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RESULTS

• Curli characterization

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• 
  Five complementary tests were performed to evaluate the ability of the modified cells to assemble functional curli: 1) determination of the percentage of adherent cells to polystyrene in 24 wells-plates, 2) crystal violet staining of biofilm formed on polystyrene in 24 wells-plates, 3) ability to bind the congo red, 4) biofilm maximum thickness measurement and biovolumes quantification of GFP-tagged biofilm observed with a confocal microscopy and 5) curli structure observation using Transmission Electron Microscopy (MET).

  
  
  

  Adhesion test and curli production

  
  

  

  Figure 1 : Engineered bacteria Percentage of adhesion
  

  csgA-knockout E. coli strain was transformed with BBa_CsgA-WT (BBa_K1404006); BBa_CsgA-His1 (BBa_K1404007); BBa_CsgA-His2 (BBa_K1404008). The corresponding positive and negative controls are Wild-type E.coli curli producing strain transformed with with the empty vector and csgA--knockout E. coli strain transformed with the empty vector respectively.
  Strains with our parts, the positive and negative controls were cultivated in 24-wells microplate in M63 Mannitol during 24H at 30°C. The supernatant was removed and the OD600 measured, then the bacteria forming the biofilm were resuspended and the OD600 measured in order to estimate the number of cells (See protocol for details ). The percentage of adhesion was calculated as follow : (OD600 of the biofilm)/ (OD600 of the supernatant + OD600 of the biofilm)
  Significant differences are indicated using uppercase letters, and different letters indicate significant differences (Tukey’s test, p < 0.05)
  
  These results show that the percentage of adhesion is similar between the strains containing the three parts and the positive control, thus tagged CsgA were still functional. CsgA with one or two tags from the P70 promoter were sufficient to form thick biofilms.

  
  

  

  Figure 2 : Engineered bacteria Biofilm formation
  

  The cells were grown as described as figure 1.
  

  The supernatant was removed and the remaining biofilm was fixed to the microplate by heat treatment at 80°C during 1H. The violet crystal solution was added in each well in order to stain the cells and the wells were washed with water to remove crystal violet in excess (See protocol for details ).
  
  Violet crystal staining shows that the strain containing the three parts could form a biofilm like the positive control, thus tagged CsgA were still functional. CsgA with one or two tags from the P70 promoter were sufficient to form thick biofilms.

  
  

  

  Figure 3 : Engineered bacteria curli production
  

  Strains are the same as in figure 1.
  Strains with our parts, the positive and negative control were cultivated in M63 Mannitol at 30°C and 180rpm. After centrifugation, the supernatant was removed and the cell pellet was resuspended in the Congo Red solution, in order to specifically stain the curli. The samples were centrifuged again and the pellets observed (See protocol for more details).
  
  Congo Red staining shows that the CsgA with one or two tag from the P70 promoter allows to form curli fiber which are able to bind congo red.
  

  
  
  

  Confocal Laser Scanning Microscopy Analyses

  
  For the Confocal Laser Scanning Microscopy biofilm acquisitions, all the strains were cultivated in 96-wells microplate in M63 Mannitol during 16H at 30°C (See Protocol for details). See results in Figure 4.

  

  Figure 4: Engineered bacteria biofilm characterization and quantification using Confocal Laser Scanning Microscopy

  All the strains used are constitutively fluorescent to allow detection with confocal laser microscopy (ZEISS LSM510 META, 40X/1.3OILDIC, laser Argon 4 lines 30 W 458 nm, 477 nm, 488 nm, 514 nm, See Protocol). Positive control/CsgA+ (Wild-type E. coli curli producing strain); Negative control/CsgA- (csgA-knockout E. coli strain); BBa_CsgA (BBa_K1404006); BBa_CsgAHis1 (BBa_K1404007); BBa_CsgAHis2 (BBa_K1404008). A) Biofilm sections obtained by Z-stack acquisitions. B) Biofilm 3D reconstruction using IMARIS® from acquisitions in A). C) Bio-volume quantification and maximum of thickness measurement using COMSTAT2 (ImageJ). The strain marked with a star is significantly different from all others (Tukey’s test, p<0.05).

  
  As no strains carrying our parts show a significant difference with the positive control, our parts insertion doesn’t modify the biofilm formation property. The His-Tag and His2-Tag engineered CsgA doesn’t disturb the curli formation.

