Difference between revisions of "Part:BBa K4765106"

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In the aggregation experiment, bacterial solutions of aTc-induced/not induced intimin-Ag3 and intimin-Nb3, intimin-Ag2 and intimin-Nb2, intimin-Ag1 and intimin-Nb1 E.coli, were mixed in a 1:1 ratio (600μL per strain per tube) and allowed to settle. Sampling was performed at 0 and 3 hours by collecting 100μL aliquots from the upper 25% of each mixture (supernatant) in each tube. These samples were subsequently transferred to EP tubes and stored at 4℃ until the final sampling. Afterward, they were resuspended and transferred to a 96-well assay plate for OD~600~ measurement. The percentage of bacteria remaining in the supernatant at 3 hours was determined by dividing the bacterial count at 3 hours (as determined by the OD~600~ measurement) by the bacterial count at 0 hours.
 
In the aggregation experiment, bacterial solutions of aTc-induced/not induced intimin-Ag3 and intimin-Nb3, intimin-Ag2 and intimin-Nb2, intimin-Ag1 and intimin-Nb1 E.coli, were mixed in a 1:1 ratio (600μL per strain per tube) and allowed to settle. Sampling was performed at 0 and 3 hours by collecting 100μL aliquots from the upper 25% of each mixture (supernatant) in each tube. These samples were subsequently transferred to EP tubes and stored at 4℃ until the final sampling. Afterward, they were resuspended and transferred to a 96-well assay plate for OD~600~ measurement. The percentage of bacteria remaining in the supernatant at 3 hours was determined by dividing the bacterial count at 3 hours (as determined by the OD~600~ measurement) by the bacterial count at 0 hours.
  
As is shown in Figure 2 and 3 , at 3 hours, in all the aTc-induced *E. coli* samples, bacteria percentage remaining in the supernatant was significantly lower compared to the uninduced samples. And among them, the Ag3/Nb3 pairs exhibited the most favorable performance.
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As is shown in Figure 2 and 3, at 3 hours, in all the aTc-induced *E. coli* samples, bacteria percentage remaining in the supernatant was significantly lower compared to the uninduced samples. And among them, the Ag3/Nb3 pairs exhibited the most favorable performance.
 +
 
 +
As is shown in Figure 4, for aTc-induced intimin-Ag3/Nb3 pairs, bacteria remaining in the supernatant was significantly lower than the uninduced samples at 3 and 6 hours. These results collectively demonstrate that the intimin-Ag/Nb pairs can effectively promote the binding between *E. coli*.
  
As is shown in Figure 4 , for aTc-induced intimin-Ag3/Nb3 pairs, bacteria remaining in the supernatant is significantly lower than the uninduced samples at 3 and 6 hours. These results collectively shows that the intimin-Ag/Nb pairs can effectively promote the binding between *E. coli*.
 
 
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| <html><img style="width:640px" src="https://static.igem.wiki/teams/4765/wiki/yzm/intimin-pairs.jpg" alt="contributed by Fudan iGEM 2023"></html>
 
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| '''Figure 4. Bacteria Remaining in the Supernatant at 0,3,6 Hours '''  
 
| '''Figure 4. Bacteria Remaining in the Supernatant at 0,3,6 Hours '''  
The bacterial quantity in the supernatant is quantified by OD~600~ (1 OD~600~ corresponds to 10^8 bacterial particles)
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The bacterial quantity in the supernatant is quantified by OD~600~ (1 OD~600~ corresponds to 10^8 bacterial particles)
 
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Revision as of 14:22, 12 October 2023


Twister P1 + T7_RBS + intimin-Nb3 fusion + stem-loop

contributed by Fudan iGEM 2023

Introduction

We introduced a self-assembly synthetic adhesion system by transfecting initimin-Nb2 fusion into E. coli. Initimin-Nb3 fusion is composed of a surface display system (intimin) and the coding sequence of a nanobody. The surface display system, which includes a short N-terminal signal peptide to direct its trafficking to the periplasm, a LysM domain for peptidoglycan binding, and a beta-barrel for transmembrane insertion[1], possesses the outer membrane anchoring of the nanobody[2].

Usage and Biology

The surface-displayed nanobody can specifically interact with the antigen produced by BBa_K4765105 .In our project, we took full advantage of the Ag-Nb interaction to create a bacteria lawn with a programmable physical structure[3].

Characterization

To confirm biofilm formation through intimin-Ag/Nb, we employed both **aggregation experiments** and **fluorescence microscopy imaging** to demonstrate its ability to mediate biofilm formation.

