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Total RNA was extracted from the 824WT and 824ccpA strain, which were grown in the pH-controlled P2 medium containing 40 g/L d-glucose and 20 g/L d-xylose as the carbon sources, at four time points: middle exponential (time point M), late exponential (time point L), transition (time point T) and stationary phases (time point S).
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The time point M (middle exponential phase) and L (late exponential phase) were in acidogenic phase, while the time point T (transition phase) and S (stationary phase) were in shift phase (shifting from acidogenesis to solventogenesis) and solventogenic phase, respectively.
The time of harvesting cells was set at early exponential phase, middle exponential phase, late exponential phase, and stationary phase.
Conversely, exponential time is some number raised to the size of the input.
However, MILP takes exponential time to finish.
Usually, optimal solutions have exponential time complexity.
Cells were cultivated in YPDA liquid medium and harvested at middle exponential phase.
Existing approaches are restricted to processes with exponential time distribution.
Total RNA content of the suppressor mutants at middle exponential phase was approximately 40% of the control strain (Fig. 2a).
This paper develops a new family of exponential time discretization methods called exponential-Krylov (expK).
Usually, the traditional optimal solutions need exponential time complexity.
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