Core Practical 9: Antimicrobial Properties of Plants (Edexcel International AS Biology)

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Marlene

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Antimicrobial Properties of Plants

  • Certain plant species have the ability toĀ killĀ orĀ prevent the growthĀ of micro-organisms
  • TheseĀ antimicrobial propertiesĀ can be incorporated into the development of new drugs

Apparatus

  • Broth containing bacterial culture and nutrients
  • Agar plate
  • Pipette
  • Plastic spreader
  • Plant tissue
  • Pestle and mortar
  • Ethanol
  • FunnelĀ 
  • Glass beaker
  • Filter paper
  • Forceps
  • Stopwatch
  • Incubator

Method

  1. Prior to this practical, bacteria would have been grown in a mixture of distilled water and nutrients, along with a specific bacterial culture
    • This mixture is called aĀ broth
  2. TransferĀ some of the bacteria from the broth onto an agar plate (which is a petri dish filled with agar jelly that will serve as a growth medium for the bacteria) using aĀ sterile pipette
  3. Make sure the bacteria isĀ evenly spreadĀ outĀ by using aĀ sterile plastic spreader
    • Open the lid of the of the agar plateĀ as little as possibleĀ when doing this to avoid contaminating the plate with other fungi or bacteria present in the surrounding air
    • Place the lidĀ back on top of the agar plateĀ immediately afterwardĀ to prevent contamination
  4. To prepare the plant extracts, plant tissue must be dried and ground finely
  5. This should beĀ soaked in ethanolĀ to extract the antimicrobial substances, after which it should be filtered
  6. Equal sized discs cut fromĀ sterile absorbent paperĀ should be dipped in the plant extract using sterile forceps
  7. Leave the discs in the extract for theĀ same amount of timeĀ to ensure that they absorb a similar amount of the plant extract
    • The disc that will serve as theĀ controlĀ will only be dipped in ethanol
  8. Space the discs out evenly on the agar plate, before taping the lid on, inverting the plate andĀ incubating it at 25Ā°C
    • This temperature will ensure good bacterial growth without stimulating the growth of human pathogens
  9. Incubate for 24 to 48 hours

RP_ Growth 1

The same method as that shown above can be used to investigate the antimicrobial properties of plants. Just remember that the paper discs are soaked in different plant extracts (instead of different antiseptics) and the control disc should be soaked in ethanol (instead of sterile water)

Analysis

  • The area around each disc where bacteria cannot grow is known as theĀ clear zone
  • TheĀ largerĀ the clear zone, theĀ more effectiveĀ the antimicrobial properties of that plant extract was
  • The size of the clear zone can be determined byĀ measuring the diameterĀ or byĀ calculating the areaĀ (area = Ļ€r2)
  • RepeatĀ the experiment at least three times andĀ calculate the meanĀ of the results

RP Growth: Analysis

Record the diameter of each clear zone to the nearest whole mm, and remember to calculate the area using the radius (taken as half the value of the mean diameter of each zone)

Aseptic techniques

  • These techniques are important to use in order toĀ preventĀ the bacterial cultures on the agar plate fromĀ being contaminatedĀ by other micro-organisms or human pathogens from outside
  • Contamination will have aĀ negative impactĀ on the growth of the bacteria under investigation
  • When doing the investigation above, use the followingĀ aseptic techniques:
    • Keep windows and doorsĀ closedĀ to prevent air movement
    • DisinfectĀ surfaces and utensils regularly to prevent contamination
    • Ensure that you useĀ sterile equipmentĀ and discard afterwards (especially plastic instruments)
    • Work near aĀ Bunsen flameĀ when transferring bacteria to ensure that microbes in the air are drawn away by rising hot air
    • For the same reason as above, hold theĀ flameĀ close to the neck of the glass container of the broth every time it's opened or closedĀ 

Culturing microorganisms 1
Culturing microorganisms 2
Culturing microorganisms 3

To prepare an uncontaminated culture of micro-organisms, this procedure can be followed

Aseptic Techniques TableUncontaminated culture preparation table

Exam Tip

It is vital that one of the paper discs placed on the bacterial agar plate is not soaked in plant extract but in ethanol instead. This is to ensure that any differences in bacterial growth observed can be attributed to the antimicrobial properties of the plant extracts used and not some other factor (such as the paper discs themselves or the presence of ethanol, for example)

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Marlene

Author: Marlene

Marlene graduated from Stellenbosch University, South Africa, in 2002 with a degree in Biodiversity and Ecology. After completing a PGCE (Postgraduate certificate in education) in 2003 she taught high school Biology for over 10 years at various schools across South Africa before returning to Stellenbosch University in 2014 to obtain an Honours degree in Biological Sciences. With over 16 years of teaching experience, of which the past 3 years were spent teaching IGCSE and A level Biology, Marlene is passionate about Biology and making it more approachable to her students.