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Topic 2 - Biological System & Media Design
Topic 2 - Biological System & Media Design
SYSTEMS AND
MEDIA DESIGN
BIOLOGICAL SYSTEMS &
MEDIA DESIGN
Design, Formulation
Introduction to
& Optimization of
Biological System Media
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BIOLOGICAL SYSTEMS MEDIA DESIGN
Differences in general growth Media formulation based on macro-
characteristics of microorganisms and microelements in microbial,
(bacterial, yeast and fungi) plant cell and mammalian cell
processes; and
Influence of microbial
characteristic on bioreactor selection The methodologies for media
optimization
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Introduction to
Biological System
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What is asexual reproduction?
•is reproduction without sex.
•a single organism or cell makes a copy of itself.
•the original and its copy will be the same, except for rare
mutations.
•They are clones.
•The main process - mitosis.
•Many plants also reproduce asexually.
Thick wall-survive in
extremely harsh
condition
Endospore- dormant,
12 formed under condition
of stress
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➢Organisms that reproduce sexually have
two different sexes: male and female.
➢Different steps are involved in the process.
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2 phases found in life cycle;
haploid and diploid.
Each spore may
Number of chromosom in
develop into new
sporophore nucleus.
individual
s
anamorph
teleomorph
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Microorganism affects the mixing
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Viscosity dependance or independance of
shear rate
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Newtonian fluid
➢A Newtonian fluid's viscosity remains constant, no matter the
amount of shear applied for a constant temperature.
➢These fluids have a linear relationship between viscosity and shear
stress.
➢Examples:
•yeast & bacterial culture
•Water
•Mineral oil
•Gasoline
•Alcohol
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Non-Newtonian Fluids
Opposite of dilatant;
the more shear
applied, the less
viscous it becomes
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Volume of dispersed
gas per vol of gas-
Oxygen mass transfer liquid dispersion
coefficient
Oxygen Demand
•
Is the rate at which oxygen is consumed on a volumetric basis
Facultative
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microorganism?
Growth hours
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-outside the range might permit only
small no of microb to grow
Contaminating microbs is
minimum.
❖ Most organisms reduce the pH during growth.
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-not extensively
used in industry- Fast-growing
useful in open & organism
large V in colder
region, nucleation
and antifreeze
proteins
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-recombinant DNA technology, transfering and expression
plasmid at 0C /increase survival of recombinant.
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-glucose
&sucrose
,
hydrocar
bon and
CO2
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-fermentation media should not contribute to the complexity of the
downstream
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-if the bubble is not strong enough-easily destroyed, no foam.
Large bioreactor – mechanical foam breakers placed inside / outside the apparatus OR use
chemical antifoam: sprayed into the foam flow / introduced into the rotor of mechanical foam
breaker.
cGMP need no antifoam detected in the final product-increasing the use of mechanical foam
breakers
Yes, for research fermentation should under sterile condition. For very large
volume of culture, very rare contamination problem.
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