Team:Gothenburg/Parts/Part Submission
From 2014.igem.org
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For this reason, we planned to submit the degradation-tag we fused to the fluorescence proteins to make sure they are degraded and do not leak into the next cycle.<br> | For this reason, we planned to submit the degradation-tag we fused to the fluorescence proteins to make sure they are degraded and do not leak into the next cycle.<br> | ||
- | <div class="imgRight" | + | <div class="imgRight" align="center"> |
- | <img src="https://static.igem.org/mediawiki/2014/" | + | <img src="https://static.igem.org/mediawiki/2014/8/87/TeamGBG_D-Tag_SnapGene.PNG" |
- | width=" | + | width="900px" height="auto"/> |
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<p>Figure 1. Picture of the part in SnapGene. | <p>Figure 1. Picture of the part in SnapGene. | ||
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<h5>Summary</h5> | <h5>Summary</h5> | ||
<p> | <p> | ||
- | Our part submission is a 165 bp long N-terminal sequence of the S.cerevisiae protein <strong>Clb3</strong>. It is a cell cycle dependend degradation signal for proteins.</p> | + | Our part submission is a 165 bp long N-terminal sequence of the S.cerevisiae protein <strong>Clb3</strong>. It is a cell cycle dependend degradation signal for proteins. In the registry you can find our part in the entry <a href="http://parts.igem.org/Part:BBa_K1503000">BBa_K1503000</a>.</p> |
Revision as of 00:40, 17 October 2014
Part Submisson
Since our whole generation counter is based on cell cycle specific signals for activation of genes and degradation of proteins, we thought it would be beneficial to add one of the specific degradation signals for yeast into the registry. S. cerevisiae was established as one of the most researched on and industrially used organisms.
For this reason, we planned to submit the degradation-tag we fused to the fluorescence proteins to make sure they are degraded and do not leak into the next cycle. Figure 1. Picture of the part in SnapGene. Cyclins bind to cell cycle specific kinases and mediate thereby the progress of the different steps of the cell cycle. The six B-cyclins in yeast (Clb1-6) are responsible for the shift into the "M-phase bla". With increasing digit the degradation occours later in the cell cycle. This goes hand in hand with the position of the destruction box in the protein, which distance to the N-terminal increases with the digit as well. To have a suitable time point of degradation for our counter we decided on using the sequence of Clb3. SummaryOur part submission is a 165 bp long N-terminal sequence of the S.cerevisiae protein Clb3. It is a cell cycle dependend degradation signal for proteins. In the registry you can find our part in the entry BBa_K1503000. |
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