Method A - Preparing the agar plates of a colony of bacteria
Glass Petri dishes and agar gel must be sterilised in an autoclave before use or pre-sterilised plastic Petri dishes can be bought.
Reason – this will kill any bacteria that are present in the solution or on the Petri dishes.
Pour the sterile agar plates and allow to fully set.
Reason – this provides the selected bacterium with all the nutrients needed to grow.
Use a sterile pipette to add a few drops of the microorganism solution to the agar. Close the lid of the agar plate and place the pipette in disinfectant.
Reason – this solution contains the bacteria that will grow on the agar.
Unwrap a sterile spreader or sterilise a spreader in ethanol. Use the spreader to spread the microorganism solution, across the entire surface of the agar plate.
Reason – this allows a lawn of bacteria to be produced across the whole of the plate. Replace the lid as soon as possible, secure with tape.
Label and invert the plate, and store upside down.
Reason – this stops additional unwanted bacteria in the air contaminating the plate. Do not fully seal the lid, as this will stop oxygen reaching the bacterium, and this may encourage harmful anaerobic bacteria to grow. Labels are important, as this identifies the growing bacterium.
Incubate at a maximum temperature of 25°C in schools and colleges.
Reason – this reduces the chance of growing harmful pathogens. Hospital laboratories would incubate plates at 37°C (body temperature) to allow quick growth and identification.
This allows the selected bacteria to be grown under laboratory conditions, and it requires skill and experience. Additional contaminating bacteria will complicate the experiment and possibly confuse the results. Aseptic technique is vital when the effectiveness of antibacterial substances is being tested.
Method B - Adding antibiotic or antiseptic soaked patches to pre-prepared agar plates
By adding filter paper soaked in a variety of anti-microbial solutions to the pre-prepared agar plate (method A), the effective of the solutions can be tested experimentally. A clear area (zone of inhibition) indicates that the bacteria have been killed.
Soak filter paper disks in a variety of solutions, use either different concentrations of the same solution, or a variety of different solutions.
Reason - the effectiveness of the solutions at killing the bacteria can be tested.
Measure the clear area around the soaked filter paper disks. A control disk must be also included.
Reason - size of zone indicates the effect of the substance tested on the growth of the specific bacterium.