Difference between revisions of "Part:BBa K2656016"

 
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Part BBa_K2656016 is the transcription factor LuxR coding sequence [https://parts.igem.org/Part:BBa_C0062 BBa_C0062] compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/Design GoldenBraid 3.0] assembly methods. It acts on the lux promoters when activated by Acyl-homoserine-lactone. It can be combined with other compatible parts from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the <html><a href="https://static.igem.org/mediawiki/parts/b/bc/T--Valencia_UPV--protocols.pdf#page=27"> Golden Gate assembly protocol </a></html>.
 
Part BBa_K2656016 is the transcription factor LuxR coding sequence [https://parts.igem.org/Part:BBa_C0062 BBa_C0062] compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/Design GoldenBraid 3.0] assembly methods. It acts on the lux promoters when activated by Acyl-homoserine-lactone. It can be combined with other compatible parts from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the <html><a href="https://static.igem.org/mediawiki/parts/b/bc/T--Valencia_UPV--protocols.pdf#page=27"> Golden Gate assembly protocol </a></html>.
  
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This part used to construct the composite part [https://parts.igem.org/Part:BBa_K2656114 BBa_K2656114]. Composite part [https://parts.igem.org/Part:BBa_K2656114 BBa_K2656114] was then used together with [https://parts.igem.org/Part:BBa_K2656116 BBa_K2656116] in order to characterize the pLux repressible promoter [https://parts.igem.org/Part:BBa_K2656002 BBa_K2656002].
  
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By using this [http://2018.igem.org/Team:Valencia_UPV/Experiments#exp_protocol experimental protocol] and inducing at different AHL concentrations, we have obtained the following experimental measures (in blue dots). These measurements were compared with our [http://2018.igem.org/Team:Valencia_UPV/Modeling#models constitutive AHL-LuxR model] to test it.
  
 
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[[File:T--Valencia_UPV_AHL_UPV2018.png|900px|thumb|none|alt=AHL experiment.|Figure 3. AHL induction experiment and comparison with our model simulation.]]
  
 
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Latest revision as of 03:57, 18 October 2018


LuxR TF Coding Sequence

domestication.
Figure 1. DNA basic parts domestication. Third construction corresponds with CDS Basic Part adaptation into the GoldenBraid grammar.

Part BBa_K2656016 is the transcription factor LuxR coding sequence BBa_C0062 compatible with both Biobrick and [http://2018.igem.org/Team:Valencia_UPV/Design GoldenBraid 3.0] assembly methods. It acts on the lux promoters when activated by Acyl-homoserine-lactone. It can be combined with other compatible parts from our [http://2018.igem.org/Team:Valencia_UPV/Part_Collection Valencia UPV IGEM 2018 Printeria Collection] to assemble transcriptional units with the Golden Gate assembly protocol .

This part used to construct the composite part BBa_K2656114. Composite part BBa_K2656114 was then used together with BBa_K2656116 in order to characterize the pLux repressible promoter BBa_K2656002.

By using this [http://2018.igem.org/Team:Valencia_UPV/Experiments#exp_protocol experimental protocol] and inducing at different AHL concentrations, we have obtained the following experimental measures (in blue dots). These measurements were compared with our [http://2018.igem.org/Team:Valencia_UPV/Modeling#models constitutive AHL-LuxR model] to test it.

AHL experiment.
Figure 3. AHL induction experiment and comparison with our model simulation.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]