Team:Lethbridge/Project

Overall project

Reducing the Environmental Footprint of Oil Sands Extraction

Why are we interested?

As a team from Alberta, we know of the economic benefit that the oils sands have brought to the province. Many members on our team have friends and family employed around the province in the energy industry, however, we are also aware of the environmental impact of the oils sands, specifically the tailings ponds. We feel it is important not only to clean the tailings ponds, but be able to extract the potential energy of the residue bitumen concurrently. Our team has previously worked on related projects in past years providing us with experience in techniques required to complete this project and potential problems that may arise. Also, being able to work on a project where we will be able to test our bacteria on real life samples gives us a physical goal as opposed to other, more esoteric projects.

The Approach

The long term goal of our project will be to create a dry powder that will enzymatically degrade tailing ponds with no live bacteria, similar to how the pills taken for lactose intolerance contain enzymes for dealing with lactose. However this will require many intermediate steps. The initial goal of our project will be to create four separate modules for use in a bacteria test chassis. These modules will 1) degrade target contaminants into useful metabolites, 2) allow the bacteria to move towards areas of high chemical concentration, 3) induce DNA degradation and 4) concentrate the modules in microcompartments. Upon successful testing of each module, they will be combined into one cell chassis (E. coli). This chassis will then be optimized to live in a tailing pond environment by selective evolution. By combining our modules in microcompartments, we can extract the enzymes required to process tailings ponds and avoid putting live genetic organisms into the wild.

The Modules

1. Bacteria have been found in tailings ponds and even in asphault. They have been shown to be able to degrade many organic compounds in nature. The pathways responsible for degradation of aromatic hydrocarbons produce catechol, a colourless, ortho-substituted benzene with two hydroxyl groups as an intermediate. Our goal is to increase the rate of catechol degradation by optimizing the pathway for introduction into the tailings. We will use a pathway which degrades catechol into a semialdehyde which is usable by the bacteria and can be further degraded into usable resources such as ethanol or methanol.
2. Chemotaxis is the method that E. coli uses to move in its environment. Bypassing the normal cellular pathways can be achieved using a riboswitch, an RNA element that will turn on protein production at desired concentration of a target compound, which in our case will be catechol – so that the cell moves towards large concentrations of catechol and remains there until it has all been degraded.
3. Previous iGEM teams have been able to remotely activate E coli’s DNA degradation pathway which is the pathway responsible for terminating the cell and a very powerful tool. By providing the ability to destroy our custom cell's DNA, we ensure that the cell will only act as an encapsulation of our parts and not escape into the environment. The DNA will be degraded eliminating the potential for horizontal gene transfer between other species present in the tailing ponds, and the relevant enzymes will not be destroyed.
4. Our iGEM project last year was the assembly of synthetic microcompartments to isolate pathways from the rest of the cellular environment. These microcompartments will be used to house the catechol degradation pathway so that the pathway can be isolated from the cell and administered to the tailings in a powdered form.

Optimization

Using selective evolution in the presence of catechol we will engineer an E. coli which is able to live in high concentrations of catechol. This will allow for optimization of the catechol degradation pathway using. The next step will be to further use selective evolution with the tailings sample so that the pathway will be optimized for the environmental conditions that the pathway will administered to.

Our Expectations

Figure 1. A depiction of the project overview.

Short-term Goals

We expect to have the biobrick parts submitted to the registry for all of the separate modules. Once we have the biobrick parts we will then be able to assemble the proposed system of the catechol degradation pathway, chemotaxis, DNA degradation and microcompartments. We will characterize all the modules, but the catechol dioxygenase will be our priority. Our short-term goal will be to provide characterized biobricks for the degradation of catechol in tailings.

Medium-term goals

We will accomplish the optimization of the system by selective evolution. To accomplish this we will use the tailings sample provided to optimize the assembled of the optimized catechol degradation pathway.

Long-term Goals