Team:Heidelberg LSL/Project UVsensors
From 2012hs.igem.org
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+ | <h4>Sensor constructs</h4> | ||
+ | <p>Those constructs were submitted as <a href="https://2012hs.igem.org/Team:Heidelberg_LSL/Parts">parts</a>.</p> | ||
+ | <center> | ||
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+ | <div class="img"> | ||
+ | <img src="https://static.igem.org/mediawiki/2012hs/b/b7/RecA_LacZ.jpg"width="220"/> | ||
+ | <div class="desc"> Map based on <a href="https://static.igem.org/mediawiki/2012hs/0/07/RecA_LacZ_pSB1C3.gb">precA_lacZ_pSB1C3</a> sequence.</div> | ||
+ | <br> | ||
+ | <img src="https://static.igem.org/mediawiki/2012hs/a/a1/RecB_LacZ.jpg" width="220"/> | ||
+ | <div class="desc"> Map based on <a href="https://static.igem.org/mediawiki/2012hs/1/1d/RecB_LacZ_pSB1C3.gb">precB_lacZ_pSB1C3</a> sequence.</div> | ||
+ | <br> | ||
+ | <img src="https://static.igem.org/mediawiki/2012hs/6/64/SulA_LacZ.jpg" width="220"/> | ||
+ | <div class="desc"> Map based on <a href="https://static.igem.org/mediawiki/2012hs/d/d3/SulA_LacZ_pSB1C3.gb">psulA_lacZ_pSB1C3</a> sequence.</div> | ||
+ | </center> | ||
+ | </p> | ||
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Revision as of 22:45, 16 June 2012
Strategy
Sensor Construction
Description
It was intended to generate constructs that are able to sense irradiation and respond to UV light with a colorful output.
First, we looked for proper E. coli promoters known to be involved in the SOS response. While RecB, RecC and SulA promoters were generated with custom-made oligonucleotides, we took precA as biobrick BBa_J22106. We designed the oligos for precB, precC and psulA to contain BB-2 standard prefix and suffix and putative promoter sequences (approx. 50 bp upstream of the start codon of each gene) taken from the EcoliWiki. Oligos were annealed and then directly used for ligation since they already contained the required overhangs. The precA part was therefore digested with EcoRI and SpeI.
As reporters, we decided for GFP and LacZ from the biobricks BBa_E0240 and BBa_K173004, respectively. We digested those plasmids with XbaI and PStI to allow for ligation with promoters into backbone pSB1K3 via standard assembly.
Finally, constructs were transformed into E. coli strain BL21 and applied to sense UV radiation with visible output.
Prior to submission, parts were transferred into pSB1C3.
Details
The following constructs were created by the above explained strategy.
Number | Promoter | Reporter | Backbone |
01 | precA | gfp | pSB1K3 |
02 | psulA | gfp | pSB1K3 |
03 | precA | lacZ | pSB1K3 |
04 | precB | lacZ | pSB1K3 |
05 | precC | lacZ | pSB1K3 |
06 | SulA | lacZ | pSB1K3 |
07 | precA | lacZ | pSB1C3 | 08 | precB | lacZ | pSB1C3 | 09 | psulA | lacZ | pSB1C3 |
Sensor constructs
Those constructs were submitted as parts.