7a101-mt----microbial Engineering

  • Uploaded by: SRINIVASA RAO GANTA
  • 0
  • 0
  • October 2019
  • PDF

This document was uploaded by user and they confirmed that they have the permission to share it. If you are author or own the copyright of this book, please report to us by using this DMCA report form. Report DMCA


Overview

Download & View 7a101-mt----microbial Engineering as PDF for free.

More details

  • Words: 324
  • Pages: 2
NR

Code No: 7A101/MT M.Tech. – I Semester Supplementary Examinations, September, 2008 MICROBIAL ENGINEERING (Biotechnology) Time: 3hours

1.a) b) 2.a) b) c) 3.a)

b) 4.a) b)

5.a) b)

Max. Marks:60

Answer any FIVE questions All questions carry equal marks --There is a paradigm change in the processes of production of bulk chemicals from, fossil (petroleum and coal) resources to renewable resources - Enumerate. Write on the evolution of (chronological development) of modern industrial (white) biotechnology. What is sterilisation? Write on its importance. Write on the effect of dosage of toxic chemicals and the time of exposure of these chemicals on microbes. Explain various airfilters used for elimination of microorganisms. The over all reaction for microbial conversion of glucose to glutamic acid is: (not balanced reaction) C6 H12O6 + NH 3 + O2 → C5 H 9 NO4 + CO2 + H 2O What mass of oxygen is required to produce 15gm of glutamic acid? Cell is an open system and violates 2nd law of thermodynamics – enumerate. Define doubling time and number of generations. What is the relation between them? The following data is obtained from a chemostat fermentation studies. A feed containing substrate at a concentration of 0.5 kg / m3 at a rate of 111cc/sec is fed into 2.5 m3 volume of reactor. If the Ks = 50 gm/cc and µm =12 min −1 find the conversion of substrate. Discuss on the role of maintenance and maintenance coefficient during the substrate utilization. Write in detail on the different phases of growth of microorganism in batch culture. Contd….2

Code No: 7A101/MT

::2::

6.

What is a model in the context of microbial growth? Explain the differences and similarities of compartmental and metabolic growth models.

7.

Distinguish between fermentation reactions classification by a) Gaden and b) Deindoerfer. Explain with the help of figures.

8.

State and explain the various production parameters considered for production of recombinant Hepatitis-B vaccine or any other rDNA product. ******

Related Documents

Engineering
June 2020 33
Engineering
June 2020 23
Engineering
June 2020 18
Engineering
December 2019 42

More Documents from ""