Part:BBa_K3896008
The gene of recombinant PmrCAB (HAPN) two-component system.
We selected the PmrA-PmrB two-component system as a vector for the core binding domain of hAPN. This system, present in Salmonella and most strains, is initially an Fe(III)-sensitive regulatory system (Fig.1) that contains a histidine kinase (HK) on its transmembrane portion, PmrB, for sensing specific environmental stimuli, and a corresponding response regulator (RR), PmrA, for mediating cellular responses.
figure 1
The target of the assay is the S protein, a monomer of the echinoderm glycoprotein on the 229E-CoV envelope, responsible for binding to human aminopeptidase N (hAPN) [1]. By reviewing the data, we found that in the complex protein of hAPN and S protein, the core binding domain of hAPN is concentrated between Ala281 and Gly330, while the RBD of S protein is Lys201 to Ser321 (Fig.2). Therefore, we intercepted the peptide sequence of the hAPN fragment as our core detection binding domain.
figure 2
We replaced the Fe (III) sensitive domains Trp34 to Glu64 of the original PmrB with the core binding domain of hAPN protein to accept the stimulation of S protein of 229E-CoV. After detecting the S protein of 229E-CoV, the sensor kinase PmrB autophosphorylates the highly conserved histidine residue, and then transfers the phosphate group to the conserved aspartate residue in its homologous reaction regulator PmrA. Then phosphorylated PmrA protein combined with promoter PmrC sequence to activate the expression of reporter gene.
In order to verify the detection function of our engineered bacteria, we designed a protein characterization experiment. In the experiment, we added 1mM IPTG to induce the expression of PmrB and PmrA, and added extracted S protein after 2h of induced expression.When the engineered bacteria received the stimulation of S protein, the transmembrane protein PmrB containing a histidine kinase (HK) underwent autophosphorylation and subsequently transferred the phosphate group to the conserved aspartate residue in the intracellular regulator PmrA, making PmrA to activate transcription of the PmrC promoter and express the downstream reporter gene EGFP.
We transferred the plasmid into E.coli BL21(DE3) and set up the following experimental groups, which yielded results consistent with expectations.
figure(3 groups)
We also set up different concentration gradients and tested the fluorescence intensity and absorbance of the engineered bacterial solution, and processed the experimental data to arrive at the optimum concentration.
figure(result)
A series of experimental results demonstrate the feasibility of the PmrCAB system for MERS-CoV detection.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 96
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 2343
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1081
- 1000COMPATIBLE WITH RFC[1000]
| None |