Edexcel A-Level Biology B 9BI0
Biological Molecules
Cells, Viruses and Reproduction of Living Things
Classification and Biodiversity
Exchange and Transport
Energy for Biological Processes
Microbiology and Pathogens
Modern Genetics
Origins of Genetic Variation
Control Systems
Ecosystems
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.
How is optical density measured when monitoring bacterial growth?
Questions from this subtopic
Each one with the model answer underneath.
- 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
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
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
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
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
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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