Abstract
With the advent of modern genetic engineering methods, microcultivation systems have become increasingly important tools for accelerated strain phenotyping and bioprocess engineering. While these systems offer sophisticated capabilities to screen batch processes, they lack the ability to realize fed-batch processes, which are used more frequently in industrial bioprocessing. In this study, a novel approach to realize a feedback-regulated enzyme-based slow-release system (FeedER), allowing exponential fed-batch for microscale cultivations, was realized by extending our existing Mini Pilot Plant technology with a customized process control system. By continuously comparing the experimental growth rates with predefined set points, the automated dosage of Amyloglucosidase enzyme for the cleavage of dextrin polymers into d-glucose monomers is triggered. As a prerequisite for stable fed-batch operation, a constant pH is maintained by automated addition of ammonium hydroxide. We show the successful application of FeedER to study fed-batch growth of different industrial model organisms including Corynebacterium glutamicum, Pichia pastoris, and Escherichia coli. Moreover, the comparative analysis of a C. glutamicum GFP producer strain, cultivated under microscale batch and fed-batch conditions, revealed two times higher product yields under slow growing fed-batch operation. In summary, FeedER enables to run 48 parallel fed-batch experiments in an automated and miniaturized manner, and thereby accelerates industrial bioprocess development at the screening stage.
Highlights
The last decade is marked by tremendous advances in the development of highly engineered strains for bioprocess application
We show the general applicability of our microscale fed-batch approach using the model organisms, Corynebacterium glutamicum, Pichia pastoris, and Escherichia coli
The BioLector is integrated into a liquid handling system (EVO 200) provided by Tecan (Männedorf, Switzerland) with eight steel needle tips, allowing for automated dosing and sampling into each well of the microtiter plate
Summary
The last decade is marked by tremendous advances in the development of highly engineered strains for bioprocess application. To determine the best candidates for process development, these libraries need to be characterized in detail, and the number of necessary experiments can sum up to a thousand per library [4]. There is a great demand for systems allowing an increased experimental throughput without sacrificing data accuracy and reproducibility. Various stand-alone microbioreactor (MBR) systems have evolved in the last years, allowing strain phenotyping with an adequate throughput without loss of control and monitoring capabilities [5]. To further increase phenotyping capacity and decrease manual handling steps, these MBR systems
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