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Assertion (A):
In insertional inactivation using a chromogenic substrate, non-recombinant colonies appear blue.
Reason (R):
The presence of an insert results in the inactivation of the $eta$-galactosidase gene, causing the colonies to remain colorless and thus identifying them as recombinants.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
We learned the lesson of transferring genes into plants and animals from studying bacteria and viruses.
Reason (R):
Pathogens like Agrobacterium tumifaciens (in plants) and retroviruses (in animals) naturally possess the ability to deliver genes to transform eukaryotic cells.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
The tumor inducing ($Ti$) plasmid of Agrobacterium tumifaciens is used in its pathogenic form as a cloning vector for gene delivery into dicot plants.
Reason (R):
The Ti plasmid has been modified into a cloning vector that is no longer pathogenic but is still able to deliver genes of interest into a variety of plants.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Bacterial cells are treated with a divalent cation like calcium to make them 'competent' to take up DNA.
Reason (R):
The calcium treatment increases the efficiency with which the DNA enters the bacterium through pores in its cell wall.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Micro-injection is a method of introducing recombinant DNA by bombarding cells with high velocity micro-particles of gold or tungsten coated with DNA.
Reason (R):
Micro-injection is suitable for plant cells, while biolistics (gene gun) is suitable for animal cells.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
In order to cut DNA with restriction enzymes, the DNA needs to be in pure form, free from other macromolecules.
Reason (R):
DNA is contained within membranes, and we must break the cell open to release DNA along with other macromolecules such as RNA, proteins, and polysaccharides.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
To isolate DNA, bacterial cells are treated with lysozyme, plant cells with cellulase, and fungal cells with chitinase.
Reason (R):
These specific enzymes are used to break down the respective cell walls to achieve the release of DNA.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
RNA is removed from the DNA extract by treatment with ribonuclease, and proteins are removed by protease.
Reason (R):
Genes are located on long molecules of DNA intertwined with proteins such as histones.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
Agarose gel electrophoresis is used to check the progression of a restriction enzyme digestion.
Reason (R):
After digestion, the DNA is a negatively charged molecule, and it must move towards the positive electrode (anode) under an electric field.
[Biotechnology-Principles-and-Processes] [class-xii ]
Assertion (A):
In Polymerase Chain Reaction (PCR), the segment of DNA can be amplified to approximately a billion times after many repeated cycles.
Reason (R):
Such repeated amplification is achieved by using a thermostable DNA polymerase, which remains active during the high temperature denaturation steps.
[Biotechnology-Principles-and-Processes] [class-xii ]
This Page Score: 0/40