Question: The following data was shared by a previous colleague from a batch experiment where an optimised E . coli strain is producing antibiotics. The amount

The following data was shared by a previous colleague from a batch experiment where an optimised E. coli strain is producing antibiotics. The amount of substrate provided was 1.75gL reactor.
\table[[Time (min),0,6,8,10,12,13,14,15,17,20],[x(cells),120,120,120,180,450,690,1100,1800,2500,2600]]
(a) Determine the following:
Specific growth rate
Doubling time
Length of the lag phase
(b) You conduct 3 follow-up experiments with different substrate concentrations and obtain the following data.
\table[[Time (min),0,6,8,10,12,13,14,15,17,20],[S=1,120,120,120,240,420,570,780,1100,2000,2000],[S=5,120,120,120,280,1200,2800,6000,14000,30000,32000],[S=10,120,120,120,310,1500,3400,7500,17000,30000,32000]]
What is the Michaelis Menten constant for this strain?
(c) You want to achieve a specific growth rate of 14max to optimise the antibiotics production in a 10L continuous culture reactor (chemostat). What should your flow rate into the chemostat and concentration of substrate in the feed be to achieve this?
(d) You've discovered the following data from a previous experiment in trying to optimise the substrate feed for antibiotics production:
Specific substrate consumption rate ()=0.6hr-1
Maintenance requirements (m)=0.002min-1
Yield coefficient of biomass vs substrate (Yxs)=0.5
Experimental data: product vs substrate yield
\table[[Substrate fed (gL),1,1.75,5,10],[Product produced (gL),0.2,0.35,1,2]]
What would be the specific rate of product formation qp for the chemostat reactor in the previous question?
 The following data was shared by a previous colleague from a

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