Testing the effectiveness of various anti microbial agents.

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Testing the effectiveness of various anti microbial agents.

Aim: ~

        We are trying to find out what bleach solutions and other solutions will work best at killing Microcuccul luteus (safe bacteria).

Apparatus: ~

2 Petri dishes per person

Ethanol

Scalpel

Cork borer

Bleach solutions

Other substances of your own choice

Bunsen burner

Protective mat

Cotton wool

Pipette

Predictions:~

        I predict that:

Prediction 1:~

20% bleach will be the best anti-microbial agent.

Prediction 2:~

Toothpaste will have a large inhabitation zone.

Prediction 3:~

Water would have the worst inhabitation zone.

Method: ~

*Firstly you need to sterilise the whole area and all of the equipment with ethanol. This is done so that no microbes can get into the safe bacteria environment unless it is absolutely necessary. Your hands must be washed with soap so that they do not have any bacteria on them.

        *Once this is done you need to sterilise your cork borer. You do this by dipping it in ethanol and putting up against a half roaring flame. Hold the cork borer down in to the flame at an angle, as there is a risk that the flame may come up the middle of it and burn the users hand.

        *Now you need to put four holes in the agar jelly (look at diagram ‘A’). They will be the same size (ours was 10mm) and in the exact centre of each quarter to give the substance a fair chance of working.

        *Once this is done place the lid pack on to the agar plate. You now need to write down what substance is going where. Firstly put your bleach in to on one of the agar plates. Make sure that you do not spill any on to the jelly, as this will affect the results. Do not fill the holes right up to the top, otherwise when you move the agar plate it will spill over the top and ruin the experiment.

        *You now need to repeat this exercise with the other substances that you have chosen. Make sure that you do not spill it on to the jelly or fill it right to the top as before as it will ruin the experiment.

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        *The agar plates now need to be sealed; to do this use cellotape and stick it on to the lid and over the side in a crossed position (look at diagram ‘B’), and left in a controlled environment. This should be stored for 48 hours at just over room temperature. However if this is not possible then they need to be stored for a longer period of time at room temperature. If this is done however the results may not be as good as they could be.

        *At the end of the incubation period you can now need to record ...

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