Difference between revisions of "Part:BBa R0040"

(Improved by Fudan-CHINA in 2018)
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This year, Fudan-CHINA makes a mutation to Part:BBa_R0040 to improve its combination with the tTA transcriptional factor by computational simulation.Please be free to visit [[Part:BBa_K2886010]].
 
This year, Fudan-CHINA makes a mutation to Part:BBa_R0040 to improve its combination with the tTA transcriptional factor by computational simulation.Please be free to visit [[Part:BBa_K2886010]].
  
 +
===Improved by University of Groningen in 2019===
 +
University of Groningen has improved the pTet promoter in E. voli using a synthetic promoter library on pTet (BBa_R0040) in order to enhance function and inducibility. Please visit [[Part:BBa_K3171173]] for more info.
  
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_R0040 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_R0040 SequenceAndFeatures</partinfo>
 +
  
  

Revision as of 12:03, 20 October 2019

TetR repressible promoter

Sequence for pTet inverting regulator. Promoter is constitutively ON and repressed by TetR. TetR repression is inhibited by the addition of tetracycline or its analog, [http://openwetware.org/wiki/ATc aTc].


Usage and Biology

Medium strength promoter. [jb, 5/24/04]

From the reference article:
"In contrast to tetracycline, anhydrotetracycline is a particularly useful inducer. It binds Tet R with an ~35-fold higher binding constant and thus allows to operate at very low concentrations. At the same time, its antibiotic activity is ~100-fold lower and concentrations of <50 ng/ml as required for the full induction of P LtetO-1 have no effect on the growth of E.coli."

Improved by Fudan-CHINA in 2018

This year, Fudan-CHINA makes a mutation to Part:BBa_R0040 to improve its combination with the tTA transcriptional factor by computational simulation.Please be free to visit Part:BBa_K2886010.

Improved by University of Groningen in 2019

University of Groningen has improved the pTet promoter in E. voli using a synthetic promoter library on pTet (BBa_R0040) in order to enhance function and inducibility. Please visit Part:BBa_K3171173 for more info.

Sequence and Features


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]