Difference between revisions of "Part:BBa K1692024"
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<h2> References </h2>
 
<h2> References </h2>
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[1]. Waters, Christopher, and Bassler, Bonnie. "Quorum Sensing:Cell-to-Cell Communication in Bacteria." Annu. Rev. Cell Dev. Biol. 2005 (21): 319–46. Print.
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[1]. Waters, Christopher, and Bassler, Bonnie. "Quorum Sensing: Cell-to-Cell Communication in Bacteria." Annu. Rev. Cell Dev. Biol. 2005 (21): 319–46. Print.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 21:20, 22 September 2015

Autolysis

Note: Please click here if you're looking for the msA-cipA construct (BBa_K1692027)

We create an autolysis system based on the concept of quorum sensing. The idea of quorum sensing is that Gram-negative bacteria releases a special molecule known as [N-]acyl-homoserine lactones (AHL) that can bind to the luxR proteins. The complex formed from using 2 AHL molecules with 2 luxR proteins can then bind the luxpR promoter and activate any downstream gene [1]. Our construct combines the part from 2010 Tokyo NoKoGen (BBa_K317039) and our ptet-luxl generator construct (BBa_K1692023). The specific AHL molecule used is 3OC6HSL, which is found in V. fischer . Our goal is to be create an automatic means of self-lysis once the cells reach a certain cell density.

We successfully sequenced the construct and did some preliminary testing with the lysis device. The autolysis system can be used in many applications and one such application is combining autolysis with our designed P(3HB) part (BBa_K1692021) as a means of releasing plastic into the media without having to do extraction process.

References

[1]. Waters, Christopher, and Bassler, Bonnie. "Quorum Sensing: Cell-to-Cell Communication in Bacteria." Annu. Rev. Cell Dev. Biol. 2005 (21): 319–46. Print.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 875
    Illegal NheI site found at 898
    Illegal NheI site found at 3268
    Illegal NheI site found at 3291
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 717
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 2873
    Illegal AgeI site found at 2943
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1853
    Illegal SapI site found at 3524