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Transformation in Bacteria

Total questions: 30

Worksheet time: 17mins

Name
Class
Date
1.

What is recombinant DNA

a)

DNA from 2 different organisms combined

b)

DNA from 2 different ribosomes

c)

DNA that is separated out from a vector

2.

Which of the following could be used as a vector for a human gene?

a)

Bacterial Plasmid

b)

Bacteria

c)

A mitochondria

d)

mRNA

3.

A circular piece of DNA, found in bacteria, is called:

a)

A plasmid

b)

mRNA

c)

Ribosome

d)

Nucleotide

4.
Plasmids, yeast, and viruses are known as ____________.
a)
restriction enzymes
b)
vectors
c)
genetically modified organisms
d)
bacteria
5.
Any change or mistake in DNA replication can cause a ________  
a)
cancer cell 
b)
virus
c)
disease
d)
mutation
6.

The transfer of genes from one cell to another by a bacteriophage is known as

a)

Recombination

b)

Conjugation

c)

Transduction

d)

Transformation

7.

The transfer of naked DNA from one cell to another is referred to as

a)

Transduction

b)

Lysogeny

c)

Transformation

d)

Conjugation

8.
A structural gene is one that encodes for ....
a)
a binding site for a repressor
b)
 how to make DNA
c)
a binding site for RNA polymerase
d)
a protein
9.

What is competency for a cell?

a)

The insertion of a formed plasmid into the cell.

b)

The chemical process of switching the gene.

c)

Super coiled molecules formed in the plasmid of the cell.

d)

Change in the structure and permeability of the cell membrane.

10.

How might a plasmid contribute to a selective advantage for a bacterial cell?

a)

Make the cell competent.

b)

Could provide a selective advantage for that cell.

c)

Make the cell wall stronger.

d)

Does not contribute

11.

What is transformation?

a)

The use of viruses to transform or genetically


engineer cells.

b)

The measure of how well cells are transformed in a new phenotype.

c)

The insertion of a foreign plasmid into a bacterial cell which results in new acquired traits.

d)

Genetic engineering or transformation of mammalian cells.

12.

Cells are made competent by;

a)

The incubation of the bacteria at 95C

b)

A process that uses calcium chloride.

c)

A process that uses GFP

d)

A process that uses polymerases

13.

Heat shock

a)

Trap the plasmids inside the cell.

b)

Enlarges the pores of the cell.

c)

Provides for the death of the cell.

d)

Increases the disintegration of the cell wall.

14.

The exogenous DNA used in bacterial transformation can be,

a)

mRNA molecule

b)

rDNA

c)

engineered plasmid

d)

red fluorescent protein

15.

LB containing ampicillin (2nd plate) is inoculated with the E. coli bacteria that contains ampicillin resistant gene. The bacteria will;

a)

Grow on the agar plate

b)

Will not grow on the agar plate.

c)

will only grow after the plate has been incubated at 45C

d)

will only grow after the plate has been placed in a warm water bath for 2 minutes.

16.

Which of the following statement is true concerning transformation;

a)

Bacterial transformation involves the transfer of genetic material that results in the acquisition of a new trait that is stable but not inheritable.

b)

There are no bacterial species that go thru the transformation process naturally.

c)

Transformation efficiencies are a way to determine how many cells were transformed per microgram of plasmid DNA used.

d)

The promoter is the region at the end of the gene .

17.

What is the purpose of the Luria broth (LB) when performing genetic transformation?

a)

Provides resistance to antibiotics

b)

Provides nutrients needed for bacteria growth

c)

Stabilizes the plasmid being given to the host organism

d)

Sterilizes the instruments

18.

A "-ampR" cell

a)

has the ampR gene in it's plasmid and is resistant to ampicillin

b)

does not have the ampR gene in it's plasmid and is resistant to ampicillin

c)

has the ampR gene in it's plasmid and is not resistant to ampicillin

d)

does not have the ampR gene in it's plasmid and is not resistant to ampicillin

19.

