Abstract

During recombinant protein production with E. coli, the integrity of the inner and outer membrane changes, which leads to product leakage (loss of outer membrane integrity) or lysis (loss of inner membrane integrity). Motivated by current Quality by Design guidelines, there is a need for monitoring tools to determine leakiness and lysis in real-time. In this work, we assessed a novel approach to monitoring E. coli cell integrity by attenuated total reflection Fourier-transform infrared (ATR-FTIR) spectroscopy. Various preprocessing strategies were tested in combination with regression (partial least squares, random forest) or classification models (partial least squares discriminant analysis, linear discriminant analysis, random forest, artificial neural network). Models were validated using standard procedures, and well-performing methods were additionally scrutinized by removing putatively important features and assessing the decrease in performance. Whereas the prediction of target compound concentration via regression was unsuccessful, possibly due to a lack of samples and low sensitivity, random forest classifiers achieved prediction accuracies of over 90% within the datasets tested in this study. However, strong correlations with untargeted spectral regions were revealed by feature selection, thereby demonstrating the need to rigorously validate chemometric models for bioprocesses, including the evaluation of feature importance.

Highlights

  • Soluble expression of recombinant protein in Escherichia coli is often achieved by translocation of the product to the periplasm, the space between the inner membrane (IM) and outer membrane (OM)

  • This study presents a novel approach to monitoring cell integrity during recombinant protein production with E. coli via in-line attenuated total reflectance (ATR)-FTIR spectroscopy

  • Whereas regression models performed poorly due to low amounts of reference data and a possible lack of sensitivity, classification with linear discriminant analysis (LDA), random forest classifiers (RFCs), and ANN resulted in high apparent prediction accuracy

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Summary

Introduction

Soluble expression of recombinant protein in Escherichia coli is often achieved by translocation of the product to the periplasm, the space between the inner membrane (IM) and outer membrane (OM). Protein leakage through the OM to the extracellular space has a strong impact on the downstream process, either as a way for selective product release and simplified primary recovery or as unwanted loss of product. The ability to distinguish changes in OM integrity (leakiness) from a loss of IM integrity (lysis) is paramount. Lysis does lead to reduced productivity and to the release of impurities, such as host cell protein (HCP), DNA, and lipids, along with the product, thereby affecting the purification process

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