Module 3 Flashcards

1
Q

What is generation time?

A

The time it takes for binary fission to occur or the population to double.

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2
Q

What factors affect generation time?

A

Genetic control, available nutrients, environmental conditions.

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3
Q

Are generation times greater in vivo or in vitro?

A

In vivo

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4
Q

What type of bacteria does a viable count account for?

A

Only live bacteria.

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5
Q

What must be used for a viable count?

A

A colony count. Suspension is added to agar and incubated, every colony corresponds to one bacterium.

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6
Q

What type of bacteria do total counts account for?

A

Both living and dead.

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7
Q

What are the different ways to perform a total count?

A

Count under the microscope

Electron particle counters

Visual turbidity

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8
Q

What standards does visual turbidity use?

A

MacFarland standards

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9
Q

What are the components of MacFarland standards?

A

Barium chloride and sulfuric acid

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10
Q

What are the ratios of the MacFarland standards?

A

For tube 0.5, 1, 2, 3:

BaCl2- 0.05, 0.1, 0.2, 0.3

H2SO4- 9.95, 9.9, 9.8, 9.7

Bacteria (x10^8)- 1.5, 3, 6, 9

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11
Q

What does spectrophotometery measure and how does it do this?

A

It measures turbidity of bacterial suspensions. It registers the amount of light transmitted (not absorbed) by bacteria. The more bacteria, the less light is measured.

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12
Q

What does nephelometery measure?

A

The amount of light scattered by bacteria.

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13
Q

When can spectrophotometery and nephelometery counts be considered viable?

A

In log growth phase.

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14
Q

What are the phases of the bacterial growth curve and their characteristics?

A

Lag- little/no cell no. increase

Log- cells divide at a constant rate

Stationary- no increase or decrease

Decline- cell no. declines exponentially

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15
Q

When is the best time to find spores?

A

Death/decline phase

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16
Q

When is the best time to work with bacteria?

A

Log/exponential phase

17
Q

When are bacteria most susceptible to antibiotics?

A

Log/exponential phase

18
Q

How can you shorten the lag phase?

A

Take bacteria from culture actively growing in log phase

Choosing suitable medium

19
Q

Why does the number of bacteria stop increasing in the stationary phase?

A

Cells stop dividing (nutrient depletion)

Growth rate is the same as the death rate

20
Q

How can culture be maintained at log phase?

A

Using a chemostat (removes gas and old media, supplies fresh media and nutrients)

21
Q

How do bacteria reproduce?

A

Binary fission