What process increases the competency of cells?

a)

calcium chloride and an ice bath

b)

calcium chloride and heat shock

c)

Luria broth (LB) and an ice bath

d)

Luria broth (LB) and heat shock

20.

Why are cells incubated at 42o C?

a)

At 42o C, bacterial cells begin releasing DNA for other cells to take up

b)

This is a good recovery temperature after heat shock

c)

At 42o C, the membranes of bacterial cells begin to degrade, creating pores through which DNA can enter the cell

21.

Ampicillin (antibiotic) is used in the plates to

a)

isolate and select for only the bacteria that have been successfully transformed

b)

give bacteria energy to grow

c)

act as a trigger to turn on the expression of the gene of interest

d)

give the bacteria a new trait (such as fluorescence or insulin production)

22.

Arabinose is used in the plates to

a)

isolate and select for only the bacteria that have been successfully transformed

b)

give bacteria energy to grow

c)

act as a trigger to turn on the expression of the gene of interest

d)

give the bacteria a new trait (such as fluorescence or insulin production)

23.

What is the difference between a plasmid and a chromosome?

a)

Chromosomes contain circular and linear DNA.

b)

Chromosomes are covered with proteins and contain circular DNA.

c)

Plasmids are covered with protein and contain circular.DNA.

d)

Chromosomes are covered with proteins contain linear DNA

24.

LB containing ampicillin (2nd plate) is inoculated with the E. coli bacteria that contains ampicillin resistant gene. The bacteria will;

a)

Grow on the agar plate

b)

Will not grow on the agar plate.

c)

will only grow after the plate has been incubated at 45C

d)

will only grow after the plate has been placed in a warm water bath for 2 minutes.

25.

Which one of these agar plates would there be no bacteria growth?

a)

+pGLO LB/amp

b)

+pGLO LB/amp/ara

c)

-pGLO LB/amp

d)

-pGLO LB

26.
What is a cloning vector?
a)
The DNA probe used to locate a particular gene in the genome.
b)
An agent such as plasmid, used to transfer DNA from an in vitro solution into a living cell.
c)
The laboratory apparatus used to clone genes.
d)
An enzyme that cuts DNA into restriction fragments.
27.

What is the purpose of the changes in extreme temperatures?

a)

Kill off the low fitness e. coli

b)

Increase Permability of the membrane

c)

Decrease Permeability of the membrane

d)

allow bineary fission to occur easier

28.

What is a selectable marker?

a)

a specific mark on bacteria that makes it resistant to antibiotics.

b)

a specific gene that makes bacteria change it's shape.

c)

a mark that shows that bacteria has BECOME resistant to antibiotics.

d)

a gene that makes it possible to distinguish bacteria that carry the plasmid from those that don't.

29.

Bacteria that did not receive a plasmid are put on an LB plate that does NOT contain ampicillin. What do you expect to happen?

a)

The bacteria will create a lawn

b)

A few individual colonies will be seen

c)

The bacteria will not grow

30.

A scientist is using an ampicillin-sensitive strain of bacteria that cannot use lactose because it has a nonfunctional gene in the lac operon. She has two plasmids. One contains a functional copy of the affected gene of the lac operon, and the other contains the gene for ampicillin resistance. Using restriction enzymes and DNA ligase, she forms a recombinant plasmid containing both genes. She then adds a high concentration of the plasmid to a tube of the bacteria in a medium for bacterial growth that contains glucose as the only energy source. This tube (+) and a control tube (-) with similar bacteria but no plasmid are both incubated under the appropriate conditions for growth and plasmid uptake. The scientist then spreads a sample of each bacterial culture (+ and -) on each of the three types of plates indicated below.


If no new mutations occur, it would be most reasonable to expect bacterial growth on which of the following plates?

a)

1 and 2 only

b)

3 and 4 only

c)

5 and 6 only

d)

1,2,3, and 4 only