Team:UCSF/lily2
From 2013.igem.org
Line 255: | Line 255: | ||
</div> | </div> | ||
<a href="https://2013.igem.org/Team:UC_Davis/Project_Overview"><h2>Project Background</h2></a> | <a href="https://2013.igem.org/Team:UC_Davis/Project_Overview"><h2>Project Background</h2></a> | ||
- | < | + | <p>Learn about how we combine riboswitches and TALs into robust orthogonal mechanisms for inducible repression. |
- | </ | + | </p></a> |
</td> | </td> |
Revision as of 17:04, 27 September 2013
Operation CRISPR: Deploying precision guided tools to target unique species in a complex microbiome
In microbial communities, bacterial populations are commonly controlled using indiscriminate, broad range antibiotics. There are few ways to target specific strains effectively without disrupting the entire microbiome and local environment. The goal of our project is to take advantage of a natural horizontal gene transfer mechanism in bacteria to precisely affect gene expression in selected strains. We combine bacterial conjugation with CRISPRi, an RNAi-like repression system developed from bacteria, to regulate gene expression in targeted strains within a complex microbial community. One possible application is to selectively repress pathogenic genes in a microbiome, leaving the community makeup unaffected. In addition, we use CRISPRi to lay the groundwork for transferring large circuits that enable complex functionality and decision-making in cells.
Project BackgroundLearn about how we combine riboswitches and TALs into robust orthogonal mechanisms for inducible repression. |
ResultsCheck out the cool results of our experiments with RiboTALs. |
Human PracticesTake a look at how we designed a new database for better raw data characterization of Biobricks. |
Judging CriteriaHere's the criteria that we met for this year's team. |
Special Thanks to Our 2013 iGEM Team Sponsors!