3.4 microbiology Flashcards

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1
Q

What are sphere shaped bacteria called?

A

Cocci (one is coccus)

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2
Q

What are rod shaped bacteria called?

A

Bacilli (one is bacillus)

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3
Q

what are spiral shaped bacteria called?

A

spirilli (one is spirillum)

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4
Q

Things that are common to gram+ve bacteria:

A

. walls with a thick layer of peptidoglycan
. no outer lipopolysaccharide layer
. stains purple
. spherical cocci shape

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5
Q

Things that are common to gram-ve bacteria:

A

. thinner layer of peptidolycans
. does contain outer lipopolysaccharide layer
. stains red
. bacilli rod shaped

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6
Q

conditions for for growth of bacteria:

A

. nutrients such as glucose nitrogen vitamins mineral salts
. temperature- growth regulated by enzymes

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7
Q

conditions for growth of bacteria:

A

PH- alkaline conditions
Oxygen-
obligate aerobes- microorganisms that must have oxygen for metabolism
facultative aerobes- microorganisms that can grow with or without oxygen (but they grow better in oxygen)
obligate anaerobes- microorganisms that will only grow in the absence of oxygen

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8
Q

What does total count mean?

A

include both living+dead cells

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9
Q

What does viable count mean?

A

count only living cells

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10
Q

What does autoclave do and the conditions?

A

.dispose of bacterial culture plates
.at 121 degrees for 15 mins

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11
Q

How do you carry out a viable count?
(using the serial dilution and agar plates)

A
  • take sterile agar plates (however many tubes there are)
  • transfer said amount cm3 of each to separate plate
  • spread with sterile spreader
  • incubate plates at suitable temp 25degrees
  • count colonies 1 colony= 1 cell
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12
Q

How to work out the dilution factor?

A

for example: you put in 0.1cm of the stock solution in the test tube that has 9.9cm3 of water in it
then you do 0.1/(0.1+9.9)= 10 to the minus two

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13
Q

Why did we work near the bunsen in the bacteria colony experiment?

A
  • working in the updraft
  • convection current carries bacteria + fungal spores away from plates preventing contamination
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14
Q

why are the plates never sealed in the experiment?

A

maintain aerobic conditions- prevent growth of anaerobic human pathogens

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15
Q

Why incubate plates at 21 degrees in experiment?

A

prevent growth of human pathogenic bacteria

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16
Q

If there’s a small amount of colonies on plate what can we say?

A

not enough colonies to count to make a reliable estimate of concentration

17
Q

If there’s too many colonies on plate what can we say?

A

too many colonies to count/ overlap therefore we cannot make a reliable estimate of concentration

18
Q

If there’s just enough colonies on the plate what do we say?

A

enough colonies that don’t overlap to make a reliable estimate of concentration

19
Q

to calculate number of colonies in original sample:

A

no of colonies x dilution factor(POSITIVE) divided by volume put on plate