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Microbiology and Pathogens

Measuring bacterial growth

  • 2 things to know
  • Papers 1 and 3

Overview

Recall questions on total and viable counts, dilution plating, turbidity, and the haemocytometer.

What you need to know

Answer each one before you reveal it.

Your recallNot started
Evaluation

Describe the principle of dilution plating for counting bacteria.

Key term

How is optical density measured when monitoring bacterial growth?

Questions from this subtopic

Each one with the model answer underneath.

  1. 1

    What is a limitation of direct cell counting using a haemocytometer?

    Model answer

    It includes both living and dead cells in the count, so does not distinguish viable cells.

  2. 2

    How does a haemocytometer enable direct cell counting?

    Model answer

    It has a counting chamber of known volume, allowing cell concentration to be determined by counting cells in a defined space.

  3. 3

    Describe the principle of dilution plating for counting bacteria.

    Model answer

    A culture is serially diluted, then known volumes are spread onto agar plates to count colony-forming units.

  4. 4

    Why does dilution plating count only viable cells?

    Model answer

    Because each colony arises from one living cell or group of cells; dead cells cannot form colonies.

  5. 5

    How is dry mass measurement of bacterial growth carried out?

    Model answer

    Culture samples are centrifuged, the pellet is dried, and the dry mass is measured.

  6. 6

    How does turbidity measurement indicate bacterial growth?

    Model answer

    A colorimeter or spectrophotometer measures light absorbance, which increases as cell density increases.

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Biological Molecules
Cells, Viruses and Reproduction of Living Things
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ALag phase shows no increase.
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Oxidation means loss of electrons or hydrogen.
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