Part:BBa_K3611002

The gene of recombinant PmrCAB twocomponent system.

We chose the PmrA-PmrB two-component system as the carrier of our detection module. As carrier of the core binding domain of ACE2, PmrA-PmrB system exists in Salmonella and most strains. The system is a regulatory system sensitive to Fe (III) originally (Fig. 1), which contains a histidine kinase (HK) on the membrane part PmrB to sense specific environmental stimuli, as well as a corresponding response regulator (RR) PmrA to mediate cellular responses.

Figure. 1 The PmrB Fe(III) binding motif was replaced by ACE2 core binding domain, which give the PmrB the ability of sensing S protein.

The target of detection is S protein, the monomer of homotrimeric spike glycoprotein on the envelope of SARS-CoV-2, which is responsible for binding to human cell receptor angiotensin-converting enzyme 2 (ACE2) [2]. The S1 subunit of S protein, responsible for recognizing ACE2, is an essential part of the virus in fusing its own envelope with the cell membrane. By reviewing the data, we found that in the complex protein of ACE2 and S protein, the core binding domain of ACE2 was concentrated between Thr20 and Asn90, while the RBD of S protein was Thr333 to Gly526 of its S1 subunit (Fig. 2). Therefore, we intercept the polypeptide sequence of this segment of ACE2 as our core detective binding domain.

Figure. 2 Binding domain of S protein and ACE2. The Thr333-Gly526 of S1 subunit is responsible for binding to ACE2.

We replaced the original PmrB ’s Fe (III) sensitive domains Trp34 to Glu64 with the core binding domain of ACE2 protein in order to receive stimulation from the S protein of SARS-CoV-2. Upon sensing S protein of SARS-CoV-2, the sensor kinase PmrB autophosphorylates a highly conserved histidine residue and subsequently transfers the phosphoryl group to a conserved aspartate residue in its cognate response regulator PmrA. Then the phosphorylated PmrA protein binds to the promoter PmrC sequence to active the expression of the reporter gene. In order to verify the detection function of our engineered bacteria, we designed a bacteria co-culture experiment. We constructed three groups of bacteria: engineered bacteria with detection function, prey bacteria expressing S protein and empty vectors. These cells were cultured at 37 ℃ overnight, and then diluted to OD600 = 0.2 with volume of 5ml.Then cultivated at 37℃ for 1h to make their OD600 reach 0.4~0.6. We designed one test group and two different control groups:  I Detection bacteria + Prey bacteria  II Detection bacteria + Empty Vector  III Empty Vector + Empty Vector The volume of each group was 10ml (mix in 1:1). After 2h 0.5mmol/L IPTG induction, the prey bacteria expressed S protein into the medium, where the detection engineered bacteria also constructed its recombinant PmrCAB system. Once the detection engineered bacteria capture the S protein, the recombinant PmrCAB system will be activated to express the enhanced green fluorescent protein. We observed the three groups of bacteria with fluorescence microscope after the induction. Strong green fluorescent can be obviously notice at the group of detection bacteria and prey bacteria. And other two groups have less or no fluorescent signal (Fig. 3).

Fig. 3 Fluorescence microscopy photos of detection bacteria. EV, bacteria with empty vector. The S protein is the Thr333-Gly526 of S protein of SARS-CoV-2, which were expressed by E. coli BL21.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  INCOMPATIBLE WITH RFC[12]

  Illegal NheI site found at 1909
  
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BamHI site found at 2337
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal AgeI site found at 1156
  
• 1000
  COMPATIBLE WITH RFC[1000]