Difference between revisions of "Part:BBa K3520019"
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==Type IIS assembly design== | ==Type IIS assembly design== | ||
− | [[File:T--Athens--Level_1_design.png|800px|thumb|center|Figure | + | [[File:T--Athens--Level_1_design.png|800px|thumb|center|Figure 2: Type IIS for level 1 Golden Gate assembly with SapI.]] |
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+ | ==Gene circuitry== | ||
+ | |||
+ | [[File:T--Athens--bc_gene_circuit.png|800px|thumb|center|Figure 3: The interactions regulating the production of bacterial cellulose under the bcs operon.]] | ||
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+ | ==Athens 2020== | ||
+ | <br> | ||
+ | |||
+ | The current part is designed by iGEM Athens 2020 team during the project MORPHÆ. In this project, Flavobacteria were used to produce a non-cellular structurally coloured biomaterial which would require the secretion of a biomolecule that Flavobacteria 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. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K3520019 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3520019 SequenceAndFeatures</partinfo> |
Latest revision as of 03:43, 28 October 2020
pHimarEm1+TUs of BcsA,B,C,D
Usage and Biology
The pMORPHÆ plasmid, consists of the pHimarEm1 vector (BBa_K3520009) containing the transcriptional units of the bcs operon’s genes (A. xylinous). More specifically, this composite vector was designed in order to permanently insert these genes into the Flavobacterium’s genome, as to produce cellulose. This plasmid was made by connecting the parts BBa_K3520013, BBa_K3520014, BBa_K3520015, BBa_K3520016, designed by iGEM Athens.
Plasmid map
The present plasmid is used to insert the Bcs operon genes (X54676.1) to a bacterium of the Flavobacterium genus through conjugation using an Escherichia coli strain for conjugation. Each gene has its own transcriptional unit that will allow their constitutive expression. These genes will all intergrated into the genome of the target Flavobacterium with the help of the Mariner transposon and then the Cellulose is produced by the recombinant bacteria.
Type IIS assembly design
Gene circuitry
Athens 2020
The current part is designed by iGEM Athens 2020 team during the project MORPHÆ. In this project, Flavobacteria were used to produce a non-cellular structurally coloured biomaterial which would require the secretion of a biomolecule that Flavobacteria 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.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 16429
Illegal suffix found in sequence at 9767 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 16429
Illegal NheI site found at 10096
Illegal SpeI site found at 9768
Illegal PstI site found at 9782
Illegal NotI site found at 9775
Illegal NotI site found at 16435 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 16429
Illegal BglII site found at 10418
Illegal BglII site found at 12957
Illegal BglII site found at 13616
Illegal XhoI site found at 10053
Illegal XhoI site found at 13254 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 16429
Illegal suffix found in sequence at 9768 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 16429
Illegal XbaI site found at 16444
Illegal SpeI site found at 9768
Illegal PstI site found at 9782
Illegal NgoMIV site found at 11082
Illegal AgeI site found at 12649 - 1000COMPATIBLE WITH RFC[1000]