Difference between revisions of "Part:BBa K613010:Experience"

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This shows that the promoter can be induced for BBa_K2281001,BBa_K2281002,and BBa_K2281003
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This shows that the promoter can be induced for  
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<a href="https://parts.igem.org/Part:BBa_K2281001">BBa_K2281001</a>,
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<a href="https://parts.igem.org/Part:BBa_K2281002">BBa_K2281002</a>,
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and <a href="https://parts.igem.org/Part:BBa_K2281003">BBa_K2281003</a>
  
 
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Revision as of 09:14, 1 November 2017

This experience page is provided so that any user may enter their experience using this part.
Please enter how you used this part and how it worked out.

Applications of BBa_K613010

Experience of the ITB_Indonesia iGEM 2015 team.

The iGEM 2015 ITB Indonesia used this promoter and RBS to express BBa_K653000 for rhamnolipid production in E. coli BL21(DE3). After IPTG induction, the separated supernatant was tested for surfactant activity.
Supernatant from empty cell, either induced or not, had no / little surfactant activity. The uninduced transformant had little activity, but the induced transformant had higher surfactant activity.
This shows that the promoter can be induced for BBa_K653000 expression.

Experience of the CIEI-BJ iGEM 2017-High school team.

The iGEM 2017 CIEI-BJ team used this promoter and RBS to express BBa_K2281003 for Old Yellow Enzyme production which is the reductase which bolsters the production of cireonellol from geraniol in E. coli BL21. and then combined 2A and GES, After IPTG induction, the protein was tested by SDS-PAGE and western blot.
This shows that the promoter can be induced for BBa_K2281001, BBa_K2281002, and BBa_K2281003

Characterization of Designed Variants by EPFL 2011

For each family, we tested the randomers and the designed variants separately. To characterize the promoter strengths, we used RFP as the reporter gene and used a platereader to test for fluorescence during and after induction with IPTG.

Non random response.png

The six designed T7 promoter variants are named as a function of their predicted promoter efficiency, relative to the wildtype. For example, T7 14 has a predicted efficiency of 14% compared to the consensus T7 promoter, whereas T7 111 is predicted to be 111% more efficient than the wildtype. In the chart above, each of the designed promoter variants for both the T7 with and without the lac operator are arranged in increasing predicted efficiency. Contrary to our expectation, some variants that were designed to have a lesser efficiency than the wildtype (e.g. T7 54) seem to have a much higher strength (as measured by fluorescence at saturation, normalized by the optical density). The data for this graph was produced in triplicate, so the error bar represents the standard error across those three measurements.


User Reviews

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