UTechBiotech.org, Kolkata, India

IPR, Bioethics, and Bioprocess Engineering

  Credits: 3  
     
  IPR  
      12 lectures
 

 

Why IPR is necessary, Various forms of IPR, TRIPS and IPR, IPR- National and International scenario, Issues related to IPR protection of software and database, IPR protection of life forms.

 
   
 
  BIOETHICS  
   
6 Lectures
   
Necessity of bioethics, Origin and Evolution of ethics into bioethics, Different paradigms of bioethics- National and International.
 
   
 
  BIOPROCESS ENGINEERING  
    6+10+8 = 24 Lectures  
    Module 1: Introduction to Process Engineering Calculations  
       
   

Physical Variables, Dimensions and Units, Unit Conversion, Dimensional Homogeneity in Equations. Errors in Data and Calculations, Statistical Error Analysis – Mean and Standard Deviation, Data Analysis – Trends in data - Linear and Nonlinear; Testing data for trends by fitting standard models; Transformation of nonlinear models to linear form; Least-Squares Analysis and Linear Regression. Stoichiometry – Limiting Reactant, Excess Reactant, Conversion, Yield and Selectivity. Introduction to material and energy balances for processes (with and without reaction).

 
       
  Module 2: Bioprocess Computations, Bioreaction Engineering and Bioreactor design  
       
   

Stoichiometry of cell growth – cell formula and growth equation; respiratory quotient; ATP gain and ATP-based cell yield; Formulation of culture media. Basic concepts – yield coefficients, maintenance coefficient, true and apparent yield. Macro-energetics of cell growth - metabolic heat evolution, energetic efficiency and heat of reaction.

Phases of microbial growth – growth curve; specific growth rate; kinetics of cell growth; dependence of specific growth rate on limiting substrate concentration – shifting order kinetics; Monod model; Other models; Inhibition of cell growth by inhibiting agents, excess substrate and product. Kinetics of microbial product synthesis – dependence on cell growth – Leudeking-Piret model. Sterilization and the kinetics of thermal death of cells.

Modes of microbial growth – shake-flask cultures, fermentor/bioreactor – batch, fed-batch and continuous-flow types. Chemostat - dilution rate and specific cell growth rate – steady state and cell wash-out; Estimation of yield/maintenance coefficients using steady chemostat data. Effect of environmental conditions on growth – dissolved oxygen (DO), temperature and pH; Oxygen transfer – transfer coefficient, OUR, OTR and OSR. Bioreactors – types, selection, design

 
       
  Module 3: Bioseparations  
     
    Introduction and scope.    Solids removal operations - settling, centrifugation and filtration. Product isolation - adsorption and extraction. Purification techniques - precipitation, ultrafiltration, chromatography and electrophoresis; membrane bioseparations.Product polishing operations - crystallization and drying. Scale-up of bioseparations.  
       
 

Recommended Texts:

 
  1>   Pauline Doran; Bioprocess Engineering Principles (Academic Press - Elsevier India).  
  2>   Richard Felder & Ronald Rouisseau; Elementary Principles of Chemical Processes (Wiley).  
  3>   Christie Geankoplis;Transport Processes & Separation Process Principles: Includes Unit Operations (Prentice Hall India, 4th Edition). Formerly, Transport Processes & Unit Operations.  
       

 

3 Credit (Theory) means 3 lecture hours each week or 42 lectures per semester.
2 Credit (Lab) means at least 40 hours of lab work per semester.