Producing human insulin in bacteria
1. Lyse human cells and cut out insulin gene from its chromosome using a restriction enzyme
2. Lyse bacteria cells to obtain bacteria plasmid. Cut bacteria plasmid with the same restriction enzyme to obtain complementary sticky ends
3. Mix the extracted insulin gene with the cut plasmid and add DNA ligase to join the insulin gene to the plasmid
4. Mix the recombinant DNA with E.coli bacteria and apply temporary heat shock or electric shock for the bacteria to take in the recombinant DNA
5. Transgenic bacteria are isolated and grown in fermenters for mass production of insulin
6. Bacteria cells are lysed to obtain insulin which is extracted and purified for use