Team:HokkaidoU Japan/Promoter/Methods
From 2013.igem.org
Line 36: | Line 36: | ||
<div>Fig.4</div> | <div>Fig.4</div> | ||
</div> | </div> | ||
- | + | <div class="clearfix"></div> | |
<h2>Assay</h2> | <h2>Assay</h2> | ||
<p> | <p> |
Revision as of 01:26, 28 September 2013
Maestro E.coli
Promoter
Method
Promoter family
As our first step for constructing original promoter family, we synthesized theoretically ideal consensus sequence to bind σ factor. This should ensure that promoter will form the most stable complex with σ factor. We synthesized such a consensus promoter showed in the figure above, originated from consensus sequence and lac operon promoter (pLac) [Fig. 1].
We constructed consensus promoter by primer annealing. [Fig. 2]. For mutating hexamer at -35 region, a promoter randomize primer which has random hexamer (NNNNNN) at -35 region was used, but other sequence in the primer is same with consensus promoter [Fig.3]. We designed reverse promoter, promoter isolation primer, that is to isolate randomized promoter by annealing downstream of it [Fig.4].
Assay
To measure transcription activities, we prepared two popular reporter genes and one antibiotics resistance gene, mRFP1, lacZ&alpha ;, and Kanamycin resistance gene.