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AQA Biology 4.1.1.6

Culturing microorganisms

Bacteria double, again and again. Set up a plate safely, measure the clear zones around antibiotic discs, then work out how many bacteria there will be.

Biology required practical 2

Start here

Two slices of bread.

Two slices from the same loaf. One goes in a bag on the kitchen worktop, the other in a bag in the fridge. A week later, you check them.

If you had to guess, would mould and bacteria grow faster somewhere warm, or somewhere cold?

Binary fission

One becomes two, every division.

Bacteria multiply by simple cell division, called binary fission, as often as once every 20 minutes if they have enough nutrients and a suitable temperature. They can be grown in a nutrient broth solution or as colonies on an agar gel plate. Each division doubles the number. Press Divide and watch the count.

0 min: 1

One bacterium at the start.

Aseptic technique

Keep the culture pure, and keep yourself safe.

Uncontaminated cultures are needed to investigate disinfectants and antibiotics. Tap each step for the reason.

Biology required practical 2

Which antibiotic works best?

Investigate the effect of antiseptics or antibiotics on bacterial growth using agar plates and measuring zones of inhibition. Spread bacteria evenly over the agar. Add paper discs soaked in each antibiotic, and a control disc soaked in sterile water. Use the same disc size, concentration and incubation time for a fair test. Incubate at 25 °C. Tap a disc to measure its clear zone.

Tap a disc.

Equation · area of a clear zone

You measure the diameter, but the equation needs the radius. Halve it first, as its own line:

r = diameter ÷ 2

Keep every length in mm, so the area comes out in mm2: cm × 10 gives mm. π is a fixed number, about 3.14. Tap the quantity you want to find.

Equation

Area of a circle

Side by side: multiply.
One over the other: divide.

Tap the quantity you want to find.

Written out

A = π r²

A
area
mm²
π
pi, about 3.14
r
radius
mm

Two steps · how many bacteria after a time?

Step 1 finds how many times the bacteria divide, using the triangle below. Time and mean division time must be in the same unit: hours × 60 gives minutes. Step 2 doubles the starting number once for each division, one line per division, just as you did with the Divide button.

Equation

Number of divisions

Side by side: multiply.
One over the other: divide.

Tap the quantity you want to find.

Written out

number of divisions = time ÷ mean division time

t
time
min
n
number of divisions
no unit
d
mean division time
min

bacteria = starting number × 2 for each division

Think again · body temperature?

“Incubate at 37 °C: that’s body temperature, so they’ll grow best.”

Your call

Choose

Why are school cultures incubated at no more than 25 °C?

Sort

Do it, or don’t?

Place each action.

Tap a card, then tap the box it belongs in. Tap a placed card to take it back.

Command words in this lesson

Explain why
Each step, then what it prevents.
Calculate
Halve, then πr². Or divide, then double.
Compare
Zone sizes, in a fair test, against the control.

Key fact

Bacteria multiply by binary fission, as often as every 20 minutes. The bigger the clear zone around a disc, the more effective the antibiotic or antiseptic.

Key note · AQA 4.1.1.6

Culturing microorganisms

  1. Bacteria multiply by binary fission, as often as once every 20 minutes with enough nutrients and a suitable temperature.
  2. Grow them in nutrient broth or as colonies on an agar gel plate.
  3. Aseptic technique: autoclave dishes and media; flame the loop; lift the lid slightly; tape the lid with a few strips; store upside down; incubate at 25 °C in school.
  4. Required practical 2: the bigger the clear zone, the more effective the antibiotic or antiseptic. Use a control disc.
  5. Area of a clear zone: halve the diameter, then A = πr².
  6. Bacteria after a time: number of divisions = time ÷ mean division time, then double once for each division.

Photograph this card. Tomorrow, cover it and say each line first.

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