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Match the features of the cloning vector pBR322 (List-I) with their characteristic function (List-II):
| List-I (Gene/Site) | List-II (Feature/Antibiotic) |
| A. tetR gene | I. Gene involved in the replication of the plasmid |
| B. ampR gene | II. Ligation of foreign DNA at BamH I site inactivates this resistance |
| C. rop gene | III. Selectable marker; transformants selected on medium containing this antibiotic |
| D. BamH I site | IV. Restriction site where foreign DNA can be ligated |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the restriction sites in List-I with their general location relative to the genes in the pBR322 vector (List-II), based on Figure 9.4:
| List-I (Restriction Site) | List-II (Location in pBR322 - based on Figure 9.4) |
| A. BamH I | I. In or near ampR gene |
| B. Pst I | II. In or near tetR gene |
| C. EcoR I | III. Outside antibiotic resistance genes/In cloning region |
| D. Hind III | IV. In or near rop gene |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the Polymerase Chain Reaction (PCR) step in List-I with the corresponding process or outcome in List-II:
| List-I (PCR Step) | List-II (Process/Action) |
| A. Denaturation | I. DNA polymerase extends the primers |
| B. Primer Annealing | II. Uses high temperature to separate double stranded DNA |
| C. Extension of Primers | III. Two sets of chemically synthesised oligonucleotides bind to template |
| D. Amplification | IV. Achieves synthesis of approximately 1 billion copies of DNA segment |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the type of cell in List-I with the corresponding enzyme used to break the cell open during DNA isolation (List-II):
| List-I (Target Cell Type) | List-II (Enzyme Used for Lysis) |
| A. Bacterial Cells | I. Cellulase |
| B. Plant Cells | II. Lysozyme |
| C. Fungal Cells | III. Chitinase |
| D. Animal Tissue | IV. No specific cell wall enzyme mentioned |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the bioreactor systems in List-I with the parameter they are designed to manage or control in List-II:
| List-I (Control System) | List-II (Parameter Controlled) |
| A. Agitator System | I. Foam |
| B. Foam Control System | II. Mixing and Oxygen availability |
| C. Temperature Control System | III. Heat |
| D. Oxygen Delivery System | IV. Oxygen levels (sparging) |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the DNA feature/element in List-I with its result or function in List-II:
| List-I (DNA Feature) | List-II (Result/Consequence) |
| A. Integration into genome | I. Transfer of malarial parasite into human body |
| B. Plasmid DNA vector | II. Alien DNA can multiply and be inherited along with host DNA |
| C. Sticky Ends | III. Acts as a vehicle to transfer the piece of DNA attached to it |
| D. Mosquito Vector | IV. Form hydrogen bonds with complementary cut counterparts, facilitating ligation |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the enzyme in List-I with its function or common reference in List-II:
| List-I (Enzyme) | List-II (Common Name/Action) |
| A. DNA Ligase | I. Cuts DNA at specific locations (Molecular Scissors) |
| B. Restriction Endonuclease | II. Joins cut DNA molecules (Molecular Glue) |
| C. DNA Polymerase | III. Replicates DNA using the host's enzyme (E. coli) |
| D. Ribonuclease | IV. Used to remove RNA from DNA preparation |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the treatment component in List-I related to making host cells competent with its effect in List-II:
| List-I (Treatment Component) | List-II (Result/Purpose) |
| A. Divalent Cation (e.g., $ ext{Ca}^{2+}$) | I. Hydrophilic property of DNA |
| B. Heat Shock (42°C) | II. Makes the bacterial cell competent to take up DNA |
| C. Inability of DNA to cross membrane | III. Increases the efficiency with which DNA enters the bacterium through cell wall pores |
| D. Ice incubation before and after heat shock | IV. Forces the bacteria to take up the recombinant DNA |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the vector type or element (List-I) with its natural or engineered action in List-II:
| List-I (Vector Source/Type) | List-II (Natural/Engineered Action) |
| A. Ti plasmid | I. Modified for gene delivery into a variety of plants |
| B. Retroviruses | II. Naturally transform normal animal cells into cancerous cells |
| C. $ ext{T-DNA}$ | III. Piece of DNA delivered to transform plant cells into a tumor |
| D. Disarmed Retroviruses | IV. Used to deliver desirable genes into animal cells |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the DNA element in List-I with its function related to replication and multiplication in List-II:
| List-I (DNA Element) | List-II (Requirement for Multiplication) |
| A. Alien Piece of DNA | I. Autonomous replication property |
| B. Chromosome | II. Needs to be linked with the origin of replication |
| C. Plasmid/Bacteriophage DNA | III. Has the ability to replicate (needed for inheritance) |
| D. Origin of replication | IV. Specific DNA sequence responsible for initiating replication |
[Biotechnology-Principles-and-Processes] [class-xii ]
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