  
  
  

  Transmission Electron Microscopy

  
  

  For the Transmission Electron Microscopy, all the strains were cultivated in conditions that allow the formation of the curli : 48h (for a 50 mL culture), 28⁰C temperature and low agitation. The ammonium molybdate was used as a negative colorant (Microscope: MET PHILIPS CM120).

  
  

  Figure 5: Engineered bacteria curli structure observation using Transmission Electron Microscopy

  The bacteria cultures we used are a csgA-knockout strain as negative control, and the three engineered csgA constructions, the WT, the His1-Tag and His2-Tag.

  
  

  The images show that there is no significant difference between our positive control and our constructions. Thus, we can conclude that our parts insertions don’t affect the structure of the amyloid fibers and the configuration of the curli formation.

  
  
  

  General Conclusion

  
  The expression of CsgA derivatives from the p70 csg promoter carried by the psb1c3 plasmid leads to functional CsgA, and allows E. coli to stick and form biofilm. Moreover, our results show that the addition of one or two His-Tag on C-term of CsgA doesn’t disturb the normal properties of curli (sturdiness, adhesion, structure and folding of CsgA).

  
  

• Nickel chelation

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• Nickel(II) chelation was evaluated in a CsgA- MG1655 background (in order to have only our modified or unmodified curlis at the surface of the strain) for each of the constructions (BBa_CsgA-WT (BBa_K1404006), BBa_CsgA-His1 (BBa_K1404007),or BBa_CsgA-His2 (BBa_K1404008)). Dimethylglyoxime (DMG) was used as a complexing reagent, which forms a pink-colored complex (peak absorption at 554nm) in the presence of Ni(II).

  
  Figure 1 : DMG-Ni complex formation with or without chelating bacteria
  

  Firstly, a calibration curve of the formation Nickel and DMG complexes was established.

  Then, strains were assayed for biofilm nickel absorption on liquid cultures using the calibration curve, measuring the OD of the complex formed for each strain at 554nm. (See Protocol for details)
  Although quantification is possible, this technique lacks precision and is more suited for qualitative studies. However, it is a cheaper alternative to ICP-MS.

  
  Figure 2 : Calibration set picture
  
  Figure 3 : Calibration set : DMG-Ni complex OD554 (optical density)=f([Ni(II)]
  

  
  

  Nickel-DMG complex colorimetry measurement follows a linear regression from a concentration of 20uM to 100uM, linked to the gradient from transparency (at [20uM]) to pink (at [100uM]). This visual method allows us to compare the Ni chelation between our strains. The more pale the color is, the more Ni has been chelated. The culture supernatant of CsgA- bacteria from strain with the part BBBa_CsgA-His2 is less colored than the others, which shows that only this part allows to capture more nickel. These results show that the part BBa_CsgA-His2 confers increased chelation to strain CsgA-. It is shown that it chelates more than part BBa_CsgA-WT and part BBa_CsgA-His1.

  A second method has been used, more quantitative and more precise (but more expensive) : ICP-MS . (See Protocol for more details)
  The metal content of the bacterial pellets were assayed. The quantity of chelated nickel for each strain has been compared to the quantity of curlis formed by each strain.

  
  Figure 4 : ICP-MS results : Ni(II) chelated for each construction linked to the quantity of curlis
  

  Significant differences are indicated using lowercase letters, and different letters indicate significant differences (Tukey’s test, p < 0.05). Error bars represent standard deviations.

  Taken together, these results show that the CsgA- Strain with part BBa_CsgA-His2 chelates twice more than strain CsgA- with part BBa_CsgA-His1. That means that only two His-tags on C-term can improve the natural nickel chelation capacities of CsgA . CsgA with a single His-tag did not perform better than a wild-type CsgA. Potentially, further increasing the amount of His-tags could improve the nickel accumulation capacities of CsgA.

  
  

• Survival after UV and high temperature exposure

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• To adress biosafety issues linked with GMOs, we worked on destroying our bacteria after letting them grow in a biofilm. As the captured metal is extracellular and Curli proteins are very resistant to environmental changes, live bacteria are not needed for our biofilter. Our goal was to obtain a biomaterial made out of modified Curli able to chelate nickel.

