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Team:BostonU/Repressors
From 2014.igem.org
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Our current MoClo library of parts does not contain enough orthogonal repressors and promoters to flush this design out. Based on this limitation, we began a literature search to find five new repressor and promoter pairs that could work together in one system. Early on in our search we found the 2014 article by Stanton <i>et al.</i> [1] where they built and tested a library of 73-TetR family repressors from various prokaryotic genomes. From these parts, they showed that 20 of them had strong transfer curves when turned on (Figure 4 below). From that subset, we chose five repressors that had desirable but slightly different transfer curves from one another: LmrA, SrpR, PhlF, BetI, and BM3R1. For our definition of desirable, we wanted to see a clear on and off function across at least two decades of REU with varying peak fluorescence as measured by Stanton <i>et al.</i>. | Our current MoClo library of parts does not contain enough orthogonal repressors and promoters to flush this design out. Based on this limitation, we began a literature search to find five new repressor and promoter pairs that could work together in one system. Early on in our search we found the 2014 article by Stanton <i>et al.</i> [1] where they built and tested a library of 73-TetR family repressors from various prokaryotic genomes. From these parts, they showed that 20 of them had strong transfer curves when turned on (Figure 4 below). From that subset, we chose five repressors that had desirable but slightly different transfer curves from one another: LmrA, SrpR, PhlF, BetI, and BM3R1. For our definition of desirable, we wanted to see a clear on and off function across at least two decades of REU with varying peak fluorescence as measured by Stanton <i>et al.</i>. | ||
| - | <center><img src="https://static.igem.org/mediawiki/2014/f/f2/BU14_tetR_orthologs_transfer_curves.jpg" width=" | + | <center><img src="https://static.igem.org/mediawiki/2014/f/f2/BU14_tetR_orthologs_transfer_curves.jpg" width="50%"></center> |
| + | <center><capt>Figure 4 from Stanton et al.(2014) where each repressor (noted in bottom left of each graph) was under control of an IPTG-inducible promoter and the corresponding repressor promoter controlled YFP fluorescence.</center></capt> | ||
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<h3>Design and Assembly</h3> | <h3>Design and Assembly</h3> | ||
Revision as of 21:28, 15 October 2014
Why Repressor Proteins?In order to build and test the priority encoder below, we will need to create new basic parts for new repressors and their corresponding promoters. The diagram below shows an Abstract Genetic Regulatory Network, or AGRN, where only the function is outlined without any specific parts assigned to the promoters, repressors, or small molecules (with the exception of the fluorescent proteins GFP, RFP, and BFP). Our current MoClo library of parts does not contain enough orthogonal repressors and promoters to flush this design out. Based on this limitation, we began a literature search to find five new repressor and promoter pairs that could work together in one system. Early on in our search we found the 2014 article by Stanton et al. [1] where they built and tested a library of 73-TetR family repressors from various prokaryotic genomes. From these parts, they showed that 20 of them had strong transfer curves when turned on (Figure 4 below). From that subset, we chose five repressors that had desirable but slightly different transfer curves from one another: LmrA, SrpR, PhlF, BetI, and BM3R1. For our definition of desirable, we wanted to see a clear on and off function across at least two decades of REU with varying peak fluorescence as measured by Stanton et al..  Design and Assembly TestingReferences |
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