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Recombinant DNA Technology

Total questions: 16

Worksheet time: 8mins

Name
Class
Date
1.

Recombinant DNA technology is used:

a)

For production of herbicide-resistant plant.

b)

To make a particular protein.

c)

To clone a specific piece of DNA

d)

All of the above.

2.

Restriction enzymes found in bacterial cells are naturally used:

a)

During DNA replication.

b)

To degrade the bacterial cell's DNA.

c)

To degrade viral DNA that enters the cell.

d)

To attach pieces of DNA together.

3.

Which of the following is correct about host cell?

a)

Plasmid is an example of host cell.

b)

Unable to receive DNA molecule through transformation.

c)

An organism that prevents cloning vectors from multiplying.

d)

An organism that is used to receive recombinant DNA for cloning purposes.

4.

What is the purpose of amplification?

a)

To screen for recombinant bacteria.

b)

To join the rDNA with the host cell.

c)

To produce multiple copies of the desired gene.

d)

To prevent the bacteria from reproducing.

5.

Which of these pairs is incorrectly matched?

a)

DNA ligase – mapping human chromosomes

b)

Target DNA – gene of interest

c)

Taq polymerase – PCR

d)

Plasmid as a vector – isolated from bacteria

6.

Which of these might be a biotechnology product?

a)

Vaccine.

b)

Modified enzyme.

c)

Protein hormone.

d)

All of the above.

7.

Plants are more readily manipulated by genetic engineering than are animals because:

a)

Plant genes do not contain introns.

b)

A somatic plant cell can often give rise to a complete plant.

c)

Genes can be inserted into plant cells by microinjection.

d)

Plant cells have larger nuclei.

8.

The following are steps involved in gene cloning procedures. Rearrange them into the correct sequence:

I. Transformation and amplification.

II. Screen for bacteria that contain recombinant

DNA.

III. Insert DNA fragment into the cut bacterial

plasmid.

IV. Cleave the plasmid and human DNA with the same restriction enzyme.

V. Isolate the bacterial plasmid and human DNA.

a)

A. I, II, III, IV, V

b)

B. V, IV, III, I, II

c)

C. V, IV, III, II, I

d)

D. IV, V, III, I, II

9.

Which of the following is true regarding screening by using antibiotics and X-gal?

I. Antibiotics will prevent the growth of bacteria

without plasmid.

II. Bacterial cells with recombinant plasmids are

resistant to antibiotics and are unable to hydrolyse

X-gal.

III. Bacterial cells which contain non-recombinant

plasmids are resistant to antibiotics and are unable

to hydrolyse X-gal.

a)

I only

b)

I and II only

c)

II and III only

d)

I, II and III

10.

Which best describes plasmids?

a)

Plasmids are enzymes used to cut DNA at specific locations

b)

Plasmids are transgenic bacteria

c)

Plasmids are circular pieces of DNA that can be used to carry foreign DNA into cells such as bacteria

d)

Plasmids are clones of bacteria or DNA segments.

11.

Which of the following statements is true about developing cDNA?

a)

mature mRNA directs the formation of the DNA

b)

mature mRNA does not contain introns

c)

DNA taken from the nucleus is used to produce the cDNA

d)

Both a and b are true

12.

The unpaired nucleotides produced by the action of restriction enzymes are referred to have

a)

sticky ends

b)

single strands

c)

restriction fragments

d)

ligases

13.

Restriction endonucleases cut DNA at a specific site called

a)

ligation site

b)

ori

c)

recognition sequence

d)

replication site

14.

Which one of the following statements about Restriction Endonuclease is true

a)

all restriction endonucleases cut DNA at specific sites

b)

all restriction endonucleases cut DNA at random sites

c)

all restriction endonucleases join DNA segments at specific sites

d)

all restriction endonucleases join DNA at random sites

15.

In genetic engineering, DNA ligase is used as:

a)

a probe

b)

a sealing enzyme

c)

a restriction enzyme

d)

a mutagen

16.

In screening process, colonies that were white in the presence of X-gal contained:

a)

Plasmid DNA only

b)

Foreign DNA only

c)

Both foreign DNA and plasmid

d)

Neither plasmid nor foreign DNA