Advertisements
Advertisements
प्रश्न
Explain the roles of the following with the help of an example each in recombinant DNA technology :
Restriction Enzymes
Advertisements
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.
APPEARS IN
संबंधित प्रश्न
Explain briefly:
Restriction enzymes and DNA
Answer the following question.
Explain the significance of palindromic nucleotide sequence in the formation of recombinant DNA.
The total number of nucleotide sequences of DNA that code for a hormone is 1530. The proportion of different bases in the sequence is found to be Adenine = 34%, Guanine = 19%, Cytosine = 23%, Thymine = 19%.
Applying Chargaff’s rule, what conclusion can be drawn?
Which of the following radioisotope is not suitable for DNA labeling based studies?
DNA strands on a gel stained with ethidium bromide when viewed under UV radiation, appear as ______
A specific recognition sequence identified by endonucleases to make cuts at specific positions within the DNA is ______
Restriction enzymes that are used in the construction of recombinant DNA are endonucleases which cut the DNA at ‘specific-recognition sequence’. What would be the disadvantage if they do not cut the DNA at specific-recognition sequence?
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?
In the restriction endonuclease EcoRI, what do the letter 'R' and the Roman numeral 'I' represent?
How are separated DNA bands visualized following agarose gel electrophoresis?
