Sample Question Paper Class: XII Biotechnology (Theory) (2016-17) Sub Code: 045 Time: 3 Hours Max. Marks: 70 General Instructions

Sample Question Paper
Class: XII
Biotechnology (Theory) (2016-17)
Sub Code: 045
Time: 3 Hours Max. Marks: 70
General Instructions
All questions are compulsory

Question paper consists of 4 sections A,B,C and D
Question numbers 1 to 6 are very short answer questions each carrying one mark
Question numbers 7 to 14 are short answer questions each carrying two marks
Question numbers 15 to 25 are also short answer questions each carrying three
marks
Question numbers 26 to 28 are long answer questions each carrying five marks
There is no overall choice. However an internal choice has been provided in one
question of three marks and two questions of five marks. You have to attempt only
one of the choices in such questions.
Use of calculators is not permitted. However, you may use log tables, if necessary.
Section A
1. How is oxygen provided in fermentors? 1

2. Why is a pilot plant essential in microbial culture works? 1
3. As a biotechnologist, what would you suggest to a farmer for successful 1
pollination or fertilization in plants.
4. Why do plant cells in culture require nutrient media for growth. 1
5. Why is splitting of animal cells essential? 1

6. Name the first drug to be produced by mammalian cell culture? 1
Section B
7. Which type of restriction enzymes are used in RDT and why? 2

8. Explain in brief any two types of non-covalent interactions found in 2
proteins.
9. Which type of DNA library would you prefer for liver cells. Give proper 2
explanation for making such a library.
10. How can you maximize protein stability during purification?Write any 2
two parameters for the same.
11. Number of genes is not related to the complexity of an organism.Give 2

reasons.
Sample Question Paper -2 pg. 1

12. Calculate the generation time of a bacterial population in which the 2
number of bacteria increase from 104/ml to 107/ml during four hours of
exponential growth.
13. Ti plasmid vector of Agrobacteriuntumefaciens is disarmed.Where is the 2

gene of interest incorporated in Ti plasmid?
14. Why are serum and antibiotics essential as growth supplements for 2
animal cells in culture?
Section C
15. How are pUC 19 vectors used for the selection of recombinants? 3
16. Yeast cells have been transformed with Yep vector containing our gene 3
of interest. How would you select the recombinants over cells not
containing the plasmid?
17. Describe the principle of MALDI technique. Write its two main uses in 3
protein studies.
OR
What are the principles behind Iso electric focusing and SDS PAGE
techniques? Why is 2D electrophoresis better than single dimension
electrophoresis?
18. How is an extracellular protein purified from a fermentation medium? 3

Illustrate the steps with a flowchart.
19. What are SNPs?Explain the relevance of studying these citing any two of 3
their important applications.
20. Graphically differentiate between fed batch and continuous cultures. 3

Which type of culture system is most suitable for obtaining maximum
amount of cellular products?
21. How does the metagenomics approach help to identify novel genes 3
present in the environment? Explain the process.
22. What are edible vaccines? How are they better than conventional 3
vaccines?Give any two points.
23. What are somatic hybrids?How are they produced? 3

24. Give a brief outline of the technique for production of monoclonal 3
antibodies.Why are monoclonal antibodies preferred over serum
antibodies in diagnostics and therapeutics?
25. How would you scale up kidney cells grown in culture? 3

Section D
26. Give reasons for the following: 3+2

a) BCAA enriched diet is recommended to atheletes before and
after exercise.
b) Give the scientific relevance of usefulness of whey.
27. Why do ddNTPs cause chain termination during Sangers DNA (1+1+1+1+1)
sequencing method? Write the DNA fragments formed by chain
termination for the given original DNA strand. 3 ATGCTAGC 5
OR
How would you detect a specific microbial contamination from a 1+4
given water sample using PCR. Give a brief explanation of the
process.
28. Explain how cDNA microarray technique can be used to study 3+2
cellular response to the environment? Support your answer with a
flowchart for the same.
OR
a) Which information can be retrieved from the following
databases? 3+2
i) EMBL
ii) PDB
iii) PALI
b) Give two reasons for completely sequencing a genome.

Sample Question Paper Class: XII Biotechnology (Theory) (2016-17) Sub Code: 045 Time: 3 Hours Max. Marks: 70 General Instructions

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Sample Question Paper Class: XII Biotechnology (Theory) (2016-17) Sub Code: 045 Time: 3 Hours Max. Marks: 70 General Instructions

Uploaded by

Copyright:

Available Formats

Sample Question Paper

Time: 3 Hours Max. Marks: 70

All questions are compulsory

1. How is oxygen provided in fermentors? 1

4. Why do plant cells in culture require nutrient media for growth. 1

5. Why is splitting of animal cells essential? 1

7. Which type of restriction enzymes are used in RDT and why? 2

11. Number of genes is not related to the complexity of an organism.Give 2

Sample Question Paper -2 pg. 1

13. Ti plasmid vector of Agrobacteriuntumefaciens is disarmed.Where is the 2

18. How is an extracellular protein purified from a fermentation medium? 3

20. Graphically differentiate between fed batch and continuous cultures. 3

23. What are somatic hybrids?How are they produced? 3

25. How would you scale up kidney cells grown in culture? 3

Sample Question Paper -2 pg. 2

26. Give reasons for the following: 3+2

Sample Question Paper -2 pg. 3

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