Abstract

BackgroundEscherichia coli is one of the most widely used hosts for recombinant protein production in academia and industry. Strain BL21(DE3) is frequently employed due to its advantageous feature of lacking proteases which avoids degradation of target protein. Usually it is used in combination with the T7-pET system where induction is performed by one point addition of IPTG. We recently published a few studies regarding lactose induction in BL21(DE3) strains. BL21(DE3) can only take up the glucose-part of the disaccharide when fed with lactose. However, initially additional glucose has to be supplied as otherwise the ATP-related lactose uptake barely happens. Yet, as lactose is an inexpensive compound compared to glucose and IPTG, a new induction strategy by a lactose-only feed during induction seems attractive. Thus, we investigated this idea in the galactose metabolizing strain HMS174(DE3).ResultsWe show that strain HMS174(DE3) can be cultivated on lactose as sole carbon source during induction. We demonstrate that strain HMS174(DE3) exhibits higher product and biomass yields compared to BL21(DE3) when cultivated in a lactose fed-batch. More importantly, HMS174(DE3) cultivated on lactose even expresses more product than BL21(DE3) in a standard IPTG induced glucose fed-batch at the same growth rate. Finally, we demonstrate that productivity in HMS174(DE3) lactose-fed batch cultivations can easily be influenced by the specific lactose uptake rate (qs,lac). This is shown for two model proteins, one expressed in soluble form and one as inclusion body.ConclusionsAs strain HMS174(DE3) expresses even slightly higher amounts of target protein in a lactose fed-batch than BL21(DE3) in a standard cultivation, it seems a striking alternative for recombinant protein production. Especially for large scale production of industrial enzymes cheap substrates are essential. Besides cost factors, the strategy allows straight forward adjustment of specific product titers by variation of the lactose feed rate.

Highlights

  • Escherichia coli is one of the most widely used hosts for recombinant protein production in academia and industry

  • The system is based on the T7 promoter, which features exceptionally high transcription rates as the target protein is transcribed by the T7 polymerase which is faster compared to native E. coli polymerases [1, 10, 11]

  • Lactose uptake in HMS174(DE3), JM109(DE3) and BL21(DE3) In order to investigate our hypothesis that cultivation on lactose as C-source and inducer was possible when employing the T7 system and strains that are able to metabolize galactose, we initially tested two strains that carried the λ prophage but had no deletions of enzymes in the Leloir pathway: JM109(DE3) and HMS174(DE3)

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Summary

Introduction

Escherichia coli is one of the most widely used hosts for recombinant protein production in academia and industry. Strain BL21(DE3) is frequently employed due to its advantageous feature of lacking proteases which avoids degradation of target protein. It is used in combination with the T7-pET system where induction is performed by one point addition of IPTG. As lactose is an inexpensive compound compared to glucose and IPTG, a new induction strategy by a lactose-only feed during induction seems attractive We investigated this idea in the galactose metabolizing strain HMS174(DE3). Its advantages result from comprehensive knowledge about the prokaryote coming along with many and comparably fast tools for genetic manipulation [1, 5] It can be cultivated on inexpensive media up to high cell densities allowing exceptionally high product titers [2, 7]. Our research group recently published several studies using the comparably

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