Team:Wageningen UR/Project/DevicesMeasuringOscillations

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(Customary fluidic device designed by Team Wageningen UR to measure oscillations)
(Customary fluidic device designed by Team Wageningen UR to measure oscillations)
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After letting the bacteria grow in this manner for 2-3 hours, the PBS was removed with the same syringe that was used to inoculate. The chamber was then let to dry out over night. The two pictures seen below show the micro-dish with a ptet-GFP strain growing in the wells directly before and after removal of the PBS.
After letting the bacteria grow in this manner for 2-3 hours, the PBS was removed with the same syringe that was used to inoculate. The chamber was then let to dry out over night. The two pictures seen below show the micro-dish with a ptet-GFP strain growing in the wells directly before and after removal of the PBS.
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[[File:ptetGFP_PBS.jpg|300px]][[File:ptetGFP_PBSremoved.jpg]]
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[[File:ptetGFP_PBS.jpg|400px]]   [[File:ptetGFP_PBSremoved.jpg|400px]]

Revision as of 12:33, 19 September 2011

Building a Synchronized Oscillatory System

Customary fluidic device designed by Team Wageningen UR to measure oscillations

Measuring oscillations

Measuring GFP WUR.jpg

By chance an oscillatory behaviour of transfomed E.coli containing the streamlined construct was observed in one of the experiments performed with a plate reader. This suggested oscillations could occur even without applying any flow over the wells. Letting the modeling tool iterate over a range of cell desities while keeping the flow rate constant at 0 confirmed that oscillations could occur at high cell densities. Therefore the measurements for oscillatory behaviour of the construct were taken without applying any flow.


For the experiments, an overnight culture of the cells containing the relevant construct was spun down and resuspended in PBS. The resuspended culture was inoculated in the device and left the cells where left in the chamber to settle down for a while. Since the bacteria were bottom fed with LB as seen in the set up section in figure X+2, only the bacteria which settled down in the wells survived, while the bacteria in PBS starved. This is shown in the short video below. The pictures were taken every ten minutes.

The video shows the micro-dish directly after inoculation, when the bacteria are still floating around everywhere in the chamber. After that the bacteria which are only in PBS start to die, whereas the bacteria in the wells survive.

After letting the bacteria grow in this manner for 2-3 hours, the PBS was removed with the same syringe that was used to inoculate. The chamber was then let to dry out over night. The two pictures seen below show the micro-dish with a ptet-GFP strain growing in the wells directly before and after removal of the PBS.

PtetGFP PBS.jpg PtetGFP PBSremoved.jpg


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