Methods of Measuring Growth Flashcards

1
Q

True or false. The higher the OD, lesser light is absorbed.

A

False. The more the light is absorbed.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Reduces bacterial load

A

Serial dilution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Method in viable count in which culture and media are mixed

A

Pour-plate method (microaerophilic: reduced need for oxygen)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Medium used in 3rd phase of most probable no. technique

A

Eosin Methylene Blue (EMB)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Where to get samples for most probable no. technique

A

Water, food, air

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Three phases in most probable no. technique

A

Presumptive, confirmatory, completed

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Downside of direct cell count

A

Reveal higher no. compared to viable as it considers both dead and alive (great plate count anomaly)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Medium used in 1st phase of most probable no. technique

A

Lauryl Sulfate Tryptone Broth (LSTB)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Optical density measures

A

the amount of light unscattered

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Durham tubes are used to

A

Check turbidity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

The standard range in serial dilution

A

30 - 300

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

No. of cells in grids in counted

A

Direct cell count

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is measured in spectrophotometer?

A

Optical density (OD)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Downside of spread-plate method

A

Affected by the environment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Method in viable count in which agar is in plate already

A

Spread-plate method

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

In direct cell counting, sample is placed into a?

A

Petroff-Hauser counting chamber (haemocytometer)

17
Q

Downside of serial dilution

A

Tedious process

18
Q

Solution for great plate count anomaly

A

Use highly selective media (depending on goal), vary culture conditions

19
Q

Advantage and disadvantage of spectrophotomerer

A

ADV: Quick (~10 mins.)
DIS: Counts dead cells

20
Q

Basis for results of most probable no. technique

A

Gas production, turbidity

21
Q

Types of diluent

A

NSS, PBS

22
Q

True or false. Colony growth on plate reflects no. of cells in sample.

A

True

23
Q

Use of membrane filters w/ specific pores

A

Filtration

24
Q

Medium used in 2nd phase of most probable no. technique

A

Brilliant Green Lactose Bile Broth (BGLB) [45 deg. C, 24H, turbidity]