S0
|
glucose supply |
2000 μg ml−1
|
D0
|
basal concentration of drug D |
0.15 μg ml−1
|
E0
|
basal concentration of drug E |
9 μg ml−1
|
|
maximal carbon uptake rate |
|
|
of bacterial type i (μg cell−1 h−1) |
|
K |
bacterial half-saturation constant |
0.0527 μg ml−1
|
c |
resource to biomass conversion |
2.851×104 cell μg−1
|
d |
drug D binding rate |
1.469×10−9 μg cell−1
|
e |
drug E binding rate |
1.44×10−9 μg cell−1
|
|
inhibition of Bs (ml µg−1, ml µg−1, (ml µg−1)2, resp.) |
|
|
inhibition of Be (ml µg−1, ml µg−1, (ml µg−1)2, resp.) |
|
|
inhibition of Bd (ml µg−1, ml µg−1, (ml µg−1)2, resp.) |
|
|
inhibition of Bm (ml µg−1, ml µg−1, (ml µg−1)2, resp.) |
|
ε |
rate of point mutations |
10−4 per locus per cell per division |
η |
dilution parameter |
1% of biomass |