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Microbiology ch 9 growth

Total questions: 56

Worksheet time: 28mins

Name
Class
Date
1.

What does the bacterial cell cycle involve?

a)

The formation of new cells through the replication of RNA

b)

The formation of new cells without the replication of DNA

c)

The formation of new cells through the replication of DNA and partitioning of cellular components into two daughter cells

d)

The formation of new cells through the exchange of DNA with other cells

2.

How do prokaryotes reproduce?

a)

Sexually

b)

Through spore formation

c)

Through budding

d)

Asexually

3.

What is the typical structure of bacterial chromosomes?

a)

They have multiple linear chromosomes

b)

They have a single circular chromosome

c)

They have a single linear chromosome

d)

They have multiple circular chromosomes

4.

What is the most common mechanism of cell replication in bacteria?

a)

Mitosis

b)

Meiosis

c)

Binary fission

d)

Budding

5.

What does the cell do before dividing?

a)

It decreases its number of cellular components.

b)

It detaches from the inner cell membrane.

c)

It grows and increases its number of cellular components.

d)

It replicates its DNA.

6.

Where does the replication of DNA start in bacterial cells?

a)

At the terminus

b)

At the origin of replication

c)

At the cell wall

d)

At the nuclear membrane

7.

How does replication proceed after it starts?

a)

In the same direction until the origin is reached again.

b)

In random directions along the chromosome.

c)

In opposite directions along the chromosome until the terminus is reached.

d)

It stops immediately after it starts.

8.

What is the first step in binary fission in bacteria?

a)

Formation of division septum

b)

Cell elongation

c)

DNA replication

d)

Cell separation

9.

During binary fission in bacteria, what forms in the center of the cell?

a)

A new nucleus

b)

A division septum

c)

A cell membrane

d)

A spindle fiber

10.

What do the two daughter cells receive after a binary fission event?

a)

A copy of the original cell membrane

b)

A copy of the original ribosomes

c)

A copy of the original chromosome

d)

A copy of the original cytoplasm

11.

What do FtsZ proteins assemble to form during binary fission?

a)

A Y ring

b)

A Z ring

c)

A cleavage furrow

d)

A septum

12.

Where is the Z ring anchored in the process of binary fission?

a)

To the nucleus

b)

To the cell wall

c)

To the plasma membrane

d)

To the cytoplasm

13.

What is the role of the Z ring in binary fission?

a)

It duplicates the DNA.

b)

It synthesizes new proteins.

c)

It pinches the cell envelope.

d)

It expands the cell size.

14.

What is the result of the Z ring pinching the cell envelope in binary fission?

a)

Fusion of two cells

b)

Creation of a single larger cell

c)

Separation of the cytoplasm of the new cells

d)

Destruction of the cell membrane

15.

What is the generation time in eukaryotic organisms?

a)

The time it takes for the population to double through one round of binary fission.

b)

The time between the same points of the life cycle in two successive generations.

c)

The time it takes for a single organism to reach maturity.

d)

The time it takes for an organism to reproduce asexually.

16.

In prokaryotes, what is the generation time also known as?

a)

Replication time

b)

Maturation time

c)

Doubling time

d)

Division time

17.

How quickly can Escherichia coli double under optimal growth conditions in the laboratory?

a)

Between 15 and 20 hours

b)

In as little as 20 minutes

c)

In exactly 30 minutes

d)

In 14 days

18.

How many cells will there be in the fourth generation if each division doubles the number of cells?

a)

8

b)

12

c)

16

d)

32

19.

What does each division of a cell result in?

a)

One new cell

b)

Two new cells

c)

Three new cells

d)

Four new cells

20.

What is a growth curve?

a)

A method to measure the size of cells

b)

A graph modeling the number of cells in a culture over time

c)

A type of bacteria

d)

A statistical model for population growth

21.

What is known as a batch culture?

a)

A culture where nutrients are continuously added

b)

A culture where waste is continuously removed

c)

A culture where no nutrients are added and most waste is not removed

d)

A culture that cannot be reproduced

22.

