Difference between revisions of "Part:BBa K2505008"
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− | <span style="margin-left: 25px;">The gene(<i>traR</i>) generates the <i>A. Tumefaciens</i> TraR trans-activator. This part constitutively produces TraR, a reporter portion of Quorum Sensing signaling molecules ([N-]acyl-homoserine lactones, AHLs), 3OC8 HSL (hereafter C8). | + | <span style="margin-left: 25px;">The gene(<i>traR</i>) is derived from <i>A. Tumefaciens</i> and optimized for <i>E. coli</i> codon in reference to the codon usage. <i>traR</i> generates the <i>A. Tumefaciens</i> TraR trans-activator. This part constitutively produces TraR, a reporter portion of Quorum Sensing signaling molecules ([N-]acyl-homoserine lactones, AHLs), 3OC8 HSL (hereafter C8). |
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Revision as of 18:20, 29 October 2017
Ptet-rbs-traR-tt
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]
The gene(traR) is derived from A. Tumefaciens and optimized for E. coli codon in reference to the codon usage. traR generates the A. Tumefaciens TraR trans-activator. This part constitutively produces TraR, a reporter portion of Quorum Sensing signaling molecules ([N-]acyl-homoserine lactones, AHLs), 3OC8 HSL (hereafter C8).
Contents
Characterization
In our project, we use a kind of Quorum Sensing signaling molecules ([N-]acyl-homoserine lactones, AHLs), 3OC8 HSL (hereafter C8) as a signaling molecule of inter-kingdom communication from bacteria to human cells. Therefore, we searched the way to detect that C8 was synthesized by E. coli introduced C8 synthesis gene, traI. To evaluate Tra system (a kind of Quorum Sensing derived from Agrobacterium tumefaciens), our team constructed the plasmids that constitutively express TraR (C8 reporter protein) and, C8-TraR inducible promoter, Ptra and subsequence gfp.
Result
The results showed that the value of RFU of GFP / Turbidity of samples and that of negative controls were same. This indicated that GFP expression was not induced by TraR-C8 complex.
RFU of GFP / Turbidity of TraR Reporter Assay
Discussion
From the results, Tra reporter system did not work in E. coli even though the temperature conditions were changed. This is because the tra box where TraR-C8 complex binds upstream Ptra is essential to active transcription and the number of this region is not enough for non-A. tumefaciens creatures to activate transcription.
Material and Method
Plasmids
Sample A. Ptet – rbs – traR (pSB6A1) B. Ptra – rbs – gfp (pSB3K3)
Negative control C. pSB6A1 D. pSB3K3
Construction
Strain All the plasmids were prepared in DH5a strain.
Medium LB medium A: LB medium containing ampicillin (50 µg/ mL) and kanamycin (50 µg/ mL).
Assay Protocol
The following experiments are performed at 37˚C unless otherwise stated.
1. Prepare overnight cultures for each sample in 3 mL LB medium A at 37˚C with vigorous shaking.
2. Dilute the overnight cultures to 1 / 60 in fresh LB medium A (1.2 mL).
3. Incubate the fresh cultures for 1 h at 37˚C or 30˚C with vigorous shaking.
4. Add 80 mM C8 or DMSO to each 800 µL sample at the final concentration 20 µM.
5. Incubate the samples for 4 h at 37˚C or 30˚C with vigorous shaking.
6. Add 100 µL of the samples to each well of a plate reader.
7. Measure RFU of GFP at 490 nm as an excitation wavelength, 525 nm as an emission wavelength.
8. Measure the turbidity at 600 nm.