Difference between revisions of "Part:BBa K3634005:Design"

 
(→‎References)
 
(2 intermediate revisions by the same user not shown)
Line 7: Line 7:
  
 
===Design Notes===
 
===Design Notes===
−
Due to the two-phase nature of our project, the selected promoter and RBS used may be subject to change after wet lab application in 2021 to maximise shinorine production. Golden gate assembly methods will facilitate this optimisation if necessary. It may also be required to include more than one single promoter for adequate expression of NRPS compared to the other enzymes involved in the shinorine pathway. It is also worth noting that the third enzyme (ATPG) may be included on plasmid A with NRPS instead of on plasmid B such that mycosporine glycine, which also absorbs UV radiation to a certain degree, is not produced in a bacteria which by chance has taken up plasmid B and would thereafter exploit UV resistance to confer a survival advantage in the environment.
+
Due to the two-phase nature of our project, the selected promoter and RBS used may be subject to change after wet lab application in 2021 to maximise shinorine production. Golden gate assembly methods will facilitate this optimisation if necessary. It may also be required to include more than one single promoter for adequate expression of NRPS compared to the other enzymes involved in the shinorine pathway.
−
 
+
−
 
+
  
 
===Source===
 
===Source===
Line 16: Line 14:
  
 
===References===
 
===References===
 +
 +
Minnesota iGEM 2012 - https://parts.igem.org/Part:BBa_K814001
 +
 +
Minnesota iGEM 2012 - https://parts.igem.org/Part:BBa_K814003
 +
 +
Balskus, E.P, Walsh, C.T. 2010. The Genetic and Molecular Basis for Sunscreen Biosynthesis in Cyanobacteria. Science. 329 (5999): p1653-1656. DOI: 10.1126/science.1193637

Latest revision as of 10:57, 3 September 2020


ATPG and NRPS Composite (E.coli Optimised)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 1561
    Illegal NheI site found at 1584
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2059
    Illegal BamHI site found at 4112
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

Due to the two-phase nature of our project, the selected promoter and RBS used may be subject to change after wet lab application in 2021 to maximise shinorine production. Golden gate assembly methods will facilitate this optimisation if necessary. It may also be required to include more than one single promoter for adequate expression of NRPS compared to the other enzymes involved in the shinorine pathway.

Source

The initial genomic sequence came from Anabaena variabilis ATCC 29413 which can be obtained from part K8140003 (Minnesota iGEM, 2012) before being optimised using the IDT optimisation tool. The promoter and RBS were selected from each respective Anderson catalogue based on their relative strength. The terminator BBa_B0015 sequence can also be taken from the iGEM registry.

References

Minnesota iGEM 2012 - https://parts.igem.org/Part:BBa_K814001

Minnesota iGEM 2012 - https://parts.igem.org/Part:BBa_K814003

Balskus, E.P, Walsh, C.T. 2010. The Genetic and Molecular Basis for Sunscreen Biosynthesis in Cyanobacteria. Science. 329 (5999): p1653-1656. DOI: 10.1126/science.1193637