Team:UC Chile/Cyanolux/Biobricks

From 2012.igem.org

(Difference between revisions)
 
(15 intermediate revisions not shown)
Line 4: Line 4:
<h2>pSB1C3_IntK (BBa_K743006)</h2>
<h2>pSB1C3_IntK (BBa_K743006)</h2>
 +
Neutral recombination plasmid backbone. Kanamycin resistance as a selectable marker for integration. EcoRI restriction site in RS2. Plasmid backbone designed for Gibson Assembly.
 +
[[File:UC Chile-IntKplasmidResult.jpg | 400px ]]
[[File:UC Chile-IntKplasmidResult.jpg | 400px ]]
-
<br />
 
-
<br />
 
-
<br />
 
<br />
<br />
<h2>pSB1C3_IntS (BBa_K743010)</h2>
<h2>pSB1C3_IntS (BBa_K743010)</h2>
 +
Suceptibility generating plasmid backbone. Spectinomycin resistance as a selectable marker for integration. mRFP1 under constitutive promoter in E.coli for negative selection of standard assembly.
[[File:UC Chile-IntSplasmidResult.jpg | 600px ]]
[[File:UC Chile-IntSplasmidResult.jpg | 600px ]]
-
<br />
 
-
<br />
 
-
<br />
 
<br />
<br />
<h1>Biobricks and Constructs</h1>
<h1>Biobricks and Constructs</h1>
 +
<br />
<h2>BBa_K743000</h2>
<h2>BBa_K743000</h2>
-
[[File:UC Chile-BBa_K743000.jpg | 250px ]]
+
<br />
 +
First recombination site of IntK plasmid backbone.
 +
 
 +
[[File:UC Chile-BBa_K743000.jpg | 230px ]]
 +
 
 +
<br />
<h2>BBa_K743001</h2>
<h2>BBa_K743001</h2>
 +
<br />
 +
Second recombination site of IntK plasmid backbone. Illegal EcoRI restriction site present. As it always is used as a downstream part, illegal site does not interfere with Standard Assembly.
 +
[[File:UC Chile-BBa_K743001.jpg | 250px ]]
[[File:UC Chile-BBa_K743001.jpg | 250px ]]
 +
 +
<br />
<h2>BBa_K743002</h2>
<h2>BBa_K743002</h2>
 +
<br />
 +
<i>Synechocystis</i> PCC. 6803 Citocrome C promoter.
 +
[[File:UC Chile-BBa_K743002.jpg | 250px ]]
[[File:UC Chile-BBa_K743002.jpg | 250px ]]
-
<h2>BBa_K743004 or BBa_K743005</h2>
+
<br />
-
[[File:UC Chile-BBa_K743004.jpg | 250px ]]
+
<h2>BBa_K743009</h2>
 +
<br />
 +
pSB1C3_IntK(BBa_K743006) with mRFP1 under <i>Synechocystis</i> PpsaAB promoter.
-
<html><center><img src="https://static.igem.org/mediawiki/2012/a/a2/UC_Chile-BBa_K743004_OR_BBa_K743005.png" align="middle" width="800"></center></html>
+
[[File:UC Chile-BBa_K743009.jpg | 500px ]]
-
<br>
+
-
Integrative plasmid designed for the expression of RFP under synechocystis psbAB or psaA2 promoter also with a kanamycin resistance cassette for selection in cyanobacteria. The construct is flanked by neutral recombination sites RS1 and RS2, homologous to synechocystis chromosome.
+
-
<h2>BBa_K743009 or BBa_K743016</h2>
+
<br />
-
[[File:UC Chile-BBa_K743009.jpg | 250px ]]
+
<h2>BBa_K743016</h2>
 +
<br />
 +
pSB1C3_IntK(BBa_K743006) with mRFP1 under <i>Synechocystis</i> PpsbA2 promoter.
-
<html><center><img src="https://static.igem.org/mediawiki/2012/1/1e/UC_Chile-BBa_K743009_or_BBa_K743016.png" align="middle" width="800"></center></html>
+
[[File:UC Chile-BBa_K743016.jpg | 500px ]]
 +
 
 +
<br />
<h2>BBa_K743014</h2>
<h2>BBa_K743014</h2>
-
[[File:UC Chile-IntKplasmidLuxABxl.jpg | 400px ]]
+
<br />
 +
pSB1C3_IntK(BBa_K743006) with LuxAB genes from Photorhabdus luminescent under <i>Synechocystis</i> Transaldolase promoter.
 +
[[File:UC Chile-IntKplasmidLuxABxl.jpg | 600px ]]
 +
 
 +
<br />
<h2>BBa_K743015</h2>
<h2>BBa_K743015</h2>
 +
<br />
 +
pSB1C3_IntK(BBa_K743006) with LuxAB genes from Vibrio fisherii under <i>Synechocystis</i> Transaldolase promoter.
 +
[[File:UC Chile-IntKfullplasmidResult.jpg | 600px ]]
[[File:UC Chile-IntKfullplasmidResult.jpg | 600px ]]
 +
 +
<br />
<h2>BBa_K743018</h2>
<h2>BBa_K743018</h2>
-
[[File:UC Chile-BBa_K743018sfGFPtag.jpg | 400px ]]
+
<br />
 +
pSB1C3_IntK(BBa_K743006) with sfGFP gene with rapid degradation tag under <i>Synechocystis</i> Transaldolase promoter.
 +
[[File:UC Chile-BBa_K743018sfGFPtag.jpg | 600px ]]

Latest revision as of 09:55, 26 October 2012

Project: Luxilla - Pontificia Universidad Católica de Chile, iGEM 2012