Microbiology Flashcards

1
Q

What do genetic differences of bacteria produce?

A

Different metabolic features and different surfaces molecules, so they have different antigenic properties

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2
Q

What is the smallest bacterium?

A

Archaea

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3
Q

What is the largest bacterium?

A

The sulphur bacterium/ thiomargarita namibiensis.

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4
Q

What are the 3 shapes of bacteria?

A

Bacillus
Coccus
Spiral/spirillum

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5
Q

What are the types of grouping of bacteria and give examples

A

Single, Helicobacter
Pairs, Diplococcus pneumoniae
Chains, Streptococcus
Clusters, Staphylococcus

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6
Q

What does gram-staining allow?

A

Distinguishment between gram-positive and gram-negative bacteria

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7
Q

What colour do gram-negative go?

A

Red

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8
Q

What colour do gram-positive go?

A

Purple

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9
Q

Describe the first step in gram staining

A

Use crystal violet which is a basic dye, it binds to peptidoglycan so all bacteria stain purple

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10
Q

Describe the second step in gram staining

A

Use lugols iodine, it is a mordant.
It binds the crystal violet more strongly

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11
Q

Describe the third step in gram staining

A

Use ethanol, a decolouriser.
It removes unbound crystal violet and lipopolysaccharides.
Gram-positive stay purple.
Gram-negative become colourless

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12
Q

Describe the fourth step in gram staining

A

Use safranin, a counter-stain.
It dyes gram-negative red

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13
Q

What is the structure of gram positive bacteria and what does it mean?

A

Has no outer lipopolysaccharide layer so stain binds more efficiently.
Lack of lipopolysaccharide layer means bacteria is more susceptible to penicillin and lysozyme.

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14
Q

What does lysozyme do?

A

It is an antibacterial enzyme, it hydrolyses the bonds holding the peptidoglycan molecule together.

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15
Q

What does penicillin do?

A

Prevents the bonds inter-linking peptidoglycan molecules from forming.
Therefore makes cell walls weak and prone to collapse.

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16
Q

What is the structure of gram negative bacteria and what does it mean?

A

Has a layer of lipopolysaccharide which protects the cell.
Not affected by lysozyme and are resistant to penicillin.

17
Q

What nutrients are needed for culturing bacteria and how are they supplied?

A

Supplied in a nutrient media either agar or nutrient broth.
Contain:
Glucose
Nitrogen for amino acid synthesis
Vitamins, Na+, Mg2+, Cl- etc

18
Q

What is the temp needed to culture bacteria?

A

37 degrees for bacterial enzymes.

19
Q

What pH is needed to culture bacteria?

A

pH 7.4

20
Q

What is clostridium bacteria?

A

Obligate anaerobes that produce toxins in wounds, they destroy body tissue.

21
Q

What does a defined medium mean?

A

Contains only known ingredients

22
Q

What does an undefined medium mean?

A

A medium where all the components are not known, because they include yeast or beef peptone

23
Q

What is a selective medium and give an example

A

A medium that only allows certain bacteria to grow.
MacConkey agar only allows gram-neg bacteria to grow

24
Q

What is an aseptic technique?

A

A technique to maintain sterility of equipment and prevents contaimination.

25
Q

What are some methods in aseptic techniques?

A

Flame the necks of bottles before opening
Flame inoculating loops before and after use
Sterilise work surface before and after using 3% lysol.
Flame the mouth of bottle
Incubate at 25 degrees

26
Q

What is an autoclave?

A

A sealed container in which equipment is heated at 121 degrees and under pressure.

27
Q

What is a viable count?

A

Counts living cells only

28
Q

What is a total count?

A

Counts dead and living cells

29
Q

What is a colony?

A

A cluster of cells which arises from a single bacterium

30
Q

Read and do 3 questions on counting colonies

A

PG 60

31
Q

Describe a dilution experiment

A

Use 9cm3 sterile distilled water in each test tube, transfer 1cm3 bacterial sample to first test tube. Bung and invert to ensure mixed.
Transfer 1cm3 sample from test tube 1 into the second test tube, using sterile methods etc.
Continue until dilution is reached.

32
Q

Describe experiment to culture bacteria from dilution experiment

A

Take a sample from each dilution test tube and put into separate petri dishes with a nutrient medium.
Incubate at 37 degrees for 24hrs, count colonies.
1 colony is one cell/one bacterium.