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Question

A thermostable DNA polymerase is isolated from:

The correct answer is

Thermus aquaticus

Understanding Thermostable DNA Polymerase Source

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).

Why Thermostable DNA Polymerase is Needed in PCR

The Polymerase Chain Reaction involves cycling through different temperatures to amplify DNA. Key steps include:

  • Denaturation: Heating the DNA to around ${94-96}^\circ\text{C}$ to separate the double strands.
  • Annealing: Lowering the temperature to allow primers to bind to the DNA template.
  • Extension: Raising the temperature to an optimal level (often around ${72}^\circ\text{C}$) for the DNA polymerase to synthesize new DNA strands.

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.

Source Organism: Thermus aquaticus

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.

Analysis of Options

  • Thermus aquaticus: This is a bacterium found in hot springs. It is the source of Taq polymerase, a well-known thermostable DNA polymerase vital for PCR. This aligns with the need for an enzyme that can withstand high temperatures.
  • Agrobacterium tumefaciens: This is a bacterium known for its ability to genetically engineer plants, often used as a vector in biotechnology. It is not primarily known as a source of thermostable enzymes for PCR.
  • E. coli: Escherichia coli is a common bacterium widely used in molecular biology research. While it has DNA polymerases, its standard DNA polymerases are not thermostable and would be denatured during the high-temperature steps of PCR.
  • Salmonella typhimurium: This is a pathogenic bacterium known to cause food poisoning. It is not a source for the thermostable DNA polymerase used in molecular biology techniques like PCR.

Based on the biological source and the requirements of molecular biology techniques like PCR, the thermostable DNA polymerase is isolated from Thermus aquaticus.


Revision Table: Key Concepts

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)

Additional Information: Thermostable Enzymes and Biotechnology

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.

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Similar Questions

  1. Which of the following is not a step of Polymerase Chain Reaction?

  2. Which of the following statements is not correct for Restriction enzymes?

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    Statement II: In downstream processing, the products formulated with suitable preservatives are ready for marketing without testing of their quality.

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  4. Which one of the following is not a process of DNA recombinant technology?

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    (B) Treatment with divalent cations

    (C) Heat shock treatment

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Important Questions from Biotechnology : Principles and Processes

  1. The first restriction endonuclease to be isolated was:

  2. Arrange the following steps of PCR in correct sequence:

    1. (A) Denaturation of ds DNA
    2. (B) Annealing
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    4. (D) Extension of Primer
    5. (E) Use of DNA polymerase and deoxynucleotides

    Choose the correct answer from the options given below:

  3. The process of cutting out DNA fragments from agarose gel and their extraction from gel piece is known as:

  4. Arrange the following steps of rDNA technology in correct sequence. 

    (A) Amplification of gene by PCR 

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