Recombinant DNA technology: Bacterial Transformation
1. Plasmids are removed from a bacterium
2. Plasmid is cut using a restriction enzyme
3. Gene of interest (e.g. Insulin gene) is removed from a human cell
4. Same restriction enzyme is used to cut gene out
5. Human gene is inserted into plasmid using Ligase enzyme to form recombinant plasmid
6. Recombinant plasmid is put into a bacterium via process of bacterial transformation
7. Bacterial cells multiply rapidly and make multiple copies of gene and produce protein of interest