Topic Summaries

Culturing microorganisms

Previous Module
Next Module

Plant disease and monoclonal antibodies

The brain and the eye

Reproductive hormones and plant hormones

Genetic engineering and modification

Resource cycles and environmental change

  • Bacteria multiply by cell division (binary fission) as frequently as once every 20 minutes, but only if they have enough nutrients and a suitable temperature.
    • Bacteria can be grown in a nutrient broth solution.
    • Bacteria can be grown as colonies on an agar gel plate.
  • Uncontaminated cultures of microorganisms are used to investigate the action of disinfectants and antibiotics. They are prepared using aseptic technique:
    • Petri dishes and culture media must be sterilised before use to prevent growing foreign microorganisms.
    • Inoculating loops must be sterilised by passing them through a flame before being used to transfer microorganisms to the petri dish.
    • The Petri dish should be stored upside down with the lid secured with adhesive tape to reduce the contamination risk from airborne microorganisms and stop condensation from pooling.
    • Cultures should be incubated at 25 °C to encourage growth of the microorganisms without growing contaminating microorganisms from humans (which grow best at 37 °C).

Effect of three antibiotics (A, B and C) on bacterial growth:
A = No effect
B = Inhibits growth weakly
C = Inhibits growth strongly

Unlock Culturing microorganisms

Subscribe to SnapRevise+ to get immediate access to the rest of this resource.

Premium accounts get immediate access to this resource.

Previous Module
Next Module