Result
Our lab experience enabled us to create the final Biobrocks of our project which are a siderophore Desferrioxamine B producer and a flagellin producer.
Mobilisation results
Protein production
Test of our biobrick proteins production using a SDS page and comassie. - : no induction ; + : induction with 0.02% arabinose at Abs(600nm)=0.4
We investigated if the DesA, DesB, DesC and DesD proteins were well produced by our biobrick using SDS PAGE.
To do this we performed SDS PAGE and stained with comassie blue using cells containing this biobrick in plasmid backbone Find here the protocol From an over night starter, cells were diluted and grown from Abs(600nm)=0.2 to Abs(600nm)=1.
Then 1UOD of cells (1.67ml at 0.6OD) was collected and centrifuged at 5000g for 5min.
After removal of the supernatant, the cell pellet was resuspended in 50µL SDS-PAGE sample buffer.
We heated the mix at 95°C during 15min
Find here the protocol
The mixture was loaded onto a polyacrylamide gel and migrated during 50min at 180V.
Staining was done using coomassie blue.
We compared the production of proteins in different background :
- E. coli Tg1 strain without any plasmide (negative temoin)
- E. coli Tg1 strain with pSB1C3 containing the RFP coding sequence (negative temoin)
- E. coli Tg1 strain complemented with our biobrick Bba_K1951011 before and after induction. (you can observe the production of the 4 proteins on the figure below on the left; right : before induction, left : after induction)
Results showed the production of the 4 proteins DesA, DesB, DesC and DesD, all involved in the desferrioxamine B biosynthesis pathway.
Proof of fonctionnality
We investigated if DesA (Lysine decarboxylase) was fonctionnal, by measurement of cadaverine using HPLC with C18 column and proofed our biobrick is a producer of this protein and makes it fonctionnal.
Investigation of the cadaverine production by the lysine decarboxylase DesA. Production has been detected by HPLC using C18 column after induction of the strain. Different backgrounds were analysed : wild type
Escherichia coli Tg1 strain (yellow column), cadA mutant from keio bank (blue column), complemented cadA mutant from keio bank with Bba_K1951004(orange column), complemented cadA mutant from keio bank with Bba_K1951011(grey column).
Results showed cadaverine detection in the wild type meaning the original strain well produces the cadaverine.
In cadA mutant from Keio bank, cadaverine was also produced in a least quantity showing that an other pathway is responsible for the production of cadaverine.
In the cadA mutant complemented by Bba_K1951004, the amount of cadaverine was recovered and even beyond the wild type production.
Moreover, in the cadA mutant complemented by Bba_K1951011, the cadaverine level produced was even over the wild type and complemented Bba_K1951004 production. We explain this result because of the higher stability of this big composite part.
To conclude, we made a big composite part able to produce every proteins involved in the biosynthetic pathway of the desferrioxamine B.
In the futur
- siderophore production (HPLC and absorption spectroscopy)
- Improve the siderophore production if needed (cofactors, protein stability, metabolic engineering)
- Binding affinity for platinum by our siderophore
- ICPAES (ion coupled plasma atomic emission spectroscopy)
- Importation of the siderophore in Streptomyces coelicolor
Biosorption result
Proof of protein production
Test of our biobrick proteins production using a SDS page and comassie
We investigated if the FliC protein was well produced by our biobrick using SDS PAGE.
To to do this we performed SDS PAGE and stained with coomassie blue using cells containing this biobrick in plasmid backbone SDS page and coomassie blue.
From an over night starter, cells were diluted and grown from Abs(600nm)=0.2 to Abs(600nm)=0.6.
Then 1UOD of cells (1.67ml at 0.6OD) was collected and centrifuged at 5000g for 5min.
After removal of the supernatant, the cell pellet was resuspended in 50µL SDS-PAGE sample buffer.
SDS page and coomassie blue The mixture was loaded onto a polyacrylamide gel and migrated during 50min at 180V.
Staining was done using coomassie blue.
The FliC is at mass 51,3kDa, and can be clearly seen in the gel photograph.
Proof of swimming recovery
We have made a biobrick BbaK1951008 ables to produce Flagellin (FliC protein of the flagellum). In the aim to test the flagellin integrity, we made a fliC mutant in a E.coli W3110 strain by transduction using phage P1 (protocol available on our website).
In the figure the deletion mutant (lower left sector) shows no swimming motility as expected and a small white colony.
In contrast the wild-type colony (lower right) has a diffuse halo due to swimming cells around the central white colony.
Finally the complemented strain, the deletion mutant complemented with our biobrick, (top panel) shows two colonies with intense
halos surrounding them.
This illustrated clearly that our biobrick can restore motility and is functional.
The intensity of the halo suggests that a greater proportion of the cells are mobile or swimming is in someway better than the wild-type.
We investigated if swimming motility was recovered by a knockout FliC strain. To test complementation with our biobrick strains were stabbed into soft (0.3%) LB agar plates, and incubated at 37°C for 4 hours. Three strains are shown:
Escherichia coli W3110 wild-type strain, which has a good swimming capacity (lower right); a fliC deletion mutant of W3110 (lower left); and the fliC mutant complemented with BBa_K1951008(top).
Microscopie of the flagellum
This check the flagella assembly and the integration of the flagellin protein expressed from our biobrick BBa_K1951008 we have observed bacteria with an electron microscope.
The image shows mutiple polar flagella in an E.coli fliC deletion mutant containing our biobrick. We saw that these cells had more flagella than wild-type (W3110) cells and that the fliC deletion mutant did not have flagella.
In the futur
- Adsorption of platinum by our flagella
- election microscopy observation
- Finalise the insertion of platinum specific peptide
- directed mutagenesis introducing a Bbs1 restriction site
- insertion by annealing
- Metal recovery by calcination or proteolysis
- Extend to other precious metals (other peptides : gold, silver, palladium)
Improvement of FliC E. coli [http://parts.igem.org/Part:BBa_K1463604 BBa_K1463604]
This biobrick is an improvement on the biobrick designed by the Glasgow 2014 team.
[http://parts.igem.org/Part:BBa_K1463604 K1463604]
The improvement of this part is multiple.
- First there is no mutation in the promotor or RBS of our part so the flagellin is well expressed and functional. Unfortunately when the Glasgow team trie to make this part they picked up a mutation in the promotor.
- Second the sequence that we have used it a synthetic gene with codon optimisation, designed specifically for high level expression in E.coli. Thus as an expression part is improved over the initial design.
- Third in the functional swimming assay, we see evidence for improved swimming (denser halo), in cells expressing our biobrick, a phenotype not observed by the Glasgow team in 2014.
Futur plan for our project
Now that every biobricks have been created and are available, make proofs of concept could allow to envisage investigation about possibilities of an industrial application.
Maquette of our process in the futur
The biologic production of high and specific adsorber could reduce environnemental impact of the metal production and its cost while renew essential precious metals like platinum, for a sustainable production.
Igem Aix Marseille 2016 in a sustainable circle
Project Achievements
