Polymerase Chain Reaction (PCR) is a technique used to amplify specific segments of DNA. The process involves repeated cycles of heating and cooling:
Because the cycle involves high temperatures during the denaturation step, the DNA polymerase used must be thermostable (heat-stable) so that it doesn't get denatured and inactivated after each heating cycle.
The first widely used and still very common thermostable DNA polymerase for PCR is Taq polymerase.
This enzyme was isolated from a thermophilic bacterium that thrives in hot springs.
Let's look at the options:
Therefore, Taq polymerase used in PCR is obtained from Thermus aquaticus.
Taq polymerase, essential for the Polymerase Chain Reaction (PCR), is derived from the thermophilic bacterium Thermus aquaticus. This enzyme's thermostability allows it to withstand the high temperatures required during PCR, enabling efficient DNA amplification.
The correct answer is (A) : Thermus aquaticus.
Answer the following questions:
(a) [(i)] Explain how some strains of Bacillus thuringiensis produce proteins that kill certain insects such as lepidopterans but do not kill the Bacillus.
[(ii)] How is the above mechanism exploited for the production of Bt cotton plant by biotechnologists?
(b) [(i)] Explain how the amplification of gene of interest is done using PCR.
[(ii)] State two applications of the desired amplified fragment of DNA.
The basic scheme of the essential steps involved in the process of recombinant DNA technology is summarised below in the form of a flow diagram. Study the given flow diagram and answer the questions that follow.
(a) What is the technical term used for Step 4 in the above process?
(b) Which of the given two combinations of restriction enzyme should be used in Step 1? Justify your answer.
(i) EcoR I to cut the plasmid and Hind III to cut the alien DNA.
(ii) EcoR I to cut both the plasmid and alien DNA.
In the given graph, \( E_a \) for the reverse reaction will be