Difference between revisions of "Part:BBa K2279000"
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2279000 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2279000 SequenceAndFeatures</partinfo> | ||
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+ | ===plasmid construction=== | ||
+ | We used PCR to produce AimR gene fragment. | ||
+ | [[file:T--TMMU-China--aimr1.jpeg]] | ||
+ | |||
===Biological function=== | ===Biological function=== |
Revision as of 12:34, 31 October 2017
AimR
AimR is a transcription factor.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI site found at 429
Illegal SapI.rc site found at 169
Illegal SapI.rc site found at 492
plasmid construction
We used PCR to produce AimR gene fragment.
Biological function
The B.subtilis bacteriophage phi3T encode the Aim system to make lysis-lysogeny decision. The AimR is a transcription factor, the AimP is the propeptide of the mature signal peptide. However, binding of AimP to the AimR will disrupt the dimer forms of AimR. After that, the AimR can no longer bind to the promoter of AimX, a potential non coding RNA involved in the process of lysis-lysogeny.
The AimR-AimP system and its role in the phage lysis-lysogeny decision, cited from reference [1].
Design
By combining the expression of AimR and AimP components, we want to develop a synthetic QS system in B. subtilis for target gene autoinhibition.
A synthetic communication pathway between B. subtilis strains by co-culturing AimP-producing “sender” cells with AimR-sensing “receiver” cells to inhibit gene expression was also designed.
Reference
[1] Erez, Z., Steinberger-Levy, I., Shamir, M., Doron, S., Stokar-Avihail, A., Peleg, Y., Melamed, S., Leavitt, A., Savidor, A., Albeck, S., et al. (2017). Communication between viruses guides lysis-lysogeny decisions. Nature 541, 488-493.