Difference between revisions of "Part:BBa K3745000"
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The following graph demonstrates the validity of this part. With higher rhamnose concentration, the concentration of the bacteria fluid tends to be greater, indicated by a high absorbance at OD600. The absorbance of culture with 0/20/40/60/80ul rhamnose added is measured every hour after liquid inoculation. | The following graph demonstrates the validity of this part. With higher rhamnose concentration, the concentration of the bacteria fluid tends to be greater, indicated by a high absorbance at OD600. The absorbance of culture with 0/20/40/60/80ul rhamnose added is measured every hour after liquid inoculation. | ||
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+ | <img src="https://2021.igem.org/wiki/images/a/ae/T--BNDS_China--Results_BBa_K3745000.png" width=700> | ||
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Revision as of 05:36, 21 October 2021
Prha-Amp
This part is a rhamnose-induced genetic circuit that contains a Rhamnose promoter, an RBS, an ORF of AmpR, and a terminator. It is improved from BBa_K1493501 by using Gibson assembly to replace the GFP with AmpR.
Usage and Biology
In our project, it is a vital part of the biosensor. After rhamnolipid is hydrolysis to rhamnose, rhamnose could induce this genetic circuit to express the ampicillin resistance gene. This mechanism increases the evolutionary fitness of the strains that have a high rhamnolipid yield (which means more rhamnose could be hydrolysis and induce the expression of AmpR) in culture with ampicillin and enables the strains with favorable mutations to be automatically selected.
Qualititive Characterization
The following graph demonstrates the validity of this part. With higher rhamnose concentration, the concentration of the bacteria fluid tends to be greater, indicated by a high absorbance at OD600. The absorbance of culture with 0/20/40/60/80ul rhamnose added is measured every hour after liquid inoculation.
<img src="" width=700>
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 869