Difference between revisions of "Part:BBa K2315034"
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When AHL is added with concentration higher than a critical value, the constitutively expressed LasR will bind to the AHL molecule 3OC12-HSL, dimerize and bind to the pLas regulatory sequence to activate GFP expression. | When AHL is added with concentration higher than a critical value, the constitutively expressed LasR will bind to the AHL molecule 3OC12-HSL, dimerize and bind to the pLas regulatory sequence to activate GFP expression. | ||
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==<b>Fluorescent Response to cognate 3OC12-HSL</b>== | ==<b>Fluorescent Response to cognate 3OC12-HSL</b>== |
Latest revision as of 21:52, 1 November 2017
LasR-pLas-GFP HSL inducible fluorescent actuator
Group: Shanghaitech iGEM 2017
The AHL receiver LasR from P.aeruginosa activates expression of GFP protein in response to 3OC12-HSL.
This Receiver can be easily replaced by other AHL receivers in our collection. A full collection could be found in: http://2017.igem.org/Team:Shanghaitech/Library
Usage and Biology
When AHL is added with concentration higher than a critical value, the constitutively expressed LasR will bind to the AHL molecule 3OC12-HSL, dimerize and bind to the pLas regulatory sequence to activate GFP expression.
Fluorescent Response to cognate 3OC12-HSL
To test this part, we used standard 3OC12HSL (HSL produced by LasI in P.aeruginosa) to determine the response curve.
Orthogonality test against non-cognate inducers
We have characterized crosstalk response of LasR to several non-cognate AHLs:
Furthermore, we test it under fluorescence microscope. Fig. 3 shows four testing samples.
It has shown that LasR is sensitive to it's cognate HSL and has obvious crosstalk with 3OC8-HSL in Tra System in relatively high concentration.
Usages in our Project
We developed a measurement protocol using the fluorescent protein coupled AHL receiver germs to measure the actual AHLs concentration in high precision and sensitivity in compared with LC-MS.
AHL receiver from P.aeruginosa, actives expression of GFP protein.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30
Illegal NheI site found at 979 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 375
Illegal AgeI site found at 572 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1740