Team:Lyon-INSA/datapage

From 2012.igem.org

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<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802001" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>Dispersin generator for <i>B. subtilis</i></b> BBa_K802001 : This part associates the <i>Bacillus subtilis</i> Constitutive Promoter (P<sub>veg</sub>) with the dispersin B gene (<i>dspB</i>). In our plasmid collection, this part is named pBK33 in the Chloramphenicol backbone and pBKH41 in the shuttle vector <i>E. coli</i> – <i>B. subtilis</i>. We worked with the plasmid pBKH41 for the tests and we tried two different genetic backgrounds : the NM522 strain to make test in <i>E. coli</i> and the 168 strain to make test in <i>Bacillus subtilis</i>.<br>
<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802001" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>Dispersin generator for <i>B. subtilis</i></b> BBa_K802001 : This part associates the <i>Bacillus subtilis</i> Constitutive Promoter (P<sub>veg</sub>) with the dispersin B gene (<i>dspB</i>). In our plasmid collection, this part is named pBK33 in the Chloramphenicol backbone and pBKH41 in the shuttle vector <i>E. coli</i> – <i>B. subtilis</i>. We worked with the plasmid pBKH41 for the tests and we tried two different genetic backgrounds : the NM522 strain to make test in <i>E. coli</i> and the 168 strain to make test in <i>Bacillus subtilis</i>.<br>
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<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802002" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>P<sub>lac</sub>(<i>B. subtilis</i>)-RBS(<i>E. coli</i>)-GFP</b>  BBa_K802002 : This part is used to determine if the promoter P<sub>lac</sub> works or not and especially how it works when it is activated by different concentration of the inductor IPTG. Within this part there is P<sub>lac</sub> from <i>Bacillus subtilis</i> which is the promoter that induces production of XylR to form a positive biofilm. Then a RBS from <i>E coli</i> is added to finally enable production of GFP which is an easy measurable parameter using the amount of fluorescence.<br>
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<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802002" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>P<sub>lac</sub>(<i>B. subtilis</i>)-RBS(<i>E. coli</i>)-GFP</b>  BBa_K802002 : This part is used to determine if the promoter P<sub>lac</sub> works or not and especially how it works when it is activated by different concentration of the inducer IPTG. Within this part there is P<sub>lac</sub> from <i>Bacillus subtilis</i> which is the promoter that induces production of XylR to form a positive biofilm. Then a RBS from <i>E coli</i> is added to finally enable production of GFP which is an easy measurable parameter using the amount of fluorescence.<br>
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<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802003" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>Shuttle vector for <i>E. coli</i> and <i>B. subtilis</i> </b>BBa_K802003 : This part is a shuttle vector of 6.5kb which is Ampicillin resistant in <i>E. coli</i> and Erythromycin resistant in <i>B. subtilis</i>. It is a <b>low</b> copy number plasmid in <i>B. subtilis</i> and a high copy number plasmid in <i>E. coli</i>. It has a polylinker containing all 4 of the iGEM restriction sites. <br>
<a href="http://partsregistry.org/wiki/index.php?title=Part:BBa_K802003" target="_blank"><font color="purple"><b>Main Page</b></font></a>: <b>Shuttle vector for <i>E. coli</i> and <i>B. subtilis</i> </b>BBa_K802003 : This part is a shuttle vector of 6.5kb which is Ampicillin resistant in <i>E. coli</i> and Erythromycin resistant in <i>B. subtilis</i>. It is a <b>low</b> copy number plasmid in <i>B. subtilis</i> and a high copy number plasmid in <i>E. coli</i>. It has a polylinker containing all 4 of the iGEM restriction sites. <br>

Revision as of 13:45, 26 September 2012


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Main Page: Lysostaphin generator for B. subtilis BBa_K802000 : This part associates the Bacillus subtilis Constitutive Promoter (Pveg) with the lysostaphin gene. In our plasmid collection, this part is named pBK23 in the pSB1C3 backbone (CmR) and pBKL28 in the shuttle vector E. coliB. subtilis. The pBKL28 plasmid was transformed in the NM522 strain to perform tests in E. coli and in the 168 strain to perform tests in Bacillus subtilis.

Main Page: Dispersin generator for B. subtilis BBa_K802001 : This part associates the Bacillus subtilis Constitutive Promoter (Pveg) with the dispersin B gene (dspB). In our plasmid collection, this part is named pBK33 in the Chloramphenicol backbone and pBKH41 in the shuttle vector E. coliB. subtilis. We worked with the plasmid pBKH41 for the tests and we tried two different genetic backgrounds : the NM522 strain to make test in E. coli and the 168 strain to make test in Bacillus subtilis.

Main Page: Plac(B. subtilis)-RBS(E. coli)-GFP BBa_K802002 : This part is used to determine if the promoter Plac works or not and especially how it works when it is activated by different concentration of the inducer IPTG. Within this part there is Plac from Bacillus subtilis which is the promoter that induces production of XylR to form a positive biofilm. Then a RBS from E coli is added to finally enable production of GFP which is an easy measurable parameter using the amount of fluorescence.

Main Page: Shuttle vector for E. coli and B. subtilis BBa_K802003 : This part is a shuttle vector of 6.5kb which is Ampicillin resistant in E. coli and Erythromycin resistant in B. subtilis. It is a low copy number plasmid in B. subtilis and a high copy number plasmid in E. coli. It has a polylinker containing all 4 of the iGEM restriction sites.

Main Page: Shuttle vector for E. coli and B. subtilis BBa_K802004 : This is a shuttle vector of 6.5kb which is Ampicillin resistant in E. coli and Erythromycin resistant in B. subtilis. It is a high copy number plasmid in both B. subtilis and E. coli. It has a polylinker containing all 4 of the iGEM restriction sites.

Main Page: iGEM linker for shuttle vectors BBa_K802003 and BBa_K802004 BBa_K802005 : This part is a custom designed polylinker which was cloned into the shuttle vectors BBa_K802004 and BBa_K802003 so that the plasmids would correspond to the iGEM format.



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