Difference between revisions of "Part:BBa K3747201:Experience"
 
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[[File:T--Wageningen_UR--wetlab_1.png|thumb|center|<b>Figure 1</b> GFP is under control of the lux pR promoter which is activated by the luxR-AHL complex. LuxR is constitutively expressed. In this construct, no AHL is produced, so the lux pR promoter should only be induced when AHL is present in the medium. ]]
 
[[File:T--Wageningen_UR--wetlab_1.png|thumb|center|<b>Figure 1</b> GFP is under control of the lux pR promoter which is activated by the luxR-AHL complex. LuxR is constitutively expressed. In this construct, no AHL is produced, so the lux pR promoter should only be induced when AHL is present in the medium. ]]
  
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The results show that conditioned medium rich in AHL activates the production of GFP in the reporter strain. The positive control strain did not show increased production of GFP as it produces AHL itself. 
  
 
===Protocol plate reader experiments===
 
===Protocol plate reader experiments===

Latest revision as of 02:36, 22 October 2021


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Applications of BBa_K3747201

This biobrick can be used to make an AHL reporter strain. The strain produces LuxR which binds to AHL. Upon high cell densities, the concentration of AHL increases, activating the lux pR promoter. When activated, GFP is produced which can be measured using plate reader experiments.

Figure 1 GFP is under control of the lux pR promoter which is activated by the luxR-AHL complex. LuxR is constitutively expressed. In this construct, no AHL is produced, so the lux pR promoter should only be induced when AHL is present in the medium.

The results show that conditioned medium rich in AHL activates the production of GFP in the reporter strain. The positive control strain did not show increased production of GFP as it produces AHL itself.

Protocol plate reader experiments

Day 1:

  • Make a preculture of a AHL producing strain in LB.

Day 2:

  • Make precultures of the positive control (link naar biobrick PC-pR-GFP), reporter and wild type strain in LB.
  • Wash the preculture of day 1 in the media that will be used for the plate reader experiment and make a new preculture in that medium. As initially M9 media gave growth issues, we used 80% M9 (supplemented with 0.2% glucose) and 20% LB.

Day 3:

  • Spin off the preculture of the posivite control in 80% M9 medium and filtersterilze the supernatant. Spike the medium with 0.2% glucose. This conditioned medium (CM) is rich in AHL. Dilutions of the CM medium were made by adding fresh 80% M9 + 20% LB medium.
  • Wash the LB precultures of the positive control, reporter and wild type strain in 80% M9 + 20% LB medium.
  • A 96 wells plate was prepared with the three strains (inoculated with OD=0.5) in triplicates and with different dilutions of the CM. Blanks were used to correct the OD for background absorption. The fluorescence of the positive control and reporter strain was corrected by substracting the fluorescence of the wildtype strain.


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