Reporter
Part:BBa_K1021020
Designed by: Swati Sureka Group: iGEM13_Cornell (2013-09-13)
PT7+GFP
The gene for green fluorescent protein sits downstream of the T7 constitutive promoter. This gene can be naturally expressed in Escherichia coli BL21-A1 in conjunction with T7 polymerase and can be expressed in Escherichia coli DH5α after co-transformation.
Usage and Biology
- The part was constructed from BBa_I712074 and BBa_E0040.
- This construct was modified to contain a bacterial RBS so that we could characterize its transcriptional functionality. A fluorescence assay was run using a 96 well plate as described in the protocol section. T7+RBS+GFP and T7+GFP (BBa_K1021020) constructs in E. coli BL21-A1 were examined for their relative fluorescence (fluorescence/OD600). A T7 construct in E. coli BL21-A1 without downstream elements was utilized as a control along with the use of the aforementioned constructs in E. coli DH5α. As can be seen from the graph there were evident differences in peak fluorescence between the T7+RBS+GFP construct and the T7+GFP construct and controls. The T7+GFP+RBS construct appears to have a 20 fold higher relative fluorescence than the T7+GFP construct or the controls.
Sequence and Features
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 696
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Categories
Parameters
None |