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This blog is to distribute jntu biotech prev papers ,GRE ,IELETS BOOKS to every one.if u want to give any suggestion..mail to vagdevi2k5@gmail.com...regards P.Vagdevi,B.I.E.T(Bharat Institue)

Friday, October 17, 2008

METABOLIC ENGINEERING-REG 2K5

Code No: RR412311 Set No.1
IV B.Tech. I Semester Regular Examinations, November -2005
METABOLIC ENGINEERING
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
? ? ? ? ?
1. Write short notes on:
(a) Passive diffusion
(b) Facilitated diffusion [16]
2. Describe in detail the primary screening involved in strain selection with example.
[16]
3. Describe
(a) Differential regulation by ISO enzymes.
(b) Gene dosage. [16]
4. Explain mixed or sequential Bioconversions with suitable examples. [16]
5. Describe Induction / Repression phenomena in E.coli with examples. [16]
6. Describe Enzyme inhibition and factors involved in it. [16]
7. How does mutation effect the enzyme production? List out the factors involved in
optimization of mutants for high yield protein production? [16]
8. Explain the Fermentation parameters involved in production of wine from yeast.
[16]
? ? ? ? ?
1 of 1
Code No: RR412311 Set No.2
IV B.Tech. I Semester Regular Examinations, November -2005
METABOLIC ENGINEERING
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
? ? ? ? ?
1. Write short notes on:
(a) Feed back repression
(b) CAMP [16]
2. Describe in detail the secondary screening involved in strain selection with example.
[16]
3. Detail the regulation of Enzyme synthesis at Fermentor level. [16]
4. Define Bioconversion and describe in detail the conversion of insoluble substances
by sequential bioconversion. [16]
5. Describe induction and Repression phenomena in yeast, citing Alcohol production
as example. [16]
6. Describe in detail the various modes of diffusion? [16]
7. What is enzyme inhibition and detail the various modes of enzyme inhibition.[16]
8. Distinguish and differentiate concerted feed back regulation and cumulative feed
back regulation with examples. [16]
? ? ? ? ?
1 of 1
Code No: RR412311 Set No.3
IV B.Tech. I Semester Regular Examinations, November -2005
METABOLIC ENGINEERING
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
? ? ? ? ?
1. Write short notes on:
(a) Cometabolism during Bioconversion
(b) Feed back regulation. [16]
2. List out and describe the parameters involved in scale up of Fermentation (large
scale) from pilot scale. [16]
3. What is bio conversion and what are the advantages of molecules generated by bio
conversion to industry. [16]
4. Explain gene regulation by Jacob and Monad model citing lac operon as example.
[16]
5. Evaluate catabolite regulation with tryptophan operon as example. [16]
6. Explain how gene dosage is evaluated and how does gene dosage effect Fermentation
process. [16]
7. List out the biotechnological application of enzymes (eg:- Proteases, Amylases etc)
Produced by Fermentation. [16]
8. Distinguish and differentiate concerted and cumulative feed back regulation with
examples. [16]
? ? ? ? ?
1 of 1
Code No: RR412311 Set No.4
IV B.Tech. I Semester Regular Examinations, November -2005
METABOLIC ENGINEERING
(Bio-Technology)
Time: 3 hours Max Marks: 80
Answer any FIVE Questions
All Questions carry equal marks
? ? ? ? ?
1. Write short notes on:
(a) Strain selection
(b) Isozymes. [16]
2. How can Metabolic pathways be genetically controlled with examples. [16]
3. What is Bioconversion and describe the factors involved in Bioconversion? [16]
4. Describe:
(a) Concerted feed back regulation
(b) Amino acid regulation. [16]
5. Describe the factors contributing to catalytic efficiency of an enzyme. [16]
6. Define Mutation and various modes of generating mutations in improving industrial
biotechnology of an organism? [16]
7. Compare and contrast direct and indirect fermentations citing amino acid synthesis
as example? [16]
8. Describe
(a) Precursor effects in biosynthesis of secondary metabolites.
(b) Producers of secondary metabolites. [16]
? ? ? ? ?
1 of 1

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