OVERVIEW

To ensure the ability of our system, it is composed of four main biological components. The parts we are using are bacteriophage, a host bacteria, an elastin-like-polymer ( ELP), and a metal binding protein.

Together, the four components will work together to sequester and remove metal ions from a solution.

BACTERIAL HOST

When considering a potential bacteria host that would be compatible with our system, the following criteria must be met.

I) The host can be parasitized by a bacteria-phage amenable to engineering.
II) The host can survive in high metal concentrations.
III) The host can resist temperature fluctuations and aggregation.

Chosen accordingly to the criteria, we have decided to explore the host bacteria: Escherichia. coli as our proof of concept as it is a well-studied model organism with defined methods of genetic manipulation and is easily accessible in our lab.

In real-life applications of our system, we will be using methanotrophic bacteria as it is one of the few natural organisms that can survive in the detrimental environment of tailings ponds. By using the methanotrophic bacteria it also ensures a cost-efficient and sustainable system as the bacteria already naturally exists in the tailings pond. The additional benefit of working with E. coli is that results obtained in the system will inform in silico modelling, allowing us to design other phage systems for different organisms.

In summary, the choice of host defines numerous properties of the system in terms of energy input, phage production, and efficiency of removing the metal ions from the oil and mining tailings ponds. Our initial efforts with E. coli will inform our design of other host-phage systems, and alter the way in which our device works to capture and sequester ions in mining and oil tailings ponds.

BACTERIOPHAGE CASPID PROTEIN

The T4 Bacteriophage capsid is an icosahedron with proteins Gp23, 24, and 31 contributing to its assembly. The Highly antigenic and small outer capsid proteins serve as accessory proteins on the outer shell. Capsid proteins from this bacteriophage will be used as a proof of concept for further usage in the finalized construct.

PHAGE SELECTION

In future design application, we have looked at phages that have a host range corresponding to our potential hosts: E. coli as the proof of concept and the methanotrophic bacteria as the real-life bacteria application.

Through the utilization of phage display technology, we will attempt to express ELPs fused to metal binding proteins on the surfaces of the T4 phage capsid for E. coli and in later experimentation, the M4 phage for the methanotrophic bacteria.

The T4 bacteriophage belongs to the phage family Myoviridae and interacts with E. coli[1]. The capsid of this phage has been successfully modified to display peptides and protein domains on the surface[1]. In past experiments, biologically active, full-length foreign proteins were displayed by fusion to SOC (small outer capsid protein) and HOC (highly antigenic outer capsid protein) accessory protein genes found on the T4 capsid surface. In fact, a bipartite T4 SOC–HOC protein display system allowed two different proteins to be displayed on one T4 particle simultaneously[2]. The high abundance of these proteins (960 SOC and 160 HOC molecules per phage capsid) increases the efficiency with which potential metal-binding proteins may function, once attached to this phage[2].

The M4 bacteriophage will be used in the real-life application of our system in the mining and oil tailing ponds as it is a natural occurring phage that can survive in the environment of the tailings pond.

As a proof of principle, we will be using the capsid protein taken from the T4 phage: gp23, 24 and 31. The proteins gp23 and gp24 are coat proteins making up the phage capsid, and gp31 acts as a chaperone in the gp23 folding process[3]. These proteins will produce an empty viral capsid to test the parts individually with the bacteria. This will allow for further experimentation with the full bacteriophage construct including the other parts.

ELASTIN LIKE POLYMERS

The purpose of elastin-like polymers (ELPs) is to remove the metal ion-laden phage from the solution[4]. At a certain temperature, ELPs will aggregate and drop out of solution. This transition temperature (Tt) is influenced by factors such as the heavy metal concentration, concentration of ELP, the length of the ELP chain, and the variable amino acids in each monomer. We will be altering the length and the concentration of ELP to achieve our goal Tt. We plan for the ELP to have a Tt between 45^οC to 50^oC as this will allow the ELP to remain in solution while maintaining the optimal efficiency of our chosen bacteria[4]. The length and the Tt have an inverse relationship; when we increase the length of the ELP, the transition temperature decreases. Using this information we intend to keep the guest residue the same while altering the length to achieve the goal Tt.

To influence the characteristics of our ELP, we can experiment with the variable amino acid in each monomer. All ELPs contain the amino acid sequence Val-Pro-Gly-X-Gly, with X representing the variable amino acid. For our project, we want to use a hydrophobic amino acid, specifically valine, glycine, or alanine. By using a hydrophobic amino acid, we can destabilize the ELP and it will more readily drop out of solution. There are several residues that are found to work well with the precipitation of ELP; valine is found to be the most effective for protein aggregation. We will add standardized linker sequences to the N- and C-termini of the ELP to allow for easy fusion to other functional proteins. In our case, we will be fusing the capsid protein of the bacteriophage and the metal-binding peptide to either end of the ELP.

METAL PROTEIN BINDING

The use of the CutA protein is employed as a proof of concept because it is found in E. coli and binds to copper well. This protein ensures that ion homeostasis is preserved within the cell, whereby the excess of copper ions is removed by this protein[5]. There will also be a hexahistidine tag for purification purposes. The CutA protein has three binding sites allowing for three copper ions to be bound per protein.

Our primary proof of concept proteins to be used are CutA and Cup1. Both are copper binding proteins to be used in the final construct attached to the ELP N or C terminal in order to effectively bind to ions. For protein purification, a hexahistidine tag will be used in the constructs for either protein.

In further applications of our project, there are many different proteins that can be used in our final system for the tailings ponds that are able to bind varying metal ions. By using the CutA as well as Cup1 proteins as a proof of concept, this shows that our system is able to work properly with a binding protein.

CONTRUST

REFERENCES

1. Yap, M.L. and Rossmann, M.G. (2014). Structure and function of bacteriophage T4. Future Microbiol Volume 9, 1319-1327.

2. Ren, Z.J. and Black, L.W. (1998). Phage T4 SOC and HOC display of biologically active, full-length proteins on the viral capsid. Gene Volume 15, 439-444

3. Bakkes P.J, Faber B.W, Heerikhuizen H.V. and Van der Vies S.M (2005). The T4-encoded cochaperonin, gp31, has unique properties that explain its requirement for the folding of the T4 major capsid protein. Proceedings of the National Academy of Sciences Volume 23, 8144-8149

4. Meyer D. and Chilkoti A. (2004) Quantification of the Effects of Chain Length and Concentration on the Thermal Behaviour of Elastin-like Polypeptides. Biomacromolecules Volume 5, 846-851

5. Rensing C. and Grass G. (2003) Escherichia. Coli mechanisms of copper homeostasis in a changing environment. FEMS Microbiology Reviews, Volume 27, 197-213