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-1 promoter in the absence of | + | 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-1 | + | The tetR protein is used to inhibit pLtetO-1. It is part of the circuit designed to prevent engineered bacteria in the detection instrument from escaping. |
− | <table><tr><th>[[File:T--XMU-CHINA--circuit--circuit.png|thumb|600px|Fig | + | <table><tr><th>[[File:T--XMU-CHINA--circuit--circuit.png|thumb|600px|'''Fig 1.''' Kill switch of the detection part]]</th><th></table> |
− | In this circuit, LacI can repress pTrc-2 promoter and pTrc-2 derivative | + | 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 combines with tetR, so that pLtetO-1 promoter can’t be repressed. Then LacI which is controlled by pLtetO-1 can repress the 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, the expression of MazF often lead to the death of bacteria. 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 the mazF, but when the ''E.coli'' escape from our detection instrument, the effect can be reversed. That is to say, the ''E.coli'' will be killed by MazF. In the same way, we can see that in the presence of IPTG, MazF can be expressed and kill the''E.coli''. | ||
===Sequence and Features=== | ===Sequence and Features=== |
Revision as of 16:25, 27 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. It is part of the circuit designed to prevent engineered bacteria in the detection instrument from escaping.
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 combines with tetR, so that pLtetO-1 promoter can’t be repressed. Then LacI which is controlled by pLtetO-1 can repress the 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, the expression of MazF often lead to the death of bacteria. 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 the mazF, but when the E.coli escape from our detection instrument, the effect can be reversed. That is to say, the E.coli will be killed by MazF. In the same way, we can see that in the presence of IPTG, MazF can be expressed and kill theE.coli.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE 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