Code No: 33028

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II B.Tech I Semester Supplimentary Examinations,Nov/Dec 2009 MICROBIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? 1. Discuss the role of Lazarro Spallanzani and Ferdinand Cohn in disproving the doctrine of spontaneous generation of microorganisms. [16] [16]

3. Discuss general steps in viral replication.

[16]

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2. Explain why Whittaker’s Fivekingdom classification was disproved.

4. What is the relationship between retrovirus and oncogenes.

[16]

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5. Explain various media that are used for preservation of stock cultures. Discuss agar slants, sterile soil, spore preparations. [16]

6. What is culture media? Classify culture media based on function and composition. [16]

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7. How can you find virus concentration both directly and indirectly by particle counts and measurement of infectious unit concentration. Define plaque forming units, lethal dose and infectious dose. [16] 8. Describe phenols, alcohols and halogens in terms of their chemical nature, mechanism of action, mode of application, common uses and effectiveness and advantages and disadvantages. [16]

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Code No: 33028

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1. Explain some common virus groups and their characteristics.

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II B.Tech I Semester Supplimentary Examinations,Nov/Dec 2009 MICROBIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? [16]

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2. Write the effect of the following environmental factors on the growth of microorganisms. (a) Solutes. (b) PH (d) Osmotic pressure.

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(c) Oxygen

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3. What are pure cultures and why they are important? How are spread plate, streak plate and pour plates prepared. [16]

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4. As a microbiologist what is your concern about public health.

[16]

5. How does a plant +ve strand virus replicate and express its genome in plants. [16] 6. Describe the structure and chemistry of cell wall in Archaea.

[16]

7. How will you measure the killing rates of microorganisms? Explain some tests for measurement of killing rates. [16]

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8. Discuss the relationship between viruses and retrograde evolution.

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[16]

Code No: 33028

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Set No - 3

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II B.Tech I Semester Supplimentary Examinations,Nov/Dec 2009 MICROBIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? [16]

2. Define assay. Explain various types of viral assays.

[16]

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1. Discuss the general characters of domain Bacteria, with suitable examples.

3. Write short notes on: (a) Tobacco Mosaic Virus (b) Poliovirus.

[8+8] [16]

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4. Explain the contributions of Louis Pasteur towards industrial microbiology.

5. What is pure culture? How do you obtain pure culture from mixed cultures? Explain three plating techniques for isolating individual cells. [16]

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6. What is radiation. Give the advantages and disadvantages of ultra violet light and ionizing radiation as sterilizing agents. Provide a few examples of how each is used for this purpose. [16] 7. Explain the reverse transcription process.

[16]

8. Define water activity and briefly discuss how it can be determined. Why is it diffcult for microorganisms to grow at low water activity (aw) values. [16]

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Code No: 33028

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II B.Tech I Semester Supplimentary Examinations,Nov/Dec 2009 MICROBIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? 1. What are nutrients? Describe major nutritional types of microorganisms.

[16]

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2. Discuss the discoveries of Redi, Needham, Spallanzani, and Ferdinand in disproving the theory of spontaneous generation. [16] 3. Discuss about the antimicrobial drugs and their uses.

[16]

4. How does a -ve strand virus replicate and express its genome.

[16]

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5. Write about the following: (a) Tissue culture cultivation of viruses. (b) Bacterial culture if viruses.

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6. Describe the structural properties of virus.

7. Briefly discuss about the three domains of life given by Woese etal.

[8+8] [16] [16]

8. What is numerical taxonomy and why are computers so important to this approach. [16]

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R05 Set No - 1

How can you find virus concentration both directly and indirectly by particle counts · and measurement of infectious unit concentration. Define plaque forming ...

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