Difference between revisions of "Part:BBa K553001"
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==Improvement and Characterization == | ==Improvement and Characterization == | ||
− | Group: <b>Tokyo Tech 2017</b> | + | Group: [http://2017.igem.org/Team:TokyoTech <b>Tokyo Tech 2017</b>] |
Author: Takuma Yasue | Author: Takuma Yasue | ||
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The result of C8 production using the wild type TraI and mutants is shown in Figure 6. | The result of C8 production using the wild type TraI and mutants is shown in Figure 6. | ||
The RFU value of the TraI (K34G)-expressing cells was approximately 3-fold higher than the TraI-expressing cells. Other mutant didn’t show improvement of 3OC8HSL production. When these RFU values were converted to 3OC8HSL concentrations using the calibration curve obtained in the reagent assay (see the TraI Assay), they were calculated as 28 nM and 42 nM, respectively. | The RFU value of the TraI (K34G)-expressing cells was approximately 3-fold higher than the TraI-expressing cells. Other mutant didn’t show improvement of 3OC8HSL production. When these RFU values were converted to 3OC8HSL concentrations using the calibration curve obtained in the reagent assay (see the TraI Assay), they were calculated as 28 nM and 42 nM, respectively. | ||
− | |||
+ | For more information, visit our page[http://2017.igem.org/Team:TokyoTech/Experiment/TraI_Improvement]. | ||
+ | <br style="clear: both" /> | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 06:35, 1 November 2017
A. tumefaciens TraI - OC8 HLA synthase
The Agrobacterium tumefaciens TraI synthase generates the OC8 HLA.
The gene is located on the Ti plasmid together with TraR (BBa_K553000), the other regulatory component of A. Tumefaciens quorum sensing.
Download Datasheet
Improvement and Characterization
Group: [http://2017.igem.org/Team:TokyoTech Tokyo Tech 2017]
Author: Takuma Yasue
Summary of Improvement and Characterization
We found that the wild type TraI(BBa_K553001) did not suit for our final circuits because enzyme activity was weak for our project. Thus, we constructed the improved TraI(BBa_K2505033) appropriate to our final circuits. Our purpose is to enhance the activity of TraI for our final genetic circuits.
Result
The result of C8 production using the wild type TraI and mutants is shown in Figure 6. The RFU value of the TraI (K34G)-expressing cells was approximately 3-fold higher than the TraI-expressing cells. Other mutant didn’t show improvement of 3OC8HSL production. When these RFU values were converted to 3OC8HSL concentrations using the calibration curve obtained in the reagent assay (see the TraI Assay), they were calculated as 28 nM and 42 nM, respectively.
For more information, visit our page[http://2017.igem.org/Team:TokyoTech/Experiment/TraI_Improvement].
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 385
- 1000COMPATIBLE WITH RFC[1000]