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12 questions
Plates should be incubated
agar side on top
agar side on bottom
it doesn't matter
The inoculating loop should be sterilized in what part of the Bunsen burner flame?
in the bright blue cone
just above the bright blue cone
above the flame
at the base of the flame
Why do you heat the inoculating loop?
to kill all bacteria on it
to kill just the harmful bacteria on it
to sterilize it
to make it hot enough to melt the agar
What is the first thing to do in this practical? (after washing hands)
Heat the inoculating loop
Open the bacteria bottle
Take the lid off the petri dish
Wipe surfaces with disinfectant
Why is aseptic technique used to transfer bacteria?
To get as many pathogens as possible in the petri dish
To transfer only the wanted bacteria onto the petri dish
To kill as many bacteria as possible
To get a variety of different microorganisms in the culture
At what angle should the petri dish lid be kept when spreading bacteria onto the plate?
25°
35°
45°
55°
What is the maximum temperature for incubation?
15°C
30°C
25°C
40°C
How would you know if the petri dish had been contaminated in the practical?
Only one colour would be seen on the plate
More than one colour would be on the plate
Furry fungi could be seen
The plate smells bad
Which is NOT a reason why we only tape the lid in 2 places
so no other harmful bacteria form
so the conditions do not become anaerobic
to save the school money on tape
why is there a maximum temperature for incubation?
To save money on powering the autoclave
to stop from melting the petri dish
So that only non pathogenic bacteria are cultured
To prevent damage to the agar
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