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Edexcel A Level (IAL) Biology -6.2 Measuring the Growth of Microorganisms- Study Notes- New Syllabus

Edexcel A Level (IAL) Biology -6.2 Measuring the Growth of Microorganisms- Study Notes- New syllabus

Edexcel A Level (IAL) Biology -6.2 Measuring the Growth of Microorganisms- Study Notes -Edexcel A level Biology – per latest Syllabus.

Key Concepts:

  • 6.2 understand the different methods of measuring the growth of microorganisms, as illustrated by cell counts, dilution plating, mass and optical methods (turbidity)

Edexcel A level Biology-Study Notes- All Topics

Methods for Measuring the Growth of Microorganisms

🌿 Introduction

Microorganisms multiply quickly, so we need reliable techniques to measure their growth. Different methods measure different things: total cells, living cells, biomass or turbidity. These techniques are widely used in research labs, food microbiology, medicine and industry.

1. Cell Counts (Direct Microscopic Counting)

What this measures

  • Total number of cells, including both living and dead.

How it is done

  • A sample is placed on a haemocytometer, a special slide with a ruled grid.
  • Cells within selected squares are counted using a microscope.
  • Calculations convert these counts into cells per unit volume.

Advantages

  • Quick results.
  • No incubation needed.
  • Useful when immediate estimates are required.

Limitations

  • Cannot distinguish live from dead cells.
  • Difficult if cells clump together.
  • Accuracy depends on even distribution of cells on the slide.

2. Dilution Plating (Viable Count Method)

What this measures

  • Number of living cells that are capable of forming colonies.

How it is done

  • The sample is diluted in steps (e.g., 1 in 10 serial dilutions).
  • A known volume from each dilution is spread on nutrient agar.
  • After incubation, colonies are counted.
  • Each colony arises from a single viable cell.
  • Colony count × dilution factor gives the number of living cells in the original culture.

Advantages

  • Measures only viable cells.
  • Very accurate for assessing living population size.

Limitations

  • Time-consuming because of incubation.
  • Some microbes do not grow well on agar.
  • Requires clean, aseptic handling.

3. Mass Measurement (Biomass Estimation)

What this measures

  • Total mass of microbial material, either wet or dry.

Wet Mass

  • Cells are collected and weighed without removing water.
  • Quick but less accurate due to variable water content.

Dry Mass

  • Cells are filtered and dried completely in an oven.
  • The remaining solid mass is weighed.
  • More accurate but takes longer.

Advantages

  • Suitable for organisms that grow as clumps or filaments (e.g., fungi).
  • Good for large-scale cultures.

Limitations

  • Destructive method.
  • Wet mass is unreliable.
  • Dry mass requires extra equipment and time.

4. Optical / Turbidity Method

What this measures

  • Cloudiness (turbidity) of a culture, which increases as cell numbers increase.

How it is done

  • A colorimeter or spectrophotometer passes light through the culture tube.
  • Microbial cells scatter the light.
  • Higher turbidity means more cells.
  • Turbidity values can be converted to estimated cell numbers using a calibration graph.

Advantages

  • Very fast and non-destructive.
  • Allows continuous monitoring of growth over time.
  • Easy to perform.

Limitations

  • Measures both living and dead cells.
  • Needs a calibration curve for accuracy.
  • Not reliable with organisms that form clumps or biofilms.

Summary Table

MethodMeasuresStrengthLimitation
Cell countTotal cells under microscopeQuick, no incubationCannot separate live/dead
Dilution platingLiving, viable cellsVery accurateSlow, needs sterile technique
Wet/Dry massBiomassGood for fungiDestructive, wet mass unreliable
TurbidityCloudiness linked to cell numberFast and easyIncludes dead cells, needs calibration

Quick Recap
Cell counts → microscope → total cells.
Dilution plating → colonies → living cells only.
Mass measurement → weigh biomass → best for fungi.
Turbidity → light scattering → quick but includes dead cells.
Choose the method based on speed, accuracy, and organism type.

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