Aggregation Asssay

In the aggregation experiment, bacterial solutions of aTc-induced/not induced intimin-Ag3 and intimin-Nb3, intimin-Ag2 and intimin-Nb2, intimin-Ag1 and intimin-Nb1 E.coli, were mixed in a 1:1 ratio (600μL per strain per tube) and allowed to settle. Sampling was performed at 0 and 3 hours by collecting 100μL aliquots from the upper 25% of each mixture (supernatant) in each tube. These samples were subsequently transferred to EP tubes and stored at 4℃ until the final sampling. Afterward, they were resuspended and transferred to a 96-well assay plate for OD~600~ measurement. The percentage of bacteria remaining in the supernatant at 3 hours was determined by dividing the bacterial count at 3 hours (as determined by the OD~600~ measurement) by the bacterial count at 0 hours.

As is shown in Figure 2 and 3, at 3 hours, in all the aTc-induced *E. coli* samples, bacteria percentage remaining in the supernatant was significantly lower compared to the uninduced samples. And among them, the Ag3/Nb3 pairs exhibited the most favorable performance.

As is shown in Figure 4, for aTc-induced intimin-Ag3/Nb3 pairs, bacteria remaining in the supernatant was significantly lower than the uninduced samples at 3 and 6 hours. These results collectively demonstrate that the intimin-Ag/Nb pairs can effectively promote the binding between *E. coli*.

contributed by Fudan iGEM 2023
Figure 2. Bacteria Percentage Remaining in the Supernatant at 3 Hours.The bacterial quantity in the supernatant is quantified by measuring the OD~600~ (1 OD~600~ corresponds to 10^8 bacterial particles).
contributed by Fudan iGEM 2023
Figure 3. Aggregation Experiment Results at 3 Hours

From left to right: aTc-induced intimin-Ag1/Nb1, not-induced intimin-Ag1/Nb1, aTc-induced intimin-Ag2/Nb2, not-induced intimin-Ag2/Nb2 and aTc-induced intimin-Ag3/Nb3, not-induced intimin-Ag3/Nb3.

contributed by Fudan iGEM 2023
Figure 4. Bacteria Remaining in the Supernatant at 0,3,6 Hours

The bacterial quantity in the supernatant is quantified by OD~600~ (1 OD~600~ corresponds to 10^8 bacterial particles)

Fluorescence Microscopy Imaging

We also employed microscopy imaging to observe the growth and expansion of biofilm. Glass slides were treated with PDL (Poly-D-Lysine) for 10 seconds, followed by mixing *E. coli* expressing intimin-Ag3 and intimin-Nb3-mScarlet on these slides. After several washes with LB KanR medium, 100 μL of LB KanR medium was added. The location of the founder cell was determined, and imaging was initiated on the microscope stage at 25°C, with video recordings captured at 5-minute intervals,and photographs taken at 0, 2, and 5.5 hours.

As illustrated in figure 5, the presence of Ag/Nb pairs on the surface enables two different strains of bacteria to coexist harmoniously by attaching to each other in an appropriate ratio. This coexistence is evident even at 5.5 hours, as both strains of bacteria remain within the field of view.

In the video that follows, we present additional evidence of bacterial growth and division within our biofilm, where bacteria bound by Ag/Nb pairs can be observed continuously dividing. The fluorescent cells in the video consistently undergo cell division throughout the entire recording.

These results collectively demonstrate that intimin-Ag/Nb fusion can mediate specific binding between *E. coli* and effectively promote biofilm formation.

contributed by Fudan iGEM 2023
Figure 5. Biofilm Growth at 0, 2, and 5.5 Hours.

Images were captured under a 150x objective lens in brightfield and fluorescence.

contributed by Fudan iGEM 2023
Figure 6. Visualization of Biofilm Formation through Microscopy Imaging.

Magnification: 150x Video Duration: Captured at 5 min intervals


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
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1305
    Illegal BsaI.rc site found at 2201


  1. Piñero-Lambea, C., Bodelón, G., Fernández-Periáñez, R., Cuesta, A. M., Álvarez-Vallina, L., & Fernández, L. Á. (2015). Programming controlled adhesion of E. coli to target surfaces, cells, and tumors with synthetic adhesins. ACS Synthetic Biology, 4(4), 463–473. https://doi.org/10.1021/sb500252a
  2. Glass, D. S., & Riedel-Kruse, I. H. (2018). A Synthetic Bacterial Cell-Cell Adhesion Toolbox for Programming Multicellular Morphologies and Patterns. Cell, 174(3), 649-658.e16. https://doi.org/10.1016/j.cell.2018.06.041
  3. Kim, H., Skinner, D. J., Glass, D. S., Hamby, A. E., Stuart, B. A. R., Dunkel, J., & Riedel-Kruse, I. H. (2022). 4-bit adhesion logic enables universal multicellular interface patterning. Nature, 608(7922), 324–329. https://doi.org/10.1038/s41586-022-04944-2