Difference between revisions of "Part:BBa K3814075:Design"

 
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===Design Notes===
 
===Design Notes===
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n/a
 
  
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In USYD 2021's project, we have used recombineering to insert 5kb chunks of DNA into E. coli. The particular recombineering strategy we have employed in our design is the bacteriophage λ Red recombineering system, and we are inserting our gene clusters into the fliK gene.
 +
 +
- In a study by Juhas and Ajioka (2016), the fliK gene in the E. coli was shown to be an optimal location for recombineering, and 15kb was successfully inserted there in one iteration.
 +
- The bacteriophage λ Red recombineering system is described in the diagram below, and many strains of E. coli have these systems already in place (Sharan et al., 2009). We have decided to use the JM109 strain and the recombineering functions were going to be brought in by the pKD46 plasmid.
 +
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[[File:T--Sydney_Australia--recombineering.png|500x500px|Caption]]
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'''Figure 1.''' Recombineering system using the bacteriophage λ Red system. According to Sharan et al. (2009), the homology arms need to be only 50bp for successful recombination, Additionally, only three genes, gam, bet and exo, are involved. The gene product of gam “prevents an E. coli nuclease, RecBCD, from degrading linear DNA fragments”, which allows for linear DNA to survive in vivo for recombination. The roles of exo and bet are shown above, with the gene product of bet, Beta, being an “ssDNA binding protein” and exo having “5′ to 3′dsDNA exonuclease activity”.
 +
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We devised a strategy called '''Babushka Blocks'''. See below an images that showcase how the homology arm (red and purple) would help in inserting a section of DNA into the fliK gene:
 +
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[[File:T--Sydney_Australia--recombineering0.png|700px|Caption]]
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'''Figure 2.''' Babushka block design. To insert Cluster 1 into the fliK landing pad, Cluster 1 must be first hybridised with the primer, which contains the red homology arm (Step 1). Afterwards, there will be two matching homology arms between the landing pad and Cluster 1: the red and purple arms. As a result, Cluster 1 is able to be inserted into the landing pad, and the end result has the genes of interest inside the landing pad (Step 2).
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Clusters like Cluster 1 will be inserted, and the recombineered cells will be selected for using antibiotic resistance genes within each cluster. This will repeat until all eight clusters have been inserted.
  
  
 
===Source===
 
===Source===
  
−
n/a
+
iGEM USYD 2021
  
 
===References===
 
===References===
 +
 +
Juhas, M., & Ajioka, J. W. (2016). Lambda Red recombinase-mediated integration of the high molecular weight DNA into the Escherichia coli chromosome. Microbial Cell Factories, 15(1). https://doi.org/10.1186/s12934-016-0571-y
 +
 +
Sharan, S. K., Thomason, L. C., Kuznetsov, S. G., & Court, D. L. (2009). Recombineering: a homologous recombination-based method of genetic engineering. Nature Protocols, 4(2), 206–223. https://doi.org/10.1038/nprot.2008.227

Revision as of 00:39, 22 October 2021


Cluster 7


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 716
    Illegal NheI site found at 739
    Illegal NheI site found at 1970
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 2805
    Illegal XhoI site found at 75
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 420
    Illegal AgeI site found at 1106
    Illegal AgeI site found at 2271
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

In USYD 2021's project, we have used recombineering to insert 5kb chunks of DNA into E. coli. The particular recombineering strategy we have employed in our design is the bacteriophage λ Red recombineering system, and we are inserting our gene clusters into the fliK gene.

- In a study by Juhas and Ajioka (2016), the fliK gene in the E. coli was shown to be an optimal location for recombineering, and 15kb was successfully inserted there in one iteration. - The bacteriophage λ Red recombineering system is described in the diagram below, and many strains of E. coli have these systems already in place (Sharan et al., 2009). We have decided to use the JM109 strain and the recombineering functions were going to be brought in by the pKD46 plasmid.

Caption

Figure 1. Recombineering system using the bacteriophage λ Red system. According to Sharan et al. (2009), the homology arms need to be only 50bp for successful recombination, Additionally, only three genes, gam, bet and exo, are involved. The gene product of gam “prevents an E. coli nuclease, RecBCD, from degrading linear DNA fragments”, which allows for linear DNA to survive in vivo for recombination. The roles of exo and bet are shown above, with the gene product of bet, Beta, being an “ssDNA binding protein” and exo having “5′ to 3′dsDNA exonuclease activity”.

We devised a strategy called Babushka Blocks. See below an images that showcase how the homology arm (red and purple) would help in inserting a section of DNA into the fliK gene:

Caption

Figure 2. Babushka block design. To insert Cluster 1 into the fliK landing pad, Cluster 1 must be first hybridised with the primer, which contains the red homology arm (Step 1). Afterwards, there will be two matching homology arms between the landing pad and Cluster 1: the red and purple arms. As a result, Cluster 1 is able to be inserted into the landing pad, and the end result has the genes of interest inside the landing pad (Step 2).

Clusters like Cluster 1 will be inserted, and the recombineered cells will be selected for using antibiotic resistance genes within each cluster. This will repeat until all eight clusters have been inserted.


Source

iGEM USYD 2021

References

Juhas, M., & Ajioka, J. W. (2016). Lambda Red recombinase-mediated integration of the high molecular weight DNA into the Escherichia coli chromosome. Microbial Cell Factories, 15(1). https://doi.org/10.1186/s12934-016-0571-y

Sharan, S. K., Thomason, L. C., Kuznetsov, S. G., & Court, D. L. (2009). Recombineering: a homologous recombination-based method of genetic engineering. Nature Protocols, 4(2), 206–223. https://doi.org/10.1038/nprot.2008.227