Cargando…

Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips

Microbial cells in industrial large-scale bioreactors are exposed to fluctuating conditions, e.g., nutrient concentration, dissolved oxygen, temperature, and pH. These inhomogeneities can influence the cell physiology and metabolism, e.g., decelerate cell growth and product formation. Microfluidic s...

Descripción completa

Detalles Bibliográficos
Autores principales: Ho, Phuong, Westerwalbesloh, Christoph, Kaganovitch, Eugen, Grünberger, Alexander, Neubauer, Peter, Kohlheyer, Dietrich, von Lieres, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518007/
https://www.ncbi.nlm.nih.gov/pubmed/31010155
http://dx.doi.org/10.3390/microorganisms7040105
_version_ 1783418373879627776
author Ho, Phuong
Westerwalbesloh, Christoph
Kaganovitch, Eugen
Grünberger, Alexander
Neubauer, Peter
Kohlheyer, Dietrich
von Lieres, Eric
author_facet Ho, Phuong
Westerwalbesloh, Christoph
Kaganovitch, Eugen
Grünberger, Alexander
Neubauer, Peter
Kohlheyer, Dietrich
von Lieres, Eric
author_sort Ho, Phuong
collection PubMed
description Microbial cells in industrial large-scale bioreactors are exposed to fluctuating conditions, e.g., nutrient concentration, dissolved oxygen, temperature, and pH. These inhomogeneities can influence the cell physiology and metabolism, e.g., decelerate cell growth and product formation. Microfluidic systems offer new opportunities to study such effects in great detail by examining responses to varying environmental conditions at single-cell level. However, the possibility to reproduce large-scale bioreactor conditions in microscale cultivation systems has not yet been systematically investigated. Hence, we apply computational fluid dynamics (CFD) simulations to analyze and compare three commonly used microfluidic single-cell trapping and cultivation devices that are based on (i) mother machines (MM), (ii) monolayer growth chambers (MGC), and (iii) negative dielectrophoresis (nDEP). Several representative time-variant nutrient concentration profiles are applied at the chip entry. Responses to these input signals within the studied microfluidic devices are comparatively evaluated at the positions of the cultivated cells. The results are comprehensively presented in a Bode diagram that illustrates the degree of signal damping depending on the frequency of change in the inlet concentration. As a key finding, the MM can accurately reproduce signal changes that occur within 1 s or slower, which are typical for the environmental conditions observed by single cells in large-scale bioreactors, while faster changes are levelled out. In contrast, the nDEP and MGC are found to level out signal changes occurring within 10 s or faster, which can be critical for the proposed application.
format Online
Article
Text
id pubmed-6518007
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-65180072019-05-31 Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips Ho, Phuong Westerwalbesloh, Christoph Kaganovitch, Eugen Grünberger, Alexander Neubauer, Peter Kohlheyer, Dietrich von Lieres, Eric Microorganisms Article Microbial cells in industrial large-scale bioreactors are exposed to fluctuating conditions, e.g., nutrient concentration, dissolved oxygen, temperature, and pH. These inhomogeneities can influence the cell physiology and metabolism, e.g., decelerate cell growth and product formation. Microfluidic systems offer new opportunities to study such effects in great detail by examining responses to varying environmental conditions at single-cell level. However, the possibility to reproduce large-scale bioreactor conditions in microscale cultivation systems has not yet been systematically investigated. Hence, we apply computational fluid dynamics (CFD) simulations to analyze and compare three commonly used microfluidic single-cell trapping and cultivation devices that are based on (i) mother machines (MM), (ii) monolayer growth chambers (MGC), and (iii) negative dielectrophoresis (nDEP). Several representative time-variant nutrient concentration profiles are applied at the chip entry. Responses to these input signals within the studied microfluidic devices are comparatively evaluated at the positions of the cultivated cells. The results are comprehensively presented in a Bode diagram that illustrates the degree of signal damping depending on the frequency of change in the inlet concentration. As a key finding, the MM can accurately reproduce signal changes that occur within 1 s or slower, which are typical for the environmental conditions observed by single cells in large-scale bioreactors, while faster changes are levelled out. In contrast, the nDEP and MGC are found to level out signal changes occurring within 10 s or faster, which can be critical for the proposed application. MDPI 2019-04-19 /pmc/articles/PMC6518007/ /pubmed/31010155 http://dx.doi.org/10.3390/microorganisms7040105 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ho, Phuong
Westerwalbesloh, Christoph
Kaganovitch, Eugen
Grünberger, Alexander
Neubauer, Peter
Kohlheyer, Dietrich
von Lieres, Eric
Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title_full Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title_fullStr Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title_full_unstemmed Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title_short Reproduction of Large-Scale Bioreactor Conditions on Microfluidic Chips
title_sort reproduction of large-scale bioreactor conditions on microfluidic chips
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518007/
https://www.ncbi.nlm.nih.gov/pubmed/31010155
http://dx.doi.org/10.3390/microorganisms7040105
work_keys_str_mv AT hophuong reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT westerwalbeslohchristoph reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT kaganovitcheugen reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT grunbergeralexander reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT neubauerpeter reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT kohlheyerdietrich reproductionoflargescalebioreactorconditionsonmicrofluidicchips
AT vonliereseric reproductionoflargescalebioreactorconditionsonmicrofluidicchips