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LAUNCH · GCSE Biology · Lesson 3 of 18 Enrichment · Do

Amylase Rate, Graph and Topic 1 Consolidation

Learning objective

I can calculate and graph relative amylase rates, judge what the evidence supports, and use enzyme and transport ideas in an exam-style explanation.

Success looks like

  • Show relative-rate working using 1 ÷ time with the unit s⁻¹.
  • Read or plot the pH–rate pattern and limit the conclusion to the evidence.
  • Link a method limitation to an improvement, then distinguish digestion from diffusion.

We will observe, work together, then use the evidence ourselves.

Arrival task

Arrival task

Choose a route. Think first, then check the answers together.

1. Time and rate

Explain why 90 s gives a larger relative rate than 180 s under matched conditions.

Relative rate = 1 ÷ time, for the same starting amount and endpoint.

2. Read the endpoint

At 60 s starch is detected; at 90 s it is not. What endpoint value is used in the rate calculation?

Use the first observed endpoint, not an invented time between samples.

3. Show the working

Calculate relative rate for an endpoint of 120 s; show the equation, substitution and unit.

Relative rate = 1 ÷ time. A value to three significant figures is sufficient here.

4. Match the instruction

Distinguish DESCRIBE from EXPLAIN when answering about a graph.

Describe = state the pattern. Explain = link that pattern to scientific reasons.

Starter

Starter · reverse the time

Matched amounts, same iodine endpoint: reaction A reaches the endpoint in 90 s; B takes 180 s. Which is faster?

Compare the rates.

Relative rate = 1 ÷ time, for matched starting amounts and endpoints. Unit: s⁻¹, read “per second”.

I do

I do · time becomes relative rate

Turn an endpoint into a relative rate

pHEndpoint / s
6120

1 · Identify the measured endpoint time: 120 s.

1/time is a comparative rate estimate, not grams of product per second.

We do

We do · build an evidence chain

Drag a card, or select it then choose its destination.

Choose a card, then a destination. You can change your mind.

Choose a card, place it, then explain the clue. Discuss one placement together before checking the rest.

I do

I do · read the graph honestly

Build the axes, then use the evidence

0.0000.0020.0040.0060.0080.0100.01245678pH (no unit)Relative rate / s⁻¹

pH on x; relative rate / s⁻¹ on y. Equal numerical steps have equal spacing.

Five illustrative single runs, not mean rates. Points show what was sampled; do not claim an exact optimum between them.

We do

We do · repair and transfer

Digestion: chemical breakdownStarch chain → smaller sugarsDiffusion: net movementHigher → lower concentrationAmylase catalyses starch digestion. Moving particles does not itself split their molecules.

Draft explanation: “Enzymes are killed at pH 4. pH 7 is the exact optimum for every amylase, and diffusion breaks starch into sugar.”

Reference: enzymes are biological catalysts, not living organisms. Digestion breaks molecules down; diffusion is net movement from higher to lower concentration. pH can affect enzyme activity.

Which revision is supported?

You do

You do · make the evidence answer

Use the supplied evidence. Write, draw, point, explain or direct an adult.

Open evidence and reference diagrams

Enzyme: biological catalyst; speeds a reaction without being used up. Substrate: substance it acts on. pH: a measure of acidity or alkalinity. Amylase acts on starch, producing smaller sugars.

pHEndpoint / sRelative rate / s⁻¹
42400.00417
51800.00556
61200.00833
7900.0111
81500.00667

Supplied illustrative observations — not your practical results. Single runs; equal starting amounts and the same iodine endpoint. Samples every 30 s. pH 7: blue-black at 30/60 s, orange-brown at 90 s. Record 90 s.

0.0000.0020.0040.0060.0080.0100.01245678pH (no unit)Relative rate / s⁻¹Digestion: chemical breakdownStarch chain → smaller sugarsDiffusion: net movementHigher → lower concentrationAmylase catalyses starch digestion. Moving particles does not itself split their molecules.

Complete the reference graph: pH 4, 5 and 8 are shown; add pH 6 and pH 7. Stretch: add the separate repeat with a distinct symbol.

