Difference between revisions of "Part:BBa K5508008"
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K5508008 SequenceAndFeatures</partinfo> | <partinfo>BBa_K5508008 SequenceAndFeatures</partinfo> | ||
+ | ==Results== | ||
+ | ===(1)Plasmid Construction=== | ||
+ | The target gene mCherry was amplified with HsLF-mCherry-F(CACCATCACCACCACTAATAAAAGCTTatggtgagcaagggcgaggag) and HsLF-mCherry-R(GGATCTTAGCTAGCCGCGGTACCttacttgtacagctcgtccatg), and the BBa_K5508000 vector was digested with Hind3 and Kpn1, followed by Gibson assembly. | ||
+ | <html> | ||
+ | <style> | ||
+ | .bild {max-width: 35% ; height: auto;} | ||
+ | </style> | ||
+ | <p> | ||
+ | <img class="bild" src="https://static.igem.wiki/teams/5508/hangzhoumedx-parts/29.png"> | ||
+ | <div class="unterschrift"><b> Electrophoretic detection of PCR results</b> | ||
+ | </div> | ||
+ | </p> | ||
+ | </html> | ||
+ | |||
+ | <html> | ||
+ | <style> | ||
+ | .bild {max-width: 35% ; height: auto;} | ||
+ | </style> | ||
+ | <p> | ||
+ | <img class="bild" src="https://static.igem.wiki/teams/5508/hangzhoumedx-parts/30.png"> | ||
+ | <div class="unterschrift"><b>Results of E. coli plasmid transformation</b> | ||
+ | </div> | ||
+ | </p> | ||
+ | </html> | ||
+ | |||
+ | <html> | ||
+ | <style> | ||
+ | .bild {max-width: 35% ; height: auto;} | ||
+ | </style> | ||
+ | <p> | ||
+ | <img class="bild" src="https://static.igem.wiki/teams/5508/hangzhoumedx-parts/31.png"> | ||
+ | <div class="unterschrift"><b>Sequencing results</b> | ||
+ | </div> | ||
+ | </p> | ||
+ | </html> | ||
+ | |||
+ | ===(2)Fluorescence detection=== | ||
+ | After the correctness of the recombinant plasmid was verified, it was transferred into BY4741 for culture. After 48 hours of adding the inducer galactose, the results are shown. | ||
+ | <html> | ||
+ | <style> | ||
+ | .bild {max-width: 35% ; height: auto;} | ||
+ | </style> | ||
+ | <p> | ||
+ | <img class="bild" src="https://static.igem.wiki/teams/5508/hangzhoumedx-parts/32.png"> | ||
+ | <div class="unterschrift"><b>Results of plasmid transformation in Saccharomyces cerevisiae </b> | ||
+ | </div> | ||
+ | </p> | ||
+ | </html> | ||
+ | |||
+ | |||
+ | <html> | ||
+ | <style> | ||
+ | .bild {max-width: 35% ; height: auto;} | ||
+ | </style> | ||
+ | <p> | ||
+ | <img class="bild" src="https://static.igem.wiki/teams/5508/hangzhoumedx-parts/33.png"> | ||
+ | <div class="unterschrift"><b>Expression of fluorescent protein:The figure shows from left to right: negative control, negative control, pESC-mCherry, pESC-HsLF-mCherry </b> | ||
+ | </div> | ||
+ | </p> | ||
+ | </html> | ||
+ | |||
+ | It can be seen that after induction, the strain shows a pink colour when illuminated by UV light. However, this colour can only be seen after centrifugation of the collected bacteria and cannot be observed directly by the naked eye in the liquid. In particular, pESC-HsLF-mCherry/BY4741 was lighter in colour compared to pESC-mCherry/BY4741. This may be due to the expression of HsLF in Saccharomyces cerevisiae low. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Latest revision as of 21:07, 30 September 2024
Gal1,10-HsLF-mCherry-CYC1
We combined BBa_K4335004 with BBa_K5508001 to verify whether lactoferrin was successfully expressed.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 1833
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 1833
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2248
Illegal BglII site found at 2372
Illegal BglII site found at 3359 - 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 1833
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 1833
Illegal NgoMIV site found at 3215
Illegal AgeI site found at 1247 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 2712
Results
(1)Plasmid Construction
The target gene mCherry was amplified with HsLF-mCherry-F(CACCATCACCACCACTAATAAAAGCTTatggtgagcaagggcgaggag) and HsLF-mCherry-R(GGATCTTAGCTAGCCGCGGTACCttacttgtacagctcgtccatg), and the BBa_K5508000 vector was digested with Hind3 and Kpn1, followed by Gibson assembly.
(2)Fluorescence detection
After the correctness of the recombinant plasmid was verified, it was transferred into BY4741 for culture. After 48 hours of adding the inducer galactose, the results are shown.
It can be seen that after induction, the strain shows a pink colour when illuminated by UV light. However, this colour can only be seen after centrifugation of the collected bacteria and cannot be observed directly by the naked eye in the liquid. In particular, pESC-HsLF-mCherry/BY4741 was lighter in colour compared to pESC-mCherry/BY4741. This may be due to the expression of HsLF in Saccharomyces cerevisiae low.