Part:BBa_K2027000:Design
Recombinant Apoptosis-Inducing Protein (L-lysine Alpha Oxidase)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1004
Illegal BglII site found at 1032
Illegal BamHI site found at 767 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 25
Design Notes
As far as design goes, this is mostly just a native Scomber japonicus enzyme codon-optimized for Escherichia coli. The conjugated tag should allow for purification and visualization with anti-FLAG antibodies, visualization with Lumio™ Green, and purification with nickel columns. Tani et al. characterized this enzyme in their quest for synthesis of L-pipecolic acid from racemic lysine after nickel column purification,1 and we verified the function of our part in a similar way. More information can be found on the experience page for this part. Below is the forward sequencing verification for the part; enzyme functionality and successful purification indicate that the carboxy-terminus is also intact.
Source
Tani, Y., Miyake, R., Yukami, R. et al. Appl Microbiol Biotechnol (2015) 99: 5045. doi:10.1007/s00253-014-6308-0
References
1. Tani, Y., Miyake, R., Yukami, R. et al. Appl Microbiol Biotechnol (2015) 99: 5045. doi:10.1007/s00253-014-6308-0