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Biotechnology : Principles and Processes: Class-XII


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MCQs on Biotechnology : Principles and Processes: Class-XII for NEET Practice


Match the historical concept/figure in List-I with its description in List-II:

List-I (Concept/Figure)List-II (Description/Source)
A. Rene DescartesI. Twentieth century off-shoot of modern biology
B. BiotechnologyII. French philosopher, mathematician, and biologist of the seventeenth century
C. Anthropocentric ApproachIII. Understanding natural phenomena directed towards human comfort and welfare
D. Physics and Chemistry disciplinesIV. Gave rise to engineering, technologies, and industries

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-I, C-III, D-IV
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-I, C-III, D-IV ]

    Remark: Rene Descartes was a 17th-century philosopher [1, II].
    Biotechnology is a 20th-century off-shoot of modern biology [2, I].
    The anthropocentric approach guides science toward human comfort [1, III].
    Physics and chemistry gave rise to engineering and industries [1, IV].

Match the large scale culture process or condition in List-I with its description in List-II:

List-I (Culture System)List-II (Characteristic)
A. Used mediumI. Large biomass leading to higher yields
B. Log/Exponential phaseII. Drained out from one side in continuous culture
C. Continuous Culture System resultIII. Physiologically most active phase of cells
D. Small scale laboratory culture limitationIV. Cannot yield appreciable quantities of products

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-III, C-I, D-IV
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-III, C-I, D-IV ]

    Remark: Used medium is drained out in continuous culture [49, II].
    Log phase is the physiologically most active phase of cells [49, III].
    Continuous culture leads to large biomass and higher yields [49, I].
    Small scale culture cannot yield appreciable quantities [51, IV].

Match the principle of gel electrophoresis (List-I) with the underlying mechanism or observation (List-II):

List-I (Principle)List-II (Mechanism/Feature)
A. DNA migration directionI. Smaller fragments travel farther
B. Fragment separation basisII. Sieving effect provided by the agarose gel
C. Relationship between size and movementIII. Towards the anode (positive electrode)
D. Agarose gel matrix functionIV. According to their size

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-III, B-IV, C-I, D-II
  • A-I, B-II, C-III, D-IV
  • A-II, B-I, C-IV, D-III
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-III, B-IV, C-I, D-II ]

    Remark: DNA moves towards the anode [23, III].
    Fragments separate according to size [23, IV].
    Smaller fragments move farther than larger ones [23, I].
    Agarose gel provides the sieving effect [23, II].

Match the three primary steps of Polymerase Chain Reaction (PCR) in List-I with their corresponding action or outcome in List-II:

List-I (PCR Cycle Step)List-II (Action/Condition)
A. DenaturationI. Annealing (binding) of primers to the template DNA
B. AnnealingII. High temperature induced separation of double stranded DNA
C. ExtensionIII. DNA polymerase synthesizes DNA segment
D. Repeated CyclesIV. Amplification to approximately billion times

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-I, C-III, D-IV
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-I, C-III, D-IV ]

    Remark: Denaturation uses high temperature to separate strands [45, II].
    Annealing is the binding of primers [44, I].
    Extension involves DNA polymerase synthesizing DNA [44, III].
    Repeated cycles achieve billion-fold amplification [44, IV].

Match the process or product in List-I with its classification or mechanism in List-II:

List-I (Product/Process)List-II (Classification/Mechanism)
A. Making curdI. Microbe-mediated process
B. Synthesis of a geneII. Modern biotechnology
C. Developing a DNA vaccineIII. Also considered a form of biotechnology (traditional sense)
D. Using genetically modified organisms (restricted sense)IV. Modern biotechnology (focused on engineered organisms)

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-III, B-II, C-II, D-IV
  • A-I, B-III, C-II, D-IV
  • A-II, B-I, C-III, D-IV
  • A-IV, B-III, C-I, D-II
  • Correct Option: A  [ A-III, B-II, C-II, D-IV ]

    Remark: Making curd is a microbe-mediated process and a form of traditional biotechnology [5, I, III].
    Synthesizing a gene is part of modern biotechnology [6, II].
    Developing a DNA vaccine is part of modern biotechnology [6, II].
    Using genetically modified organisms is the restricted sense of modern biotechnology [5, IV].

