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Team:Wageningen UR/Project/IntroductionProj1
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=== Abstract === | === Abstract === | ||
| - | One aim of synthetic biology is to re-engineer naturally occurring gene circuits to produce artificial systems that behave predictably. Our project involved providing additional functionality and also streamlining a recently published synchronized oscillatory circuit in an attempt to reproduce and further characterize its dynamics. Our genetic circuit consists of modified (and BioBricked) elements of the Vibrio fischeri lux quorum sensing system composed to form interconnected positive and negative feedback loops, which dynamically regulate the expression of GFP. In order to provide our ''E. coli'' host with the right environment required for population-wide oscillations, we designed and manufactured a custom flow-chamber capable of maintaining a defined cell population while independently varying the growth conditions. The chamber was specifically designed for time-lapse studies with a fluorescence microscope. We detected synchronized oscillatory gene expression under zero-flow conditions, suggesting an unexpected level of robustness. This should facilitate its integration with more advanced genetic circuits. | + | One aim of synthetic biology is to re-engineer naturally occurring gene circuits to produce artificial systems that behave predictably. Our project involved providing additional functionality and also streamlining a recently published synchronized oscillatory circuit in an attempt to reproduce and further characterize its dynamics. Our genetic circuit consists of modified (and BioBricked) elements of the ''Vibrio fischeri'' lux quorum sensing system composed to form interconnected positive and negative feedback loops, which dynamically regulate the expression of GFP. In order to provide our ''E. coli'' host with the right environment required for population-wide oscillations, we designed and manufactured a custom flow-chamber capable of maintaining a defined cell population while independently varying the growth conditions. The chamber was specifically designed for time-lapse studies with a fluorescence microscope. We detected synchronized oscillatory gene expression under zero-flow conditions, suggesting an unexpected level of robustness. This should facilitate its integration with more advanced genetic circuits. |
[[Team:Wageningen_UR/Project/CompleteProject1Description| Read more]] | [[Team:Wageningen_UR/Project/CompleteProject1Description| Read more]] | ||
Revision as of 21:43, 20 September 2011
