Difference between revisions of "Part:BBa K389016:Design"
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===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 | * double terminator (forward) to keep expression of mRFP by the constitutive promoter low | ||
** double terminator <partinfo>BBa_B0017</partinfo> instead of <partinfo>BBa_B0015</partinfo> because of problems mentioned with <partinfo>BBa_B0012</partinfo> | ** 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 | * mRFP gene to show the activity of the ''vir'' promoter | ||
* this BioBrick is for measuring the natural virA/G system | * this BioBrick is for measuring the natural virA/G system | ||
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===Source=== | ===Source=== | ||
Revision as of 13:08, 16 October 2010
VirA/G reporter device mRFP
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE 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 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1632
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 4260
Illegal AgeI site found at 4372 - 1000INCOMPATIBLE 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 (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
- virA from A. tumefaciens C58 (BBa_K389001)
- virG gene synthesized by Mr. Gene (BBa_K389002)
- vir promoter from A. tumefaciens C58 (BBa_K389003)
- constitutive promoter, RBS, double terminator and mRFP from parts.igem (BBa_J23110, BBa_B0034, BBa_B0017, BBa_E1010)