Large food molecules are digested by enzymes into smaller molecules and these products of digestion are then absorbed into the bloodstream.
Enzymes catalyse (speed up) chemical reactions.
The activesite is where the substrate attaches to.
The enzyme now breaks down the substrate into the products.
If the substrate does not fit perfectly into the activesite, the enzyme cannot break down this substrate.
Enzymes are specific. The substrate must fit perfectly into the active site (the lock and key theory).
Proteins are broken down by enzymes called proteases and we find these in the stomach, pancreas and small intestine.
Proteins are long chains of chemicals called aminoacids.
When we digest the proteins, the protease enzymes convert the protein back to the individual amino acids, which are then absorbed into the bloodstream.
When the amino acids are absorbed by the body cells, they are joined together in a different order to make humanproteins.
Starch (type of carbohydrate) consists of a chain of glucosemolecules.
Carbohydrates are brokendown by enzymes called carbohydrases. In the case of starch this is called amylase.
When carbohydrates like starch are digested, we produce simple sugars.
Amylase is found in the saliva and pancreas.
A lipid molecule consists of a molecule of glycerol attached to three molecules of fatty acids.
Lipid molecules are digested by the enzyme lipase. This produces glycerol and fatty acids.
Bile is made in the liver and it is stored in the gallbladder.
Bile helps to speed up the digestion of lipids but bile is not an enzyme.
Bile converts large lipid droplets into smaller droplets.
Bile emulsifies the lipid. This massively increases the surface area of the lipid droplets.
This increases the rate of lipid breakdown by lipase.
Bile is also alkaline. This allows it to neutralise stomach acid, creating alkaline conditions in the small intestine.
This increases the rate of lipid digestion by lipase.