Part:BBa_K233321:Design
Turing Machine - Unary Adder 2
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1982
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1982
Illegal NheI site found at 877
Illegal NheI site found at 900 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1982
Illegal BglII site found at 719 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1982
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1982
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 2731
Illegal BsaI.rc site found at 1855
Design Notes
This part is designed to respond to two chemical inputs 1) Lactose/ iptg 2) AHL (acyl homoserine lactone and its derivatives used in quorum sensing)
If cells containing this construct are placed in an environment containing lactose/ IPTG ONLY, the cells show no difference.
If the cells are placed in an environment containing AHL ONLY, they begin to produce their own AHL. This is acheived in the following manner. AHL binds to LuxR (which is constitutively produced). The AHL-LuxR complex, activates the promoter pLuxR. This initiates the transcription of the LuxI gene responsible for production of AHL. The reporter gene (Lysis Cassette) however is not transcribed since the repressor protein is bound to LacO binding site (downstream of the pLuxR promoter) in absence of Lactose. This prevents transcription of the reporter gene since RNA polymerase is unable to bind to the promoter.
In presence of BOTH AHL and Lactose. The reporter gene is ALSO activated along with the gene for AHL production. This causes cell lysis.
The construct if coded in a proper manner responds to chemical inputs AHL and Lactose, and behaves like a Turing Machine (Unary Adder).
Source
made from parts listed in the registry