Difference between revisions of "Part:BBa K411001:Design"

(Source)
(Design Notes)
 
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===Design Notes===
 
===Design Notes===
We want to choose a kind of riboswitch which has the following characteristics:  
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This riboswitch has the following characteristics:  
The inducer cannot metabolize in E. coli.  
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* The inducer (Theophylline) cannot metabolize in ''E. coli''.  
It does not exist in naturally occurring E. coli  
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* Both the inducer (Theophylline) and the riboswitch itself does not naturally occur in ''E. coli ''.
It does not have EcoRI,X,S, or PstI cutting site
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* It did not originally have EcoRI, XbaI, SpeI, and PstI cutting sites, so no point mutations were needed.
 
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See [http://2010.igem.org/Team:NYMU-Taipei NYMU-Taipei's Design page]
 
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===Source===
 
===Source===

Latest revision as of 08:43, 18 October 2010

Theophylline-inducible Riboswitch


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE 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'

References