Chapter 3 Flashcards

1
Q

Kilo meter = 10^ — of a m

A

10^3 (1000m)

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2
Q

1 decimeter = 10^ — of a Meter

A

10^-1 (.1m)

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3
Q

1 centimeter = 10^— m

A

10^- 2 (.01) m

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4
Q

1 millimeter = 10^— m

A

10^ -3 (.001 m )

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5
Q

1 micrometer = 10^—- m

A

10^ -6 (.000001)m

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6
Q

1 nanometer = 10^—-

A

10^-9 m

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7
Q

1 picometer = 10^— m

A

10^-12 m

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8
Q

Larger to smaller conversion number (increases or decrease)

A

Increase

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9
Q

What the ocular lens does

A

(Eyepiece) remagnifies image formed by objective lens

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10
Q

Body tube, what it does

A

Transmitts image from obj lens to ocular lens

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11
Q

Primary lenses that magnify specimen

A

Objective lenses

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12
Q

Part of microscope that holds slide

A

Stage

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13
Q

What the condenser does

A

Focuses light thro specimen

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14
Q

What the iris diaphragm does

A

Controls amount of light entering condenser

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15
Q

The light source on the microscope is called the

A

Illuminator

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16
Q

Define magnification

A

How large something appears when compared to actual size

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17
Q

Define resolution

A

Ability of light microscope to distinguish fine details (or distinguish two points a specified distance apart)

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18
Q

Total magnification =

A

Magnification of ocular lens (10x) x obj lens

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19
Q

Ability of subs to bend light

A

Refractive index

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20
Q

Why we use immersion oil

A

Oil has same refractive index as glass, without it the light would refract and be lost

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21
Q

What is a smear

A

Single layer of cells on slide

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22
Q

What is does fixing mean (step in creating stain)

A

Apply heat briefly to underside of slide, attaches cells to slide

23
Q

How to create a simple stain

A
  1. Create smear
  2. Fixing
  3. Stain
  4. Rinse primary stain off and expose to mordant
24
Q

define staining (how it works)

A

When a salt dissociates into cation and anion, stain is attached to one of them

25
If the pigment is attached to the cation the dye is called
A positive chromophore, “basic dye”
26
If the pigment is attached to the anion, the dye is called
Negative chromophore, “acidic dye”
27
What is a mordant (give example)
Anything that increases affinity of primary stain to cells (increases ability to stick), like heat Also coats structures (like flagella) to make easier to see
28
A simple stain + several other steps used to distinguish between cell types
Differential stain
29
Different kinds of differential stains
Gram stain, acid fast stain
30
Describe how to do a gram stain
1. Primary stain, crystal violet (all steps included) apply iodine mordant 2. Add decolorizer (alcohol) to remove primary stain from some cells 3. Add counter stain safranin
31
In a gram stain, the recolorized cells are gram neg or pos | Bacteria that retain the color during decolonization are
``` Gram negative ( lose color during decolonization ) Gram positive ```
32
Acid fast stain procedure
1. primary stain w/ carbolfuchsin, heat applied 2. Decolorize (acid alcohol, removed red stain from bacteria that are not acid fast) 3. Counter stain (methylene blue) stains non acid fast
33
Acid fast stains are used to
Identify mycobacterium or Norcardia bacteria, Bc have waxy material in cell wall that stain binds to
34
What is a negative staining
Mix bacteria solution w suspension of colored particles (India ink or nigrosin) to create contrasting background, dye bacteria w simple stain (safranin) capsules won’t retain dye, appear as halos
35
What a negative stain can tell us ab a bacteria
Presence of a capsule, therefore virulence
36
What is an endospore
When cell detects adverse environmental conditions, forms an endospore within it that protects it from conditions
37
How to endospore stain
1. Primary stain(malachite green), heat(stream 5min), rinse. Dyes the endospores 2. Counterstain=safranin, stains all other cell parts except endospores (pink/red)
38
Why capsules of a negative stain appear as halos surrounding cells
Capsules don’t accept most biological dyes
39
Flagella stain procedure
Primary stain (carbolfuchsin) and mordant applied over and over again. Layers build up on flagella like mascara
40
The short the wave length of the light, the ______ the resolution
Greater
41
Light passing thro two different materials, w two different refractive indexes, would cause the light to
Bend
42
In an acid fast stain, the bacteria who lose color during decolorization (appear blue after recolor)
Are non-acid fast, lack lipid components in cell wall.
43
In an acidfast stain, the bacteria that retain color during decolorization (red)
Are acid fast, contain lipid in cell wall (carbolfuchsin more soluble in cell walls than in acid alcohol)
44
Differential stains are
Gram or acid fast stain
45
Primary stain for acid fast stain Mordant Decolorizer Counter stain
Primary: carbolfuchsin (red) Mordant: heat Decolorizer: acid alcohol Counter: methylene blue
46
Stains and decolorizers for gram stain in order
- crystal violet (primary) - iodine (mordant) - alcohol acetone (decolorizer) - safranin (counter stain)
47
Special stains
Negative, endospore, flagella
48
Which stains use safranin | Which use carbolfuchsin
Safranin: gram, endospore, negative, Carbolfuchsin: acid fast, flagella
49
Obj power magnifications
Scanning= 4x Low=10x High =40x Oil= 100x
50
Negative staining often uses what kind of dye
Acid dye
51
Why gram neg bacteria lose color during gram stain (don’t retain crystal violet)
Alcohol disrupts outer lipopplysaccaride layer, Less peptidoglycan in cell wall, Crystal violet iodine complex washed out
52
Which is harder to kill, gram positive or gram negative bacteria
Negative (have more impenetrable walls and an outer membrane surrounding wall)
53
Why gram positive don’t lose crystal violet iodine complex
CV-I complex bigger than the CV molecule that entered the cell, can’t be washed out of intact thick peptidoglycan layer