Difference between revisions of "Team:Arizona State"

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         <h1 class = "center"> Our Project </h1>
 
         <h1 class = "center"> Our Project </h1>
 
         <p class = "big home-text">Quorom sensing (QS) allows bacteria to sense the surrounding
 
         <p class = "big home-text">Quorom sensing (QS) allows bacteria to sense the surrounding
             cell population and "communicate" with their neighbors. Bacteria do this by
+
             cell population density and communicate with their neighbors. They do this by producing
             releasing an inducer protein, such as a N-acyl homoserine lactone (AHL), which upon
+
             N-acyl homoserine lactones (AHLs), which can diffuse back into the bacteria at high concentrations.
             reaching a certain concentration, will activate genes that increase cell
+
             In the cell they bind to receiver proteins, which then activate gene expression in a coordinated manner. There are many natural QS systems, but only four in popular use by synthetic biologists. Some of these systems use AHLs that can activate multiple receiver systems or "crosstalk" between networks. This can cause problems when using QS in higher level designs. Our project aims to characterize a variety of AHL networks,
            density. Our project aims to characterize a variety of AHL networks,
+
 
             increasing the number of functional QS systems with minimal crosstalk in
 
             increasing the number of functional QS systems with minimal crosstalk in
 
             synthetic biology. </p>
 
             synthetic biology. </p>

Revision as of 00:13, 19 October 2016


Ringtones

Diverse homoserine lactone systems for cellular communication

Our Project

Quorom sensing (QS) allows bacteria to sense the surrounding cell population density and communicate with their neighbors. They do this by producing N-acyl homoserine lactones (AHLs), which can diffuse back into the bacteria at high concentrations. In the cell they bind to receiver proteins, which then activate gene expression in a coordinated manner. There are many natural QS systems, but only four in popular use by synthetic biologists. Some of these systems use AHLs that can activate multiple receiver systems or "crosstalk" between networks. This can cause problems when using QS in higher level designs. Our project aims to characterize a variety of AHL networks, increasing the number of functional QS systems with minimal crosstalk in synthetic biology.


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