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Assertion (A):
Each restriction endonuclease functions by binding to the DNA and cutting each of the two strands of the double helix at specific points in their sugar-phosphate backbones.
Reason (R):
Each restriction endonuclease recognizes a specific palindromic nucleotide sequence in the DNA by inspecting the length of the DNA sequence.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Restriction enzymes cut the DNA strands a little away from the center of the palindrome sites, leaving single-stranded portions called sticky ends.
Reason (R):
These sticky ends form strong covalent bonds with their complementary cut counterparts, which facilitates the action of DNA ligase.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Recombinant molecules of DNA are composed of DNA from different sources/genomes.
Reason (R):
Normally, the vector and the source DNA must be cut by the same restriction enzyme to ensure that the resultant fragments have the same kind of sticky ends.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
DNA fragments are separated in gel electrophoresis according to their size.
Reason (R):
The agarose matrix provides a sieving effect, causing smaller DNA fragments to move farther through the gel towards the anode.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Pure DNA fragments are visible in the gel only after staining with ethidium bromide and exposure to UV radiation.
Reason (R):
Pure DNA fragments are not visible in visible light and without staining.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
The process of cutting out the separated bands of DNA from the agarose gel and extracting them from the gel piece is known as elution.
Reason (R):
The DNA fragments purified through elution are then used in constructing recombinant DNA by joining them with cloning vectors.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
The origin of replication ($ori$) sequence in a vector is responsible for controlling the copy number of the linked DNA.
Reason (R):
If a scientist wants to recover many copies of the target DNA, it should be cloned in a vector whose origin supports a high copy number.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Vectors need to have very few, preferably single, recognition sites for commonly used restriction enzymes.
Reason (R):
Presence of more than one recognition site within the vector will complicate the gene cloning process by generating several fragments.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
If a foreign DNA is ligated at the $Pst$ I site in the vector pBR322, the recombinant plasmid loses resistance to ampicillin.
Reason (R):
The $Pst$ I restriction site is present within the coding sequence of the $tet^R$ gene of pBR322.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Selection of recombinants using insertional inactivation of the $eta$-galactosidase gene is often preferred because it avoids the cumbersome procedure of simultaneous plating on two plates having different antibiotics.
Reason (R):
The general principle of insertional inactivation is that the foreign DNA is inserted within the coding sequence of a gene, making it non-functional.
[Biotechnology-Principles-and-Processes] [class-xii ]
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