Chapter 3 Flashcards

(15 cards)

1
Q

What do the terms magnification and resolving power refer to?

A

Magnification makes objects appear larger.

Resolving power refers to ability to show details.

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2
Q

Why do we use oil at high magnification?

A

Oil immersion helps to improve resolving power at high magnification.

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3
Q

– What is the difference between transmission electron microscopy and scanning electron microscopy?

A

TEM- Are thin slices that are from inside of the cell.

SEM- Visualize surfaces of cell.

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4
Q

Be familiar with each of the six “I’s”

A
  • -Inoculation
  • -Incubation
    • Isolation
    • Inspection
    • Information Gathering
    • Identification
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5
Q

Why does the light microscope have a resolving power that is limited to 0.2-0.5 µm? Why can’t we
improve the resolving power of the light microscope?

A

Wavelength of visible light is 400-700 nanometers. The longer wavelength, lower resolving power.

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6
Q

Why is electron microscopy capable of much greater resolution than light microscopy?

A

Because the wavelengths are much shorter

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7
Q

Be able to describe two ways in which we can view live specimens

A

Wet Mount & Hanging drop slides

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8
Q

Why do we add dyes to our slides when viewing bacteria?

A

Because it is extremely difficult to see cells without the dye.

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9
Q

What is the difference between positive staining with a basic dye and negative staining with an acidic
dye (think about what the dye molecules attach to and what the final image looks like)

A

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10
Q

What is the difference between a simple and a differential stain?

A

Simple stain- type of positive staining technique that uses a single dye to add color to cells so that they are easier to see.

Differential stain- a technique that utilizes two dyes to distinguish between different microbial groups of cell parts by color reaction.

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11
Q

Be familiar with how the Gram stain works, and what would happen if a Gram stain were performed
and one of the reagents were forgotten

A

The gram stain steps

  1. Add crystal violet (primary dye)
  2. Gram’s Iodine (mordant)
  3. Alcohol (decolorizer)
  4. Safranin (red dye counterstain)
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12
Q

What are three ways in which bacteria can be isolated from the environment and grown in pure
culture?

A

streak plate, pour plate, & spread plate

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13
Q

Why would one use solid, semisolid and liquid media? What purposes do each of these media serve?

A

Solid- Isolation (plates) maintenance (slants)
Liquid- we use for fermentation study’s
Semisold- motility study (shows the movement of bacteria)

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14
Q

What is the difference between a defined, or simple medium, and a complex, or undefined, medium?

A

Defined (simple)- what makes it defined we know the Structure of the media. We can assign a molar value to all ingredients. It also is usually restricted range of organisms.

Undefined (complex)- Can’t put a number of molar value so makes it undefined. Grows wide range of organisms ( due to so many nutrients it can grown a lot faster)

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15
Q

What are each of the following media used for?

    • General purpose media
    • Selective media
    • Differential media
A

General purpose media- Good for growing organisms.

Selective media- Only certain organisms grow in this medium.

Differential media- Allows you to tell the difference between what grows often it will be a color change.

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