Rate: 1 ÷ endpoint time. At pH 7: 1 ÷ 90 = 0.0111 s⁻¹ (3 significant figures). These are single-run rates, not means. Highest among tested: pH 7; exact optimum is not established. The extra pH 7 repeat (120 s) is a separate trial, not silently averaged.

Topic 1 transfer: digestion breaks large molecules into smaller molecules. Diffusion is net particle movement from higher to lower concentration; it does not break a starch molecule apart. Enzymes are catalysts, not living organisms. pH changes can alter activity; slower timing alone does not prove permanent denaturation.

Describe = give a pattern; explain = link cause and effect; evaluate = use evidence and limits. An unobserved endpoint by 300 s establishes no exact reciprocal rate.

Standard

1. Calculate relative rate for pH 6 and pH 7, showing equation, substitution and units. Check that shorter time gives a larger value.

Help with this question

Write the formula first. We use 1/t throughout; no mixed 1000/t scale.

2. Complete the five-point graph using the two calculated rates and three supplied points. Label both axes and state the rise-and-fall pattern.

Help with this question

Use the supplied axes and three reference points; complete the two missing points without redrawing the whole graph.

3. Use one numerical comparison to identify the highest tested activity in the first series. Explain how pH can affect the enzyme’s active site.

Help with this question

Separate DESCRIBE (numbers/pattern) from EXPLAIN (active-site reasoning). Slower activity alone does not prove permanent denaturation.

4. Give one strength, one limitation and one linked improvement for the endpoint method. Use the separate pH 7 repeat of 120 s to qualify your confidence.

Help with this question

Use “A strength is …; a limit is …; therefore …”. Keep the 120 s repeat separate from the first series.

5. Exam-style transfer: distinguish enzyme digestion from diffusion in the supplied two-step diagram. Explain why movement from high to low concentration does not itself break starch into sugars.

Help with this question

Use the printed definitions. A catalyst speeds a reaction; a concentration gradient describes distribution.

Exit

Exit ticket

Use your book OR one ticket. Show your explanation with the supplied evidence. Say it, write it, draw it, sign it, choose it or show it; an adult can scribe it.

Illustrative matched-condition data: pH 6 endpoint 120 s; pH 7 endpoint 90 s. A separate pH 7 repeat gave 120 s. Relative rate = 1 ÷ time in seconds (s⁻¹). Samples were 30 s apart; pH 4–8 were tested.

1. Calculate both first-series relative rates and use them for a bounded comparison.

Help with this question

Show 1 ÷ time and s⁻¹. End with “in this series”.

2. Use the repeat or sampling interval to give one limitation and a justified next investigation change.

Help with this question

Name the limitation before an improvement. A shorter interval must be authorised and feasible.

Pause

Take a quiet pause.

You can look away from the screen. Come back when you are ready.

The lesson and your work are still here. Close this box to return.

Cold Call

Give thinking time. Invite a response by voice, pointing or showing work. A pupil can pass; check in privately when useful.

Lesson tools

W8L2 · Amylase and pH: Continuous-Sampling Investigation

W8L1 · Enzyme Action: Preparing the pH Investigation

Choose a slide or a print route.

Knowledge organiser

Teacher Print Tools

Print a complete pupil pack here, or print just the selected arrival questions from the Arrival task slide. Each pack includes the organiser, supported questions and the selected exit route. Teacher answers are separate in TA Brief.

Knowledge organiser

One A4 reference sheet for your book.

LAUNCH W8L3 Knowledge Organiser ... LAUNCH SCIENCE | W8L3 | Enzyme rates and evidence Knowledge organiser Learning objective I can calculate and graph relative amylase rates, judge what the evidence supports, and use enzyme and transport ideas in an exam-style explanation. Success criteria 1. Show relative-rate working using 1 ÷ time with the unit s⁻¹. 2. Read or plot the pH–rate pattern and limit the conclusion to the evidence. 3. Link a method limitation to an improvement, then distinguish digestion from diffusion. 0.000 0.002 0.004 0.006 0.008 0.010 0.012 4 5 6 7 8 pH (no unit) Relative rate = 1 / time (s⁻¹) Calculate a reciprocal Relative rate = 1/time. For 120 s: 1/120 = 0.00833 s⁻¹. For 90 s: 1/90 = 0.0111 s⁻¹. A shorter endpoint time gives a larger reciprocal, for matched amounts and the same stopping rule. Describe then qualify These illustrative first-series points rise from pH 4 to 7 and fall at pH 8. pH 7 is highest among the values tested here. A separate pH 7 repeat gives 120 s (0.00833 s⁻¹); it shows variation, not a new pH value. Explain and evaluate pH can alter substrate binding and catalysis. The graph does not directly show active-site shape or prove permanent denaturation. Matched conditions support comparison; 30 s sampling limits precision. A shorter feasible authorised interval narrows that timing window. Transfer the science Enzyme digestion chemically breaks large molecules into smaller ones. Diffusion is net particle movement from higher to lower concentration. Diffusion does not itself chemically break starch into sugars. Made by Matt | Use the reference to explain, calculate and evaluate.

