Difference between revisions of "Part:BBa K322211:Design"
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===Design Notes=== | ===Design Notes=== | ||
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+ | This biobrick was made from BBa_I712019. 6 bases upstream of the start codon, which were presumably present in BBa_I712019 to make a proper eukaryotic context for the start codon, were removed for improved expression in ''E. coli''. | ||
+ | Note that the luciferase is temperature sensitive. Growing the chassis at 30°C will result in considerably increased brightness. | ||
===Source=== | ===Source=== | ||
− | Photinus pyralis | + | Photinus pyralis, from BBa_I712019 |
===References=== | ===References=== | ||
+ | Increase in bioluminescence intensity of firefly luciferase using genetic modification. ''Analytical Biochemistry'' '''366''', 131-136. Fujii, H., Noda, K., Asami, Y., Kuroda, A., Sakata, M. & Tokida, A. (2007). |
Latest revision as of 17:54, 25 October 2010
Red emitting firefly luciferase mutant (356K)
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 SapI.rc site found at 808
Design Notes
This biobrick was made from BBa_I712019. 6 bases upstream of the start codon, which were presumably present in BBa_I712019 to make a proper eukaryotic context for the start codon, were removed for improved expression in E. coli.
Note that the luciferase is temperature sensitive. Growing the chassis at 30°C will result in considerably increased brightness.
Source
Photinus pyralis, from BBa_I712019
References
Increase in bioluminescence intensity of firefly luciferase using genetic modification. Analytical Biochemistry 366, 131-136. Fujii, H., Noda, K., Asami, Y., Kuroda, A., Sakata, M. & Tokida, A. (2007).