Reporter
Part:BBa_E0051:Design
Designed by: Austin Che Group: iGEM06_MIT (2009-03-01)
lacZa.GFP fusion
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 878
Design Notes
LacZa was placed first in discussion with Joey Davis (Sauer lab). The subunit interfaces of lacZ are at the N-terminal residues and also lacZa is shorter and doesn't have any potential internal translation start sites wheras GFP might have some in-frame RBS and ATG which could possibly lead to translation of lacZa without GFP if GFP were first.
The amino acid linker AGGSEGGGSEHHHHHHGSE is between the lacZa and GFP. The 6-his can also facilitate detection on a Western blot, for purification, etc. The start codon from GFP was removed.
Source
amino acids 1-60 from lacZ and amino acids 2-end of GFP (BBa_E0043)