, we obtain it by syntetisation. For a better unerstanding, go [https://2010.igem.org/Team:EPF_Lausanne/Project_immuno there]. | ||
Revision as of 11:02, 25 October 2010
Cloning
We performed all the cloning in E.coli, and did experiments on Asaia transformation, growth and resistance to antibiotics in parallel.
As E. coli origin does not work in Asaia, we added an origin that was compatible with this bacteria (which was recovered from a GFP-plasmid transformed into the Asaia we received from Italy). On the opposite, Asaia's origin does work in E. coli, which is very useful for our sets of experiments.
BioBricks
All our parts are in the pSB1C3 backbone vector (abbreviate C3). When you click on the part's name, you are redirected to the partsregistry corresponding page.
First the legend:
- Ori = Origin of replication for Asaia and E. coli
- S = Strong Promoter
- W = Weak Promoter
- Immu = immunotoxin
- P25 = Pfs25 protein
- P28 = Pfs28 protein
- Kan = Resistance to Kanamycin
- Tet = Resistance to Tetracycline
We made basic parts to build the complexest one.
[http://partsregistry.org/Part:BBa_K320000 *C3 + Ori] We made this plasmid because we needed an origin of replication that works in Asaia. After experiences we conclued that it also work with E. coli.
[http://partsregistry.org/Part:BBa_K320001 *C3 + Immu] The immunotoxine is the main part of the project, we obtain it by syntetisation. For a better unerstanding, go there.
[http://partsregistry.org/Part:BBa_K320002 *C3 + S] We made a new strong promoter permitting use to test teh expression of the immunotoxine. We called it strong because we used the constitutive sequence which should give the biggets level of expression.
[http://partsregistry.org/Part:BBa_K320010 *C3 + W] This promoter has been made to have a second level of expression for our proteins, which is lower than the strong one.
We made the following BioBricks from the aboves :
[http://partsregistry.org/Part:BBa_K320003 *C3 + Ori + Tet]
[http://partsregistry.org/Part:BBa_K320004 *C3 + Ori + Kan]
[http://partsregistry.org/Part:BBa_K320005 *C3 + S + CFP]
[http://partsregistry.org/Part:BBa_K320006 *C3 + S + Immu]
[http://partsregistry.org/Part:BBa_K320007 *C3 + S + P25]
[http://partsregistry.org/Part:BBa_K320008 *C3 + S + Immu + ori + Kan]
[http://partsregistry.org/Part:BBa_K320009 *C3 + S + P28 + Ori + Tet]
[http://partsregistry.org/Part:BBa_K320011 *C3 + Ori + Amp]
[http://partsregistry.org/Part:BBa_K320012 *C3 + W + Immu]
[http://partsregistry.org/Part:BBa_K320013 *C3 + W + P25]
