Aseptic Technique: RP Flashcards

1
Q

What is aseptic technique?

A
  • Working in sterile conditions to prevent contamination of sample and infection of others.
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2
Q

Before inoculation, what sort of steps should we do to prevent contamination of our bacteria sample?

A
  • Sterilise al equipment to kill microbes.
  • Sterilise work surfaces with disinfecant to kill microbes.
  • Wash hands with soap to kill microbes.
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3
Q

During inoculation, what sort of steps should we do to prevent contamination of our bacteria sample?

A
  • Work near bunsen burner, convection currents will sterilise the air.
  • Only open petri dish SLIGHTLY/ at angle.
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4
Q

After inoculation, what sort of steps should we do to prevent contamination of our bacteria sample?

A
  • Sterilise all equipment to kill microbes (ie. place in disinfectant.)
  • Sterilise work surfaces with disinfectant to kill microbes.
  • Wash hands with soap to remove microbes.
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5
Q

What do we pass through bunsen burner roaring flame whilst preparing lawn plate culture of bacteria?

A
  • Neck of the bottle (that had bacteria in it.)
  • After you have transferred certain volume of bacteria using a sterile pipette, flame the neck of bottle again!
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6
Q

What is a petri dish with bacteria culture in known as?

A
  • Known as a lawn plate.
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7
Q
A
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8
Q

Why do we leave our lawn plate for 5-10 minutes after spreading bacteria evenly across the agar?

A
  • Allows for broth to be absorbed into the agar.
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9
Q

Why do you GENTLY use forceps to press down the antibiotic multi-test ring onto the lawn plate? Where do you press down?

A
  • Press down on parts between different antibiotics, not on the antibitoics directly as this will lead antibiotic to be released instantly!!
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10
Q

Why do we only slightly tape the agar plate down? ie. not all the way.

A
  • Prevents growth of harmfu, anaerobic bacteria.
  • Bacteria need the oxygen to replicate.
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11
Q

What do we meaure after we have incubated the agar plate for 72 hours with antibiotic multi-use ring?

A
  • Measure diamaters of zones of inhibition.
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12
Q

What graph do we plot for this RP?

A
  • Bar chart
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13
Q

How would we conclude that a certain antibiotic is SIGNIFICANTLY more effective than other antibiotics from this practical?

A
  • Mean diameter of zone of inhibition is largest AND it’s standard deviation doesn’t overlap.
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14
Q

Areas of innacuracy from this practical?

A
  • Only tested on 1 bacteria.
  • Only tested 8 antibiotics.
  • Don’t know of any side-effects anitbiotic may have on humans.
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15
Q

What do we use to spread the bacteria culture in this RP?

A
  • Plastic, sterile spreader.
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