(Paper) Class - XII Sample Paper Biotechnology 2008 - 3
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Class - XII Sample Paper Biotechnology (Set - 3) 2008
Sample Paper - 2008
Class – XII
Subject – Biotechnology
Time
allowed : 3 hours
Maximum Marks: 70
General
Instructions :
(i) All questions are compulsory.
(ii) There is no overall choice. However, an internal choice has been provided in one question of two marks and two questions of five marks. You have to attempt only one of the choices in such questions. Question paper contains four sections -A, B, C and D.
(iii) Question numbers 1 to 5 are very short answer questions, carrying 1 mark
each.
(iv) Question numbers 6 to 15 are short answer questions, carrying 2 marks each.
(v) Question numbers 16 to 25 are also short answer questions, carrying 3 marks each.
(vi) Question numbers 26 to 28 are long answer questions, carrying 5 marks each.
(vii)
Use of calculators is not permitted. However, you may use log tables, if
necessary.
SECTION
A
1.
Give
the sequence of the two primers (5 nucleotides long) required to amplify the
following DNA sequence by PCR :
5' GCACCTAGATCGATCC 3'
2. What is lyophilization ?
3. Why is the nutrient medium autoclaved before using it for culturing microbes?
4. Which future vaccine holds promise of bypassing the need to visit the doctor regularly for childhood immunisations ?
5.
Why
is ‘Golden rice’ nutritionally superior to normal rice?
SECTION
B
6. You wish to introduce the human insulin gene into a bacterial host in the hope of producing large amounts of human insulin. Should you use genomic DNA or cDNA ? Explain.
7. What are ESTs ? How are they useful in genome analysis ?
8.
Which of the following
proteins would be expected to migrate fastest through SDS-PAGE gel, and why ?
Protein
MW (daltons)
Transferrin
90,000
Cytochrome
c
13,400
a-antitrypsin 45,000
Serum albumin 69,000
Myoglobin 17,000
9. Give two distinguishing features of pBR322 and BAC vectors.
10. How can SNPs be used to predict susceptibility to diseases ?
11. Why are type II restriction endonucleases (RE) extensively used in recombinant DNA technology ? Why do bacteria make RE ?
12.
What is the IUPAC code for T or C ? Write the complementary sequence of
the following sequence :
5' - A T G A Y C G B T - 3'
13. rythropoietin (EPO) is included in the list of banned substances for sportsmen. What is this substance ? How does it act ?
OR
Embryonic
cells during development not only commit along different lineages but also
retain a population of cells that are present only at strategic locations in the
adult organism. Name these specialized cells and why they are maintained in
undifferentiated state?
15.
Study the following enzyme purification table and answer the questions
that follow:
Step
Procedure
Total protein (mg)
Activity (units)
1.
Crude extract
20,000
4,000,000
2.
Precipitation (salt)
5,000
3,000,000
3.
Precipitation (pH)
4,000
1,000,000
4. Ion exchange chromatography 200 800,000
(a)
Which step in the purification is most effective, and why ?
(b) Which of the procedures is least effective and why ?
SECTION
C
16. What is OKT-3 ? Why is it administered to patients undergoing organ transplantation ? What is the relevance of fusing an antibody producing B-cell with myeloma cells in hybridoma technology ?
17. What is ‘Molecular Pharming’ ? Suggest any four advantages of expressing transgenic proteins in milk ?
18. Name any three resources available from the NCBI and their uses.
19. What is fed-batch culture and what are its benefits in microbial technology ? How is it different from a batch culture ?
20. Name the special DNA polymerase used in PCR reactions. What are the three basic steps of a PCR cycle ?
OR
Using a single template molecule, how many DNA molecules are generated after 10 cycles of amplification ?
21. Suggest any four reasons why complete genome sequencing projects should be undertaken ? Describe the advantage of using bacterial artificial chromosomes (BAC) in such sequencing programmes.
22. What is downstream processing ? What strategy would you use to purify a recombinant protein that is secreted into the growth medium ?
23. Name any four physical and/or chemical properties of enzymes which might be useful to change by site-directed mutagenesis. Support your answer by taking an example of an engineered protein/enzyme.
24. Explain how DNA “microarray” technique can be used to study cellular response to environment. Also depict major steps diagrammatically.
25.
A
Chronic Myelogenous Leukemia (CML) patient has been put on a combination drug
therapy for the past 2 months. How can the FISH technique be used to monitor the
effect of chemotherapy ?
SECTION
D
26.
(a)
What is the principle of protein fingerprinting ? Illustrate major steps.
(b)
Who developed this technique ?
(c)
What are prions ?
27.
(a) How will
you select bacterial cells carrying a recombinant plasmid ?
(b)
Explain briefly a technique for visual screening of transformed bacteria.
(c) How can E. coli cells be made competent and who developed this method ?
OR
(a)
Enlist the four major steps in a recombinant DNA experiment.
(b)
What is the advantage of having a polylinker in a cloning vector ?
(c) Name a cloning vector that can be used to clone large DNA fragments (> 1 MB).
28.
(a)
Describe vector-mediated and vector-less gene transfer in plants.
(b) Why is Agrobacterium tumefaciens regarded as nature’s genetic engineer ? 5
OR
(a)
Enlist the six major steps in plant tissue culture.
(b)
Name a medium commonly used for culturing plant parts and what factors dictate
the choice of media.
NAVODAYA
VIDYALAYA SAMITI, BHOPAL REGION
(1ST PRE – BOARD EXAMINATION – 2007 – 08)