Intermediate
Part:BBa_K933002
Designed by: Hannah Jepsen-Burger Group: iGEM12_Penn_State (2012-10-01)
short leader sequence with mCherry and GFP reporters
This sequence has the available space to insert repeating codon sequences in an effort to determine codon optimization in E.coli. It is prefaced by a weak RBS, a short leader sequence, and contains restriction enzyme sites that allow for the insertion of the repeat sequences. Two reporters-mCherry and GFP-show the degradation of tRNA as the repeated sequences interfere with natural translation. mCherry should change with changing sequences, and GFP should remain constant.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 71
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 71
Illegal NheI site found at 99
Illegal NheI site found at 122
Illegal NotI site found at 77 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 71
Illegal BamHI site found at 202 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 71
- 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 71
Illegal XbaI site found at 86 - 1000COMPATIBLE WITH RFC[1000]
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Categories
Parameters
None |