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Autores principales: Ida Dinges, Ina Depentori, Lisa Gans, Dirk Holtmann, Siegfried R. Waldvogel, Markus Stöckl
Formato: Artículo Open Access
Publicado: Wiley 2024
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Acceso en línea:https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.202301721
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author Ida Dinges
Ina Depentori
Lisa Gans
Dirk Holtmann
Siegfried R. Waldvogel
Markus Stöckl
author_facet Ida Dinges
Ina Depentori
Lisa Gans
Dirk Holtmann
Siegfried R. Waldvogel
Markus Stöckl
Ida Dinges
Ina Depentori
Lisa Gans
Dirk Holtmann
Siegfried R. Waldvogel
Markus Stöckl
collection Wiley Open Access
contents Coupling of CO2 Electrolysis with Parallel and Semi‐Automated Biopolymer Synthesis – Ex‐Cell and without Downstream Processing Ida Dinges Ina Depentori Lisa Gans Dirk Holtmann Siegfried R. Waldvogel Markus Stöckl ChemSusChem AbstractImportant improvements have been achieved in developing the coupling of electrochemical CO2 reduction to formate with its subsequent microbial conversion to polyhydroxybutyrate (PHB) by Cupriavidus necator. The CO2 based formate electrosynthesis was optimised by electrolysis parameter adjustment and application of Sn based gas diffusion electrodes reaching almost 80 % Faradaic efficiency at 150 mA cm−2. Thereby, catholyte with the high formate concentration of 441±9 mmol L−1 was generated as feedstock without intermediate downstream processing for semi‐automated formate feeding into a fed‐batch reactor system. Moreover, microbial formate conversion to PHB was studied further, optimised, and successfully scaled from shake flasks to semi‐automated bioreactors. Therein, a PHB per formate ratio of 16.5±4.0 mg g−1 and a PHB synthesis rate of 8.4±2.1 mg L−1 OD−1 h−1 were achieved. By this process combination, an almost doubled overall process yield of 22.3±5.5 % was achieved compared to previous reports. The findings allow a detailed evaluation of the overall CO2 to PHB conversion, providing the basis for potential technical exploitation. 10.1002/cssc.202301721 http://creativecommons.org/licenses/by/4.0/
doi_str_mv 10.1002/cssc.202301721
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id wiley_oa_10_1002_cssc_202301721
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by/4.0/
publishDate 2024
publisher Wiley
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spellingShingle Coupling of CO2 Electrolysis with Parallel and Semi‐Automated Biopolymer Synthesis – Ex‐Cell and without Downstream Processing
Ida Dinges
Ina Depentori
Lisa Gans
Dirk Holtmann
Siegfried R. Waldvogel
Markus Stöckl
ChemSusChem
Coupling of CO2 Electrolysis with Parallel and Semi‐Automated Biopolymer Synthesis – Ex‐Cell and without Downstream Processing Ida Dinges Ina Depentori Lisa Gans Dirk Holtmann Siegfried R. Waldvogel Markus Stöckl ChemSusChem AbstractImportant improvements have been achieved in developing the coupling of electrochemical CO2 reduction to formate with its subsequent microbial conversion to polyhydroxybutyrate (PHB) by Cupriavidus necator. The CO2 based formate electrosynthesis was optimised by electrolysis parameter adjustment and application of Sn based gas diffusion electrodes reaching almost 80 % Faradaic efficiency at 150 mA cm−2. Thereby, catholyte with the high formate concentration of 441±9 mmol L−1 was generated as feedstock without intermediate downstream processing for semi‐automated formate feeding into a fed‐batch reactor system. Moreover, microbial formate conversion to PHB was studied further, optimised, and successfully scaled from shake flasks to semi‐automated bioreactors. Therein, a PHB per formate ratio of 16.5±4.0 mg g−1 and a PHB synthesis rate of 8.4±2.1 mg L−1 OD−1 h−1 were achieved. By this process combination, an almost doubled overall process yield of 22.3±5.5 % was achieved compared to previous reports. The findings allow a detailed evaluation of the overall CO2 to PHB conversion, providing the basis for potential technical exploitation. 10.1002/cssc.202301721 http://creativecommons.org/licenses/by/4.0/
title Coupling of CO2 Electrolysis with Parallel and Semi‐Automated Biopolymer Synthesis – Ex‐Cell and without Downstream Processing
topic ChemSusChem
url https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.202301721