Team:Virginia/Parts
From 2013.igem.org
(Difference between revisions)
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<p><a href="https://2013.igem.org/Team:Virginia/Results">Results</a></p> | <p><a href="https://2013.igem.org/Team:Virginia/Results">Results</a></p> | ||
<p><a href="https://2013.igem.org/Team:Virginia/Modeling">Modeling</a></p> | <p><a href="https://2013.igem.org/Team:Virginia/Modeling">Modeling</a></p> | ||
- | <p><a href="https://2013.igem.org/Team:Virginia/ | + | <p><a href="https://2013.igem.org/Team:Virginia/Chassis_Improvements">Chassis Improvements</a></p></span> |
</li> | </li> | ||
<li> | <li> |
Revision as of 22:28, 26 October 2013
Parts
BBa_K1011000 encodes the FtsZ gene. When overexpressed, the FtsZ gene leads to z-ring formation at the cell poles rather than along the cell midline, leading to minicell production.
BBa_S05211 encodes a strong RBS and the GFP gene. This part was produced as an intermediate.
BBa_S05212 encodes a strong RBS, the GFP gene, and a double terminator. This part was produced as an intermediate, although it is particularly useful as a reporter gene construct for insertion behind the target gene.
BBa_S05213 encodes an IPTG-inducible promoter, a strong RBS, and the FtsZ gene. This part was produced as an intermediate.
BBa_K1011001 encodes our final construct: an IPTG-inducible promoter, a strong RBS, the FtsZ gene, a strong RBS, the GFP gene, and a double terminator. As overexpression of FtsZ induces minicell formation, GFP serves as a reporter. Use of the ITPG promoter grants control over the level of FtsZ overproduction, which may thus be tuned to optimal minicell production.
Submitted BioBricks