This mini-lesson walks you through Enzymes & Digestion: enzymes as biological catalysts (the active site & lock-and-key model), how temperature and pH change enzyme activity (denaturation), the human digestive system, the digestive enzymes (amylase, protease/pepsin, lipase), the role of bile, and absorption in the villi.
Work through each screen, answer the questions as you go (some are wordy, some are calculations) and collect ⭐ stars. Press Start when you're ready.
Enzymes · catalysts
Enzymes are biological catalysts
An enzyme is a biological catalyst: a protein that speeds up the rate of a reaction without being used up, so it can be reused again and again.
Enzymes let reactions happen quickly at the low temperatures of the body (around 37 °C) instead of needing lots of heat.
Each enzyme has a specially shaped part called the active site, where the reacting molecule — the substrate — fits and reacts.
Enzymes are specific: one enzyme works on one type of substrate, because the active site only fits that molecule's shape.
Watch out: because they are proteins, enzymes have a precise 3-D shape. If that shape is destroyed the enzyme can no longer work.
Enzymes · lock-and-key
The lock-and-key model
The lock-and-key model explains enzyme specificity. The substrate (the key) fits exactly into the enzyme's active site (the lock). They join to form an enzyme–substrate complex, the reaction happens, then the products are released and the enzyme is free to work again.
Substrate fits the active site → enzyme–substrate complex → products released → enzyme reused.
Key idea: only a substrate with the complementary shape fits the active site — this is why each enzyme is specific to one reaction.
Quick check
What is an enzyme?
?Which statement best describes an enzyme?
Enzymes · temperature
Effect of temperature
As temperature rises, enzyme-controlled reactions get faster — molecules move more and collide more often. But above an enzyme's optimum temperature the rate falls sharply.
Rate peaks at the optimum (about 37 °C in humans), then drops as the enzyme denatures.
Above the optimum, the heat breaks the bonds holding the enzyme's shape together. The active site changes shape, the substrate no longer fits, and the enzyme is denatured. Denaturing is permanent — it does not reverse on cooling.
Misconception: a denatured enzyme is not "killed" — enzymes are not alive. Its shape is changed so the active site no longer fits the substrate.
Enzymes · pH
Effect of pH
Each enzyme also has an optimum pH at which it works fastest. If the pH is too high or too low, the enzyme denatures — again the active site changes shape.
Stomach protease (pepsin) works best in acid (≈pH 2); enzymes in the small intestine work best in alkaline conditions (≈pH 8).
Link it up: the stomach makes hydrochloric acid to give pepsin its acidic optimum and to kill microbes; bile later neutralises this acid so the small intestine's enzymes have their alkaline optimum.
Sort it
What happens to the enzyme?
Tap a condition, then the box that describes the enzyme's activity.
⚡ Fastest (at optimum)
🔥 Denatured (shape lost)
🐢 Slow (but still works)
Calculate
Your turn — rate of reaction
1An enzyme breaks down 30 mg of substrate in 2 minutes. Calculate the mean rate of reaction in mg per minute.
mg/min
Hint: rate = amount ÷ time = 30 ÷ 2.
Calculate
Your turn — rate from a graph reading
2In an experiment, 18 cm³ of gas is produced by an enzyme reaction in 90 seconds. Calculate the mean rate in cm³ per second.
cm³/s
Hint: rate = volume ÷ time = 18 ÷ 90.
Digestion · the gut
The human digestive system
Digestion breaks large, insoluble food molecules into small, soluble ones that can be absorbed into the blood. Food passes along the gut in order:
Order: mouth → oesophagus → stomach → small intestine → large intestine.
Amylase (a carbohydrase) breaks starch → sugars (e.g. glucose/maltose). Made in the salivary glands and pancreas.
Protease breaks proteins → amino acids. Pepsin is the stomach protease that works in acid; more protease is made by the pancreas.
Lipase breaks lipids (fats) → fatty acids + glycerol. Made in the pancreas and small intestine.
Match it
Match each enzyme to what it does
Tap a statement on the left, then its matching enzyme on the right.
Job
Enzyme
Quick check
Which products?
?Lipase acts on a fatty meal. What are the products of lipid digestion?
Digestion · bile
Bile — not an enzyme
Bile is made in the liver, stored in the gall bladder, and released into the small intestine. Bile is alkaline and it is not an enzyme — but it has two important jobs:
Neutralises the acid that arrives from the stomach, making conditions alkaline — the optimum pH for enzymes in the small intestine.
Emulsifies fats: it breaks large fat droplets into many tiny droplets, giving a much bigger surface area for lipase to work on. This speeds up fat digestion.
Emulsification: bigger surface area = faster lipase action (but bile itself does no chemical digestion).
Exam trap: bile does not digest fat — lipase does the chemical breakdown. Bile only emulsifies (physical change) and neutralises acid.
Quick check
What does bile do?
?Which statement about bile is correct?
Absorption · the villi
Absorption in the villi
The digested food is absorbed in the small intestine, whose inner lining is covered in millions of tiny finger-like villi (singular: villus). Villi are beautifully adapted for fast absorption:
Villi give a large surface area, a thin (one-cell) wall and a good blood supply for rapid absorption.
Large surface area — millions of villi (with micro-villi) mean more room for absorption.
Thin walls — only one cell thick, so molecules diffuse across a short distance.
Good blood supply — capillaries carry absorbed glucose and amino acids away, keeping a steep concentration gradient.
Link it up: the same adaptations (big surface area, thin wall, short diffusion path) make any good exchange surface efficient — like the alveoli in the lungs.
Quick check
Why villi?
?Villi have thin walls that are only one cell thick. How does this help absorption?
Recap
The big ideas to know
Enzymes: protein catalysts; active site + lock-and-key; specific to one substrate
Conditions: optimum temperature (≈37 °C) & pH; too hot / wrong pH → denatured (active site changes shape, permanent)
Gut order: mouth → oesophagus → stomach → small intestine → large intestine