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explain examples of aseptic techniques that could be used
- wash hands with soap / disinfect surfaces to prevent contamination
- sterilise pipette / spreader / boil agar growth medium → kill microbes / prevent contamination
- flame neck of bottle of bacteria to kill microbes / prevent contamination
- bunsen burner close → upward current of air draws air-borne microbes away to prevent contamination
- lift lid of petri dish slightly / minimise opening to prevent entry of microbes / contamination
describe a method to investigate effect of antimicrobial substances e.g antibiotics on microbial growth
- prepare area using aseptic techniques
- use a sterile pipette to transfer bacteria from broth to agar plate using aseptic techniques
- use a sterile spreader to evenly spread bacteria over agar plate
- use sterile forceps to place same size discs that have been soaked in different types / concentrations of
antimicrobials for same length of time, onto agar plate (at equal distances)
- lightly tape lid onto plate (not fully sealed), invert and incubate at 25C for 48 hours
- measure diameter of inhibition zone around each disc and calculate area using πr^2
why is it important to maintain a pure culture of bacteria?
- bacteria may outcompete bacteria being investigated
- or could be harmful to humans
why hold lid with 2 pieces of tape instead of sealing it completely?
- allows oxygen in preventing growth of anaerobic bacteria
- which are more likely to be pathogenic
why use a paper disc with water?
- act as a control
- ensuring antimicrobial prevented growth, not paper disc
why incubate upside down?
condensation drips onto lid rather than surface of agar
what if inhibitation zones are irregular?
repeat readings in different positions, calculate a mean
why not use higher antimicrobial conc?
more bacteria killed so clear zones may overlap
why incubate at 25C or less?
below human body temp to prevent growth of pathogens
describe how data about the effect of antimicrobial substances can be presented as a graph
- categorical data: bar chart (x axis = type of antimicrobial, y axis = area of zone of inhibition mm3)
- continuous data: line graph joined by line of best first (x axis = concentration of antibiotic, y axis area of zone of inhibition mm3)
explain the presence and absence of clear zones
- clear zones: antimicrobial diffuses out of disc into agar, killing / inhibiting growth of bacteria
- larger clear zones: more bacteria killed so more effective antimicrobial
- no clear zones: if antibiotic used, bacteria may be resistant or antibiotic may not be effective against that specific bacteria