Difference between revisions of "Part:BBa K3031019:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | The OxyR protein transcription factor was designed using principles relating to statistical data of structural features of reactive cysteines in a wide variety of proteins. | |
− | + | Constitutive promoter was chosen for the production of the OxyR protein in order to reach a high enough level to be able to bind with H2O2 and induce the downstream genes controlled by TrxC promoter. | |
Revision as of 04:55, 21 October 2019
Constitutive promoter + OxyR + TrxC promoter + GFP generator
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 781
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 734
Illegal BsaI.rc site found at 1894
Design Notes
The OxyR protein transcription factor was designed using principles relating to statistical data of structural features of reactive cysteines in a wide variety of proteins. Constitutive promoter was chosen for the production of the OxyR protein in order to reach a high enough level to be able to bind with H2O2 and induce the downstream genes controlled by TrxC promoter.
Source
Yang Ming University iGEM team 2013
OxyR sequence from Uniprot and then sequenced by Genscript.