Team:HokkaidoU Japan/Promoter/Methods

From 2013.igem.org

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<h2>Assay</h2>
<h2>Assay</h2>
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To measure transcription activities, we prepared two popular reporter genes and one antibiotics resistance gene, mRFP1, lacZ&alpha;, and Kanamycin resistance gene.
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To measure transcription activities, we prepared two popular reporter genes and one antibiotics resistance gene, mRFP1, LacZ&alpha;, and Kanamycin resistance gene.
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Revision as of 07:48, 20 October 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).

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).

fig.2
fig.3
fig.4

Assay

To measure transcription activities, we prepared two popular reporter genes and one antibiotics resistance gene, mRFP1, LacZα, and Kanamycin resistance gene.