Procedure for genetically engineering bacteria to produce human insulin
1. Obtain DNA segment with insulin gene
2. Obtain plasmid, cut with same restriction enzyme
3. Mix plasmid and insulin DNA, bind by complementary base pairing
4. Add DNA ligase to seal insulin gene into plasmid (recombinant plasmid)
5. Mix recombinant plasmid with E.coli, apply heat shock to allow entry
6. Isolate and grow transgenic bacteria in fermenter, extract and purify insulin