Difference between revisions of "Part:BBa K649101:Experience"
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===Applications of BBa_K649101===
 
===Applications of BBa_K649101===
  
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To confirm LsrR represses lsrA promoter, we constructed BBa_K649105. If you want to see detailed infomation, please click [https://parts.igem.org/Part:BBa_K649105:Experience here].
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To confirm LsrR represses lsrA promoter, we constructed BBa_K649105.
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We characterized BBa_K649105 in <i>E.coli</i> MG1655.
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[[Image:LsrRBA.png|thumb|center|500px|Fluorescence intensity is decreased by LsrR repression.<br>This work is done by Hiroki Yoshise.]]
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We confirmed that LsrR represses lsrA promoter. We measured LsrR repression activity by using a plasmid (BBa_K649105) which have a <i>lsrR</i> gene downstream of lsrA promoter-<i>gfp</i>.By the LsrR repression, the fluorescence intensity decreased 3-fold. This result shows that LsrR successfully repressed lsrA promoter. The working part we created allow the use of AI-2 as a signaling molecule, which is a very powerful tool to build complex Synthetic Biology systems.
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[Sample]
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Ptet-<i>gfp</i> on pSB6A1(JM2.300)(positive control)
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Promoterless-<i>gfp</i> on pSB6A1(JM2.300)(negative control)
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PlsrA-<i>gfp</i> on pSB3K3(MG1655)
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PlsrA-<i>gfp</i>-PlsrR-<i>lsrR</i> on pSB3K3(MG1655)
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[Method]
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1. Overnight cultures of reporter strains grown at 37&deg;C in LB medium containing appropriate antibiotics were diluted 1:100 into 3 ml of LB medium and were incubated at 37&deg;C as fresh cultures.
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2. After their OD590 reached 0.15, the fresh cultures were diluted 1:10.
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3. After 4-hour incubation at 37&deg;C, 1 ml of each culture was moved to 1.6ml tube and its fluorescence intensity was measured with a flow cytometer.
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[[Image:lsrO.png|thumb|center|500px|After four hours from OD590 reaching 0.15, we measured OD.<br>This work is done by Hiroki Yoshise.]]
  
 
===User Reviews===
 
===User Reviews===

Latest revision as of 15:12, 28 October 2011

Applications of BBa_K649101

To confirm LsrR represses lsrA promoter, we constructed BBa_K649105.

We characterized BBa_K649105 in E.coli MG1655.

Fluorescence intensity is decreased by LsrR repression.
This work is done by Hiroki Yoshise.


We confirmed that LsrR represses lsrA promoter. We measured LsrR repression activity by using a plasmid (BBa_K649105) which have a lsrR gene downstream of lsrA promoter-gfp.By the LsrR repression, the fluorescence intensity decreased 3-fold. This result shows that LsrR successfully repressed lsrA promoter. The working part we created allow the use of AI-2 as a signaling molecule, which is a very powerful tool to build complex Synthetic Biology systems.


[Sample]

Ptet-gfp on pSB6A1(JM2.300)(positive control)

Promoterless-gfp on pSB6A1(JM2.300)(negative control)

PlsrA-gfp on pSB3K3(MG1655)

PlsrA-gfp-PlsrR-lsrR on pSB3K3(MG1655)

[Method]

1. Overnight cultures of reporter strains grown at 37°C in LB medium containing appropriate antibiotics were diluted 1:100 into 3 ml of LB medium and were incubated at 37°C as fresh cultures.


2. After their OD590 reached 0.15, the fresh cultures were diluted 1:10.


3. After 4-hour incubation at 37°C, 1 ml of each culture was moved to 1.6ml tube and its fluorescence intensity was measured with a flow cytometer.

After four hours from OD590 reaching 0.15, we measured OD.
This work is done by Hiroki Yoshise.

User Reviews

UNIQ82575f25823ad80c-partinfo-00000000-QINU UNIQ82575f25823ad80c-partinfo-00000001-QINU