Principles of Micro 2 Flashcards

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1
Q

describe the experiment by Louis Pasteur

A

he did the experiment with the swan neck flask where he boiled broth to get rid of all the microorganism and it stayed sterile because microorganism were trapped in the neck of the flask

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2
Q

what happened to the broth when the neck of the flask was broken

A

it became contaminated once exposed to the air

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3
Q

describe the work of Robert Koch

A

he wanted to figure out how disease occurred using pure culture from a diseased mice and infecting a healthy mice

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4
Q

what are Koch’s postulates

A
  1. the suspected causative organisms should always be present with the specific disease and absent in healthy animals
  2. the suspected organism can be grown in pure culture
  3. organisms taken from pure culture should cause disease in healthy animal
  4. the suspected organism can be re-isolated and shown to be the same as the original
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5
Q

what were problems with Koch’s postualtes

A
  • not all microorganisms are culturable
  • some microorganisms are opportunistic - so they can be present in a healthy individual and not cause disease unless under the right conditions
  • re-isolated microorganisms might not be the same as original
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6
Q

who is John Snow

A
  • father of epidemiology

- showed contaminated pump handles were contaminating water causing cholera

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7
Q

who is Edward Jenner

A
  • he inoculated a young boy with cowpox to create immunity against smallpox
  • brought about the concept of vaccination
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8
Q

what is Ignaz Semmelweiss known for

A

washing hands between patients can reduce incidence of infections (though his idiot companions paid him no mind)

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9
Q

describe the work of Anthon von Leeuwenhoek

A

he came up with the early microscope

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10
Q

what is magnification, resolution, and resolving power

A

magnification - enlarging of object
resolution - degree to which detail is maintained in object
resolving power - minimum spacing between two points where can be clearly as separate entities

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11
Q

factors the limit microscopic magnification of microorganisms

A

resolution, resolving power, wavelength

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12
Q

light source and max magnification for brightfield

A

visible

1500x

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13
Q

light source and max magnification for fluorescence

A

UV

1500x

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14
Q

light source and max magnification for TEM

A

electrons

500,000 - 1,000,000 x

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15
Q

light source and max magnification for SEM

A

electrons

10,000 - 1,000,000x

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16
Q

what are two different ways to prep specimen for microscopic viewing

A
  • placing live specimen on surface then putting a coverslip
  • kill specimen then put coverslip

for both preparation one can put dye or stain

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17
Q

when will one use a live vs. killed specimen

A

live: motility, cell behavior, short term
killed: physical appearance, longer term storage

18
Q

what does the positive stain stick to

A
  • the actual specimen providing color

- basic (neg aspect)

19
Q

what does the negative stain stick to

A
  • settles around the specimen to form a silhouette so sticks to the background
  • acidic (positive)
20
Q

what color does the gram positive and gram negative stain

A

gram + - purple

gram neg - pink

21
Q

when does one gram stains

A

for some bacterias but it can’t stain all

22
Q

what is Paul Ehrlich known for?

A

the stain method called acid fast - ziehl neelsen method

23
Q

how does the acid fast-ziehl neelsen method work

A

carbol fuschin –> heat five mins –> decolourise –> methylene blue

24
Q

what are the colors of the stain in acid fast-ziehl neelsen method

A

the acid-fast bacteria stains pink/red

while the non-acid fast bacteria stains blue

25
Q

what species uses acid fast-ziehl neelsen method and why?

A

mycobacterium sp because of its waxy outer coat

26
Q

how does the fungal stain work

A

skin scraping –> 10% KOH –> heat gently –> keratin dissolves –> fungi visible

27
Q

do prokaryotes have cell wall

A

yes except in mycoplasma sp

28
Q

nuclear membrane and nucleolus is present in what?

A

eukaryotes but def not in prokaryote or viruses

29
Q

difference in ribosomes between prokaryotes, eukaryotes, and viruses

A

prokaryotes - small 70S (30 and 50)
eukaryotes - large 80S (40 and 60)
virus - absent

30
Q

what type of DNA do plasmids have

A

circular DNA

31
Q

how does bacteria genome differ from fungi and viruses

A
  • they are mainly circular with the exception of one
  • smaller in size
  • single chromosome with no associated proteins
32
Q

what separates the surface structures from the internal structures in bacteria?

A

cell wall – also keeps cells rigid

33
Q

importance of capsule

A

helps to temporarily escape phagocytosis

prevent bacteriophage attachment

34
Q

importance of fimbriae/common pili

A

help attach to surfaces or tissue

help bacteria attach to each other for urinary system

35
Q

importance of flagellae

A

for motility

36
Q

different between gram positive and gram negative surface structure

A

gram positive - cytoplasmic membrane and peptidoglycan

gram negative - cytoplasmic membrane, peptidoglycan, and outer membrane

37
Q

difference in peptidoglycan between gram positive and gram negative

A

gram negative has a thinner peptidoglycan layer

38
Q

what does gram positive have that gram negative does not

A

techoic acid and lipotechoic acid

39
Q

importance of cell wall in bacteria when it comes to antibiotic treatment

A

cell wall of bacteria is made up of peptidoglycan only found in bacteria so can be used as a unique target for antibiotics

40
Q

other than antibiotic factor, what is the importance of cell wall in bacteria

A

contributes to symptoms of disease
defines cell shape
maintains osmotic integrity