Difference between revisions of "Part:BBa K4137008"

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<partinfo>BBa_K4137008 short</partinfo>
 
<partinfo>BBa_K4137008 short</partinfo>
  
This construct contains a T7 promoter, a RBS, a mleR coding complex, a mleR purification tag—6xHis, and a terminator B1006. This construct produce and purifies mleR, the regulator of CcdA, which produces when malate acid is presented.
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This construct produces and purifies mleR, the malate-induced regulator that binds to p_mleS promoter for the production of ccdA antitoxin.
  
 
[[File:t7-mler-his.png|800px|thumb|center|Fig.1 Malate-binding transcriptional activator + 6x His-Tag complete construct.]]
 
[[File:t7-mler-his.png|800px|thumb|center|Fig.1 Malate-binding transcriptional activator + 6x His-Tag complete construct.]]

Revision as of 05:37, 9 October 2022


mleR expressing construct

This construct produces and purifies mleR, the malate-induced regulator that binds to p_mleS promoter for the production of ccdA antitoxin.

Fig.1 Malate-binding transcriptional activator + 6x His-Tag complete construct.

Construct Designs

We attached a 6x His-Tag downstream of the mleR sequence for purification purposes. A T7 and RBS are attached upstream to the side of the open reading frame. The terminator BBa_B1006 is attached downstream of the sequence.

Characterization

Sequence and Features

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 49
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]