Word help

enzyme

A biological catalyst that speeds a reaction without being used up.

substrate

The substance an enzyme acts on.

active site

The region where the substrate binds and the reaction is catalysed.

specificity

An enzyme acts on particular substrates because of its complementary active site.

endpoint

The agreed observable point at which timing is recorded.

control variable

A factor kept the same to make the comparison valid.

denaturation

A change in an enzyme’s three-dimensional structure that disrupts the active site and its function. Unsuitable pH or high temperature can cause this.

TA Brief

Current stage

Objective mapping: Retains calculation, graph work, evaluation and Topic 1 transfer; labels 1/time as endpoint-based relative rate and supplies all prerequisite definitions. Fifteen minutes of independent work are preserved.

Preparation

Use the supplied models, cards, data and booklet. W8L1 plans only. In W8L2, handle reagents only with the centre-approved method, prepared equipment, local risk assessment and trained supervision. The supplied-observation route needs no reagents and teaches the same interpretation; it does not certify physical practical completion. Do not infer concentrations, heating arrangements or disposal from lesson cards.

Real-world link

Choose a route at each task using what the pupil shows. Switching adds no task, record or label.

Teacher answers

Shared activities

Starter · reverse the time: 90 s is faster than 180 s for matched amounts and the same endpoint. 1/90 ≈ 0.0111 s⁻¹; 1/180 ≈ 0.00556 s⁻¹. Doubling the time halves the relative rate. Worked rate and graph point: Relative rate = 1/time = 1/120 = 0.00833 s⁻¹. Plot pH 6 at 0.00833 s⁻¹; pH has no unit. Build an evidence chain: Calculation checks: a reciprocal value; shorter time gives larger rate. Pattern/conclusion: pH 7 has the highest first-series rate among tested values; rate rises to pH 7 then falls at pH 8. Evaluation: colour judgement, shorter sampling intervals, and transparent treatment of repeats/anomalies. Graph and claim repair: First-series rates are 0.00417, 0.00556, 0.00833, 0.0111 and 0.00667 s⁻¹ for pH 4–8. The separate pH 7 repeat is 0.00833 s⁻¹, plotted with a distinct symbol at x = 7. These values do not prove an exact universal optimum or permanent denaturation. Topic 1 process labels: Starch chemically breaking into smaller sugars is enzyme digestion. Net movement of particles from higher to lower concentration is diffusion. Movement does not itself chemically break starch into sugars.

Supported arrival

  • 1. 90 s is faster.
  • 2. Orange-brown.
  • 3. 1 ÷ 100 = 0.0100 s⁻¹ (0.01 s⁻¹ is also correct).
  • 4. EVALUATE.

Supported independent task

  • 1. pH 6: 1/120 = 0.00833 s⁻¹. pH 7: 1/90 = 0.0111 s⁻¹.
  • 2. Plot (6, 0.00833) and (7, 0.0111), pH on x-axis, relative rate/s⁻¹ on y-axis. Accept equivalent pupil-directed placement.
  • 3. pH 7 is fastest in the first series, because 0.0111 s⁻¹ is the highest measured relative rate (or 90 s the shortest time).
  • 4. The exact endpoint between samples is unknown. A shorter fixed interval could narrow the timing window if authorised and feasible; it does not remove every uncertainty.
  • 5. Starch breaking into smaller sugars: digestion. Particles moving down a concentration gradient: diffusion.

Supported exit

  • 1. 1/120 = 0.00833 s⁻¹; pH 7 is faster in the first series (90 s).
  • 2. The first statement is supported. Only pH 4–8 in these conditions were tested; the repeat also shows variation.

