Team:UCL London/Approach

Biochemical Engineering

As a team, we have a vision that our cells can detect external changes in the environment and hence be programmed to response to them, instead of us manually having to detect and resonse. Our project is based primarily on biochemical engineering processes and it's essential that the audience understands what us Biochemical Engineers are about and what we do, especially as this is unfamiliar territory to many.

In our department, we believe that extraordinary advances in the life sciences have great potential to improve our quality of life, this is ultimately achieved through better medicines and a cleaner environment. We provide the foundations for the transforming of such extraordinary next discoveries into products and processes leading to the improvement of health and welfare state of the nation.

Fermenters

For the first time, UCL iGEM 2010 will be implementing the use of its sophisticated class of 1 litre fermenters. In the biopharmaceutical industry, protein expression takes place on a large scale in these devices although at scales by far larger than the ones to be put into use during this project. The recombinant E.coli cells are grown under a controlled environment within the fermenters whose scales can be as large as 10,000 L. A medium is firstly created containing vital chemicals which will ensure that the cells have the vital requirements to maintain growth Fermentation Protocol.

The diagram shows one of the 1 litre fermenters that will be used to test one of our strains. The main parts have been labeled and are as follows;

Main Fermentation Chamber: This is where our E.Coli cells are grown and where the fermentation process takes place

Impellers

Temperature probe

pH probe

Base

Acid

In let air

Compressor

Out let air

Sampling tube

Inoculation opening

Protein Expression

E.coli is essentially one of the most widely applied in-vivo expression systems. The reason for its wide application is the fact that it is so well developed and the E. coli genome is fully developed and well understood. In biotechnology, as an example, a DNA sequence for a protein of interest could be inserted into a high copy-number plasmid containing the lac promoter, which is then transformed into the bacterium Escherichia coli. Addition of IPTG (a lactose analog) activates the lac promoter and causes the bacteria to express the protein of interest.

One technique of insuring high levels of a protein is to clone the gene downstream of a well-characterized regulated promoter. In our case, we will be using pTAC, the tac promoter, a very widely used expression system. Being the strong hybrid promoter it is, it is repressed by the LacI protein, and on addition of IPTG, the lacI repressser is inactivated. This inactivtation breaks the strong repression of pTAC resulting in expression of pTAC. It has been shown that high expressions of pTAC is directly proportional to the concentration of IPTG added. And so by varying the concentratrion of IPTG added, you can regulate the rate of the expression of the desired protein downstream. That’s essentially the biology behind protein expression. The engineering side is where our project really gets interesting.