How is culture density defined?

a)

The size of cells per unit volume

b)

The number of cells per unit weight

c)

The number of cells per unit volume

d)

The speed of cell growth per unit time

23.

Do infections of the body always follow the growth curve?

a)

Yes, in all cases

b)

No, but correlations can exist depending on the site and type of infection

c)

Yes, but only in closed environments

d)

No, infections are not related to the growth curve

24.

What is the first phase of the bacterial growth curve where there is no increase in the number of living bacterial cells?

a)

Log phase

b)

Stationary phase

c)

Lag phase

d)

Death phase

25.

During which phase of the bacterial growth curve does the number of living bacterial cells increase exponentially?

a)

Log phase

b)

Stationary phase

c)

Lag phase

d)

Death phase

26.

What is the phase called where the plateau in the number of living bacterial cells occurs due to the rate of cell division and death being roughly equal?

a)

Log phase

b)

Stationary phase

c)

Lag phase

d)

Death phase

27.

Which phase of the bacterial growth curve is characterized by an exponential decrease in the number of living bacterial cells?

a)

Log phase

b)

Stationary phase

c)

Lag phase

d)

Death phase

28.

Where does the growth curve pattern of a bacterial culture take place according to the text?

a)

In an open environment

b)

In a closed environment

c)

In a semi-closed environment

d)

Outside of a laboratory setting

29.

What is NOT added or removed from a bacterial culture in a closed environment as mentioned in the text?

a)

Nutrients and waste

b)

Oxygen and carbon dioxide

c)

Antibiotics and proteins

d)

Enzymes and water

30.

Why is it advantageous to maintain cells in the logarithmic phase of growth?

a)

To slow down the growth rate

b)

To maintain genetic stability

c)

To increase the growth rate

d)

To ensure rapid nutrient depletion

31.

What is the purpose of a chemostat in sustaining microbial growth?

a)

To sterilize the culture

b)

To maintain a continuous culture with nutrients supplied at a steady rate

c)

To introduce new strains of bacteria

d)

To periodically remove all cells from the culture

32.

What is the purpose of a chemostat as described in Figure 9.7?

a)

To maintain a culture in the stationary phase of growth

b)

To maintain a culture in the logarithmic phase of growth

c)

To prevent the growth of aerobic bacteria

d)

To increase the concentration of toxic wastes and dead cells

33.

What does the effluent in a chemostat do?

a)

Adds nutrients to the culture

b)

Removes toxic wastes and dead cells from the culture

c)

Provides suitable oxygen levels for anaerobic bacteria

d)

Stops the growth of bacteria

34.

How is the growth of aerobic bacteria sustained in a chemostat?

a)

By preventing the addition of nutrients

b)

By maintaining suitable oxygen levels

c)

By keeping the culture in the stationary phase

d)

By allowing the accumulation of toxic wastes

35.

What is the purpose of performing bacterial counts by microbiologists?

a)

To identify the type of bacteria in a sample

b)

To estimate the number of bacterial cells in a sample

c)

To determine the size of bacterial cells

d)

To discover new species of bacteria

36.

What does the number of bacteria in a clinical sample indicate?

a)

The age of the bacterial culture

b)

The temperature at which bacteria grow best

c)

The extent of an infection

d)

The antibiotic resistance of the bacteria

37.

Which of the following is a direct method used to measure bacterial cell number?

a)

Estimating the weight of the bacterial culture

b)

Measuring the turbidity of the bacterial culture

c)

Counting the cells

d)

Analyzing the genetic material of the bacteria

38.

What do indirect methods of measuring bacterial growth depend on?

a)

The measurement of cell presence or activity without counting individual cells

b)

The direct visualization of bacteria under a microscope

c)

The counting of bacterial colonies on an agar plate

d)

The measurement of the nutrient consumption by bacteria

39.

