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.
The cloning site present in the \( \textit{rop}\) site of \(\textit{E. coli}\) cloning vector pBR322 is:
The cloning site present in the ampicillin resistance gene of \( \textit{E. coli}\) cloning vector pBR322 is :
A block of certain mass is placed on a rough floor. The coefficients of static and kinetic friction between the block and the floor are 0.4 and 0.25 respectively. A constant horizontal force \( F = 20 \, \text{N} \) acts on it so that the velocity of the block varies with time according to the following graph. The mass of the block is nearly (Take \( g = 10 \, \text{m/s}^2 \)):
A wooden block of mass M lies on a rough floor. Another wooden block of the same mass is hanging from the point O through strings as shown in the figure. To achieve equilibrium, the coefficient of static friction between the block on the floor and the floor itself is