Match the detailed requirements of Polymerase Chain Reaction (PCR) in List-I with their function or characteristic in List-II:

List-I (PCR Component)List-II (Role/Requirement)
A. PrimersI. Template for DNA synthesis
B. Genomic DNAII. Small chemically synthesised oligonucleotides
C. Nucleotides (dNTPs)IV. Provided in the reaction for enzyme extension
D. Thermostable DNA PolymeraseIII. Remain active during high temperature denaturation

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-I, C-IV, D-III
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-I, C-IV, D-III ]

    Remark: Primers are small chemically synthesised oligonucleotides [44, II].
    Genomic DNA serves as the template [44, I].
    Nucleotides are provided in the reaction for extension [44, IV].
    Thermostable polymerase remains active during high temperature denaturation [44, 45, III].

Match the specific feature of the pBR322 vector in List-I with its function or location in List-II:

List-I (pBR322 Feature)List-II (Role/Example)
A. ampR geneI. Protein involved in replication of the plasmid
B. Pst I siteII. Selectable marker conferring Ampicillin resistance
C. rop geneIII. Specific location within the tetR gene
D. BamH I siteIV. Restriction site located within the ampR gene

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-IV, C-I, D-III
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-IV, C-I, D-III ]

    Remark: *ampR* is a selectable marker for Ampicillin resistance [28, 31, II].
    Pst I is listed as a restriction site on pBR322, specifically shown in the *ampR* region [31, IV].
    *rop* codes for proteins involved in the replication of the plasmid [31, I].
    BamH I site is located in the tetracycline resistance gene [29, 31, III].

Match the part of the Restriction Enzyme name (EcoRI) in List-I with the convention it represents in List-II:

List-I (Naming Part of EcoRI)List-II (Represents)
A. EI. Species of the prokaryotic cell
B. coII. Order in which the enzyme was isolated
C. RIII. Genus of the prokaryotic cell
D. IIV. Name of the strain

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-III, B-I, C-IV, D-II
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-III, B-I, C-IV, D-II ]

    Remark: E comes from the genus (*Escherichia*) [17, III].
    co comes from the species (*coli*) [17, I].
    R is derived from the strain name (RY 13) [17, 18, IV].
    I (Roman numeral) indicates the order of isolation [18, II].

Match the scope or definition of Biotechnology in List-I with its description in List-II:

List-I (Definition/Process)List-II (Scope)
A. Traditional BiotechnologyI. Integration of natural science and organisms/cells/molecular analogues for products/services
B. Restricted sense of BiotechnologyII. Use of live organisms or enzymes to produce products/processes useful to humans
C. EFB Definition of BiotechnologyIII. Processes using genetically modified organisms
D. Making curd, bread, or wineIV. Microbe-mediated processes

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-III, C-I, D-IV
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-III, C-I, D-IV ]

    Remark: Traditional biotechnology is defined by using organisms/enzymes for useful products [5, II].
    The restricted sense refers to processes using genetically modified organisms [5, III].
    EFB definition encompasses integration of natural science and molecular analogues [6, I].
    Curd/bread/wine making are microbe-mediated processes [5, IV].

Match the method of introducing alien DNA into host cells (List-I) with its corresponding description (List-II):

List-I (Method)List-II (Description/Host Type)
A. Micro-injectionI. Bombarding cells with high velocity micro-particles of gold or tungsten
B. Gene Gun (Biolistics)II. Direct injection of RDNA into the nucleus of an animal cell
C. Chemical treatment (Ca++)III. Used to make bacterial cells competent to take up plasmid DNA
D. Disarmed Pathogen VectorsIV. Used to infect the host cell, transferring the recombinant DNA

[Biotechnology-Principles-and-Processes] [class-xii ]

  • A-II, B-I, C-III, D-IV
  • A-I, B-II, C-IV, D-III
  • A-III, B-IV, C-I, D-II
  • A-IV, B-III, C-II, D-I
  • Correct Option: A  [ A-II, B-I, C-III, D-IV ]

    Remark: Micro-injection involves direct injection into the nucleus of an animal cell [37, II].
    Biolistics/Gene Gun bombards cells with micro-particles [38, I].
    Divalent cations (like Ca++) treat bacterial cells to make them competent [36, III].
    Disarmed pathogens infect the cell to transfer RDNA [38, IV].