Genetic Engineering – Check Test

 

1.         Genetic engineering is the

            A    swapping of genes between organisms.

            B    construction of new genetic codes on DNA.

            C    hybridising of different species.

            D    transfer of DNA from one organism to another.

 

2.         The genes of an organism are made up of

            A    DNA.

            B    chromosomes.

            C    plasmids.

            D    cell nuclei.

 

3.         The normal control of activity in a bacterium

            depends on

            A    foreign genes.

            B    inserted plasmids.

            C    chromosomes.

            D    simple proteins.

 

4.         Plasmids are used to

            A    cut genes out of chromosomes.

            B    carry genes into bacterial cells.

            C    make proteins in animal cells.

            D    join genes together.

 

5.         The organisms currently most commonly used in

            genetic engineering to make useful products are

            A    plants.

            B    animals.

            C    yeasts.

            D    bacteria.

 

6.         Which line in the table describes the advantages of genetic

            engineering over selective breeding.

           

 

Product

quantity

Product

quality

Product

separation

A

small

pure

easy

B

large

contaminated

hard

C

large

pure

easy

D

small

contaminated

hard

 

7.         Selective breeding has disadvantages compared to

            genetic engineering because

            A    the improvements produced are gradual.

            B    the hybrids only show desired characteristics.

            C    completely different species can be crossed.

            D    it is a relatively new development.

 

8.         A disadvantage of current genetic engineering is that

            A    bacteria cannot make certain complex proteins.

            B    products may be contaminated by bacteria.

            C    it is impossible to insert genes into plant cells.

            D    plasmids cannot be inserted into bacterial cells.