Target Exam

CUET

Subject

Biology

Chapter

Biotechnology -Principles and Processes

Question:

Read the following passage carefully and answer the given questions.

The separated DNA fragments can be visualized only after staining the DNA with ethidium bromide followed by exposure to UV radiation. Bright orange colored bands of DNA in ethidium bromide stained gel exposed to UV light can be seen. The separated bands of DNA are cut out from the agarose gel and extracted from the gel piece. This step is known as elution. The DNA fragments purified in this way are used in constructing recombinant DNA by joining them with a cloning vector.

The natural polymer used in the agarose gel is extracted from:

Options:

Sea weeds

Desert plants

Soil microbes

Vegetable peels

Correct Answer:

Sea weeds

Explanation:

The correct answer is Option (1) → Sea weeds 

The process of cutting DNA using restriction endonucleases results in the formation of DNA fragments. These fragments can be separated using a technique called gel electrophoresis.

Since DNA fragments are negatively charged molecules, they can be separated by applying an electric field, causing them to move towards the anode through a medium or matrix. Agarose, a natural polymer extracted from seaweeds, is commonly used as the matrix. The DNA fragments separate based on their size due to the sieving effect provided by the agarose gel. Smaller fragments move farther compared to larger fragments.

The separated DNA fragments can be visualized only after staining the DNA with a compound called ethidium bromide, followed by exposure to UV radiation. Without staining, the pure DNA fragments cannot be seen in visible light. After staining, you can observe bright orange-colored bands of DNA in an ethidium bromide stained gel exposed to UV light.

Once the DNA fragments are separated, they can be cut out from the agarose gel and extracted from the gel piece. This step is known as elution. The purified DNA fragments obtained through elution are then used in constructing recombinant DNA by joining them with cloning vectors.