Drugs from genetically modified organisms

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Spec 8.17
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Drugs from genetically modified organismsSpec 8.17

In short

Genetically modified organisms can make human drugs. The human gene is inserted into a microorganism such as a bacterium or yeast, a plant or an animal, which makes the protein. Bacteria produce human insulin in fermenters, and transgenic animals and plants can make proteins in milk or leaves.

Making drugs with GMOs
OrganismHow it is usedExample
Microorganisms (bacteria, yeast)The human gene is inserted on a plasmid; the cells are grown in large fermenters and the protein is purified from the cultureHuman insulin for diabetes; human growth hormone
PlantsA human gene is inserted into plant cells, and the protein is extracted from leaves or seedsAntibodies and vaccine antigens made in tobacco or other plant leaves
AnimalsThe gene is joined to a promoter that works in the mammary gland, so the protein is secreted in milkHuman antithrombin (a protein that prevents unwanted blood clotting) in the milk of transgenic goats; human clotting factor IX in the milk of transgenic sheep

Advantages of making human insulin in GM microorganisms rather than extracting it from animals:

  • The insulin is identical to human insulin, so it is less likely to cause an immune response.
  • It can be made in large amounts, quickly and cheaply, in fermenters.
  • There are fewer ethical objections than using animals, and a reliable supply that does not depend on slaughter of animals.

Bacteria cannot remove introns and cannot modify proteins after translation in the way eukaryotic cells do (for example by adding carbohydrate groups). So a human gene for bacteria is supplied as cDNA, and proteins that need these modifications to work are made in yeast, plants or animals instead.

Exam tip:

A ‘how are drugs produced using GMOs’ answer needs the sequence: isolate the human gene, insert it into a vector, put the vector in the host, express the gene and purify the protein.

Written and checked against the Edexcel International A Level Biology (YBI11) specification · Updated October 2026

Frequently asked questions

How is recombinant DNA made?

A restriction endonuclease cuts the gene and a plasmid at the same recognition sequence, leaving complementary sticky ends. The gene and plasmid are mixed, so the sticky ends pair by complementary base pairing. DNA ligase then forms phosphodiester bonds between the sugar–phosphate backbones, producing a recombinant plasmid that can be put into a host cell.

What do restriction enzymes and DNA ligase do?

Restriction enzymes (restriction endonucleases) cut DNA at specific base sequences, hydrolysing phosphodiester bonds and often leaving single-stranded sticky ends. DNA ligase does the opposite job, forming phosphodiester bonds to join DNA fragments together. Together they allow a gene to be cut out and joined into a vector.

How are genes put into bacteria and plant cells?

Bacteria take up plasmids after treatment with calcium chloride and a heat shock, which makes their membranes permeable. Plant cells can be transformed by Agrobacterium, which transfers DNA from its Ti plasmid, or by a gene gun that fires DNA-coated metal particles into the cells.

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