Team:Chiba/Project
From 2009.igem.org
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LuxR proteins, the AHL-LuxR complex activates the Lux promoter. The | LuxR proteins, the AHL-LuxR complex activates the Lux promoter. The | ||
threshold [AHL] at which switching occurs is determined by the | threshold [AHL] at which switching occurs is determined by the | ||
- | affinity of AHL for the particulr LuxR ortholog | + | affinity of AHL for the particulr LuxR ortholog. |
[[Team:Chiba/Project/Quorum_Sensing|(more about quorum sensing)]] | [[Team:Chiba/Project/Quorum_Sensing|(more about quorum sensing)]] | ||
Revision as of 07:59, 2 September 2009
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AbstractIntroductionProject DesignSignaling SystemIn this project, we use acylated homoserine lactones (AHLs), signaling molecules used for quorum sensing in gram negative bacteria. Senders express LuxI or similar enzymes, which catalyze the production of AHLs, under the control of a constitutive (Tet) promoter. Each cell thus generates AHL more or less at a constant rate. AHL can freely permeate cell membranes and are detected by neighboring cells. Receivers constitutively express LuxR proteins (or a similar ortholog), the protein that detects AHL concentrations. When AHLs bind LuxR proteins, the AHL-LuxR complex activates the Lux promoter. The threshold [AHL] at which switching occurs is determined by the affinity of AHL for the particulr LuxR ortholog. (more about quorum sensing) 1, parallel communication2, Series communicationConclusions |