W4-lecture 2: Microbial growth Flashcards
What is the name of the enzyme that will destruct the peptidoglycan wall during cell division?
Autolysin
What is the name of the enzyme allows peptidoglycan subunit to be exported across the cytoplasmic membrane
Bactoprenol
What is the name of the ring that contains the autolysin?
the FtsZring
What are the scars that you can see near the septum on the bacteria
the wall bands, they separate the old and new peptidoglycan
What is a selective medium?
medium that allow the growth of only some kind of bacteria can grow on it
What is a differential medium?
medium that helps to differentiate the different kind of bacteria that grow on it
Give two example of selective medium ?
MacConkey Mannitol-salt
What does the macconkey medium help differentiate?
Differentiate (differential media) between Lactose fermenters (Pink) and Lactose non‐fermenters (colorless).
What does the bile salts inhbits in the macconley medium?
The gram+ and it is permissive for the gram enteric pathogens.
What does the mannitol-salt is selective for
Selective medium, high NaCl concentration: inhibits most Gram‐and many Gram+.
Name one use of the mannitol-salt medium
Used for isolation or detection of Staphylococcus.
What does the mannitol-salt help differentiate?
Mannitol fermenters: +, yellow; ‐, pink.
T or F : staphylococcus aureus is mannitol.
false, is is a mannitol fermenter.
Where will the microorganisms grow on the spread-plate technique
on the agar (2D)
Where will the microorganisms grow on the pour-plate method?
in 3 dimensions.
What is the advantage of the pour-plate method?
you can grow anaerobes.
What is used to make the count under the microscope ?
the counting chamber
If there is 159 colonies on a plate that is diluted at 10^-3, what will be the CFU?
CFU is the number of colonie per mL. Since there is 159 colonies in 10^-3, plate count x dilution factor is (10^3x159) so the CFU is 1.59x10^5 cells per mL of original sample
What are the pros and cons of the counting chamber?
• Pros: Fast, no need to wait until bacteria has grown (so can be done on bacteria that can’t grow). • Cons: Small cells can be missed, motile cells are hard to count and must be immobilized.
What counting technique would you use if you have a microorganisms that can’t grow because it is dead?
The microscopic count pr flow cytometry
what is viability staining?
viability staining : stains to know which cells are dead and which ones are alive
T or F : you can use the turbidity method to quantify only for living cells
false