Preprint Article Version 1 This version is not peer-reviewed

Accelerated Bioprocess Development of Endopolygalacturonase-Production with Saccharomyces cerevisiae Using Multivariate Prediction in a 48 Mini-Bioreactor Automated Platform

Version 1 : Received: 16 October 2018 / Approved: 17 October 2018 / Online: 17 October 2018 (06:19:46 CEST)

A peer-reviewed article of this Preprint also exists.

Sawatzki, A.; Hans, S.; Narayanan, H.; Haby, B.; Krausch, N.; Sokolov, M.; Glauche, F.; Riedel, S.L.; Neubauer, P.; Cruz Bournazou, M.N. Accelerated Bioprocess Development of Endopolygalacturonase-Production with Saccharomyces cerevisiae Using Multivariate Prediction in a 48 Mini-Bioreactor Automated Platform. Bioengineering 2018, 5, 101. Sawatzki, A.; Hans, S.; Narayanan, H.; Haby, B.; Krausch, N.; Sokolov, M.; Glauche, F.; Riedel, S.L.; Neubauer, P.; Cruz Bournazou, M.N. Accelerated Bioprocess Development of Endopolygalacturonase-Production with Saccharomyces cerevisiae Using Multivariate Prediction in a 48 Mini-Bioreactor Automated Platform. Bioengineering 2018, 5, 101.

Journal reference: Bioengineering 2018, 5, 101
DOI: 10.3390/bioengineering5040101

Abstract

Mini-bioreactor systems enabling automatized operation of numerous parallel cultivations have been used to accelerate and optimize bioprocess development. As implementation of fed-batch conditions, multiple options of process control and sample analysis are possible, these systems represent valuable screening tools for large-scale production. However, the dynamic behavior of cultivations has not yet been considered regarding data evaluation and decision making during high-throughput screening in mini-bioreactors. In this study, the characterization of Saccharomyces cerevisiae AH22 secreting recombinant endopolygalacturonase is performed in 48 parallel fed-batch cultivations regarding 16 experimental conditions. Automated parallel process control, frequent sampling and analysis were implemented. Data-driven multivariate methods were developed to allow for fast, automated decision making as well as online predictive data analysis regarding endopolygalacturonase production. Using dynamic process information, a cultivation with abnormal behavior could be detected by principal component analysis as well as two clusters of similarly behaving cultivations, later classified according to the feeding rate. By decision tree analysis, cultivation conditions leading to an optimal recombinant product formation could be identified automatically. The developed method is easily adaptable and suitable for automatized process development reducing the experimental times and costs.

Subject Areas

mini-bioreactors; parallelization; automation; digitalization; multivariate analysis; dynamic processes

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