This Page Score: 0/40
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. Agarose | I. Charge carried by DNA fragments |
| B. Ethidium Bromide | II. Natural polymer extracted from sea weeds, used as matrix |
| C. Negative | III. Staining compound that allows visualization under UV radiation |
| D. UV Radiation Exposure | IV. Leads to bright orange coloured DNA bands |
[Biotechnology-Principles-and-Processes] [class-xii ]
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 it | I. 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 genes | III. Ultimate aim of almost all recombinant technologies |
| D. Producing a desirable protein | IV. Modern biotechnology |
[Biotechnology-Principles-and-Processes] [class-xii ]
Match the Bioreactor specifications in List-I with their description in List-II:
| List-I (Bioreactor Type/Feature) | List-II (Description/Range) |
| A. Volume capacity | I. Cylindrical or with a curved base |
| B. Stirred-tank reactor shape | II. Most commonly used bioreactors |
| C. Stirring type bioreactors | III. Provides optimum growth conditions (Temp, pH, substrate, $ ext{O}_2$) |
| D. Bioreactor goal | IV. 100-1000 litres of culture |
[Biotechnology-Principles-and-Processes] [class-xii ]
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 step | I. Maintenance of introduced DNA in the host and transfer to progeny |
| B. Second step | II. Introduction of the identified DNA into the host |
| C. Third step | III. Culturing host cells at large scale and product extraction |
| D. Subsequent step after host introduction | IV. Identification of DNA with desirable genes |
[Biotechnology-Principles-and-Processes] [class-xii ]
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 ]
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 Marker | I. $eta$-galactosidase gene |
| B. Chromogenic Substrate Marker | II. Helps identify and eliminate non-transformants |
| C. Example of Antibiotic Resistance Marker | III. 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 ]
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/wine | I. Modern biotechnology |
| B. Developing a DNA vaccine | II. Traditional biotechnology (microbe-mediated) |
| C. Using genetically modified organisms (restricted sense) | III. Qualitative improvement in health and food production |
| D. Overall impact of modern biotechnology | IV. Part of biotechnology/genetic engineering |
[Biotechnology-Principles-and-Processes] [class-xii ]
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 Reproduction | I. Preserves the genetic information |
| B. Asexual Reproduction | II. Provides opportunities for variations and formulation of unique combinations |
| C. Traditional Hybridisation | III. Overcome the limitation of including undesirable genes |
| D. Genetic Engineering | IV. Often leads to inclusion and multiplication of undesirable genes |
[Biotechnology-Principles-and-Processes] [class-xii ]
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-injection | I. Plants |
| B. Biolistics (Gene Gun) | II. Bacteria (for transformation) |
| C. $ ext{Ca}^{2+}$ (Divalent Cation) Treatment | III. Animal cells (nucleus) |
| D. Retroviruses (Disarmed) | IV. Animal cells (general) |
[Biotechnology-Principles-and-Processes] [class-xii ]
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 preservatives | I. Downstream Processing |
| B. Separation and purification | II. Clinical Trials |
| C. Thorough testing (as in case of drugs) | III. Formulation |
| D. Strict testing for each product | IV. Quality Control Testing |
[Biotechnology-Principles-and-Processes] [class-xii ]
This Page Score: 0/40