  
  

  To find the best way to degrade bacteria and DNA, the following protocol was used to test the influence of UV light and temperature separately :
  

  • Wells containing M63 cultures of strain 227 were put under UV light or at 60 or 70°C for different lengths of time. Well contents were then gradually transferred into Eppendorf and diluted (100, 300, 900 and 2700 fold).
    
  • LB plates (without antibiotic) corresponding to UV/temperature exposure times (+ one plate for control) were then spotted with s227 different concentrations in order to be able to count survival bacteria after incubation at 37°C.
    
  • Genomic DNA was extracted from s227 concentrated culture. From the solution obtained, Curli promoter(750 bp) was amplified by PCR with Q5 polymerase and designed primers.
    
  • Epifluorescence observations were made after Back Light coloration with 200µL s227 liquid cultures.
    
    
    

  UV light influence

  
  

  LB plates

  
  

  
  

  No bacteria grew on LB plate after 15 minutes UV light exposure.
  Bacterian growth can be stopped this way.

  
  

  DNA extraction

  
  Bacterian DNA seemed to be degraded after 10 min UV light exposure.
  ⇒ In consequence, UV light can be used to destroy DNA.

  
  

  Backlight

  
  

  
  Still some green-colored bacteria could be seen after 20 min UV exposure.
  ⇒UV light isn’t enough to kill bacteria.

  
  
  

  Temperature influence

  
  

  LB plates

  
  

  
  Bacteria grew on LB plates even 45 min after being heated to 60°C.
  ⇒ 60°C isn't enough high to kill bacteria.

  
  

  So we tried experiments with a temperature of 70°C.

  
  

  LB plates

  
  

  ⇒Bacterian growth can be stopped as well as with UV light.

  
  

  DNA extraction

  
  

  
  No DNA degradation at all.
  ⇒ In consequence, temperature doesn't enable to destroy DNA, in contrary to UV light.

  
  

  Backlight

  
  

  Control plate	15 min at 70°C	30 min at 70°C	45 min at 70°C

  
  No difference of coloration was observed between the control and the samples heated at 70°C : indeed a lot of green-colored bacteria remained after 45 min of heating.
  ⇒ Temperature isn’t enough to kill bacteria just like UV light.

  
  

  To solve this last problem, bacteria were put in contact with ethanol absolute. The Back Light coloration gives the following picture.
  

  Backlight after DNA extraction of bacterian culture exposed to ethanol

  
  

  These numerous experiments lead us to developp a protocol in three steps, illustrated by the drawing below :
  

  Global strategy to kill bacteria

  
  

• Promoter optimization and characterization

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• As a follow-up to the exploration of curli production and nickel chelation, we want to know the kinetics behind the 70 base-pair long promoter sequence that we used through this whole summer. In fact, it has the interesting property of being activated at 37°C instead of the 30°C of the natural 750 base-pair CsgA promoter from where it is orginially isolated. However, we explored these two promoters' kinetics at 30 and 37°C by inserting a GFP downstream. On a pKK backbone, two essential parts have been assembled: a promoter and a reporter. The reporter in this case is always the same: GFP. However, the promoter is different for each construction. One a first hand, P70 is the 70 base-pair long promoter sequence and when combined to the reporter GFP is called p70:GFP. On a second hand, P750 is the 750 base-pair long promoter sequence coding for the inter-genic regulation for curli production and combined to the report GFP is called P750:GFP.
  The idea behind the two constructions is shown in the figure below.

  
  

  Early growth stage promoter kinetics
  

  During the early growth stages at 37°C, we can observe that the P70 (orange) has a higher GFP expression level compared to the P750 (red). However at 30°C, both P70 (light blue) and P750 (dark blue) have low GFP expression levels. We conclude that P70 has the ability to prematurely activate downstream expression at 37°C

  
  

  Late growth stage promoter kinetics
  

  During the late growth stages at 37°C, we can observe that both P70 (orange) and P750 (red) have a downregulated GFP expression and are moving toward lower expressions. However at 30°C, P70 (light blue) stabilizes within the range of low GFP expressions and P750 (dark blue) reaches the highest GFP expression values. We conclude that P750 has a delayed, albeit extremely high high-leveled, GFP expression at 30°C.

  
  

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