Preparing an uncontaminated bacterial culture using aseptic technique
1. Sterilise petri dishes, culture media (such as agar) and surfaces to kill unwanted bacteria
2. Sterilise inoculating loop by passing it through a flame to kill unwanted bacteria
3. Use this to spread bacteria onto agar, minimise lifting lid of Petri dish
4. Secure lid of Petri dish with adhesive tape to prevent microorganisms from air entering
5. Store plates upside down so condensation doesn't drip onto agar, disrupting colonies
6. Incubate at 25 degrees celsius to allow growth of bacteria, preventing growth of pathogens