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Cloning Vectors

Total questions: 20

Worksheet time: 14mins

Name
Class
Date
1.
Restriction Enzymes are . . . 
a)
proteins
b)
DNA
c)
fats
d)
carbohydrates
2.
Restriction Enzymes . . . 
a)
cut DNA at precise locations
b)
help bacteria to pick up DNA
c)
move DNA through a gel
d)
copy DNA
3.

Some restriction enzymes produce "sticky ends". Sticky ends are . . .

a)

single-stranded DNA "overhangs" that can bind to complementary DNA

b)

double stranded DNA aligned with each other

c)

single-stranded DNA aligned with host DNA

d)

ends of a double stranded DNA strand

4.

How do we name restriction Enzymes ?

a)

First letter in Cap for Genus, next two letter in small for species, next one letter for strain and roman numeral for order of discovery

b)

First two letter in Cap for Genus, next one letter in small for species, next one letter for strain and English numeral for order of discovery

c)

First two letter in Cap for Genus, next one letter in capital for species, next one letter for strain and roman numeral for order of discovery

d)

First two letter in Cap for Genus, next one letter in small for species, next one letter for strain and roman numeral for order of discovery

5.

Which RE's from above make blunt cuts? (More than one answer)

a)

Alul

b)

HaeIII

c)

BamHI

d)

HindIII

e)

EcoRI

6.

Which RE's from above make sticky cuts? (More than one answer)

a)

Alul

b)

HaeIII

c)

BamHI

d)

HindIII

e)

EcoRI

7.

Restriction Enzymes were primarily used as....

a)

defense by protozoa against antibiotics

b)

tools by viruses to cleave bacterial genome

c)

defense by bacteria against bacteriophages viruses

d)

tools to cleave DNA during replication

8.

What is a palindrome?

a)

A sticky end resulting from a restriction enzyme

b)

A blunt end resulting from a restriction enzyme

c)

A sequence that reads the same forwards and backwards

d)

A sequence that is complementary to the other

9.

Identify the given plasmid.

a)

pUC19

b)

pBR322

c)

pUC119

d)

pUC18

10.

What are selectable marker ?

a)

a radium labelled marker

b)

a type of sequence

c)

resistant gene

d)

a type of protein

11.

LacZ gene is used to?

a)

Differentiate between transformant and non transformant

b)

Differentiate between clones with vector plasmids and without vector plasmids

c)

Differentiate between competent cells and non competent cells

d)

Differntiate between negative and false negative

12.

What is the origin of replication ?

a)

place of origin

b)

sequence of genome where replication starts

c)

where DNA are formed

d)

where RNA are formed

13.

What is transformation?

a)

Procedure though which a piece of protein incorporated into bacterium

b)

Procedure though which a piece of lipid incorporated into bacterium

c)

Procedure though which a piece of DNA incorporated into bacterium

d)

Procedure though which a piece of carbohydrate incorporated into bacterium

14.

In order to insert a human gene into plasmid, both must

a)

code for the same gene product.

b)

be cut by the same restriction enzyme.

c)

originate from the same type of cell.

d)

have identical sequences.

15.

The alternative selectable marker _______________ and chromogenic substrate __________________ that selects recombinants on the basis of their ability to produce colour are

a)

LacZ gene , X-gal

b)

α-galactosidase and X-gal

c)

Amp R gene and X-gal

d)

β-galactosidase and X-gal

16.

The colonies of recombinant bacteria appear white in contrast to blue colonies of non-recombinant bacteria because of

a)

Insertional inactivation of β-galactosidase gene in recombinant bacteria

b)

Inactivation of glycosidase gene in recombinant bacteria

c)

Incompetence of recombinant bacteria containing β-galactosidase

d)

insertional inactivation of α-galactosidase gene in non-recombinant bacteria

17.

Non essential genes/stuffer fragments are removed from bacteriophage because

a)

To increase the phage genomic DNA size

b)

To reduce the phage genomic RNA size

c)

To fit in other phage DNA

d)

To fit in the foreign gene to be cloned

18.

E.coli DH5alpha is made chemically competent by

a)

giving them a freeze shock

b)

giving them a heat shock

c)

giving them electrical current

d)

all of above

19.

What is the importance of cos sites in cosmids?

a)

to make cosmids infectious

b)

to make cosmids competent

c)

allow DNA to be packaged inside lambda phage heads

d)

permit replication as plasmid in bacteria

20.

How do you overcome vector religation problem?

a)

Use ligase enzyme

b)

Use alkaline phosphatase enzyme

c)

Use restriction enzymes

d)

Use polymerase enzyme