A thermostable DNA polymerase is isolated from:
Thermus aquaticus
A thermostable DNA polymerase is a type of enzyme that can withstand high temperatures without denaturing or losing its activity. This property is crucial for certain molecular biology techniques, most notably the Polymerase Chain Reaction (PCR).
The Polymerase Chain Reaction involves cycling through different temperatures to amplify DNA. Key steps include:
Since the enzyme is exposed to high temperatures during the denaturation step in every cycle, a standard DNA polymerase from organisms like E. coli would be denatured and become inactive. Therefore, a polymerase that remains stable and active at these high temperatures is essential for PCR.
The first and most commonly used thermostable DNA polymerase, known as Taq polymerase, was isolated from the bacterium Thermus aquaticus. This bacterium is an extremophile, meaning it thrives in extreme environments, specifically hot springs and hydrothermal vents. Its enzymes, including DNA polymerase, have naturally evolved to function optimally at high temperatures.
Based on the biological source and the requirements of molecular biology techniques like PCR, the thermostable DNA polymerase is isolated from Thermus aquaticus.
| Term | Definition/Significance | Source Organism |
|---|---|---|
| Thermostable DNA Polymerase | Enzyme active at high temperatures; essential for PCR | N/A (Property, not organism) |
| Taq Polymerase | A specific, commonly used thermostable DNA Polymerase | Thermus aquaticus |
| PCR (Polymerase Chain Reaction) | Technique to amplify DNA using temperature cycles | N/A (Technique) |
| Thermus aquaticus | Extremophile bacterium found in hot springs | N/A (Organism) |
The discovery of thermostable enzymes from extremophile organisms like Thermus aquaticus has revolutionized molecular biology. These enzymes are stable under harsh conditions, making them invaluable for various industrial and research applications. Beyond DNA polymerases, other thermostable enzymes like proteases and amylases are also isolated from thermophilic (heat-loving) organisms and used in industries such as detergents, food processing, and textiles.
While Taq polymerase is the most famous, other thermostable DNA polymerases have been isolated from different thermophilic organisms, such as Pfu polymerase from Pyrococcus furiosus. Pfu polymerase is known for its high fidelity (accuracy) compared to Taq polymerase, although it can be slower.
Understanding the source of these enzymes is crucial in biotechnology as it directly relates to their unique properties and applications.
Which of the following is not a step of Polymerase Chain Reaction?
Which of the following statements is not correct for Restriction enzymes?
Given below are two statements:
Statement I: In a bioreactor, small volumes of cultures are developed in which useful bio-products are produced.
Statement II: In downstream processing, the products formulated with suitable preservatives are ready for marketing without testing of their quality.
In the light of the above statements, choose the correct answer from the options given below:
Which one of the following is not a process of DNA recombinant technology?
Downstream processing method involves:
Arrange the following steps involved in the transformation of bacteria in a sequence from initiation to end:
(A) Incubation of rDNA with bacterial cell on ice
(B) Treatment with divalent cations
(C) Heat shock treatment
(D) Selection on antibiotic-containing agar plate
(E) Placed them again on ice
Which of the following statements are incorrect?
(A) Fragments of DNA can be separated by ELISA.
(B) Transformation is a procedure through which a piece of DNA is introduced into a host bacterium.
(C) Recombinant DNA technology does not involve isolation of a desired DNA fragment.
(D) DNA ligases are used for stitching DNA fragments into a vector.
The first restriction endonuclease to be isolated was:
Arrange the following steps of PCR in correct sequence:
Choose the correct answer from the options given below:
The process of cutting out DNA fragments from agarose gel and their extraction from gel piece is known as:
Arrange the following steps of rDNA technology in correct sequence.
(A) Amplification of gene by PCR
(B) Insertion of rDNA into host cell using vector
(C) Isolation of the genetic material from the cell
(D) Cutting the DNA at specific location
In biolistic method, the cells are bombarded with high velocity microparticles of: