Team:TPHS SanDiego/Project

From 2013hs.igem.org

(Difference between revisions)
 
Line 44: Line 44:
<div align="justify">
<div align="justify">
<p style="font-family:Georgia;color:black;font-size:16px;">
<p style="font-family:Georgia;color:black;font-size:16px;">
-
<h1>Overview</h1>
 
-
Our project focuses on promoter engineering. Our goal is to characterize a set of promoters (of our design) by moving the repressor and/or activator binding sites with respect to the -10 and -35 regions of the promoter. Ideally, we would like to show that by moving an activator binding site it can become a repressor and that by moving a repressor binding site it may become either irrelevant to transcription rate or even boost it. We also want to see if there is a steep decline in repressor/activator function as the binding site move along the promoter or if it is a gradual/linear change. We believe this project could have application to genetic circuits by allowing a single protein to either activate or repress a promoter depending on where the binding sites are placed on the promoter.
 

Latest revision as of 23:21, 21 June 2013

header
Mercury