Team:Calgary/Project/Promoter

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<p>Naphthenic acids are comprised of many different carboxylic acids. Little is known about the natural biological NA-degradation pathways of <i>Pseudomonas</i> or microalgae, and therefore it was difficult to pinpoint a good starting point to find a promoter. We decided to pursue two different methods in order to search for a promoter that was sensitive to naphthenic acids, to increase the chances of a positive result.</p>
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<p>Naphthenic acids are comprised of many different carboxylic acids. Little is known about the natural biological NA-degradation pathways of <i>Pseudomonas</i> or microalgae, and therefore it was difficult to identify a good starting point to find a promoter. We decided to pursue two different methods in order to search for a promoter that was sensitive to naphthenic acids and to increase the chances of a positive result.</p>
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<td><a href="https://2011.igem.org/Team:Calgary/Project/ProjectPseudomonas"><img style="width: 150px;" src="https://static.igem.org/mediawiki/2011/0/01/UCalgary2011_PromoterFredFishing.png"></img></a></td>
<td><a href="https://2011.igem.org/Team:Calgary/Project/ProjectPseudomonas"><img style="width: 150px;" src="https://static.igem.org/mediawiki/2011/0/01/UCalgary2011_PromoterFredFishing.png"></img></a></td>
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<h2>A Novel Approach to Biotinylation/ChIP-SEQ: "Promoter Fishing"</h2>
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<h2>A Novel Approach to Biotinylation/ChIP-SEQ: "Sensory Element Fishing"</h2>
<p>This is a novel approach to the biotinylation of small molecules (namely, naphthenic acids) to interact with proteins or DNA sequences in both <i>Pseudomonas</i> and microalgae that responded to naphthenic acids.<a href="https://2011.igem.org/Team:Calgary/Project/ProjectPseudomonas"> Click here to read more</a>.</p>
<p>This is a novel approach to the biotinylation of small molecules (namely, naphthenic acids) to interact with proteins or DNA sequences in both <i>Pseudomonas</i> and microalgae that responded to naphthenic acids.<a href="https://2011.igem.org/Team:Calgary/Project/ProjectPseudomonas"> Click here to read more</a>.</p>
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<h2>A Bioinformatics and qRT-PCR Approach to Finding NA-Sensitive Promoters</h2>
<h2>A Bioinformatics and qRT-PCR Approach to Finding NA-Sensitive Promoters</h2>
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<p>We decided to pursue a second method of searching, which was conducted simultaneously with the Promoter Fishing. We narrowed down a list of candidate genes using a number of bioinformatics web programs and then produced primers for those genes for use in quantitative reverse-transcriptase PCR. <a href="https://2011.igem.org/Team:Calgary/Project/Promoter/Bioinformatics">Click here to read more</a>.</p>
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<p>We decided to pursue a second method of searching, which was conducted simultaneously with the Promoter Fishing. We narrowed down a list of candidate genes using a number of bioinformatics web programs and then produced primers for those genes for use in quantitative real-time PCR. <a href="https://2011.igem.org/Team:Calgary/Project/Promoter/Bioinformatics">Click here to read more</a>.</p>
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Latest revision as of 01:38, 29 September 2011


Searching for a Naphthenic Acid-Sensitive Promoter

Naphthenic acids are comprised of many different carboxylic acids. Little is known about the natural biological NA-degradation pathways of Pseudomonas or microalgae, and therefore it was difficult to identify a good starting point to find a promoter. We decided to pursue two different methods in order to search for a promoter that was sensitive to naphthenic acids and to increase the chances of a positive result.

A Novel Approach to Biotinylation/ChIP-SEQ: "Sensory Element Fishing"

This is a novel approach to the biotinylation of small molecules (namely, naphthenic acids) to interact with proteins or DNA sequences in both Pseudomonas and microalgae that responded to naphthenic acids. Click here to read more.

A Bioinformatics and qRT-PCR Approach to Finding NA-Sensitive Promoters

We decided to pursue a second method of searching, which was conducted simultaneously with the Promoter Fishing. We narrowed down a list of candidate genes using a number of bioinformatics web programs and then produced primers for those genes for use in quantitative real-time PCR. Click here to read more.

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