Reporter
Part:BBa_K2451015
Designed by: Jared Clements Group: iGEM17_UT-Knoxville (2017-10-26)
Lac-RBS-xylR-Terminator-Pu-RBS-xylA-RBS-xylM-T-Lac-RBS-xylB-T
Catalytic sites of xylA, xylM, and xylB from P. putida were added in place of GFP from part BBa_K2451013. This creates a circuit for expression of monooxygenases xylA and xylM under the control of xylR (regulatory protein) and aromatic substrates. Additionally, dehydrogenase xylB is transcribed under a Lac promoter as the initial constructs (BBa_K1966000 and BBa_K1966001) were ligated together in the 2016 project. See https://parts.igem.org/Part:BBa_K2451013 for usage information.
Testing utilizing IPTG and 1 mM m-xylenes revealed the following gas chromatography data for alcohol and aldehyde conversions in M9 media.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 2190
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 4681
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 3966
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 5333
[edit]
Categories
Parameters
None |