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NEET-UG Biology · Class 12

PCR and the steps of recombinant DNA technology — NEET & JEE Questions

PCR and the steps of recombinant DNA technology is a topic in Biotechnology: Principles and Processes, a Class 12 Biology chapter of the NEET-UG syllabus. TestBudy holds 17 published NEET-UG questions on PCR and the steps of recombinant DNA technology, each with the marking scheme of the real paper.

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PCR and the steps of recombinant DNA technology MCQs with solutions

10 of the 17 published questions on this topic, exactly as they appear in a test. Answers and worked solutions come with your result rather than on this page.

  1. Question 1 · difficulty L1 · recall

    PCR is primarily used to

    • A. amplify a selected DNA sequence
    • B. separate proteins by mass
    • C. translate DNA into protein
    • D. destroy all template DNA
  2. Question 2 · difficulty L2 · understanding

    Polymerase chain reaction (PCR) amplifies DNA following the equation.

    • A. 2n+12 n+1
    • B. 2 N22 \mathrm{~N}^2
    • C. N2\mathrm{N}^2
    • D. 2n2^n
  3. Question 3 · difficulty L2 · understanding

    During PCR, what happens during the annealing step?

    • A. Restriction enzymes cut the amplified DNA
    • B. DNA strands are separated by high temperature
    • C. DNA polymerase synthesises new strands at maximum temperature
    • D. Primers bind to complementary sequences on the template DNA
  4. Question 4 · difficulty L2 · understanding

    During PCR, the denaturation step mainly

    • A. separates the two DNA strands
    • B. allows primers to bind
    • C. extends primers with DNA polymerase
    • D. ligates vector and insert
  5. Question 5 · difficulty L3 · understanding

    Identify the correct sequence of steps in each cycle of Polymerase Chain Reaction :

    • A. Extension → Annealing → Denaturation
    • B. Annealing → Denaturation → Extension
    • C. Denaturation → Extension → Annealing
    • D. Denaturation → Annealing → Extension
  6. Question 6 · difficulty L3 · understanding

    Following are the steps involved in the process of PCR. A. Annealing B. Amplification (~1 billion times) C. Denaturation D. Treatment with Taq polymerase and deoxynucleotides E. Extension Choose the correct sequence of steps of PCR from the options given below :

    • A. C→A→D→E→B\mathrm{C} \rightarrow \mathrm{A} \rightarrow \mathrm{D} \rightarrow \mathrm{E} \rightarrow \mathrm{B}
    • B. A→B→E→D→C\mathrm{A} \rightarrow \mathrm{B} \rightarrow \mathrm{E} \rightarrow \mathrm{D} \rightarrow \mathrm{C}
    • C. A→C→E→D→B\mathrm{A} \rightarrow \mathrm{C} \rightarrow \mathrm{E} \rightarrow \mathrm{D} \rightarrow \mathrm{B}
    • D. D→B→E→C→A\mathrm{D} \rightarrow \mathrm{B} \rightarrow \mathrm{E} \rightarrow \mathrm{C} \rightarrow \mathrm{A}
  7. Question 7 · difficulty L3 · understanding

    Thermostable DNA polymerase used in PCR was isolated from :

    • A. Thermus aquaticus
    • B. Escherichia coli
    • C. Agrobacterium tumifaciens
    • D. Bacillus thuringiensis
  8. Question 8 · difficulty L3 · understanding

    Given below are two statements : one is labelled as Assertion (A) and the other is labelled as Reason (R). Assertion (A) : Polymerase chain reaction is used in DNA amplification. Reason (R) : The ampicillin resistant gene is used as a selectable marker to check transformation. In the light of the above statements, choose the correct answer from the options given below :

    • A. Both (A) and (R) are correct and (R) is the correct explanation of (A)
    • B. Both (A) and (R) are correct but (R) is not the correct explanation of (A)
    • C. (A) is correct but (R) is not correct
    • D. (A) is not correct but (R) is correct
  9. Question 9 · difficulty L3 · understanding

    Match List-I with List-II . List-I List-II (a) Protpolast fusion (i) Totipotency (b) Plant tissue culture (ii) Pomato (c) Meristem culture (iii) Somaclones (d) Micropropagation (iv) Virus free plants Choose the correct answer from the options given below.

    • A. (a) (b) (c) (d) (iv) (iii) (ii) (i)
    • B. (a) (b) (c) (d) (iii) (iv) (ii) (i)
    • C. (a) (b) (c) (d) (ii) (i) (iv) (iii)
    • D. (a) (b) (c) (d) (iii) (iv) (i) (ii)
  10. Question 10 · difficulty L3 · understanding

    Which of the following is not an application of PCR (Polymerase Chain Reaction)?

    • A. Detection of gene mutation
    • B. Molecular diagnosis
    • C. Gene amplification
    • D. Purification of isolated protein

Common mistakes in PCR and the steps of recombinant DNA technology

Recorded against questions in this topic that are not shown above, so none of these points at an answer you can see on this page.

  • Putting downstream processing before recombinant DNA has been created and expressed.
  • Places annealing before template strand separation.
  • Assumes any DNA polymerase tolerates repeated near-boiling temperatures.
  • Assumes DNA polymerase can initiate synthesis de novo at any desired target.

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