In industrial fermentations, why is a relatively large seed volume (about 10–40% of working fermenter volume) often used?

Difficulty: Easy

Correct Answer: To decrease the overall fermentation time by reducing lag and quickly establishing target physiology

Explanation:


Introduction / Context:
Scale-up lines use seed trains to prepare cultures with the right physiology for production vessels. Choosing an appropriate inoculum ratio affects start-up dynamics, risk of contamination, by-product profiles, and time-to-harvest economics.


Given Data / Assumptions:

  • Well-conditioned seed at late exponential phase.
  • Production fermenter inoculated at 10–40% v/v depending on organism and process.
  • Objective: minimize non-productive time and variability.


Concept / Approach:
A larger seed volume introduces a high initial viable-cell concentration with enzymes already induced for the intended substrate. This shortens or essentially eliminates lag, rapidly establishes desired metabolism, and suppresses contaminants by competitive advantage, all of which shorten the overall batch duration to reach target titer.



Step-by-Step Solution:
1) Higher starting cell density increases initial volumetric rate (dX/dt) at the same specific growth rate.2) Pre-adapted physiology reduces time needed for enzyme induction in the production medium.3) Fast dominance lowers contamination risk and stabilizes pH/DO control sooner.4) Net effect: decreased overall fermentation time to reach the desired endpoint.


Verification / Alternative check:
Process histories show that increasing inoculum ratio from 5% to, say, 20% frequently cuts several hours from batch time while preserving yield; diminishing returns appear beyond organism-specific optima.


Why Other Options Are Wrong:
Option A contradicts observed kinetics; larger inoculum shortens, not lengthens, batches.Option B: yield may improve indirectly, but the primary rationale is time reduction and robustness.Option D is opposite of process goals and is not a consequence of larger seed volume.


Common Pitfalls:
Ignoring oxygen transfer constraints at high inoculum, or assuming that larger inoculum automatically increases final titer irrespective of substrate or product inhibition.


Final Answer:
To decrease the overall fermentation time by reducing lag and quickly establishing target physiology

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