Micro Lab midterm Flashcards

(45 cards)

0
Q

Resolution

A

Ability to distinguish objects as separate from each other

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1
Q

Magnification

A

Increase in apparent size of an object

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2
Q

Why stain

A

View shape, + cellular structures

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3
Q

Glycocalyx

A

Extracellular Polly metric material (glycoproteins)

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4
Q

Purpose of the dye

A

Any die could be used instead of methane blue, the purpose of the dye is to contrast the charge of the bacteria, they have to be opposite.

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5
Q

Autolysis

A

Destruction of tissue or so buy it’s own enzyme.

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6
Q

Smear

A

A slide with microbes on it, ready to be stained

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7
Q

What is the purpose of the heat fixing smear?

A

To denature of the bacterial enzyme

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8
Q

What is a simple stain?

A

Determines morphology, size and arrangement.

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9
Q

What will a positive stain due to the bacteria?

A

Positive Stan will turn bacteria purple color because bacterial has a negative charge it will be attracted to a positive (base)

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10
Q

Negative stains

A

Stains the background, They are used for bacteria that are difficult to stain due to their size, used specifically used for Cocobacilli

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11
Q

What is the key ingredient for staining

A

Alcohol, dissolving lipids

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12
Q

Gram-positive

A

Has thick walls full with Peptidoglycan

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13
Q

Gram-negative

A

Wall has LPS layer

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14
Q

Penicillin

A

Will work on gram-positive

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15
Q

Tetracycline

A

Will work on gram-negative

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16
Q

Mycobacteria

A

No cell wall, no endospores or capsules.

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17
Q

Acid-fast stain

A

Designed to identify mycobacteria a.k.a. tuberculosis and leprosy

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18
Q

Acid fast positive

A

The cell wall lipids of the mycobacterium do not dissolve in the acid alcohol applied and thus the red stain does not wash off

19
Q

Capsule stain

A

“Sugarcoat”=Glycocalyx

Makes it more pathogenic or stronger

Where is this both stains acid and basic appears white like a halo around the cell

20
Q

Because of this capsule such as streptococcus pneumonia

A

WBC cannot phagocyte the bacteria efficiently and disease occurs

21
Q

Spore stain

A

In order for endospore just stay and we need to apply heat.

Difficult to stain you need to use steam a lot of stain visualization.

22
Q

Example of Spores

A

Anthrax, botulism, tetanus, diarrhea and Gangrene.

23
Q

Flagella stain

A

Two types of flagella:
Peritrichous (around all bacteria)
Polar (at one or both ends of the cell)

Difficult to sustain individualize

24
Culture media
what do they need to grow?
25
Used to test agar
Plate and slant
26
How to sterilize Culture Media
To sterilize we need autoclave, "little oven", it has high steam and high pressure
27
Nutrient broth vs nutrient agar
NB liquid broth, | NA solid in room temperature
28
Selective medium
Tell her you don't want to keep the rest thatt you want to grow
29
Differential medium
Use color change to tell the difference. | Example: used to examine staph
30
Enriched medium
Add extra stimulus because it's difficult to grow. Requires boiled blood vitamin minerals Ex: Neisseria Gonorrhea
31
Fastidious
Difficult
32
PE
Kills gram-negative bacteria
33
Mannitol salt agar
Rare sugar alcohol
34
S. Aureus vs. S. Epidermis
S.A-very dangerous can eat mannitol. Produces acid waste (yellow) S.E.- harmless cannot eat mannitol stays pink.
35
Streak plate technique
Separate different bacterial species from each other when they are in a mixture
36
Isolation of colonies
Hey call me represents a single bacterium and it's overnight descendants
37
Alpha
Partial breakdown of the red blood cells (greening)
38
Beta
Total distruction of RBCs Very dangerous White/ clear zone
39
Gamma
No distraction of RBCs
40
Serial dilution of cultures
This is how we count bacteria
41
To test a serial dilution of cultures
We have to get a sample to colony level meeting only one bacteria.
42
Dilution factor
How much you diluted
43
Bacteria in urine should be
Less then 10^5. If not you have to get antibiotics
44
Calculation of number of visible bacteria in the original sample
Number of colonies 1 ---------------------- X ---------------- Volume places. Dilution factor