3.4 microbiology Flashcards

1
Q

what are the 3 classifications of bacteria?

A

coccus (circular)
bacillus (rod shaped)
spirillum (curved forms)

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2
Q

what are the 3 circular bacteria?

A

diplococcus (pairs)
streptococcus (chains)
staphylococcus (clusters)

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3
Q

what are the 3 rod shaped bacteria?

A

coccobacilli (oval)
streptobacilli
mycobacteria

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4
Q

what are the 3 curved forms of bacteria?

A

vibrio (curved rod)
spirilla (coil)
spirochete (spiral)

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5
Q

conditions needed for bacterial growth

A
  • glucose nutrient
  • nitrogen nutrient
  • temperature
  • pH
  • oxygen
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6
Q

why does bacteria need glucose to grow?

A

energy source for respiration (can be on the agar)

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7
Q

why does bacteria need nirtoeg to grow?

A

synthesis of amino acids

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8
Q

what do obligate aerobes need?

A

O2 for metabolism

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9
Q

how do facultative anaerobes grow?

A

some grow best with )2 but can grow without

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10
Q

how do obligate anaerobes grow?

A

grow in absence of oxygen

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11
Q

what is the condition for growth (temp) for mesophiles?

A

20-40C - bacteria growth in labs are normally mesophiles

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12
Q

what is the condition for growth (temp) for thermophiles?

A

40C +

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13
Q

what is the condition for growth (temp) for psychrophiles?

A

below 20C

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14
Q

what is direct cell count? (equation)

A

total cell count = count living + dead cells using a haemocytometer

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15
Q

what are viable cell counts?

A

counting only living cells

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16
Q

how is viable cell counting done?

A

a known volume of organism is added to agar plates, incubated and colonies counted

17
Q

what is the assumption when doing direct cell counts?

A

that 1 cell gives rise to 1 colony

18
Q

what is the limitation of direct cell counts?

A

makes no allowance for clumping f cells which can cause an underestimation of numbers

19
Q

what can lead to an overestimate of numbers?

A

choosing a plate with too few colonies will not give a reliable estimate

20
Q

what can lead to and underestimate of numbers?

A

some plates have too many to count reliability

21
Q

what = population in 1cm3 of original culture?

A

number of colonies x dilution factor

22
Q

what do indirect cell counts measure?

23
Q

what does measuring turbidity estimate?
what is the number of microbes compared with?

A

microbe numbers by measuring cloudiness
cloudier = more microbes
compared with known standards

24
Q

what does the gram stain reaction distinguish between?

A

the 2 chemically different types of cell walls found in bacteria

25
features of Gram Positive bacteria
- thick peptidoglycan (murein) cell wall - no lipopolysaccharide layer - stains purple - e.g. Bacillus, Staphylococcus, Streptococcus
25
26
features of Gram Negative bacteria
- more complex cell wall - outer lipopolysaccharide layer - peptidoglycan (murein) cell wall - can't absorb crystal violet stain - stains red with a counterstain - e.g. Salmonella, E. coli
27
what is the lipopolysaccharide layer?
acts as an endotoxin which protects the peptidoglycan cell wall from attack by some antibiotics and the enzyme lysozyme
28
what are aseptic techniques?
handling cultures in such a way as to prevent contamination from unwanted organisms
29
what are some aseptic techniques?
- sterilise work surface before and after - pass insulating loop through flame - lift Petri dish only enough to allow loop to enter and open away from mouth - secure lid with 2 pieces of tape