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Assertion (A):
Restriction enzymes cut the strand of DNA a little away from the centre of the palindromic site, creating sticky ends.
Reason (R):
These sticky ends are necessary because they facilitate the action of the enzyme DNA ligase by forming hydrogen bonds with their complementary cut counterparts.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
The linking of the cut antibiotic resistance gene with the plasmid vector to form recombinant DNA became possible with the enzyme DNA ligase.
Reason (R):
If the vector DNA and the source DNA are cut by the same restriction enzyme, the recombinant molecule cannot be created.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Exonucleases remove nucleotides from the ends of the DNA, whereas endonucleases make cuts at specific positions within the DNA.
Reason (R):
Restriction enzymes belong to a larger class of enzymes called nucleases.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
The palindromic sequence in DNA reads the same on the two strands when the orientation of reading (e.g., 5' to 3') is kept the same.
Reason (R):
The first restriction endonuclease, Hind II, always cut DNA molecules by recognising a specific sequence of six base pairs.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
When an alien piece of DNA is transferred into an alien organism, it needs to be linked with the origin of replication (`ori`).
Reason (R):
The origin of replication sequence is responsible for initiating replication and also controls the copy number of the linked DNA.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Cloning vectors must 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 generate several fragments, which will complicate the gene cloning process.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Genes conferring resistance to antibiotics are considered useful selectable markers in cloning experiments.
Reason (R):
Selectable markers help in identifying and eliminating non-transformants by selectively permitting the growth of only the transformants.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
If a foreign DNA is ligated at the $BamH$ I site in the vector pBR322, the transformant cells will lose resistance to ampicillin.
Reason (R):
The $BamH$ I restriction site is present within the coding sequence of the tetracycline resistance gene ($tet^R$) of pBR322.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Selection of recombinants using insertional inactivation of the $eta$-galactosidase gene is often preferred over selection using two antibiotic resistance genes.
Reason (R):
Non-recombinant colonies carrying the intact $eta$-galactosidase gene appear blue in the presence of a chromogenic substrate.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Bacterial cells are made 'competent' to take up DNA by treating them with divalent cations such as calcium.
Reason (R):
DNA is a hydrophilic molecule, so it cannot pass easily through the hydrophobic cell membrane without chemical manipulation.
[Biotechnology-Principles-and-Processes] [class-xii ]
This Page Score: 0/40