Team:Tokyo Tech/Projects/RPS-game/assay
From 2011.igem.org
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<li><a href="#2.2.">2.2. Method</a></li> | <li><a href="#2.2.">2.2. Method</a></li> | ||
<li><a href="#2.3.">2.3. Result</a></li> | <li><a href="#2.3.">2.3. Result</a></li> | ||
+ | </ul> | ||
+ | <a href="#3.">3. New lasI promoter activity</a> | ||
+ | <ul> | ||
+ | <li><a href="#3.1.">3.1. Sample</a></li> | ||
+ | <li><a href="#3.2.">3.2. Method</a></li> | ||
+ | <li><a href="#3.3.">3.3. Result</a></li> | ||
</ul> | </ul> | ||
</li> | </li> | ||
Line 369: | Line 375: | ||
<h3 id="2.3.">2.3. Result</h3> | <h3 id="2.3.">2.3. Result</h3> | ||
<img src="https://static.igem.org/mediawiki/2011/6/60/LasR_repression.png" alt="LasR repression" width="500px" align="center" /> | <img src="https://static.igem.org/mediawiki/2011/6/60/LasR_repression.png" alt="LasR repression" width="500px" align="center" /> | ||
+ | <h2 id="3.">3. New lasI promoter activity</h2> | ||
+ | |||
+ | <h3 id="3.1.">3.1. Sample</h3> | ||
+ | <p> | ||
+ | <ul> | ||
+ | <li>Ptrc-rbs-lasR-TT on pBR / PlasI(BBa_I649000)-rbs-gfp-TT on pSB3K3</li> | ||
+ | <li>Ptrc-rbs-lasR-TT on pBR / promoterless-rbs-gfp-TT on pSB3K3 (negative control)</li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | <h3 id="3.2.">3.2. Method</h3> | ||
+ | <p> | ||
+ | <ol> | ||
+ | <li>Overnight cultures of sample strain grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:100 in the medium, and overnight cultures of promoterless negative control strain grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:200 in the medium , and then they were incubated at 37 °C as fresh cultures.</li> | ||
+ | <li>After their OD600 reached 0.2, we added 3 µL of 500 µM 3O-C12-HSL (3OC12-HSL+) or 3µL of DMSO (3OC12-HSL-) into the fresh cultures.</li> | ||
+ | <li>After 3-hour incubation at 37 °C (OD reached approximately 1.80.), 0.25 mL of each culture was harvested by centrifugalization and suspended by adding 1 mL of PBS (phosphate-buffered saline).</li> | ||
+ | <li>We dispensed 500 µL of each suspension into a disposable tube through a cell strainer, and its fluorescence intensity was measured with a flow cytometer of Becton, Dickinson and Company.</li> | ||
+ | </ol> | ||
+ | </p> | ||
+ | <h3 id="3.3.">3.3. Result</h3> | ||
+ | <img src="https://static.igem.org/mediawiki/2011/2/24/BBa_K649001_graph3.png" alt="LasR repression" width="500px" align="center" /> | ||
<!-- ############ End of main contents ############ --> | <!-- ############ End of main contents ############ --> |
Revision as of 10:56, 4 October 2011
RPS detailed method and result
1. Previous lasI promoter activity
1.1. Sample
- PlasI(BBa_J64010)-rbs-gfp-TT on pSB3K3 / Ptrc-rbs-lasR-TT on pBR
- promoterless-gfp on pSB3K3 / Ptrc-rbs-lasR-TT-PlasI-rbs-cI-TT on pBR (negative control)
1.2. Method
- Overnight culture of sample strain grown at 37 °C in LB medium containing carbenicillin and kanamycin, and overnight culture of promoterless negative control grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:300 in the medium, and then they were incubated at 37 °C as fresh cultures.
- After their OD600 reached 0.2, we added 3 µL of 500 µM 3O-C12-HSL (3OC12-HSL+) or 3µL of DMSO (3OC12-HSL-) into the fresh cultures.
- After 3-hour incubation at 37 °C (OD approximately reached 1.50.), 0.25 mL of each culture was harvested by centrifugalization and suspended by adding 1 mL of PBS (phosphate-buffered saline).
- We dispensed 500 µL of each suspension into a disposable tube through a cell strainer, and its fluorescence intensity was measured with a flow cytometer of Becton, Dickinson and Company.
1.3. Result
2. LasR repression
2.1. Sample
- Ptrc-rbs-lasR-TT-PlasI-rbs-cI on pBR / Pλ-rbs-gfp on pAC
- Ptrc-rbs-lasR-TT on pBR / promoterless-rbs-gfp-TT on pSB3K3 (negative control)
2.2. Method
- Overnight culture of sample strain grown at 37 °C in LB medium containing carbenicillin and chloramphenicol were diluted 1:20 in the medium, and overnight culture of promoterless negatgive control grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:300 in the medium and then they were incubated at 37 °C as fresh cultures.
- After their OD600 reached 0.2, we added 3 µL of 500 µM 3O-C12-HSL (3OC12-HSL+) or 3µL of DMSO (3OC12-HSL-) into the fresh cultures.
- After 3-hour incubation at 37 °C (OD approximately reached 1.50.), 0.25 mL of each culture was harvested by centrifugalization and suspended by adding 1 mL of PBS (phosphate-buffered saline).
- We dispensed 500 µL of each suspension into a disposable tube through a cell strainer, and its fluorescence intensity was measured with a flow cytometer of Becton, Dickinson and Company.
2.3. Result
3. New lasI promoter activity
3.1. Sample
- Ptrc-rbs-lasR-TT on pBR / PlasI(BBa_I649000)-rbs-gfp-TT on pSB3K3
- Ptrc-rbs-lasR-TT on pBR / promoterless-rbs-gfp-TT on pSB3K3 (negative control)
3.2. Method
- Overnight cultures of sample strain grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:100 in the medium, and overnight cultures of promoterless negative control strain grown at 37 °C in LB medium containing carbenicillin and kanamycin were diluted 1:200 in the medium , and then they were incubated at 37 °C as fresh cultures.
- After their OD600 reached 0.2, we added 3 µL of 500 µM 3O-C12-HSL (3OC12-HSL+) or 3µL of DMSO (3OC12-HSL-) into the fresh cultures.
- After 3-hour incubation at 37 °C (OD reached approximately 1.80.), 0.25 mL of each culture was harvested by centrifugalization and suspended by adding 1 mL of PBS (phosphate-buffered saline).
- We dispensed 500 µL of each suspension into a disposable tube through a cell strainer, and its fluorescence intensity was measured with a flow cytometer of Becton, Dickinson and Company.