Difference between revisions of "Part:BBa K3262000"
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+ | == Characterization of RFP and TAL (2019 SNU_India) == | ||
+ | <html> | ||
+ | <center> | ||
+ | <p> | ||
+ | <div style="text-align:justify;"> Following the cloning, we checked for the expression of both RFP and p-coumaric acid in bacteria. RFP was visualized by fluorescence microscopy following IPTG (0.5mM) induction for 4 hrs (Figure 8) and p-coumaric acid (Figure 9a-d) production was probed in filtered culture supernatant by mass spectrometry (Agilent Technologies 6540 UHD-Accurate Mass Q-TOF LC/MS in negative mode using methanol as solvent) | ||
+ | </div></p> | ||
+ | <p> | ||
+ | <img style="vertical-align: bottom;)" width=60% src="https://static.igem.org/mediawiki/parts/d/d4/T--SNU_India--TRT_RFP.png"> | ||
+ | </center> | ||
+ | <div style="text-align:justify;"> Figure 8: DIC and Fluorescence image of RFP expression in bacteria after induction with IPTG for 4 hrs. | ||
+ | </div></p> | ||
+ | <p> | ||
+ | <p> | ||
+ | <img style="vertical-align: bottom;)" width=60% src=" https://static.igem.org/mediawiki/parts/f/f8/T--SNU_India--TRT_RFP_Intensity.png | ||
+ | "> | ||
+ | </center> | ||
+ | <p> | ||
+ | <img style="vertical-align: bottom;)" width=60% src=" https://static.igem.org/mediawiki/parts/b/be/T--SNU_India--TRT_MS1.png"> | ||
+ | </center> | ||
+ | |||
+ | </center> | ||
+ | <div style="text-align:justify;"> Mass spectra of 1) Pure p-coumaric acid in methanol and 2) mass spectra of Induced culture supernatant | ||
+ | </div></p> | ||
+ | |||
+ | <p | ||
+ | <img style="vertical-align: bottom;)" width=60% src=" https://static.igem.org/mediawiki/parts/4/45/T--SNU_India--TRT_MS2.png"> | ||
+ | </center> | ||
+ | |||
+ | </center> | ||
+ | <div style="text-align:justify;"> Reference: | ||
+ | Schindelin, J.; Arganda-Carreras, I. & Frise, E. et al. (2012), "Fiji: an open-source platform for biological-image analysis", Nature methods 9(7): 676-682, PMID 22743772, doi:10.1038/nmeth.2019 | ||
+ | |||
+ | </center> | ||
+ | <div style="text-align:justify;"> For detailed results: https://2019.igem.org/Team:SNU_India/Experiments | ||
+ | </div></p> | ||
+ | |||
+ | |||
+ | </div></p> | ||
+ | </html> |
Latest revision as of 03:45, 22 October 2019
pT7+RFP+TAL
Tyrosine Ammonia Lyase with RFP under T7 promoter
Sequence and Features
Assembly Compatibility:
- 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 797
Illegal NgoMIV site found at 1629
Illegal AgeI site found at 593
Illegal AgeI site found at 705
Illegal AgeI site found at 892
Illegal AgeI site found at 1058 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2087
Characterization of RFP and TAL (2019 SNU_India)
Following the cloning, we checked for the expression of both RFP and p-coumaric acid in bacteria. RFP was visualized by fluorescence microscopy following IPTG (0.5mM) induction for 4 hrs (Figure 8) and p-coumaric acid (Figure 9a-d) production was probed in filtered culture supernatant by mass spectrometry (Agilent Technologies 6540 UHD-Accurate Mass Q-TOF LC/MS in negative mode using methanol as solvent)
Figure 8: DIC and Fluorescence image of RFP expression in bacteria after induction with IPTG for 4 hrs.
Mass spectra of 1) Pure p-coumaric acid in methanol and 2) mass spectra of Induced culture supernatant
Reference:
Schindelin, J.; Arganda-Carreras, I. & Frise, E. et al. (2012), "Fiji: an open-source platform for biological-image analysis", Nature methods 9(7): 676-682, PMID 22743772, doi:10.1038/nmeth.2019
For detailed results: https://2019.igem.org/Team:SNU_India/Experiments