Lecture 3 - Monod Kinetics
Lecture 3 - Monod Kinetics
Lecture 3 - Monod Kinetics
LECTURE 3:
MONOD KINETICS AND EFFECTS
OF VARIABLES
Lecturer:
ENGR. MICHAEL ALLAN G. RAMOS
Department of Chemical Engineering
Technological Institute of the Philippines
1st Semester, A.Y. 2016-2017
MONOD EQUATION
-An empirical model for quantifying specific growth rate when one of
the substrates have become limited.
-For substrate-limited growth
-Substrate concentration dependent and is similar to saturation kinetics
(similar also to Langmuir isotherm for adsorption saturation kinetics or
the Michaelis-Menten kinetics)
m .S
=
S + Ks
Where;
u = specific growth rate
S = limiting substrate concentration (g/L)
Ks = affinity constant/ saturation constant when u = 0.5 um
um = maximum specific growth per hour
0.4
0.3
0.2
Specific Growth
rate
1/2 max
0.1
Ks = 1.0 g/L
0
0
8 10 12 14 16 18 20
INTERPRETATION OF KS
Affinity constant or saturation constant is inversely proportional to
the to the affinity of the organism for its substrate
Bacteria with a high affinity for substrate has a low Ks and vice
versa. Low Ks is good for the bacteria or any other microorganism
to grow.
The higher the Ks the less growth
Recall Km for enzyme-catalyzed reactions
Substrate
Ks , mg/L
Organism
Glucose
Enterobacter aerogenes
Glucose
2-4
Escherichia Coli
Glucose
25
Saccharomyces Cerevisiae
Ribose
Hansenula polymorphia
Ammonia
0.1
Enterobacter aerogenes
MICHAELIS-MENTEN vs MONOD
Michaelis Menten
Kinetic expression is
derived (theoretical)
Constant enzyme pool
Free enzymes
Non-growing microbes
v vs. S where v is
reaction velocity
Km is half saturation
constant
Monod
Empirical expression
Growth
Enzyme concentration
increases with time,
enzyme is produced
from protein expression
Relates microbial growth
rate constant to S
u vs S
Ks is half saturation
constant
MICHAELIS-MENTEN vs MONOD
Both are saturation kinetics
First-order region,
for low S
mixed order
Center region =
mixed order (mid
range S)
Zero-order region
for high S
S, mg/L
MICHAELIS-MENTEN vs MONOD
Parameters (um and Ks) are determined by linearization
(double-reciprocal plot) or nonlinear curve fitting.
S
S
ks
=
+
m
m
Slope = 1/um; intercept = ks/ um
Relationship between dependent variable and S determined
experimentally, in the lab
Set conditions (T, chemistry, enzyme or microbe)
Measure the u for each S
Plot u vs. S; analyze data for parameter estimation
ILLUSTRATIVE EXAMPLE
A simple batch fermentation of an aerobic bacterium growing on methanol gave
the following results shown in the table:
Time, hours
0
2
4
8
10
12
14
16
18
Calculate ;
a. Maximum specific growth rate (max)
b. Growth yield (Yx/S)
c. Mass doubling time (td)
d. Estimate the saturation constant (KS)
e. Specific growth rate () at t=10h
X (g/L)
0.2
0.211
0.305
0.98
1.77
3.22
5.6
6.15
6.2
S (g/L)
9.23
9.21
9.07
8.03
6.8
4.6
0.92
0.077
0
A) COMPETITIVE INHIBITION
- Presence of a toxic compound or product becomes inhibitory to the
growth of the microorganism
u m .S
u=
k s '+ S
Where;
I = toxic compound or P = product ;
KP and KI are constants
k s ' = k s .1 +
KI
k s ' = k s .1 +
KP
B) NON-COMPETITIVE INHIBITION
- Presence of a toxic compound or product becomes inhibitory to the
growth of the microorganism
'
u m .S
u=
ks + S
Where;
I = toxic compound or P = product ; Ex. P = Ethanol Fermentation
KP and KI are constants
um
um ' =
I
1 +
KI
um
um ' =
P
1 +
KP
C) SUBSTRATE INHIBITION
- Due to high substrate concentration; presence of a maxima
u=
u m .S
S2
ks + S +
kI
[Smax]
u
D) UNCOMPETITIVE INHIBITION
'
u m .S
u=
k s '+ S
Where;
I = toxic compound; KI is a constant
ks ' =
ks
I
1 +
KI
um
um ' =
I
1 +
KI
EFFECT OF TEMPERATURE
ON CELL GROWTH
Classification
Psychrophiles (Topt < 200C)
Mesophiles (200C < Topt < 500C)
Thermophiles (Topt > 200C)
General rule: rate of reaction increases 2x for every 10 C0 increase in
temperature unless specified (rate of reaction = rate of cell growth)
An optimal growth is observed (maxima). Beyond which cell death
occur rapidly
Temperature affects yield coefficient
EFFECT OF TEMPERATURE
ON CELL GROWTH
ug =
1 dX
.
X dt
unet = u g kd
u g = A.e
kd = A'.e
Ea
R .T
Ed
R.T
REFERENCES
Shuler, Kargi, Bioprocess Engineering, Cornell University
David Shonnard, Chemical Engineering, Michigan Technological
University
DI Wang, Chemical Engineering, MIT
Loh Kai Chee, Chemical and Biomolecular Engineering, NUS
Industrial Microbiology, INDM 4005, Lecture series