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Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form

This study introduced an automated long‐term fermentation process for fungals grown in pellet form. The goal was to reduce the overgrowth of bioreactor internals and sensors while better rheological properties in the fermentation broth, such as oxygen transfer and mixing time, can be achieved. Becau...

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Autores principales: Soerjawinata, Winda, Kockler, Isabelle, Wommer, Lars, Frank, Robert, Schüffler, Anja, Schirmeister, Tanja, Ulber, Roland, Kampeis, Percy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288991/
https://www.ncbi.nlm.nih.gov/pubmed/35865648
http://dx.doi.org/10.1002/elsc.202100094
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author Soerjawinata, Winda
Kockler, Isabelle
Wommer, Lars
Frank, Robert
Schüffler, Anja
Schirmeister, Tanja
Ulber, Roland
Kampeis, Percy
author_facet Soerjawinata, Winda
Kockler, Isabelle
Wommer, Lars
Frank, Robert
Schüffler, Anja
Schirmeister, Tanja
Ulber, Roland
Kampeis, Percy
author_sort Soerjawinata, Winda
collection PubMed
description This study introduced an automated long‐term fermentation process for fungals grown in pellet form. The goal was to reduce the overgrowth of bioreactor internals and sensors while better rheological properties in the fermentation broth, such as oxygen transfer and mixing time, can be achieved. Because this could not be accomplished with continuous culture and fed‐batch fermentation, repeated‐batch fermentation was implemented with the help of additional bioreactor internals (“sporulation supports”). This should capture some biomass during fermentation. After harvesting the suspended biomass, intermediate cleaning was performed using a cleaning device. The biomass retained on the sporulation support went through the sporulation phase. The spores were subsequently used as inocula for the next batch. The reason for this approach was that the retained pellets could otherwise cause problems (e.g., overgrowth on sensors) in subsequent batches because the fungus would then show undesirable hyphal growth. Various sporulation supports were tested for sufficient biomass fixation to start the next batch. A reproducible spore concentration within the range of the requirements could be achieved by adjusting the sporulation support (design and construction material), and an intermediate cleaning adapted to this.
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spelling pubmed-92889912022-07-20 Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form Soerjawinata, Winda Kockler, Isabelle Wommer, Lars Frank, Robert Schüffler, Anja Schirmeister, Tanja Ulber, Roland Kampeis, Percy Eng Life Sci Research Articles This study introduced an automated long‐term fermentation process for fungals grown in pellet form. The goal was to reduce the overgrowth of bioreactor internals and sensors while better rheological properties in the fermentation broth, such as oxygen transfer and mixing time, can be achieved. Because this could not be accomplished with continuous culture and fed‐batch fermentation, repeated‐batch fermentation was implemented with the help of additional bioreactor internals (“sporulation supports”). This should capture some biomass during fermentation. After harvesting the suspended biomass, intermediate cleaning was performed using a cleaning device. The biomass retained on the sporulation support went through the sporulation phase. The spores were subsequently used as inocula for the next batch. The reason for this approach was that the retained pellets could otherwise cause problems (e.g., overgrowth on sensors) in subsequent batches because the fungus would then show undesirable hyphal growth. Various sporulation supports were tested for sufficient biomass fixation to start the next batch. A reproducible spore concentration within the range of the requirements could be achieved by adjusting the sporulation support (design and construction material), and an intermediate cleaning adapted to this. John Wiley and Sons Inc. 2022-05-18 /pmc/articles/PMC9288991/ /pubmed/35865648 http://dx.doi.org/10.1002/elsc.202100094 Text en © 2022 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Soerjawinata, Winda
Kockler, Isabelle
Wommer, Lars
Frank, Robert
Schüffler, Anja
Schirmeister, Tanja
Ulber, Roland
Kampeis, Percy
Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title_full Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title_fullStr Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title_full_unstemmed Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title_short Novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
title_sort novel bioreactor internals for the cultivation of spore‐forming fungi in pellet form
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9288991/
https://www.ncbi.nlm.nih.gov/pubmed/35865648
http://dx.doi.org/10.1002/elsc.202100094
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