Difference between revisions of "Part:BBa K2279001"

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This part has been improved to be functional in ''E. coli'': produce and secrete the mature arbitrium peptide of phage phi3T (SAIRGA). For this, the signal secretion of AimP was replaced by the OmpA secretion signal ([[Part:BBa_K2675002|BBa_K2675002]]).
 
This part has been improved to be functional in ''E. coli'': produce and secrete the mature arbitrium peptide of phage phi3T (SAIRGA). For this, the signal secretion of AimP was replaced by the OmpA secretion signal ([[Part:BBa_K2675002|BBa_K2675002]]).
 
Also, the AimP has been codon-optimized for ''Escherichia coli'' K12 ([[Part:BBa_K2675001|BBa_K2675001]]).
 
Also, the AimP has been codon-optimized for ''Escherichia coli'' K12 ([[Part:BBa_K2675001|BBa_K2675001]]).
For more information on the improved parts, please go to the page of http://2018.igem.org/Team:Evry_Paris-Saclay/Peptide.
+
For more information on the improved parts, please go to http://2018.igem.org/Team:Evry_Paris-Saclay/Peptide.
  
 
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Revision as of 13:48, 11 October 2018


AimP

AimP encodes a signal peptide.

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
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 58
  • 1000
    COMPATIBLE WITH RFC[1000]

Plasmid construction

We used PCR to produce AimP gene fragment.

T--TMMU-China--aimP.jpeg

Then we inserted this gene to plasmid pSB1C3. We transformed this recombinant plasmid (one contains gene AimP) into strain DH5α (E. coli). Then we picked some colonies for cultivation and extracted the recombinant plasmid, which was verified by PCR and sequencing. From the result of electrophoresis, we confirmed the transformation of AimP was success.

T--TMMU-China--aimp4.jpeg


Biological Function

The B.subtilis bacteriophage phi3T employs the AimR-AimP QS system to make the lysis-lysogeny decision. AimP is the pre-pro-peptide. It is 43aa long. The mature signal peptide of AimP is SAIRGA. Binding of the mature signal peptide to 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. T--TMMU-China--aimfu.jpeg

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. AimAuto.jpeg

Figure 1. The design of autoinhibiton system

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.

AimSR.jpeg

Figure 2. The design of AimR-AimP based Sender and Receiver cells.

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.

Improvement by Evry_Paris-Saclay 2018

This part has been improved to be functional in E. coli: produce and secrete the mature arbitrium peptide of phage phi3T (SAIRGA). For this, the signal secretion of AimP was replaced by the OmpA secretion signal (BBa_K2675002). Also, the AimP has been codon-optimized for Escherichia coli K12 (BBa_K2675001). For more information on the improved parts, please go to http://2018.igem.org/Team:Evry_Paris-Saclay/Peptide.