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RESULTS

• Curli characterization

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• 5 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 Transcription 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 more 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 more 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 Analyzes

  
  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.

  
  
  We can conclude that 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 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_K1404006, BBa_K1404007,or 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).

  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, b measuring the OD of the complex formed for each strain at 554nm.
  Although quantification is possible, this technique lacks precision and is more suited for qualitative studies. However, it is a cheaper alternative to mass spectrometry.

  

  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 BBa_K1404008 is less colored than the others, which shows that only this part allows to capture more nickel. These results show that the part BBa_K1404008 confers increased chelation to strain CsgA-. It is shown that it chelates more than part BBa_K1404006 and part BBa_K1404007.

  A second method has been used, more quantitative and more precise (but more expensive) : mass spectrometry . 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.

  

  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_K1404008 chelates twice more than strain CsgA- with part BBa_K1404007. 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 / 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

  
  

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

  
  

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

  
  

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

  
  
  

  Temperature influence

  
  

  
  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.

  
  

  
  No more bacteria on LB plate after 15min at 70°C
  ⇒Bacterian growth can be stopped as well as with UV light.

  
  

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

  
  

  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.
  image benjamin

  
  
  

  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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• Biobrick for promoter characterization
  The principal of the construction is shown in the figure below.
  
  
  

  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.
  The first promoter is P70, sequence found in the Resgistry. This construction is called p70::gfp
  The second promoter is PCurli, obtained from a PCR, sequence coding for the inter-genic regulation for curli production. This construction is called pcurli::gfp.

  
  

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