Bacteria and disease Flashcards
What are pathogens
Microorganisms that cause disease
How can you investigate microorganisms even though they are small
By culturing them
What is culturing
Growing large numbers of the microorganisms so they can be measured in some way
What are the most cultured organisms
Bacteria and fungi
Why is important to take great care when culturing
There’s a risk a mutant strain can grow that may be pathogenic
there is a risk of contamination
When culturing a pure strain anything from the air will contaminate it
What are some health and safety precautions that must be followed when culturing
Making sure the equipment is sterile
Once the culture has grown it cannot leave the lab
Sterilize culture at 121 degrees got 15mins
What are the steps needed for culturing microorganism
1) Find microorganism you want to culture
2) Right nutrients to grow microorganisms (medium)
3) Introduce microorganism to medium
4) The sterile broth in the flask
5) Flsk is then stoppered again with cotton wool
6) Flask is incubated
What is the nutrient medium
What form does it come in
Usually nutrient agar
Can come in nutrient broth (nutrients in liquid) or solid form
What is agar
Why is agar useful
A jelly extracted from seaweed
It doesn’t melt until it is heated to 90 degrees
How are most microorganisms grown
Medium enriched in good protein such as blood yeast or meat
What is a selective medium
A medium in or on which only a select group of microorganisms with particular requirements will grow
What is a selective medium important for
Identifying the particular mutant strain of microorganisms and antibiotic resistance
Identifying microorganisms that have been genetically modified
What is inoculation
Getting bacteria onto your agar or into your broth
How do you get a pure culture
isolation is needed
How does isolation take place
1) Growing a culture under anaerobic conditions
2) Indicator media that cause certain types of bacteria to change color
3) Different nutrients to grow different microorganisms
How can bacteria or single-celled fungi cultured in a nutrient broth be counted
Using a microscope and haemocytometer
What is a haemocytometer
Consists of a specialised thick microscope slide with a rectangular chamber that holds a standard volume of liquid
Why is the sample of nutrient broth diluted with trypsin blue
The dye stains dead cells blue so you can identify them and count the living organisms
What does the corner of the haemocytometer have
Squares divided into 16 smaller squares
Why is the haemocytometer calibrated
So the number of bacterial and fungal cells in one set of 16 squares equates to the number of cells X10 to the ower of 4 of broth
What is turbidimetry
What happens
An alternative way of measuring the number of cells in culture (a specialized form of colorimetry)
As the number of bacterial cells in a culture increase, it becomes increasingly cloudy)
What does a colorimeter measure
How much light passes through a sample
How is a calibration curve produced
What does it help us measure
By growing a control culture and taking samples at regular time intervals
The number microorganisms using turbidimetry
What is diluting plating
What is used to find
Another way of counting microorganisms in a culture
used to find total viable cell count
What is the technique dilution plating based on
The idea that each colony on an agar plate have grown from a single, viable microorganism on the plate
What happens if the number of colonies is multiplied by a dilution factor
Then the total viable count for the original sample can be determined
How can the accuracy of dilution plating after finding the mean measured
by using a haemocytometer to count the original culture
What is a simple way to assess the growth of a cultured fungi
To measure the diameter of the patches of mycelium
Explain the process if finding the growth of cultured fungi
1) Different petri dish at different temperature
2) measure the diameter of each fungal colony
3) The temperature that has resulted in the largest mean for growth is the optimum temperature
What is the generation time
The time between bacterial division
Do bacteria rapidly divide
Yes they always divide very quickly
Why do we use log to deal with bacteria
Because bacteria divide rapidly and log makes it easier to deal
How is log represented on the graph
Y-axis is in powers of 10 and x-axis is time/hrs
What is the exponential growth rate formula
What does each stand for
K=log10Nt -log10N0 ---------------------------- log102 x t k=exponenyial growth rate Nt=no.of organs at time t No=No.of organisms at time 0 k = exponential growth rate constant t= the time the colony has been growing
What are the 4 stages for this growth curve
- lag phase (When bacteria are adapted to their maximum environment and are not yet reproducing at their maximum rate)
- log phase (When the rate of bacterial production is close to or at theoretical maximum)
- stationary phase (As the no. of new cells formed by binary fission is equal t the no. of cells dying)
- death phase (when reproduction has almost ceased)
Give two reasons why the exponential growth of bacteria doesn’t continue
1) Reduction of nutrients available
2) Build up of waste products