What does direct cell count refer to?

a)

Estimating the number of cells based on weight

b)

Counting the cells in a liquid culture or colonies on a plate

c)

Calculating the size of cells in a sample

d)

Measuring the volume of a liquid culture

40.

What is the purpose of counting live, or viable, cells in a sample?

a)

To determine the nutritional value of the sample

b)

To assess the effectiveness of preservation methods

c)

To assess the extent of an infection, effectiveness of antimicrobial compounds and medication, or contamination of food and water

d)

To calculate the expiration date of the sample

41.

What does direct microscopic cell count involve?

a)

Estimating the number of cells using a mathematical model.

b)

Transferring a known volume of a culture to a calibrated slide and counting the cells under a light microscope.

c)

Using a chemical dye to visualize the cells on a culture plate.

d)

Counting the number of cells that grow in a culture dish after incubation.

42.

What is the name of the calibrated slide used in direct cell count?

a)

Petroff-Hausser chamber

b)

Ehrlich-Hausser chamber

c)

Neubauer chamber

d)

Fuchs-Rosenthal chamber

43.

What is the purpose of a Petroff-Hausser chamber?

a)

To measure the volume of a sample

b)

To count the bacterial cells in a measured volume of a sample

c)

To magnify bacterial cells for better visualization

d)

To stain bacterial cells for identification

44.

What is etched on the slide of a Petroff-Hausser chamber to facilitate precision in counting?

a)

A magnifying lens

b)

A grid

c)

A chemical reagent

d)

A barcode

45.

What is an advantage of using a Petroff-Hausser chamber for direct cell count?

a)

Requires complex equipment

b)

Time-consuming

c)

Inexpensive

d)

Less accurate

46.

What is a disadvantage of using a Petroff-Hausser chamber for direct cell count?

a)

It is difficult to use

b)

It is very expensive

c)

Does not work well with dilute cultures

d)

It is very slow

47.

What do newly developed fluorescence staining techniques allow scientists to distinguish between?

a)

Different species of bacteria

b)

Viable and dead bacteria

c)

Types of bacterial infections

d)

The age of bacterial cells

48.

How do primary and secondary viability stains differ?

a)

In their color under a microscope

b)

In their ability to cross the cytoplasmic membrane

c)

In their ability to bind to nucleic acids

d)

In their cost and availability

49.

What color do live cells fluoresce when stained with primary and secondary stains?

a)

Red

b)

Blue

c)

Green

d)

Yellow

50.

Under what condition can a cell be stained red by the secondary stain?

a)

When the cell is alive and well

b)

When the cell's cytoplasmic membrane is considerably damaged

c)

When the cell has not absorbed any primary stain

d)

When the cell is of a specific bacterial species

51.

What is the purpose of fluorescence staining as shown in Figure 9.9?

a)

To measure the size of bacterial cells

b)

To differentiate between viable and dead bacterial cells

c)

To identify the species of bacteria

d)

To count the total number of cells in a sample

52.

What device is used in the Direct Cell Count method to detect and count the changes in electrical resistance?

a)

Microscope

b)

Spectrophotometer

c)

Coulter counter

d)

Centrifuge

53.

What is immersed in an electrolyte solution during the Direct Cell Count method?

a)

A glass rod

b)

A plastic tube

c)

A glass tube with a small opening

d)

A metal wire

54.

What is a limitation of the Direct Cell Count method?

a)

It cannot count cells rapidly.

b)

It is not accurate.

c)

It cannot differentiate between live and dead cells.

d)

It requires a very large sample volume.

55.

What is the function of a Coulter counter?

a)

It measures the volume of cells.

b)

It counts the number of cells.

c)

It identifies the type of cells.

d)

It measures the temperature of the cell solution.

56.

How does a Coulter counter measure cell count?

a)

By detecting changes in light absorption.

b)

By measuring changes in resistance in an electrolyte solution.

c)

By counting the number of cells under a microscope.

d)

By using a chemical reaction to indicate cell presence.