Culturing Microorganisms - PRACTICAL Flashcards

Cell Biology (33 cards)

1
Q

What is the purpose of a culture medium?

A

To grow bacteria and other microorganisms

It contains carbohydrates, minerals, proteins, and vitamins needed for growth.

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2
Q

What are two types of culture media mentioned?

A
  • Nutrient broth solution
  • Solid agar jelly
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3
Q

What do bacteria form on the surface of agar plates?

A

Visible colonies or an opaque covering of bacteria

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4
Q

What is used to transfer microorganisms to the culture medium?

A
  • Inoculating loop
  • Sterile dropping pipette
  • Spreader
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5
Q

At what temperature are cultures of microorganisms typically kept in schools?

A

Above 25 °C

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6
Q

Why are pathogens more likely to grow above 25 °C?

A

Because harmful pathogens are more likely to grow at higher temperatures

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7
Q

What temperature conditions are used in industrial settings for culturing bacteria?

A

Higher temperatures to promote faster growth

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8
Q

What is the first step in testing the action of antibiotics on bacterial cultures?

A

Place paper discs soaked in different types or concentrations of antibiotics on an agar plate

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9
Q

What is the area called where bacteria die around the antibiotic disc?

A

Inhibition Zone

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10
Q

What is the purpose of using a control disc in antibiotic testing?

A

To ensure any difference in bacterial growth is due to the antibiotic alone

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11
Q

How long should the agar plate be left for after placing the antibiotic discs?

A

48 hours at 25 °C

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12
Q

What does a larger inhibition zone indicate?

A

The antibiotic is more effective against the bacteria

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13
Q

What can contamination by unwanted microorganisms lead to?

A

Affecting results and potentially causing the growth of pathogens

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14
Q

How should Petri dishes and culture medium be prepared to avoid contamination?

A

Sterilized before use, e.g., by heating to a high temperature

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15
Q

What should be done to the inoculating loop before transferring bacteria?

A

Sterilized by passing it through a hot flame

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16
Q

How should the lid of the Petri dish be secured after transferring bacteria?

A

Lightly taped on

17
Q

Why should the Petri dish be stored upside down?

A

To prevent drops of condensation from falling onto the agar surface

18
Q

What can be compared to assess the effectiveness of different antibiotics on bacteria?

A

The relative sizes of the inhibition zones

A larger inhibition zone indicates a more effective antibiotic against the bacteria.

19
Q

What does a larger inhibition zone around a disc indicate?

A

More effective antibiotic against the bacteria.

20
Q

To obtain accurate results, what should be calculated for the inhibition zones?

A

The area of the inhibition zones using their diameter.

21
Q

What is the equation for the area of a circle?

22
Q

In the equation Area = πr², what does ‘r’ represent?

A

The radius of the inhibition zone.

23
Q

How is the radius of the inhibition zone calculated?

A

It’s equal to half the diameter.

24
Q

What units are used to express the area of an inhibition zone?

A

cm² or mm².

25
What numerical value can be used for π in calculations if not available on a calculator?
3.14.
26
How do you find the radius of zone A if the diameter is 14 mm?
Radius of A = 14 mm / 2 = 7 mm.
27
What is the area of inhibition zone A if the radius is 7 mm?
Area of A = π x 7² = 154 mm².
28
How do you find the radius of zone B if the diameter is 20 mm?
Radius of B = 20 mm / 2 = 10 mm.
29
What is the area of inhibition zone B if the radius is 10 mm?
Area of B = π x 10² = 314 mm².
30
How does the area of inhibition zone B compare to zone A?
314 mm² is just over twice 154 mm².
31
True or False: The inhibition zone of antibiotic B is roughly twice the size of the inhibition zone of antibiotic A.
True.
32
What equation can also be used to calculate the area of a bacterial colony?
Area = πr².
33
What must be measured to calculate the area of a bacterial colony?
The diameter of the colony.