This Page Score: 0/40
Match the Bioreactor components/systems in List-I with their functions/goals in List-II:
| List-I (Bioreactor Component) | List-II (Function/Purpose) |
| A. Stirrer/Agitator System | I. Maintenance of sterile (microbial contamination-free) ambiance |
| B. Sampling Ports | II. Facilitates even mixing and oxygen availability throughout the vessel |
| C. Bioprocess Engineering | III. Allows small volumes of the culture to be withdrawn periodically |
| D. Continuous Culture System | IV. Produces larger biomass by maintaining cells in active log phase |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the methods of introducing alien DNA into host cells (List-I) with their defining characteristic (List-II):
| List-I (Method) | List-II (Target/Description) |
| A. Competent Cells (Heat Shock) | I. Recombinant DNA directly injected into nucleus of animal cell |
| B. Micro-injection | II. Cells are bombarded with micro-particles coated with DNA (e.g., Gold/Tungsten) |
| C. Biolistics (Gene Gun) | III. Uses treatment with divalent cation like calcium and brief exposure to 42°C |
| D. Disarmed Pathogen Vectors | IV. Modified Retroviruses or Ti plasmids used for gene delivery |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the year in List-I with the significant event in the development of RDT/Biotechnology in List-II:
| List-I (Year) | List-II (Event) |
| A. 1963 | I. Isolation and characterization of the first sequence-specific restriction endonuclease (Hind II) |
| B. 1968 | II. Stanley Cohen and Herbert Boyer accomplish the construction of the first recombinant DNA molecule |
| C. 1972 | III. Isolation of the two enzymes (one cut DNA, one methylated DNA) restricting bacteriophage growth in E. coli |
| D. 1936 | IV. Herbert Boyer was born |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the pathogen or related element in List-I with its role in natural or engineered gene transfer in List-II:
| List-I (Pathogen/Element) | List-II (Associated Vector/Disease) |
| A. Retroviruses | I. Insect vector for malarial parasite |
| B. Agrobacterium tumifaciens | III. Source of modified Ti plasmid cloning vector for plants |
| C. Mosquito | I. Insect vector for malarial parasite |
| D. T-DNA | IV. Piece of DNA delivered by bacterium to cause tumor formation in plants |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the steps involved in Downstream Processing (List-I) with their corresponding description/requirement (List-II):
| List-I (Downstream Step) | List-II (Component/Requirement) |
| A. Separation and Purification | I. Thorough testing required for drugs |
| B. Formulation | II. Collectively referred to as Downstream Processing |
| C. Clinical Trials | III. Strict testing required for each product |
| D. Quality Control Testing | IV. Product mixed with suitable preservatives |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the restriction enzyme characteristics in List-I with their description or quantification in List-II:
| List-I (Characteristic) | List-II (Feature/Number) |
| A. Palindromic Sequence | I. DNA cut at specific positions within the double helix |
| B. Restriction Endonuclease Function | II. Over 900 |
| C. Number of Restriction Enzymes Known | III. Sequence of base pairs that reads same on the two strands (5' → 3' direction) |
| D. Recognition Sequence for Hind II | IV. Specific sequence of six base pairs |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the individuals/groups in List-I with their key contributions in List-II:
| List-I (Scientist) | List-II (Contribution) |
| A. Herbert Boyer | I. Studied small ringlets of DNA called plasmids |
| B. Stanley Cohen | II. French philosopher who influenced anthropocentric approach |
| C. Rene Descartes | III. Observed restriction enzymes leaving 'sticky ends' on DNA |
| D. Combined work (1972) | IV. Construction of the first artificial recombinant DNA molecule |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the DNA type in List-I with its replication characteristic in List-II, regarding cloning vectors:
| List-I (DNA Type) | List-II (Replication/Copy Number) |
| A. Plasmid DNA | I. Replicate independent of chromosomal DNA |
| B. Bacteriophage DNA | II. Low copy number (e.g., one or two copies per cell) |
| C. Some Plasmids | III. Very high copy numbers of their genome |
| D. High Copy Number Vector | IV. Used when one wants to recover many copies of target DNA |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the component/step of Polymerase Chain Reaction (PCR) in List-I with its description in List-II:
| List-I (PCR Requirement) | List-II (Step/Function) |
| A. Primers | I. Achieves amplification to approximately billion times |
| B. DNA Polymerase | II. Small chemically synthesised oligonucleotides complementary to DNA regions |
| C. Repeated Amplification | III. Enzyme used for extension of primers using genomic DNA as template |
| D. High Temperature Step | IV. Induces denaturation of double stranded DNA |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the selection mechanism/result in List-I with the corresponding outcome or requirement in List-II:
| List-I (Selection Mechanism) | List-II (Outcome/Feature) |
| A. Insertional Inactivation | I. Colonies appear blue |
| B. Non-recombinant Colonies (chromogenic) | II. Colonies do not produce any colour (white) |
| C. Recombinant Colonies (chromogenic) | III. Requires simultaneous plating on two plates having different antibiotics |
| D. Selection using two antibiotic resistance genes | IV. Inactivation of the gene for synthesis of β-galactosidase |
[Biotechnology-Principles-and-Processes] [class-xii ]
This Page Score: 0/40