Difference between revisions of "Part:BBa K606040:Experience"
 
Line 40: Line 40:
 
|};
 
|};
 
<!-- End of the user review template -->
 
<!-- End of the user review template -->
 +
{|width='80%' style='border:1px solid gray'
 +
|-
 +
|width='10%'|
 +
<partinfo>BBa_K143064 AddReview 5</partinfo>
 +
|width='60%' valign='top'|
 +
This part was used as a part of the Bee subtilis, iGEM METU 2013 project. We simulated the production of RFP under two different IPTG concentrations to observe its basal and maximum transcription rates.
 +
|};
 +
 
<!-- DON'T DELETE --><partinfo>BBa_K606040 EndReviews</partinfo>
 
<!-- DON'T DELETE --><partinfo>BBa_K606040 EndReviews</partinfo>

Latest revision as of 02:39, 5 October 2013


The Hyperspank promoter was designed to be compatible for B. subtilis. It is shorter than the classic one, but is also recognised by E. coli polymerases.

We characterised it with an RFP expression system (PHs-RBS-RFP), into TURBO cells that express LacI to allow the promoter to be the less leacky possible. This system is inducible by IPTG.



Without IPTG


E.coli containing Hyperspank+RBS+RFP - IPTG at 37°C
-IPTG E.coli at 37°C (rfp image)
-IPTG E.coli at 37°C (trans image)
-IPTG E.coli at 37°C (rfp image)
-IPTG E.coli at 37°C (trans image)


With IPTG :

E.coli containing Hyperspank+RBS+RFP + IPTG at 37°C
+IPTG E.coli at 37°C (rfp image)
+IPTG E.coli at 37°C (trans image)
+IPTG E.coli at 37°C (rfp image)
+IPTG E.coli at 37°C (trans image)

User Reviews

UNIQc7221628bb6b35c1-partinfo-00000000-QINU

•••••

This part was used as a part of the Bee subtilis, iGEM METU 2013 project. We simulated the production of RFP under two different IPTG concentrations to observe its basal and maximum transcription rates.

;

UNIQc7221628bb6b35c1-partinfo-00000002-QINU