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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 element related to DNA separation/visualization (List-I) with its corresponding feature (List-II):

List-I (Technique/Compound)List-II (Feature/Outcome)
A. AgaroseI. Charge carried by DNA fragments
B. Ethidium BromideII. Natural polymer extracted from sea weeds, used as matrix
C. NegativeIII. Staining compound that allows visualization under UV radiation
D. UV Radiation ExposureIV. Leads to bright orange coloured DNA bands

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

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

    Remark: Agarose is a natural polymer from sea weeds used as matrix.
    Ethidium bromide is used for staining DNA.
    DNA fragments are negatively charged molecules.
    UV radiation exposure makes the stained DNA bands appear bright orange.

Match the activity/goal in List-I with the corresponding process type in List-II:

List-I (Goal/Application)List-II (Process Type)
A. Synthesising a gene and using itI. Overcoming the limitation of traditional hybridization
B. Use of genetically modified organisms (restricted sense)II. Part of biotechnology/genetic engineering
C. Introduction of only desired genesIII. Ultimate aim of almost all recombinant technologies
D. Producing a desirable proteinIV. Modern biotechnology

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

    Remark: Synthesising a gene is part of biotechnology.
    Modern biotechnology uses genetically modified organisms.
    Genetic engineering allows introduction of only desirable genes, overcoming traditional hybridization limitations.
    The ultimate aim of recombinant technologies is to produce a desirable protein.

Match the Bioreactor specifications in List-I with their description in List-II:

List-I (Bioreactor Type/Feature)List-II (Description/Range)
A. Volume capacityI. Cylindrical or with a curved base
B. Stirred-tank reactor shapeII. Most commonly used bioreactors
C. Stirring type bioreactorsIII. Provides optimum growth conditions (Temp, pH, substrate, $ ext{O}_2$)
D. Bioreactor goalIV. 100-1000 litres of culture

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

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

    Remark: Bioreactors process large volumes (100-1000 litres).
    A stirred-tank reactor is usually cylindrical or with a curved base.
    Stirring type bioreactors are the most commonly used.
    Bioreactors provide optimal conditions for achieving the desired product.

Match the basic steps in genetically modifying an organism (List-I) with their corresponding process (List-II):

List-I (Step Order)List-II (Basic Step)
A. First stepI. Maintenance of introduced DNA in the host and transfer to progeny
B. Second stepII. Introduction of the identified DNA into the host
C. Third stepIII. Culturing host cells at large scale and product extraction
D. Subsequent step after host introductionIV. Identification of DNA with desirable genes

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

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

    Remark: The three basic steps are: (i) identification of desired DNA [15, IV]; (ii) introduction into the host [15, II]; and (iii) maintenance and transfer to progeny [15, I]. Culturing host cells at large scale is a subsequent process step [39, III].

Match the components of the restriction enzyme naming convention (List-I) with their origin (List-II), using EcoRI as an example:

List-I (Name Component)List-II (Origin)
A. First Letter (E in EcoRI)I. Species of the prokaryotic cell
B. Next Two Letters (co in EcoRI)II. Genus of the prokaryotic cell
C. Letter R (in EcoRI)III. Order in which the enzymes were isolated from that strain
D. Roman Numbers (I in EcoRI)IV. Name of the bacterial strain (e.g., RY 13)

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

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

    Remark: First letter is from the genus (E from Escherichia).
    Next two letters are from the species (co from coli).
    The letter R is derived from the strain name (RY 13).
    Roman numbers indicate the order of isolation.

Match the types of selectable markers in List-I with their corresponding function or example in List-II:

List-I (Marker Type)List-II (Function/Example)
A. Selectable MarkerI. $eta$-galactosidase gene
B. Chromogenic Substrate MarkerII. Helps identify and eliminate non-transformants
C. Example of Antibiotic Resistance MarkerIII. Allows differentiation based on ability to produce color
D. Target gene for Insertional Inactivation (Color)IV. Ampicillin, tetracycline, chloramphenicol, or kanamycin resistance genes

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

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

    Remark: Selectable markers identify and eliminate non-transformants.
    Chromogenic substrate markers differentiate based on color production.
    Antibiotic resistance genes (ampicillin, tetracycline, etc.) are common markers for *E. coli*.
    The $eta$-galactosidase gene is the target for color-based insertional inactivation.

Match the biotechnological activities in List-I with their classification or impact in List-II:

List-I (Technique/Product)List-II (Classification)
A. Making curd/bread/wineI. Modern biotechnology
B. Developing a DNA vaccineII. Traditional biotechnology (microbe-mediated)
C. Using genetically modified organisms (restricted sense)III. Qualitative improvement in health and food production
D. Overall impact of modern biotechnologyIV. Part of biotechnology/genetic engineering

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

    Remark: Making curd/bread/wine is a microbe-mediated process, considered traditional biotechnology.
    Developing a DNA vaccine is included in biotechnology [6, IV].
    The restricted sense of biotechnology refers to using genetically modified organisms [5, I].
    Modern biotechnology led to qualitative improvement in health and food production.

Match the reproduction/breeding technique in List-I with its key characteristic or outcome in List-II:

List-I (Reproduction Type)List-II (Key Outcome)
A. Sexual ReproductionI. Preserves the genetic information
B. Asexual ReproductionII. Provides opportunities for variations and formulation of unique combinations
C. Traditional HybridisationIII. Overcome the limitation of including undesirable genes
D. Genetic EngineeringIV. Often leads to inclusion and multiplication of undesirable genes

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

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

    Remark: Sexual reproduction provides opportunities for variations.
    Asexual reproduction preserves the genetic information.
    Traditional hybridization often leads to inclusion of undesirable genes.
    Genetic engineering overcomes the limitation of including undesirable genes.

Match the method for introducing alien DNA (List-I) with its specific target organism (List-II):

List-I (Method/Element)List-II (Target Organism)
A. Micro-injectionI. Plants
B. Biolistics (Gene Gun)II. Bacteria (for transformation)
C. $ ext{Ca}^{2+}$ (Divalent Cation) TreatmentIII. Animal cells (nucleus)
D. Retroviruses (Disarmed)IV. Animal cells (general)

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

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

    Remark: Micro-injection injects DNA directly into the nucleus of an animal cell.
    Biolistics is suitable for plants.
    Divalent cation treatment makes bacterial cells competent for transformation.
    Disarmed retroviruses are used to deliver genes into animal cells.

Match the requirement (List-I) with the corresponding step in Downstream Processing (List-II):

List-I (Requirement)List-II (Associated Step)
A. Formulation with suitable preservativesI. Downstream Processing
B. Separation and purificationII. Clinical Trials
C. Thorough testing (as in case of drugs)III. Formulation
D. Strict testing for each productIV. Quality Control Testing

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

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

    Remark: Formulation involves adding preservatives [55, III].
    Separation and purification are collectively called Downstream Processing [55, I].
    Clinical trials are required for drugs [55, II].
    Strict testing is referred to as Quality Control Testing [55, IV].