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A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes

In the course of their development, industrial biocatalysis processes have to be optimized in small-scale, e. g., within microfluidic bioreactors. Recently, we introduced a novel microfluidic reactor device, which can handle defined reaction compartments of up to 250 μL in combination with magnetic...

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Autores principales: Heinzler, Raphael, Hübner, Jonas, Fischöder, Thomas, Elling, Lothar, Franzreb, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288360/
https://www.ncbi.nlm.nih.gov/pubmed/30564572
http://dx.doi.org/10.3389/fbioe.2018.00189
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author Heinzler, Raphael
Hübner, Jonas
Fischöder, Thomas
Elling, Lothar
Franzreb, Matthias
author_facet Heinzler, Raphael
Hübner, Jonas
Fischöder, Thomas
Elling, Lothar
Franzreb, Matthias
author_sort Heinzler, Raphael
collection PubMed
description In the course of their development, industrial biocatalysis processes have to be optimized in small-scale, e. g., within microfluidic bioreactors. Recently, we introduced a novel microfluidic reactor device, which can handle defined reaction compartments of up to 250 μL in combination with magnetic micro carriers. By transferring the magnetic carriers between subsequent compartments of differing compositions, small scale synthesis, and bioanalytical assays can be conducted. In the current work, this device is modified and extended to broaden its application range to the screening and optimization of bioprocesses applying immobilized enzymes. Besides scaling the maximum compartment volume up to 3 mL, a temperature control module, as well as a focused infrared spot were integrated. By adjusting the pump rate, compartment volumes can be accurately dosed with an error <5% and adjusted to the requested temperature within less than a minute. For demonstration of bioprocess parameter optimization within such compartments, the influence of pH, temperature, substrate concentration, and enzyme carrier loading was automatically screened for the case of transferring UDP-Gal onto N-acetylglucosamine linked to a tert-butyloxycarbonyl protected amino group using immobilized β1,4-galactosyltransferase-1. In addition, multiple recycling of the enzyme carriers and the use of increased compartment volumes also allows the simple production of preparative amounts of reaction products.
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spelling pubmed-62883602018-12-18 A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes Heinzler, Raphael Hübner, Jonas Fischöder, Thomas Elling, Lothar Franzreb, Matthias Front Bioeng Biotechnol Bioengineering and Biotechnology In the course of their development, industrial biocatalysis processes have to be optimized in small-scale, e. g., within microfluidic bioreactors. Recently, we introduced a novel microfluidic reactor device, which can handle defined reaction compartments of up to 250 μL in combination with magnetic micro carriers. By transferring the magnetic carriers between subsequent compartments of differing compositions, small scale synthesis, and bioanalytical assays can be conducted. In the current work, this device is modified and extended to broaden its application range to the screening and optimization of bioprocesses applying immobilized enzymes. Besides scaling the maximum compartment volume up to 3 mL, a temperature control module, as well as a focused infrared spot were integrated. By adjusting the pump rate, compartment volumes can be accurately dosed with an error <5% and adjusted to the requested temperature within less than a minute. For demonstration of bioprocess parameter optimization within such compartments, the influence of pH, temperature, substrate concentration, and enzyme carrier loading was automatically screened for the case of transferring UDP-Gal onto N-acetylglucosamine linked to a tert-butyloxycarbonyl protected amino group using immobilized β1,4-galactosyltransferase-1. In addition, multiple recycling of the enzyme carriers and the use of increased compartment volumes also allows the simple production of preparative amounts of reaction products. Frontiers Media S.A. 2018-12-04 /pmc/articles/PMC6288360/ /pubmed/30564572 http://dx.doi.org/10.3389/fbioe.2018.00189 Text en Copyright © 2018 Heinzler, Hübner, Fischöder, Elling and Franzreb. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Heinzler, Raphael
Hübner, Jonas
Fischöder, Thomas
Elling, Lothar
Franzreb, Matthias
A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title_full A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title_fullStr A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title_full_unstemmed A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title_short A Compartmented Flow Microreactor System for Automated Optimization of Bioprocesses Applying Immobilized Enzymes
title_sort compartmented flow microreactor system for automated optimization of bioprocesses applying immobilized enzymes
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288360/
https://www.ncbi.nlm.nih.gov/pubmed/30564572
http://dx.doi.org/10.3389/fbioe.2018.00189
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