Techniques in Microbiology Flashcards
What is the difference in biosafety level 3 and 4 - give an example of a microbe for each
Manipulations are formed in a safety cabinet
Tuberculosis and Ebola
Define a pure culture
A culture containing only a single kind of microbe
Equation including magnification
Image size = actual size*magnification
Give 2 limitations of microscopic counts
Small cells can be overlooked
Dead and alive cells cannot be distinguished
Outline the spread-plate, streak-plate and pour-plate method - what must occur before a spread and pour plate method
Streak - spreading of a mixture using an inoculating loop or swab
Spread - spreading of a mixture using a sterile bent rod
Pour - mixture of sample and liquid agar is incubated
Dilution
Give 1 limitation of the pour-plate technique
Hot agar may kill cells
What is the great plate count anomaly - give 2 reasons for it
The discrepancy in results between plate counts and microscopy
- Dead cells are counted
- Growth requirements aren’t met
Give three ways to measure cell mass - how does the 3rd one work - turbidity?
Dry weight
Concentration of a particular cell constituent
Spectrophotometry - amount of light scattered is directly proportional to cell biomass