Antimicrobial properties in plants Flashcards

1
Q

State six aseptic techniques.

A

-Wipe down surfaces with antibacterial cleaner before and after the experiment.
-Use a Bunsen burner in the workspace so convection currents draw microbes away from the culture.
-Flame the wire hoop before using it to transfer bacteria.
-Flame the neck of any bottles before using them.
-Keep all vessels containing bacteria open for the minimum amount of time.
-Close windows and doors to limit air currents.

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2
Q

How is a plant extract prepared?

A

Grind the selected plant sample into a paste and add a few cm3 of ethanol.

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3
Q

How is the control of the practical set up?

A

Dip a filter paper disc in ethanol and place it on the agar plate.

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4
Q

Why are bacteria incubated at 25°C?

A

To prevent the growth of pathogens (harmful bacteria) which occurs at higher temperatures.

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5
Q

How can you compare the effectiveness of different extracts applied to the same bacteria?

A

Measure the diameter and calculate the area of the zone of inhibition (clear zone) on the agar.

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6
Q

What does the zone of inhibition indicate?

A

It indicates the bacteria killed by the antibiotic. The larger the zone, the more effective the antimicrobial properties of the plant.

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7
Q

State the hazards and precautions of this practical.

A

Naked flame: keep away from flammable materials, tie hair up and wear goggles.
Bacteria is a biohazard, use disinfectant and wash hands.
Disinfectant is flammable, keep away from naked flame.

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8
Q

Why should the lid not be completely taped to the petri dish?

A

To allow oxygen to enter the petri dish, preventing the growth of harmful anaerobic bacteria.

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9
Q

Why is the petri dish incubated upside down?

A

To prevent condensation from forming on the lid and dripping down onto the agar.

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10
Q

Describe the graph that can be plotted from the results of this practical.

A

A bar chart of the zone of inhibition against plant extract.

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