Difference between revisions of "Part:BBa K3777029"
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<b><font size="3">Usage and Biology</font></b> | <b><font size="3">Usage and Biology</font></b> | ||
<br>Compared to our another part BBa_K3777028,this part add a gene called mphA, which can improve the detection limit of erythromycin | <br>Compared to our another part BBa_K3777028,this part add a gene called mphA, which can improve the detection limit of erythromycin | ||
| + | <br>According to the paper we reference,it is said that trapping erythromycin within Escherichia coli through phosphorylation increases the sensitivity of its biosensor (MphR) by approximately 10-fold. | ||
https://static.igem.org/mediawiki/parts/thumb/2/22/LuxR-Plux-dCas9-mphA.PNG/798px-LuxR-Plux-dCas9-mphA.PNG | https://static.igem.org/mediawiki/parts/thumb/2/22/LuxR-Plux-dCas9-mphA.PNG/798px-LuxR-Plux-dCas9-mphA.PNG | ||
<br> | <br> | ||
Revision as of 18:03, 21 October 2021
luxR-Plux-dCas9-mphA
A biosensor device that can improve the detection limit of erythromycin.
Usage and Biology
Compared to our another part BBa_K3777028,this part add a gene called mphA, which can improve the detection limit of erythromycin
According to the paper we reference,it is said that trapping erythromycin within Escherichia coli through phosphorylation increases the sensitivity of its biosensor (MphR) by approximately 10-fold.
Referernce:Miller Corwin A,Ho Joanne M,Parks Sydney E,Bennett Matthew R. Macrolide Biosensor Optimization through Cellular Substrate Sequestration.[J]. ACS synthetic biology,2021,10(2)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 2204
Illegal NheI site found at 5364
Illegal NheI site found at 5387 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 4483
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 5951
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 1022