Difference between revisions of "Part:BBa K3267001"

Line 5: Line 5:
 
Transformed cells with this construct respond to AHL-dependent quorum sensing and GFP would be expressed by the activated transcription factor protein LuxR which binds to the bidirectional promoter region (pLuxR/pLuxI).
 
Transformed cells with this construct respond to AHL-dependent quorum sensing and GFP would be expressed by the activated transcription factor protein LuxR which binds to the bidirectional promoter region (pLuxR/pLuxI).
  
===Biology and Usage===
+
==Biology and Usage==
 
This Receiver part contains the V. fischeri-intrinsic bidirectional promoter region, the LuxRS regulon. The high concentration of Acyl-homoserine lactose (AHL) binds to the LuxR protein to activate and it binds to pLuxR/pLuxS promoters. Instead of LuxS protein, we add super folder GFP in order to make this part as the reporter part of the whole system (Fig 1). The super folder GFP is followed by the PixCell degradation tag from the 2018 Imperial College team to analyze the reporter gene spatiotemporally.
 
This Receiver part contains the V. fischeri-intrinsic bidirectional promoter region, the LuxRS regulon. The high concentration of Acyl-homoserine lactose (AHL) binds to the LuxR protein to activate and it binds to pLuxR/pLuxS promoters. Instead of LuxS protein, we add super folder GFP in order to make this part as the reporter part of the whole system (Fig 1). The super folder GFP is followed by the PixCell degradation tag from the 2018 Imperial College team to analyze the reporter gene spatiotemporally.
  
Line 11: Line 11:
 
[[File:T--NYU_Shanghai--ResultsFig6.jpg|thumb|center|Figure 1: Quorum Sensing by Electric Stimulation]]
 
[[File:T--NYU_Shanghai--ResultsFig6.jpg|thumb|center|Figure 1: Quorum Sensing by Electric Stimulation]]
  
===Characterization===
+
==Characterization==
 
Two parts (Bioelectric Relay cell and QS Receiver cell) are separately transformed in E. coli. and mixed on the agar plate to cultured under electric stimulation. The GFP fluorescence level is determined by pixel intensities after a 1-hour electric shock followed by 24-hour post-culturing. There are three sets to show our model: Co-culture of both cells, only relay cell, and only receiver cell.
 
Two parts (Bioelectric Relay cell and QS Receiver cell) are separately transformed in E. coli. and mixed on the agar plate to cultured under electric stimulation. The GFP fluorescence level is determined by pixel intensities after a 1-hour electric shock followed by 24-hour post-culturing. There are three sets to show our model: Co-culture of both cells, only relay cell, and only receiver cell.
  
Line 27: Line 27:
  
 
[[File:T--NYU_Shanghai--MethodsFig5.jpeg|thumb|center|Figure 5: Making Sure that the Electric Setup has 0.5 V]]
 
[[File:T--NYU_Shanghai--MethodsFig5.jpeg|thumb|center|Figure 5: Making Sure that the Electric Setup has 0.5 V]]
 
+
==Referece==
 
<!-- -->
 
<!-- -->
 
<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 00:40, 22 October 2019


Quorum-Sensing Receiver Construct

Transformed cells with this construct respond to AHL-dependent quorum sensing and GFP would be expressed by the activated transcription factor protein LuxR which binds to the bidirectional promoter region (pLuxR/pLuxI).

Biology and Usage

This Receiver part contains the V. fischeri-intrinsic bidirectional promoter region, the LuxRS regulon. The high concentration of Acyl-homoserine lactose (AHL) binds to the LuxR protein to activate and it binds to pLuxR/pLuxS promoters. Instead of LuxS protein, we add super folder GFP in order to make this part as the reporter part of the whole system (Fig 1). The super folder GFP is followed by the PixCell degradation tag from the 2018 Imperial College team to analyze the reporter gene spatiotemporally.


Figure 1: Quorum Sensing by Electric Stimulation

Characterization

Two parts (Bioelectric Relay cell and QS Receiver cell) are separately transformed in E. coli. and mixed on the agar plate to cultured under electric stimulation. The GFP fluorescence level is determined by pixel intensities after a 1-hour electric shock followed by 24-hour post-culturing. There are three sets to show our model: Co-culture of both cells, only relay cell, and only receiver cell.

Figure 2: GFP Expression Level of Co-culture of Relay and Receiver part, Individual culture of Relay and Receiver, and No Cells. Every sample is stimulated by 0.5V potential for an hour.
Figure 3: Co-culture Plate under GFP (the right hole is positive anode; the left hole is the negative cathode)

Quantitatively, only when both Relay and Receiver cell exists (Co-culture), GFP expression is enhanced. Only the Receiver cell has lightly more expression of GFP than only Relay cell (Fig 2). This should be due to the intrinsic LuxR proteins that facilitate the GFP expression only by its own plasmid. Qualitatively, we also observed the spatial expressing of quorum sensing as most of the GFP expressing cells are located on the side positive electric potential (Fig 3).

Improvement Upon BBa_K2862021

We made this electrochemical control of Bio-parts possible with simpler equipment and a more complicated pathway. 2018 Imperial College team used a commercial potentiostat, but we handmade the electrodes connected to the simple power supply in the physics lab, which significantly saves our budget and time. The electric modulation worked properly in a more complicated setting as we discussed above. The existing part only used SoxRS regulons with the reporter gene, but our system extended the research on electric control of bacterial genes with LuxRI regulons with two layers signaling.

Figure 4: Electric Modulation On Agar Plate Setup
Figure 5: Making Sure that the Electric Setup has 0.5 V

Referece

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 AgeI site found at 1015
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 1661