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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 molecular component in List-I with its analogy or functional characteristic in List-II:

List-I (Molecular Component)List-II (Analogy/Function)
A. Restriction EndonucleasesI. Insect vector for malarial parasite
B. Plasmid DNAII. Molecular Scissors
C. MosquitoIII. Vector to transfer piece of DNA attached to it
D. Sticky EndsIV. Facilitates the action of DNA ligase

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

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

    Remark: Restriction enzymes are known as ‘molecular scissors’ [13, II].
    Plasmid DNA acts as a vector [13, III].
    Mosquito is an insect vector for malarial parasite [13, I].
    Sticky ends facilitate the action of DNA ligase [21, IV].

Match the concept regarding DNA replication and inheritance (List-I) with the essential property or mechanism (List-II):

List-I (Concept)List-II (Related Sequence/Property)
A. Multiplication of alien DNAI. Linking alien DNA with ori
B. CloningII. Making multiple identical copies of any template DNA
C. Inheritance of alien DNAIII. Ability of the chromosome to replicate
D. Initiation of replicationIV. Origin of replication (ori)

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

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

    Remark: Alien DNA multiplication requires linking with *ori* [11, I].
    Cloning is making multiple identical copies [11, II].
    Inheritance occurs when alien DNA is part of a replicating chromosome [10, III].
    *Ori* is the specific sequence responsible for initiating replication [11, IV].

Match the culture system in List-I with its description or role in List-II:

List-I (Culture System)List-II (Characteristic)
A. Small volume culturesI. Maintaining cells in their physiologically most active log/exponential phase
B. Large scale productionII. Cannot yield appreciable quantities of products
C. Continuous Culture SystemIII. Requires development of bioreactors
D. Stirred-tank bioreactorIV. Most commonly used bioreactor type

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

    Remark: Small cultures cannot yield appreciable quantities [50, II].
    Large scale production requires bioreactors [51, III].
    Continuous culture maintains cells in the log/exponential phase [49, I].
    Stirring type bioreactors are the most commonly used [52, IV].

Match the discipline or historical figure in List-I with its associated concept or age in List-II:

List-I (Discipline)List-II (Associated Field/Age)
A. Physics and ChemistryI. Twentieth century off-shoot of modern biology
B. BiotechnologyII. Gave rise to engineering, technologies and industries for human welfare
C. Anthropocentric ApproachIII. French philosopher of seventeenth century
D. Rene DescartesIV. Understanding natural phenomena directed towards human comforts

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

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

    Remark: Physics and chemistry led to industries working for human welfare [1, II].
    Biotechnology is a twentieth-century off-shoot of modern biology [2, I].
    Anthropocentric approach focuses understanding natural phenomena on human comforts [1, IV].
    Rene Descartes was a French philosopher of the seventeenth century [1, III].

Match the action or condition in List-I with its consequence or result in List-II:

List-I (Cut Type)List-II (Resulting Feature)
A. Cutting DNA away from center of palindromeI. Enables the bacteria to take up the recombinant DNA
B. Cutting at specific pointsII. Leaves single stranded portions at the ends (sticky ends)
C. Heat shock (42°C) applicationIII. Occurs in the sugar-phosphate backbone
D. Hydrogen bonding between sticky endsIV. Facilitates the action of DNA ligase

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

    Remark: Cutting away from the center of the palindrome leaves sticky ends [20, 21, II].
    Restriction enzymes cut the sugar-phosphate backbones [19, III].
    Heat shock enables bacteria to take up RDNA [37, I].
    Hydrogen bonding of sticky ends facilitates ligation by DNA ligase [21, IV].

Match the steps in product preparation (List-I) with their defining purpose (List-II) after the biosynthetic stage:

List-I (Post-Biosynthetic Step)List-II (Purpose/Requirement)
A. Downstream ProcessingI. For formulations intended as drugs
B. FormulationII. Collective term for separation and purification processes
C. Clinical TrialsIII. Required for marketing as a finished product
D. Quality Control TestingIV. Strict testing required for each product; varies from product to product

[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: Downstream processing is the collective term for separation and purification [55, II].
    Formulation is necessary before marketing the finished product [55, III].
    Clinical trials are required for drug formulations [55, I].
    Quality Control Testing involves strict, product-specific testing [55, IV].

Match the product type in List-I (traditional) with the modern biotechnological products mentioned in the source (List-II):

List-I (Traditional Product)List-II (Modern Product)
A. CurdI. Antibiotics
B. BreadII. Vaccines
C. WineIII. Enzymes
D. Microbial activity (General)IV. Recombinant proteins

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

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

    Remark: Curd, bread, and wine are listed as microbe-mediated processes. Modern products listed include antibiotics, vaccines, enzymes, and the ultimate aim is recombinant proteins. Since all are modern products, we group them accordingly. A, B, C map to I, II, III (examples of specific products mentioned), while D maps to IV (the general goal/output).

Match the enzyme action in List-I with the molecular consequence in List-II:

List-I (Enzyme action on DNA)List-II (Molecular consequence)
A. Restriction EndonucleaseI. Addition of methyl groups to DNA
B. DNA LigaseII. Cuts the two strands of the double helix at specific points in their sugar-phosphate backbones
C. Enzyme isolated in 1963 (methylating)III. Joins the ends of cut DNA molecules
D. ExonucleaseIV. Removes nucleotides from the ends of the DNA

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

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

    Remark: Restriction endonuclease cuts the sugar-phosphate backbone [19, II].
    DNA ligase joins the ends of cut DNA molecules [14, III].
    One enzyme isolated in 1963 added methyl groups to DNA [16, I].
    Exonuclease removes nucleotides from the ends of the DNA [18, IV].

Match the feature of gel electrophoresis (List-I) with the DNA behavior or application (List-II):

List-I (Feature)List-II (DNA Behavior)
A. DNA molecular sizeI. Moves toward the positive electrode (anode)
B. Negative charge of DNAII. Smaller fragments move farther
C. Sieving effect of the gelIII. Method used to check progression of restriction enzyme digestion
D. Agarose gel electrophoresisIV. Fragments separate (resolve) according to this

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

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

    Remark: DNA fragments resolve according to size [23, IV].
    Negative charge causes movement toward the anode [23, I].
    The sieving effect makes smaller fragments move farther [23, II].
    Electrophoresis checks the progression of digestion [42, III].

Match the key processes in Recombinant DNA Technology (List-I) with their primary description (List-II):

List-I (Process)List-II (Step)
A. IsolationI. Transferring RDNA into host cells
B. LigationII. Cutting of DNA by restriction endonucleases
C. FragmentationIII. Joining the gene of interest with the vector
D. TransformationIV. Obtaining the genetic material (DNA) in pure form

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

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

    Remark: Isolation is obtaining genetic material in pure form [39, 40, IV].
    Ligation is joining the DNA fragment into a vector [39, 43, III].
    Fragmentation is cutting DNA by restriction endonucleases [39, II].
    Transformation is transferring RDNA into host cells [39, I].