Lecture 1 (Saleha)

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    BIOREACTOR CONSIDERATIONS FOR

    SUSPENSION, IMMOBILIZED,ANIMAL AND PLANT CELL

    CULTURES

    ERT 314 BIOREACTOR SYSTEM

    Dr. Saleha Shamsudin

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    Course Contents

    Differences between batch and continuous system basedon productivity, modifications for batch and continuous

    bioreactor, simple bioreactor design for immobilizedcell systems, animal and plant cell cultures, solid statefermentation process.

    Chapter 9Bioprocess Engineering Basic Concepts

    Michael L. Shuler/Fikret KargiPrentice Hall International Series in the Physical and

    Chemical Engineering Sciences

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    INTRODUCTION

    The choice of reactor will determined:

    Product concentrations and purity Degree of substrate conversion/yield Whether sustainable/reliable performance

    The bioreactor consideration must be made in thecontext of the total process:

    Biocatalyst Reactor Separation Purification

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    Choosing the cultivation method(batch or continuous)

    -based on productivity-Production of cell mass or primary products

    FOUR CHARACTERISTIC PHASES OF THE GROWTH CYCLE

    1. Lag Phase adaptation of the cells to the new environment

    minimal increase in cell density

    2. Exponential (log) Growth Phase

    cells are dividing regularly

    cells divide at a constant rate

    3. (Harvesting) Stationary Phase cells stopped growing and dividing

    production of secondary metabolites

    4. (Preparation for new batch) Death Phase (Cleaning, sterilizing,filling)

    viable cell population declines

    viable cells decreases geometrically

    BATCH

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    1t Sum of times required for the lag phase, harvesting and

    preparation (vary with size and nature of fermentation) 3 to 10 h

    ct

    Total time to complete a batch cycle

    10

    ln1

    tX

    Xt

    m

    m

    c

    mX

    0X

    The maximal attainable cell concentration

    The cell concentration at inoculation

    00 SYXX

    SXm Total amount of mass cell =

    10

    0

    ln1 tXX

    SYr

    mm

    SX

    b

    The rate of cell mass

    production in one batch

    cycle,

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    Based on productivity, most of commercialbioprocesses are batch system. Why?

    *Applied to growth associated product

    *Genetic instability

    *Operability and reliability

    *Market economics

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    Operated by supplying an essential growth-limiting nutrient at a constant rate with the

    result that the culture density and growth rateadjust themselves to the supply.

    Chemostat

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    Operated by maintaining a constant cell densityby supplying fresh medium as required.

    It possesses a photocell system whichcontinuously monitors the cell density andmaintains this constant by controlling themedium inlet flowrate.

    Turbidostat