Difference between revisions of "Part:BBa K3520020"

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This part was designed during the Partnership of iGEM Athens 2020 and iGEM KU Istanbul 2020.
 
This part was designed during the Partnership of iGEM Athens 2020 and iGEM KU Istanbul 2020.
 
The latter team is creating a communication scheme between humans and biological cells by morphing cells into lasers. With this technology, they will be able to detect changes inside and around cells and tissues. These cell lasers can be employed in diagnostics and therapeutic purposes alongside as a high throughput method in basic research.
 
The latter team is creating a communication scheme between humans and biological cells by morphing cells into lasers. With this technology, they will be able to detect changes inside and around cells and tissues. These cell lasers can be employed in diagnostics and therapeutic purposes alongside as a high throughput method in basic research.
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==iGEM Athens 2020==
 
==iGEM Athens 2020==

Latest revision as of 03:43, 28 October 2020


bcsA-Bacterial Cellulose Synthase A


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]



This composite parts is assembled with TYPEIIS Assembly and it consists of the following subparts:

Promoter ompA + RBS + GFP superfolder codon optimised for Flavobacteriia + Double Terminator


iGEM KU Istanbul 2020



This part was designed during the Partnership of iGEM Athens 2020 and iGEM KU Istanbul 2020. The latter team is creating a communication scheme between humans and biological cells by morphing cells into lasers. With this technology, they will be able to detect changes inside and around cells and tissues. These cell lasers can be employed in diagnostics and therapeutic purposes alongside as a high throughput method in basic research.

iGEM Athens 2020



iGEM Athens 2020 team during the project MORPHÆ works with Flavobacteriia to produce a non-cellular structurally coloured biomaterial that will require the secretion of a biomolecule that Flavobacteriia do not normally secrete. Our hypothesis is that the formed matrix will have a structure similar to that of the biofilm and thus, it will provide the material with macroscopically the same colouration properties as the biofilm.

So these two teams above, collaborated in a creative way and iGEM Athens designed a cloning experiment in which Flavobacteriia will express reflectin with a signal peptide which will translocate it to the outer membrane and GFP superfolder. As a result, the biolaser designed by iGEM KU Istanbul will be able to track genetically modified Flavobacteriia.