Lab test 1 Flashcards

1
Q

light microscope

A
  • described as compound microscope
  • b/c it has a optical system that uses two lenses(objective lens and ocular lens)
  • light to magnify(enlarge) the object
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2
Q

object

A
  • the actual specimen

- the image is an enlargement(magnification) of the object

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3
Q

the letter e is upside down and backwards

A

the letter e is upside down and backwards

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4
Q

magnification

A

-enlargement of the object

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5
Q

resolving power(resolution)

A

-the power of the optical system the microscope to distinguish between two separate objects a certain distance apart in order to discern fine detail or structure(image not blurred)

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6
Q

limit of resolution

A

the distance between two objects at which it first becomes impossible to resolve them as separate
-the object cannot be resolved anymore by the light microscope

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7
Q

microscopists

A

always start with the 4x or 10x objective(10x objective if microscope does not have 4x objective.) b/c the 4x objective is the scanning lens, which allows one to view the entire field in order to locate the specimen

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8
Q

brightness control(rheostat or voltage regulator)

A

-functions to regulate the intensity of light from the bulb onto the specimen

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9
Q

iris diaphragm

A

-functions to control the amount of light entering the condenser lends in order to create contrast(a dark back round)

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10
Q

working distance(focal length)

A

the distance between the objective lens and the slide(specimen) when the specimen is in focus. the 4x objective has the longest working distance, while the 100x has the shortest working distance

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11
Q

parfocal

A

the lenses of the microscope are adjusted so that the specimen remains somewhat in focus when switching from a low power to a high power objective lens
-the microscope requires little adjustment with the coarse or fine adjustment knobs

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12
Q

refraction

A

refers to the bending of light rays by the convex objective and oculars lenses of the microscope which serves to magnify the specimen

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13
Q

simple stain

A

-it is important to make the smear thin so that the cells will be separated and clearly observable

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14
Q

heat fix

A
  • to kill the cells

- to ensure that the cells adhere to the microscope slide

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15
Q

methylene blue

A

a positive basic stain that attaches to negative, acidic cell parts

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16
Q

cultue tube

A

-should be held at a 45 degree angle so that microorganisms in the air cannot enter the mouth of tube and contaminate it

17
Q

morphology

A

refers to size and shape of cells

-groor groupings of cells

18
Q

growth arrangement

A
  • refers to patterns of bacterial cell divisions or grouping of cells
  • ex: diplococci(paired cells)
  • streptobacilli(chains of 4 or more rod shaped cells)
19
Q

streptobacilli

bacillus subtilus

A

chains of 4 or more large rod shaped cells(streptobacilli)

20
Q

streptococcus pneumoniae

diplococci

A

pair of spherical shaped cells

-diplococci

21
Q

e coli

A

small

single rod shaped cells

22
Q

staphylococcus aureus

staphylococci

A

grape-like clusters of spherical shaped cells(staphyloccoi)

23
Q

streptococus pyogenes

streptococci

A

chains of 4 or more spherical shaped cells(streptococci)

24
Q

gram stain

A

-differential staining technique because it uses two different colored dyes, primary stain and a counterstain, in order to distinguish between gram-positive and gram negative cell wall structure.

25
Q

primary stain

A

Crystal violet dye

26
Q

mordant

A

grams iodine

27
Q

decolorizer

A

ethyl alcohol(95%)

28
Q

counterstain

A

safranin red dye

29
Q

mordant

A
  • a chemical that fixes/ retains the crystal violet dye in the cell wall of both gram-positive and gram-negative bacteria.
  • crystal violet-iodine complex becomes trapped in the peptidoglycan layer of the cell wall
30
Q

gram positive cell wall

A

one layer: thick peptidoglycan layer bound by teichoic acids

31
Q

gram negative cell wall

A

two layers:
1-inner layer thin peptidoglycan layer
2-outer membrane layer, phospholipid bilayer, containing lipoplysaccharides
-lipopolysaccharide components contain two important parts, the O-antigen and the lipid A endotoxin

32
Q

alcohol

A

disrupts the outer lipid layer of the gram negative cell wall and removes the crystal violet stain

33
Q

gram stain

A

if the gram stain procedure was stopped after crystal violet dye was applied, but prior to decolorization, both gram negative and gram-positive bacterial cels would appear purple(violet)

34
Q

gram stain

A

if the gram stain procedure was stopped after decolorization, gram negative bacterial cells would appear colorless, while gram positive bacterial cells would appear purple(violet)

35
Q

gram stain

A

if at the end of the gram stain procedure both gram positive and gram negative bacterial cells appeared reddish pink the most likely explanation would be:

a) too much decolorized was used and was left on the slide for too long a period of time
b) the mordant(gram iodine) step was skipped

if the bacteria appear both purple and pink(gram variable), it is because the cultures are too old

36
Q

bacillus subtilus

A

the organism(bacterium) found to be gram positive(purple)

37
Q

e coli

A

the organism(bacterium) found to be gram negative(reddish-pink)

38
Q

morphology of gram positive organism(bacterium)

A
  • bacillus subtilus
  • large, rod shaped cell in chains
  • streptobacilli
39
Q

morphology of gram negative organism(bacterium)

A
  • e coli

- small single rod shaped cells