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      Polymer-based controlled-release fed-batch microtiter plate – diminishing the gap between early process development and production conditions

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          Abstract

          Background

          Fed-batch conditions are advantageous for industrial cultivations as they avoid unfavorable phenomena appearing in batch cultivations. Those are for example the formation of overflow metabolites, catabolite repression, oxygen limitation or inhibition due to elevated osmotic concentrations. For both, the early bioprocess development and the optimization of existing bioprocesses, small-scale reaction vessels are applied to ensure high throughput, low costs and prompt results. However, most conventional small-scale procedures work in batch operation mode, which stands in contrast to fed-batch conditions in large-scale bioprocesses. Extensive expenditure for installations and operation accompany almost all cultivation systems in the market allowing fed-batch conditions in small-scale. An alternative, more cost efficient enzymatic glucose release system is strongly influenced by environmental conditions. To overcome these issues, this study investigates a polymer-based fed-batch system for controlled substrate release in microtiter plates.

          Results

          Immobilizing a solid silicone matrix with embedded glucose crystals at the bottom of each well of a microtiter plate is a suitable technique for implementing fed-batch conditions in microtiter plates. The results showed that the glucose release rate depends on the osmotic concentration, the pH and the temperature of the medium. Moreover, the applied nitrogen source proved to influence the glucose release rate. A new developed mathematical tool predicts the glucose release for various media conditions. The two model organisms E. coli and H. polymorpha were cultivated in the fed-batch microtiter plate to investigate the general applicability for microbial systems. Online monitoring of the oxygen transfer rate and offline analysis of substrate, product, biomass and pH confirmed that fed-batch conditions are comparable to large-scale cultivations. Furthermore, due to fed-batch conditions in microtiter plates, product formation could be enhanced by the factor 245 compared to batch cultivations.

          Conclusions

          The polymer-based fed-batch microtiter plate represents a sophisticated and cost efficient system to mimic typical industrial fed-batch conditions in small-scale. Thus, a more reliable strain screening and early process development can be performed. A systematical scale-down with low expenditure of work, time and money is possible.

          Electronic supplementary material

          The online version of this article (10.1186/s13036-019-0147-6) contains supplementary material, which is available to authorized users.

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          The Reductive Amination of Aldehydes and Ketones and the Hydrogenation of Nitriles: Mechanistic Aspects and Selectivity Control

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            Online respiration activity measurement (OTR, CTR, RQ) in shake flasks

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              Device for sterile online measurement of the oxygen transfer rate in shaking flasks.

              The oxygen transfer rate (OTR) is the most suitable measurable parameter to quantify the physiological state of a culture of aerobic microorganisms since most metabolic activities depend on oxygen consumption. Online measurement of the oxygen transfer rate in stirred bioreactors is state of the art although technically difficult. However, the online determination of the oxygen transfer rate in shaking bioreactors under sterile conditions has not been possible until recently. A newly developed measuring device eliminates this deficit. Extremely useful information about cultivating conditions and the physiological state of microorganisms can be gained in early stages of research and bioprocess development from many reactors operated in parallel.
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                Author and article information

                Contributors
                jochen.buechs@avt.rwth-aachen.de
                Journal
                J Biol Eng
                J Biol Eng
                Journal of Biological Engineering
                BioMed Central (London )
                1754-1611
                22 February 2019
                22 February 2019
                2019
                : 13
                : 18
                Affiliations
                [1 ]ISNI 0000 0001 0728 696X, GRID grid.1957.a, AVT - Biochemical Engineering, , RWTH Aachen University, ; Forckenbeckstraße 51, 52074 Aachen, Germany
                [2 ]ISNI 0000 0001 0728 696X, GRID grid.1957.a, DWI – Leibniz Institute for Interactive Materials, , RWTH Aachen University, ; Forckenbeckstraße 50, 52074 Aachen, Germany
                [3 ]Kuhner Shaker GmbH, Kaiserstraße 100, 52134 Herzogenrath, Germany
                Article
                147
                10.1186/s13036-019-0147-6
                6387502
                30833982
                f50c5e00-68a2-4f81-a74b-6b83709a0599
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 August 2018
                : 11 February 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100006360, Bundesministerium für Wirtschaft und Energie;
                Award ID: IGF-No. 18411N
                Categories
                Research
                Custom metadata
                © The Author(s) 2019

                Biotechnology
                fed-batch,microtiter plate,escherichia coli,hansenula polymorpha,screening,high-throughput,bioprocess development

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