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प्रश्न
Explain the roles of the following with the help of an example each in recombinant DNA technology :
Restriction Enzymes
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उत्तर
Restriction enzymes are specialised enzymes that recognise and cut a particular sequence of DNA. Every restriction enzyme identifies specific sequences called recognition sequences. These recognition sequences are palindromic. Palindromes are the sequence of base pairs that read same both backwards and forwards (i.e., same in 5' → 3' and 3' → 5' direction).
Restriction enzymes are of two types:
1) Restriction endonucleases − They cut the DNA at specific positions within the DNA
2) Restriction exonucleases − They cut the DNA at the ends (remove the nucleotides at the ends of the DNA).
The restriction endonuclease is specifically important and is extensively used in recombinant DNA technology. They are capable of cutting DNA fragment in two ways, resulting in the formation of either blunt or sticky ends. Sticky ends obtained after the action of restriction enzymes are particularly important in recombinant DNA technology as they are helpful in linking the foreign DNA to the vector.
Restriction enzymes cut a little away from the centre of the palindrome site, but between the two bases on opposite strands. For example, restriction enzyme Eco-RI is one such restriction endonuclease that gives sticky ends.

Hence, structures called overhangs (or sticky ends) are generated on each strand. Overhangs are the structures obtained after palindromic sequences are cut by molecular scissors.

They are significant because these sticky ends form hydrogen bonds with their complementary counterparts with the help of DNA ligases.
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संबंधित प्रश्न
Name and describe the technique that helps in separating the DNA fragments formed by the use of restriction endonuclease
Collect 5 examples of palindromic DNA sequences. Better try to create a palindromic sequence by following base-pair rules.
Explain briefly:
Restriction enzymes and DNA
Answer the following question.
Write the use of restriction endonuclease in the formation of recombinant DNA.
There is a restriction endonudease called as EcoRI. What does co part in it stands for?
How does one visualise DNA on an agarose gel?
A mixture of fragmented DNA was electrophoresed in an agarose gel. After staining the gel with ethidium bromide, no DNA bands were observed. What could be the reason?
What is elution?
How are DNA fragments visualised once they are separated by gel electrophoresis?
Identify the activity of endonuclease and exonuclease in the given image.
