Difference between revisions of "Part:BBa K592014:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | Due to the toxic nature of HO1 and pcyA enzymatic activities, we added a very weak promoter (J23113) to the PCB chromophore module. | + | Due to the toxic nature of HO1 and pcyA enzymatic activities, we added a very weak promoter (J23113) to the PCB chromophore module. This part was designed to be inserted into the bacterial chromosome. Therefore, B1001 was used instead of B0015. |
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===Source=== | ===Source=== |
Latest revision as of 13:12, 18 September 2011
HO1-pcyA, low expression, B1001 terminator
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1607
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1160
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Due to the toxic nature of HO1 and pcyA enzymatic activities, we added a very weak promoter (J23113) to the PCB chromophore module. This part was designed to be inserted into the bacterial chromosome. Therefore, B1001 was used instead of B0015.
Source
Assembled using parts from the 2011 iGEM distribution.