Difference between revisions of "Part:BBa K411001:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | + | This riboswitch has the following characteristics: | |
− | The inducer cannot metabolize in E. coli. | + | * The inducer (Theophylline) cannot metabolize in ''E. coli''. |
− | + | * Both the inducer (Theophylline) and the riboswitch itself does not naturally occur in ''E. coli ''. | |
− | It | + | * It did not originally have EcoRI, XbaI, SpeI, and PstI cutting sites, so no point mutations were needed. |
− | + | See [http://2010.igem.org/Team:NYMU-Taipei NYMU-Taipei's Design page] | |
− | + | ||
− | + | ||
===Source=== | ===Source=== |
Latest revision as of 08:43, 18 October 2010
Theophylline-inducible Riboswitch
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This riboswitch has the following characteristics:
- The inducer (Theophylline) cannot metabolize in E. coli.
- Both the inducer (Theophylline) and the riboswitch itself does not naturally occur in E. coli .
- It did not originally have EcoRI, XbaI, SpeI, and PstI cutting sites, so no point mutations were needed.
See [http://2010.igem.org/Team:NYMU-Taipei NYMU-Taipei's Design page]
Source
Synthesized directly from two primers:
- forward primer : 5' - gaattcgcggccgcttctagag ggtgataccagcatcgtcttgatgcccttggcag - 3'
- reverse primer : 5' - ctgcagcggccgctactagta cttgttgtcttgcagcggggtgctgccaagggcatcaagac - 3'