Mastering Restriction Enzymes and DNA Analysis Techniques

Mastering Restriction Enzymes and DNA Analysis Techniques

Assessment

Interactive Video

Biology, Science, Chemistry

9th - 12th Grade

Hard

Created by

Patricia Brown

FREE Resource

The video tutorial explains the discovery and function of restriction enzymes, which are crucial in genetic engineering. It covers the types of nucleases, how restriction enzymes recognize specific DNA sequences, and the mechanisms of DNA cleavage. The tutorial also discusses the creation of recombinant DNA and the separation of DNA fragments using gel electrophoresis.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What year were the two enzymes responsible for restricting bacteriophage growth in E. coli discovered?

1953

1963

1973

1983

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary function of restriction endonucleases?

To add methyl groups to DNA

To synthesize proteins

To cut DNA at specific sequences

To replicate DNA

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What does the 'Eco' in EcoRI represent?

The recognition sequence

The type of DNA cut

The enzyme's function

The genus and species of the source organism

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a palindromic sequence in the context of DNA?

A sequence that reads the same in both directions

A sequence that is unique to each organism

A sequence that is only found in RNA

A sequence that cannot be cut by enzymes

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What type of DNA ends are generated by a staggered cut?

Blunt ends

Linear ends

Sticky ends

Circular ends

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Why are sticky ends important in DNA recombination?

They make DNA more stable

They allow DNA fragments to easily pair and join

They prevent DNA from being cut

They increase the length of DNA

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

In genetic engineering, why must the vector and source DNA be cut with the same restriction enzyme?

To ensure the DNA is not damaged

To create compatible sticky ends for recombination

To prevent the DNA from being degraded

To increase the speed of the reaction

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