Difference between revisions of "Part:BBa K389016:Design"

(References)
 
Line 7: Line 7:
 
===Design Notes===
 
===Design Notes===
 
* The ''virA'' gene is under the control a medium strong constitutive promoter so there is enough VirA receptor expressed but not too much so the cell suffers from the expression (VirA is a membrane protein)
 
* The ''virA'' gene is under the control a medium strong constitutive promoter so there is enough VirA receptor expressed but not too much so the cell suffers from the expression (VirA is a membrane protein)
* The ''virG'' gene is mutated so it works without an ''rpoA'' subunit from ''Agrobacterium tumefaciens'' (YC Jung ''et al.'', 2004)
+
 
* double terminator (forward) to keep expression of mRFP by the constitutive promoter low  
+
* The ''virG'' gene is mutated so it works without an ''rpoA'' subunit from ''Agrobacterium tumefaciens'' ([http://www.springerlink.com/content/wmq06kua5qkma1au/ YC Jung ''et al.'', 2004])
** double terminator <partinfo>BBa_B0017</partinfo> instead of <partinfo>BBa_B0015</partinfo> because of problems mentioned with <partinfo>BBa_B0012</partinfo>  
+
 
* mRFP gene to show the activity of the ''vir'' promoter
+
* Double terminator (forward) to keep expression of mRFP by the constitutive promoter low.
* this BioBrick is for measuring the natural virA/G system
+
** Double terminator <partinfo>BBa_B0017</partinfo> instead of <partinfo>BBa_B0015</partinfo> because of problems mentioned with <partinfo>BBa_B0012</partinfo>.
 +
 
 +
* mRFP gene to show the activity of the ''vir'' promoter.
 +
 
 +
* This BioBrick is for measuring the natural VirA/G system.
 +
 
  
 
===Source===
 
===Source===
  
 
* ''virA'' from ''A. tumefaciens'' C58 (<partinfo>K389001</partinfo>)
 
* ''virA'' from ''A. tumefaciens'' C58 (<partinfo>K389001</partinfo>)
 +
 
* ''virG'' gene synthesized by Mr. Gene (<partinfo>BBa_K389002</partinfo>)  
 
* ''virG'' gene synthesized by Mr. Gene (<partinfo>BBa_K389002</partinfo>)  
 +
 
* ''vir'' promoter from ''A. tumefaciens'' C58 (<partinfo>BBa_K389003</partinfo>)  
 
* ''vir'' promoter from ''A. tumefaciens'' C58 (<partinfo>BBa_K389003</partinfo>)  
* constitutive promoter, RBS, double terminator and mRFP from parts.igem (<partinfo>BBa_J23110</partinfo>, <partinfo>B0034</partinfo>, <partinfo>BBa_B0017</partinfo>, <partinfo>E1010</partinfo>)
+
 
 +
* Constitutive promoter, RBS, double terminator and mRFP from parts.igem (<partinfo>BBa_J23110</partinfo>, <partinfo>B0034</partinfo>, <partinfo>BBa_B0017</partinfo>, <partinfo>E1010</partinfo>)
 +
 
  
 
===References===
 
===References===
YC Jung ''et al.'' (2004) Mutants of ''Agrobacterium tumefaciens virG'' Gene That Activate Transcription of ''vir'' Promoter in ''Escherichia coli'', ''Current Microbiol'' 49:334-340.
+
YC Jung ''et al.'' (2004) [http://www.springerlink.com/content/wmq06kua5qkma1au/ Mutants of ''Agrobacterium tumefaciens virG'' Gene That Activate Transcription of ''vir'' Promoter in ''Escherichia coli''], ''Current Microbiol'' 49:334-340.

Latest revision as of 16:08, 25 October 2010

VirA/G reporter device mRFP


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
    Illegal NheI site found at 647
    Illegal NheI site found at 2581
    Illegal NheI site found at 2604
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 1632
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 4260
    Illegal AgeI site found at 4372
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1768


Design Notes

  • The virA gene is under the control a medium strong constitutive promoter so there is enough VirA receptor expressed but not too much so the cell suffers from the expression (VirA is a membrane protein)
  • The virG gene is mutated so it works without an rpoA subunit from Agrobacterium tumefaciens ([http://www.springerlink.com/content/wmq06kua5qkma1au/ YC Jung et al., 2004])
  • Double terminator (forward) to keep expression of mRFP by the constitutive promoter low.
  • mRFP gene to show the activity of the vir promoter.
  • This BioBrick is for measuring the natural VirA/G system.


Source


References

YC Jung et al. (2004) [http://www.springerlink.com/content/wmq06kua5qkma1au/ Mutants of Agrobacterium tumefaciens virG Gene That Activate Transcription of vir Promoter in Escherichia coli], Current Microbiol 49:334-340.