Difference between revisions of "Part:BBa K3332039"

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<partinfo>BBa_K3332039 short</partinfo>
 
<partinfo>BBa_K3332039 short</partinfo>
  
The tetR protein is able to repress PLtetO promoter in the absence of aTc.
+
The tetR protein is able to repress pLtetO-1 promoter in the absence of aTc.
 
===Usage and Biology===
 
===Usage and Biology===
The tetR protein is used to inhibit PLtetO from expressing LacI. It is part of the circut designed to prevent engineered bacteria in the detection instrument from escaping.
+
The tetR protein is used to inhibit pLtetO-1 from expressing LacI. It is part of the circut designed to prevent engineered bacteria in the detection instrument from escaping.
 
<table><tr><th>[[File:T--XMU-CHINA--circuit--circuit.png|thumb|600px|Fig.1 Circuit.]]</th><th></table>
 
<table><tr><th>[[File:T--XMU-CHINA--circuit--circuit.png|thumb|600px|Fig.1 Circuit.]]</th><th></table>
 
In this circuit, LacI can repress pTrc-2 promoter and pTrc-2 derivative promoter,while tetR can repress pLtetO-1 promoter. When ATc exits, it can combine tetR, so that pLtetO-1 promoter can’t be repressed. Then LacI which is controlled by pLtetO-1 can repress pTrc-2 promoter and pTrc-2 derivative promoter. As a result, mf-lon and MazF can’t be expressed.
 
In this circuit, LacI can repress pTrc-2 promoter and pTrc-2 derivative promoter,while tetR can repress pLtetO-1 promoter. When ATc exits, it can combine tetR, so that pLtetO-1 promoter can’t be repressed. Then LacI which is controlled by pLtetO-1 can repress pTrc-2 promoter and pTrc-2 derivative promoter. As a result, mf-lon and MazF can’t be expressed.

Revision as of 11:22, 26 October 2020


tetR

The tetR protein is able to repress pLtetO-1 promoter in the absence of aTc.

Usage and Biology

The tetR protein is used to inhibit pLtetO-1 from expressing LacI. It is part of the circut designed to prevent engineered bacteria in the detection instrument from escaping.

Fig.1 Circuit.

In this circuit, LacI can repress pTrc-2 promoter and pTrc-2 derivative promoter,while tetR can repress pLtetO-1 promoter. When ATc exits, it can combine tetR, so that pLtetO-1 promoter can’t be repressed. Then LacI which is controlled by pLtetO-1 can repress pTrc-2 promoter and pTrc-2 derivative promoter. As a result, mf-lon and MazF can’t be expressed.

As a kind of bacterial toxin, MazF can cause the bacteria death. So there comes the conclusion that as long as the engineered E.coli are cultured in the environment with ATc, it won’t be killed by MazF, but when the E.coli escape from our testing instrument, the effect can be reversed, that is to say, the E.coli will be killed by MazF. In the same way, we can conclude that in the presence of IPTG, MazF can be expressed to cause bacterial death.


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]


Reference

[1] Chan CT, Lee JW, Cameron DE, Bashor CJ, Collins JJ. 'Deadman' and 'Passcode' microbial kill switches for bacterial containment. Nat Chem Biol. 2016;12(2):82-86. doi:10.1038/nchembio.1979