Bacteriology (17) Flashcards

(38 cards)

1
Q

Flame-sterilization

A

A technique that utilizes heat, in our case from a bunsen burner, to sterilize non-flammable materials (including inoculating loops)

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2
Q

Working with bacterial cultures

A

Agar plates: remove lid only when performing the procedure, perform the procedure quickly

Bacterial broth tube: hold at 30º to 45º angle and flame the top

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3
Q

Prokaryotes

A
  1. Most are unicellular (some are colonial)
  2. No nuclear envelope
  3. DNA found in nuclear space in a naked circular molecule (sometimes a plasmid)
  4. Reproduce asexually via binary fission
  5. Cell wall is composed as peptidoglycan
  6. Sometimes, the cell wall is covered by a capsule (a sticky layer of polysaccharides or proteins)
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4
Q

Fimbriae

A

Hair-like projections that help the prokaryote stick to structures, substrates, or other members in a colony

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5
Q

Pilli

A

Longer than fimbriae

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6
Q

Punctiform (<1mm)

A

Classification of bacterial colony by shape

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7
Q

Round

A

Classification of bacterial colony by shape
Circular

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8
Q

Filamentous

A

Classification of bacterial colony by shape
Threadlike

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9
Q

Irregular

A

Classification of bacterial colony by shape

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10
Q

Smooth

A

Classification of bacterial colony by edge shape
Distinct colony edge

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11
Q

Curled

A

Classification of bacterial colony by edge shape
Almost scalloped looking

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12
Q

Wavy

A

Classification of bacterial colony by edge shape
Regular lobes

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13
Q

Lobate

A

Classification of bacterial colony by edge shape
Irregular lobes

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14
Q

Filamentous

A

Classification of bacterial colony by edge shape

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15
Q

Smooth

A

Classification of bacterial colony by surface

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16
Q

Concentric

A

Classification of bacterial colony by surface
ridges

17
Q

Wrinkled

A

Classification of bacterial colony by surface

18
Q

Contoured

A

Classification of bacterial colony by surface
ridges

19
Q

Other characteristics of classification

A

Pigmentation
Opacity
1. Opaque (no light passes through)
2. Translucent (permits light through, objects not visible)
3. Transparent (permits light through, objects visible)

20
Q

Example 1:

A

Name: Bacillus subtilis
Characteristics:
1. Irregular (shape)
2. Lobate (edges/margins)
3. Surface: unsure
4. Grey/Green color
5. Opaque

21
Q

Example 2:

A

Name: Escherichia coli (E. coli)
Characteristics:
1. Irregular (shape)
2. Lobate (edges/margins)
3. Wrinkled (surface)
4. White color
5. Transluscent

22
Q

Example 3:

A

Name: Micrococcus roseus
Characteristics:
1. Punctiform (shape)
2. Smooth (edges/margins)
3. Smooth (surface)
4. Yellow/beige in colro
5. Opaque

23
Q

Example 4:

A

Name: Rhodospirillum rubrum
Characteristics:
1. Irregular (shape)
2. Curled (? edges/margins)
3. Smooth, shiny
4. White
5. Opaque

24
Q

Example 5:

A

Name: Sarcina lutea
Characteristics:
1. Round/irregular (shape)
2. Smooth (edges/margins)
3. Smooth
4. Dark in color
5. Opaque

25
Example 6:
Name: Serratia marcescens Characteristics: 1. Round (shape) 2. Round/slight curl? (margins) 3. Concentric 4. White/yellow 5. Opaque
26
Classifying bacterial cells by morphology: Cocci
Round
27
Classifying bacterial cells by morphology: bacilli
Rod like
28
Classifying bacterial cells by morphology: spirilli
Spirals
29
Classifying bacteria by cell wall structure: Gram +
1. Simple cell wall 2. Thick peptidoglycan cell wall layer 3. No outer lipopolysaccharide wall layer 4. Retain crystal violet/iodine 5. Appear blue/purple due to rxn between crystal violet and peptidoglycan cell wall
30
Classifying bacteria by cell wall structure: Gram -
1. Complex cell wall 2. Thin peptidoglycan cell wall layer 3. Outer lipopolysaccharide wall layer 4. Retain safranin 5. Appear pink/red due to rxn between outer membrane and safranin
31
Gram Staining Technique
Procedure to differentiate bacterial "species" based on cell wall properties 1. Can be Gram + or Gram - 2. Bacteria is fixed on slide using the following procedure: - Crystal violet, rinsed with water - Iodine, rinsed with acetone - Safranin, rinsed with water
32
Streak Plate Technique
Serial dilution of bacteria across three areas of an agar plate so that bacterial colonies can be isolated, investigated, and identified Procedure: 1. Dip sterile cotton swab into bacterial culture and swab across 1/3 of agar plate 2. Flame inoculation loop and allow to cool 3. Touch loop to one end of swabbed area and zigzag to another side of the agar plate 4. Repeat step 2 5. Repeat step 3 for last remaining 1/3
33
Disinfecting agents
Decontaminate nonliving objects (surfaces, doorknobs)
34
Antiseptic agents
Slows/stops the growth of microorganisms on external surfaces of body (skin)
35
Antibiotic agents
Used to inhibit bacterial growth inside of living organisms
36
Testing the efficacy of agents used to control/stop bacterial growth
Measuring the zone of inhibition
37
Zone of inhibition procedure
1. Take sterile cotton swab and dip into liquid culture and run back and forth across the plate 2. Rotate 90 degrees and repeat 3. Place antibiotic disks onto first plate and disinfecting agents (listerine, isopropyl, and bleach) onto second plate 4. Allow space in between disks 5. Make sure to label
38
Comparing zones of inhibition
After incubation, we can compare the zone of inhibitions 1. Using a ruler, measure the diameter of the zone of inhibition (cleared areas around the disks) 2. More sensitive bacteria is to the agent, the wider the zone of inhibition (most antimicrobial efficacy)