Investigating Antibiotics And Antiseptics Flashcards

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1
Q

what is grown and cultured in growth mediums

A

bacteria and some other microorganisms

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2
Q

what does a growth medium contain

A
  • carbohydrates
  • minerals
  • proteins
  • and vitamins they need to grow
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3
Q

what are the two things the growth medium could be

A
  • a nutrient broth solution

- or solid agar jelly

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4
Q

what do bacteria grown on agar plates form

A
  • visible colonies on the surface of the jelly

- which could spread out to give an even covering

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5
Q

how do you make an agar plate

A
  • hot agar jelly is poured into petri dishes
  • when jelly cools and sets, incoulating loops are used to transfer microorganisms to the agar jelly
  • the microorganisms then multiply
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6
Q

what is a petri dish

A

a shallow round plastic dish

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7
Q

how could you alternatively place the microorganisms on the agar jelly

A
  • use a sterile dropping pipette to drop the microorganisms on to the jelly
  • and use a spreader to get an even covering of bacteria
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8
Q

why are cultures of microorganisms kept at 25C in school

A

harmful pathogens are less likely to grow at this temperature

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9
Q

how is temperature managed when growing bacteria outside of school

A
  • you may culture microorganisms at a higher temperature

- to provide the optimum conditions for growth

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10
Q

what do antibiotics simply do

A

they kill bacteria inside the body

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11
Q

what do antiseptics simply do

A

they kill bacteria outside the body

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12
Q

what can you use to investigate the effect of antiseptics and antibiotics

A

cultures of bacteria

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13
Q

what is the process of investigating the effects of antibiotics (and antiseptics alike)

A
  • soak paper disks soaked in different types of antibiotics on an agar plate with an even covering of bacteria
  • leave some space between the discs
  • the antibiotic should diffuse into the agar jelly
  • leave the plate for 48 hours at 25C
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14
Q

what will antibiotic resistant bacteria do on the agar jelly compared to non-resistant bacteria

A
  • the resistant bacteria will continue to grow on the agar around the paper discs
  • while the non-resistant bacteria will die
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15
Q

what is the inhibition zone

A

the clear area that is left where the bacteria have died

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16
Q

what is the control in this experiment and why should you use it

A
  • a paper disc that has not been soaked in an antibiotic
  • you should use it because you can be sure that any difference between the growth of the bacteria around the control disc and the antibiotic disc is due to the effect of the antibiotic alone
17
Q

how will a more effective antibiotic against the bacteria be shown after the time is up

A

the antibiotic will have a larger zone of inhibition

18
Q

how do you avoid contamination by unwanted microorganisms which can affect your results

A

by using aseptic conditons

19
Q

what are the five things you can do to make sure the bacteria is in aseptic conditons

A
  • sterilise petri dishes and growth medium
  • sterilise the incoulating loop
  • keep liquid cultures in a culture vial with a lid
  • cover the petri dish with a lid
  • store the petri dish upside down
20
Q

how do you sterilise the petri dishes and growth medium

A
  • by placing them in a machine called an autoclave

- which uses steam at a high pressure and temperature to kill any microorganisms present

21
Q

how should the incoulating loop be sterilised

A
  • by passing it through a flame

- so that any unwanted microorganisms are killed

22
Q

why should you keep liquid bacteria cultures in a cultural vial with a lid

A
  • to prevent other microbes from getting in

- you should only be briefly removing the lid when transferring the bacteria

23
Q

why should the petri dish be stores upside down

A

to stop drops of condensation falling onto the agar jelly