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Biological Molecules » Temperature Practical Investigation

What you'll learn this session

Study time: 30 minutes

  • How temperature affects enzyme activity in biological systems
  • Planning and conducting controlled temperature experiments
  • Recording and analysing experimental data accurately
  • Understanding the relationship between kinetic energy and molecular movement
  • Identifying variables and controlling experimental conditions
  • Drawing conclusions from practical investigations

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Introduction to Temperature Practical Investigation

Temperature is one of the most important factors affecting biological processes. In this session, you'll learn how to investigate the effects of temperature on biological molecules, particularly enzymes, through hands-on practical work. Understanding how temperature influences molecular behaviour is crucial for explaining many biological phenomena.

Key Definitions:

  • Enzyme: A biological catalyst that speeds up chemical reactions without being used up.
  • Substrate: The substance that an enzyme acts upon during a chemical reaction.
  • Active site: The specific region of an enzyme where the substrate binds.
  • Denaturation: The permanent change in enzyme shape that destroys its function.
  • Kinetic energy: The energy of movement that molecules possess.

🌡 Why Temperature Matters

Temperature affects how fast molecules move. Higher temperatures give molecules more kinetic energy, making them move faster and collide more often. This is why reactions speed up when it's warmer - but there's a limit!

Planning Your Temperature Investigation

A good temperature investigation needs careful planning. You'll typically use an enzyme like catalase (found in potatoes) or amylase (found in saliva) to see how temperature changes affect their activity.

Common Temperature Experiments

The most popular experiments involve testing enzyme activity at different temperatures. Here are the main types you might encounter:

🥔 Catalase Investigation

Using potato pieces in hydrogen peroxide. Measure oxygen bubbles produced at different temperatures from 10°C to 70°C.

🍞 Amylase Investigation

Testing how quickly starch breaks down into sugar at various temperatures using iodine indicator.

🧪 Lipase Investigation

Measuring pH changes as fats break down into fatty acids at different temperatures.

Setting Up Your Experiment

Proper experimental setup is crucial for getting reliable results. You need to control all variables except temperature to ensure your results are valid.

Essential Equipment List

Water baths or beakers with thermometers: For maintaining different temperatures (usually 10°C, 20°C, 30°C, 40°C, 50°C, 60°C, 70°C). Measuring cylinders: For accurate volumes of solutions. Stopwatch: For timing reactions. Test tubes: For holding your reaction mixtures. Enzyme source: Fresh potato, saliva, or commercial enzyme solutions.

Controlling Variables

In any good experiment, you must identify and control your variables properly:

Independent variable: Temperature (what you're changing)

Dependent variable: Rate of reaction (what you're measuring)

Control variables: These must stay the same:

  • Volume of enzyme solution
  • Concentration of substrate
  • pH of solutions
  • Time allowed for reaction
  • Size of potato pieces (if using catalase)

Conducting the Investigation

Follow a systematic approach to ensure accurate and reliable results. Safety is paramount when working with different temperatures and chemicals.

Safety Considerations

Always wear safety goggles when using hydrogen peroxide. Be careful with hot water baths - temperatures above 60°C can cause burns. Handle glassware carefully, especially when moving between hot and cold conditions.

Step-by-Step Method

Here's a typical procedure for investigating catalase activity:

  1. Set up water baths at your chosen temperatures (10°C, 20°C, 30°C, 40°C, 50°C, 60°C, 70°C)
  2. Prepare identical pieces of fresh potato (your enzyme source)
  3. Measure equal volumes of hydrogen peroxide into test tubes
  4. Place test tubes in water baths and allow 5 minutes to reach temperature
  5. Add potato pieces simultaneously and start timing
  6. Count oxygen bubbles produced or measure foam height after set time periods
  7. Record results in a clear table
  8. Repeat each temperature at least three times for reliability

Recording and Analysing Results

Accurate data recording and analysis are essential for drawing valid conclusions from your investigation.

Data Recording

Create a clear results table with appropriate headings and units. Always include:

  • Temperature (°C)
  • Time intervals (seconds or minutes)
  • Measurement of enzyme activity (bubbles per minute, foam height, etc.)
  • Repeat readings
  • Average/mean values

Case Study Focus: Catalase in Liver Cells

Catalase is found in nearly all living organisms. In human liver cells, it breaks down harmful hydrogen peroxide into harmless water and oxygen. This enzyme works optimally at around 37°C (body temperature) but becomes denatured above 60°C. This is why fever can be dangerous - it can damage essential enzymes!

Understanding Your Results

Your results should show a clear pattern that demonstrates how temperature affects enzyme activity.

Expected Pattern

Typically, you'll observe:

  • Low temperatures (10-20°C): Slow reaction rate due to low kinetic energy
  • Medium temperatures (30-40°C): Increasing reaction rate as molecules move faster
  • Optimum temperature (around 37-40°C): Maximum reaction rate
  • High temperatures (50°C+): Decreasing reaction rate as enzymes denature
  • Very high temperatures (60°C+): Little or no activity as enzymes are destroyed

📈 Graphing Your Results

Plot temperature on the x-axis and rate of reaction on the y-axis. You should see a curve that rises to a peak (optimum temperature) then falls sharply. This classic bell-shaped curve shows the temperature-enzyme relationship.

Explaining the Science

Understanding why temperature affects enzymes helps explain many biological processes in living organisms.

The Molecular Explanation

At low temperatures, enzyme and substrate molecules move slowly with little kinetic energy. Few successful collisions occur between enzyme active sites and substrate molecules, so reaction rates are slow.

As temperature increases, molecules gain kinetic energy and move faster. More collisions occur between enzymes and substrates, increasing the reaction rate. This continues until the optimum temperature is reached.

Beyond the optimum temperature, the enzyme's protein structure begins to change. The active site loses its specific shape and the enzyme can no longer bind effectively with its substrate. This denaturation is usually permanent.

Real-World Applications

Understanding temperature effects on biological molecules has many practical applications in medicine, food science and biotechnology.

🩸 Medical Applications

Doctors use temperature to preserve organs for transplant and understand how fever affects body chemistry.

🍽 Food Industry

Food processing uses controlled temperatures to activate or deactivate enzymes in preservation and manufacturing.

🧪 Biotechnology

Industrial processes use enzymes at specific temperatures for maximum efficiency in producing medicines and chemicals.

Common Experimental Errors

Be aware of these potential problems that could affect your results:

  • Inaccurate temperature control - use proper thermometers and allow equilibration time
  • Inconsistent timing - use stopwatches and standardise measurement intervals
  • Variable enzyme concentration - use fresh materials and consistent amounts
  • pH changes - some reactions alter pH, which can affect enzyme activity
  • Insufficient repeats - always do at least three repeats for reliable averages
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