Abstract

Recombinant protein production with Escherichia coli is usually carried out in fed-batch mode in industry. As set-up and cleaning of equipment are time- and cost-intensive, it would be economically and environmentally favorable to reduce the number of these procedures. Switching from fed-batch to continuous biomanufacturing with microbials is not yet applied as these cultivations still suffer from time-dependent variations in productivity. Repetitive fed-batch process technology facilitates critical equipment usage, reduces the environmental fingerprint and potentially increases the overall space-time yield. Surprisingly, studies on repetitive fed-batch processes for recombinant protein production can be found for yeasts only. Knowledge on repetitive fed-batch cultivation technology for recombinant protein production in E. coli is not available until now. In this study, a mixed feed approach, enabling repetitive fed-batch technology for recombinant protein production in E. coli, was developed. Effects of the cultivation mode on the space-time yield for a single-cycle fed-batch, a two-cycle repetitive fed-batch, a three-cycle repetitive fed batch and a chemostat cultivation were investigated. For that purpose, we used two different E. coli strains, expressing a model protein in the cytoplasm or in the periplasm, respectively. Our results demonstrate that a repetitive fed-batch for E. coli leads to a higher space-time yield compared to a single-cycle fed-batch and can potentially outperform continuous biomanufacturing. For the first time, we were able to show that repetitive fed-batch technology is highly suitable for recombinant protein production in E. coli using our mixed feeding approach, as it potentially (i) improves product throughput by using critical equipment to its full capacity and (ii) allows implementation of a more economic process by reducing cleaning and set-up times.

Highlights

  • Escherichia coli serves as a beloved workhorse for the production of many recombinant proteins

  • All cultivations were carried out with the strain E. coli BL21(DE3), transformed with a pET30a+ plasmid carrying the gene for the cytoplasmic protein (CP) and periplasmic

  • The potential of achieving high recombinant protein titers in repetitive fed-batch cultivation mode was shown by Luttmann et al for P. pastoris as production host (Martens et al, 2011)

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Summary

Introduction

Escherichia coli serves as a beloved workhorse for the production of many recombinant proteins. Even though IPTG induction is described as tunable, toxic effects can be observed (Wurm et al, 2016; Hausjell et al, 2018). Due to the non-toxicity and low cost of lactose compared to other inducers, this induction mechanism is tuneable and economically feasible (9.39 €/g IPTG vs 0.02 €/g lactose) (Yan et al, 2004; Briand et al, 2016). For periplasmic recombinant protein production soft induction by lactose is especially important as translocation to the periplasm is the rate limiting step (Gupta and Shukla, 2017; Karyolaimos et al, 2019; Hausjell et al, 2020)

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