Standard arrival

  • 1. The same measured change takes less time; 1/90 is larger than 1/180.
  • 2. 90 s, while acknowledging the endpoint was reached after 60 s and by 90 s.
  • 3. Relative rate = 1/120 = 0.00833 s⁻¹.
  • 4. Describe states how values change; explain uses biology, such as pH affecting the active site, to account for the pattern.

Standard independent task

  • 1. Relative rate = 1/time. pH 6: 1/120 = 0.00833 s⁻¹. pH 7: 1/90 = 0.0111 s⁻¹. The shorter time produces the larger reciprocal rate.
  • 2. x-axis pH (no unit); y-axis relative rate/s⁻¹. Points 4:0.00417, 5:0.00556, 6:0.00833, 7:0.0111, 8:0.00667. Rate rises from pH 4 to 7, then falls at pH 8.
  • 3. pH 7 has the highest first-series rate, 0.0111 s⁻¹ versus e.g. pH 4 at 0.00417 s⁻¹. pH can alter the active-site environment/shape and affect substrate binding and catalysis. The graph does not prove permanent denaturation or an exact universal optimum.
  • 4. Strength: matched starting amounts/temperature and a common endpoint support comparison. Limitation: 30 s intervals or subjective colour judgement. Improvement: shorter fixed intervals if authorised, or consistent agreed colour judgement; link it to the limitation. The pH 7 repeat gives 120 s, so variation weakens confidence from one series.
  • 5. Digestion is chemical breakdown catalysed by enzymes; amylase breaks starch into smaller sugars. Diffusion is net particle movement from higher to lower concentration. Moving particles does not itself change starch molecules chemically.

Standard exit

  • 1. pH 6: 0.00833 s⁻¹; pH 7: 0.0111 s⁻¹. pH 7 is faster in the first series under these matched conditions.
  • 2. Variation: repeat matched trials across all pH values to judge the pattern. Or 30 s timing gap: shorter fixed intervals narrow the endpoint window if authorised.

Stretch arrival

  • 1. Its relative rate halves.
  • 2. It summarises time to an observed endpoint, with sampling and colour limits. It does not continuously measure the amount changed per instant.
  • 3. 1/120 = 0.00833 s⁻¹; 1000/120 = 8.33 on that stated scaled convention. They must not be mixed on one unlabelled axis.
  • 4. For example: one trial per pH limits repeatability evidence, so repeat matched trials before treating the peak as secure.

Stretch independent task

  • 1. pH 6 = 1/120 = 0.00833 s⁻¹. First pH 7 = 1/90 = 0.0111 s⁻¹. Separate repeat pH 7 = 1/120 = 0.00833 s⁻¹; it equals the first pH 6 rate. Keep both pH 7 observations visible.
  • 2. First-series graph uses the five supplied/calculated coordinates. Repeat belongs at (7, 0.00833), as the same IV condition measured again, with its own symbol/key. Do not silently replace or average raw points.
  • 3. The claim is too broad. pH 7 is highest only in the first series among pH 4–8 tested. A 120 s repeat shows variation and matches the first pH 6 time. Untested values and other amylase sources/conditions remain unknown. pH effects on active sites are a biological explanation, not direct molecular observations from this graph.
  • 4. Matched starting amounts/temperature and common endpoint strengthen validity. A 30 s interval limits timing precision; a shorter fixed interval could narrow that gap if feasible/authorised. It does not remove subjective colour judgement, variable starting conditions or all repeat variation.
  • 5. Digestion chemically breaks large molecules down; diffusion moves particles down a concentration gradient. They are different processes. The graph measures an endpoint in starch breakdown, not membrane transport, concentration gradients across a gut wall or transport proteins.

Stretch exit

  • 1. Repeat rate = 1/120 = 0.00833 s⁻¹, matching first-series pH 6. It shows variation and weakens an exact-optimum claim.
  • 2. A shorter authorised interval narrows the timing window, or repeats clarify variation. Lower activity alone does not establish irreversible structural change; the graph does not measure active-site structure or recovery.

OpenStax: enzymes

Next teaching after W8L3: w/c 2 November, after half term.

Made by Matt