Answer: E.coli or Escherichia coli
Step-by-step explanation:
Procedure
1. Obtain the segment of DNA in a human chromosome that contains insulin gene. Cut the gene using a restriction enzyme. This enzyme cuts the restriction site at the two ends of the gene to produce sticky ends. Each sticky end is a single strand sequence of DNA bases. These bases can pair with complementary bases to form a double strand.
2.Obtain a plasmid from a bacterium. Cut the plasmid with same restriction enzyme. This produces 'sticky ends' complementary to the ends of the Insulin gene.
3. Mix the plasmid with the DNA segment containing the human insulin gene. The human insulin gene will bind to their sticky ends. Add the enzyme DNA ligase to seal the human plasmid containing DNA from two different organisms is recombinant plasmid
4. Mix the recombinant plasmid with E.coli bacterium. Apply temporary electric shock. This opens pores of cell surface membrane of the bacterium for the plasmid to enter.
5.The transgenic bacterium will use the new gene to make insulin
The insulin protein has to be extracted and purified before it can be used