Lab 1 Test Flashcards

1
Q

Cultural Characteristics

A

refers to how microorganisms appear on media

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2
Q

Filiform

A

uniform looking slant

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3
Q

Echinulate

A

Toothy uniform slant

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4
Q

Beaded

A

uniform with beads straying at the top

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5
Q

Effuse

A

spreading clumps

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6
Q

Arborescent

A

A little tree-like

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7
Q

Rhizoid

A

very tree like

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8
Q

Ring

A

Growth on sides but not center, like a donut

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9
Q

Pellicle

A

thicker growth as a layer on top, if it is thin it is membranous

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10
Q

Membranous

A

growth as a very thin layer on top

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11
Q

Flocculent

A

Floating clumps on surface

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12
Q

Turbid

A

cloudy subsurface growth

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13
Q

Granular

A

small discrete particles are seen (like salt in water)

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14
Q

Flocculent

A

floating clumps of bacteria

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15
Q

Flakey

A

large particles (flakes) are seen

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16
Q

Viscid

A

thick and sticky

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17
Q

Sabouraud agar

A

is good for fungal growth

18
Q

Nutrient agar

A

is good for bacterial growth

19
Q

Basic dyes

A

like methylene blue are positive and thus stick to negatively charged bacteria cell walls.

20
Q

Common Basic Dyes

A

methylene blue, crystal violet, safranin, and malachite green

21
Q

Acidic dyes

A

like eosin, contain negatively charged color-bearing ions and will not stick to bacteria

22
Q

Common Acidic Dyes

A

Indian ink, congo red, nigrosoine, eosin

23
Q

Ocular lens

24
Q

Body tube

A

in between ocular lens and objective lens

25
Coarse focusing knob
more general focus
26
Fine focusing knob
more finer focus
27
Objective Lenses
primary lens that magnify the specimen
28
Stage
holds slide in position
29
Condenser Focuses
focuses light through the specimen right below stage
30
Diaphragm
controls the amount of light entering the condenser
31
Simple staining
only uses one basic stain, procedure consists of taking the slide, drowning it in methylene blue for 1 minute then washing it off and blotting
32
Gram staining
separate gram negative and gram positive bacteria, with gram positive being vulnerable to antibiotics Gram positive turn purple after decoloring and gram negative lose their color So if you want to see gram negative they are counter stained with safranin to look pink Heat fix → Crystal violet (both turn purple) → iodine both stay purple (it is used as mordant by fixing the crystal violet onto it)→ Alcohol acetone gram negatives are now colorless → safranin gram-negatives turn pink
33
Acid-fast
mainly used for identification of the medically important microorganisms, like he agents that cause tuberculosis and leprosy Cover smear with carbolfuchsin→ decolorize with acd alcohol → counterstain with methylene blue → blot dry
34
Capsular staining-
used to view a gelatinous coat called a CAPSULE that is comprised of glycoproteins or polypeptides. What makes this special is because we use negative staining and stain the background as contrast nigrosine to stain background → add your sample → crystal violet for the capsule viewing
35
Schaeffer-Fulton Endospore staining
used to view endospores Prepped smear of sample , then place over boiling water while having malachite green , then cool and wash to counterstain with safranin The spores contain the green while the cells are pink
36
Dorner Endospore staining
Add drops of water onto a slide and introduce your sample , add 5 drops of carbolfuchsin and boil for 5 min, then mix onto a slide with nigrosin, use a spreader slide.
37
Peritrichous
bunch of tails all over the place
38
Lophotrichous
a bunch of flagella coming from one side
39
Monotrichous
one flagella
40
Amphitrichous
one flagella on each side