Difference between revisions of "Part:BBa K1216007"
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<b>Comparison of the pLuxR variant and pLuxR Wild-Type dose response to OHHL in liquid culture and on agar plates</b> | <b>Comparison of the pLuxR variant and pLuxR Wild-Type dose response to OHHL in liquid culture and on agar plates</b> | ||
− | [[File:facscomparisonliquid.jpg|400px|left|thumb|<b>Figure 4.</b>For the awild type we got :EC50=0.02nM, R2=0.84, n=1.7<br>For the pLuxR variant we got :EC50=6482nM, R2=0.97, n=0.8;]] | + | [[File:facscomparisonplate.jpg|400px|left|thumb|<b>Figure 5. Comparison of the sensivity of the wild type promoter and the mutated PluxR1 promoter on agar plates</b>For the wild type we got :EC50=4.45nM, R2=0.80, n=1.7<br>For the pLuxR variant we got :EC50=17814nM, R2=0.93, n=0.8]] |
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+ | [[File:facscomparisonliquid.jpg|400px|left|thumb|<b>Figure 4. Comparison of the sensivity of the wild type promoter and the mutated PluxR1 promoter in liquid culture</b>For the awild type we got :EC50=0.02nM, R2=0.84, n=1.7<br>For the pLuxR variant we got :EC50=6482nM, R2=0.97, n=0.8;]] | ||
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Revision as of 07:46, 4 October 2013
Variant of the wild-type pLuxR promoter with lower sensitivity
BBa_K1216007 is a variant of the wild-type pLuxR promoter with a lowered sensitivity for LuxR-AHL.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Site directed mutagenesis of the BBa_R0062 pLuxR wild type promoter to obtain the pLuxR variant BBa_K2126007
Our goal was to achieve mutations in the luxbox of the pLuxR BBa_R0062 promoter to shift the dose response curve of the promoter depending on the OHHL (3-oxo-hexanoyl-l-homoserine-l-lactone) concentration.
We did site directed mutagenisis of specific sites of the luxbox according to the results of the literature ()
We mutated the promoter directly in the J09855 construct and added a GFP reporter to be able to screen for differences in the dose response curves. In the end we isolate one mutated promoter which shows a 300'000 fold shift in sensivity. For more details see : Characterization of the pLuxR variant dose response to OHHL using plate reader analysis and FACS single cell analysis
Characterization of the pLuxR variant dose response to OHHL using plate reader analysis and FACS single cell analysis
Characterization and comparison to the wild type pLuxR using the plate reader analysis
The GFP reporter allows us to make fluorescence measurement in plate reader experiments as well as in single cell analysis to characterize the promoter behavior depending on [OHHL], by recording the fluorescence [au]. According to literature (Geske G.D. Evaluation of a focused library of N-aryl L-homoserine lactones reveals a new set of potent quorum sensing modulators) we could define the first experimental OHHL ranges to induce the promoter. After some fine tunning and adjusting experiment we could narrow down the ranges to obtain a dose response curve in a reasonable resolution for the BBa_R0062 wild type promoter to the OHHL (3-oxo-hexanoyl-l-homoserine-lactone) concentration. See Figure 1. This datas were obtained from plate reader experiment. Accordnig to the sensivity range of the wild type promoter we could screen for promoters, and scan the potentially shifted variants in different ranges of [OHHL]. We finally isolate one promoter variant which shows a shift compared to the wild type. See G1 on Figure 1.
Characterization of the pLuxR dose response to OHHL in liquid culture and on agar plates by FACS single cell analysis
Comparison of the pLuxR variant and pLuxR Wild-Type dose response to OHHL in liquid culture and on agar plates