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Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase

ABSTRACT: Advanced biotransformation processes typically involve the upstream processing part performed continuously and interlinked tightly with the product isolation. Key in their development is a catalyst that is highly active, operationally robust, conveniently produced, and recyclable. A promis...

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Autores principales: Kruschitz, Andreas, Peinsipp, Linda, Pfeiffer, Martin, Nidetzky, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285329/
https://www.ncbi.nlm.nih.gov/pubmed/34189615
http://dx.doi.org/10.1007/s00253-021-11411-x
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author Kruschitz, Andreas
Peinsipp, Linda
Pfeiffer, Martin
Nidetzky, Bernd
author_facet Kruschitz, Andreas
Peinsipp, Linda
Pfeiffer, Martin
Nidetzky, Bernd
author_sort Kruschitz, Andreas
collection PubMed
description ABSTRACT: Advanced biotransformation processes typically involve the upstream processing part performed continuously and interlinked tightly with the product isolation. Key in their development is a catalyst that is highly active, operationally robust, conveniently produced, and recyclable. A promising strategy to obtain such catalyst is to encapsulate enzymes as permeabilized whole cells in porous polymer materials. Here, we show immobilization of the sucrose phosphorylase from Bifidobacterium adolescentis (P134Q-variant) by encapsulating the corresponding E. coli cells into polyacrylamide. Applying the solid catalyst, we demonstrate continuous production of the commercial extremolyte 2-α-d-glucosyl-glycerol (2-GG) from sucrose and glycerol. The solid catalyst exhibited similar activity (≥70%) as the cell-free extract (~800 U g(−1) cell wet weight) and showed excellent in-operando stability (40 °C) over 6 weeks in a packed-bed reactor. Systematic study of immobilization parameters related to catalyst activity led to the identification of cell loading and catalyst particle size as important factors of process optimization. Using glycerol in excess (1.8 M), we analyzed sucrose conversion dependent on space velocity (0.075–0.750 h(−1)) and revealed conditions for full conversion of up to 900 mM sucrose. The maximum 2-GG space-time yield reached was 45 g L(−1) h(−1) for a product concentration of 120 g L(−1). Collectively, our study establishes a step-economic route towards a practical whole cell-derived solid catalyst of sucrose phosphorylase, enabling continuous production of glucosides from sucrose. This strengthens the current biomanufacturing of 2-GG, but also has significant replication potential for other sucrose-derived glucosides, promoting their industrial scale production using sucrose phosphorylase. KEY POINTS: • Cells of sucrose phosphorylase fixed in polyacrylamide were highly active and stable. • Solid catalyst was integrated with continuous flow to reach high process efficiency. • Generic process technology to efficiently produce glucosides from sucrose is shown. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-021-11411-x.
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spelling pubmed-82853292021-07-20 Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase Kruschitz, Andreas Peinsipp, Linda Pfeiffer, Martin Nidetzky, Bernd Appl Microbiol Biotechnol Biotechnological Products and Process Engineering ABSTRACT: Advanced biotransformation processes typically involve the upstream processing part performed continuously and interlinked tightly with the product isolation. Key in their development is a catalyst that is highly active, operationally robust, conveniently produced, and recyclable. A promising strategy to obtain such catalyst is to encapsulate enzymes as permeabilized whole cells in porous polymer materials. Here, we show immobilization of the sucrose phosphorylase from Bifidobacterium adolescentis (P134Q-variant) by encapsulating the corresponding E. coli cells into polyacrylamide. Applying the solid catalyst, we demonstrate continuous production of the commercial extremolyte 2-α-d-glucosyl-glycerol (2-GG) from sucrose and glycerol. The solid catalyst exhibited similar activity (≥70%) as the cell-free extract (~800 U g(−1) cell wet weight) and showed excellent in-operando stability (40 °C) over 6 weeks in a packed-bed reactor. Systematic study of immobilization parameters related to catalyst activity led to the identification of cell loading and catalyst particle size as important factors of process optimization. Using glycerol in excess (1.8 M), we analyzed sucrose conversion dependent on space velocity (0.075–0.750 h(−1)) and revealed conditions for full conversion of up to 900 mM sucrose. The maximum 2-GG space-time yield reached was 45 g L(−1) h(−1) for a product concentration of 120 g L(−1). Collectively, our study establishes a step-economic route towards a practical whole cell-derived solid catalyst of sucrose phosphorylase, enabling continuous production of glucosides from sucrose. This strengthens the current biomanufacturing of 2-GG, but also has significant replication potential for other sucrose-derived glucosides, promoting their industrial scale production using sucrose phosphorylase. KEY POINTS: • Cells of sucrose phosphorylase fixed in polyacrylamide were highly active and stable. • Solid catalyst was integrated with continuous flow to reach high process efficiency. • Generic process technology to efficiently produce glucosides from sucrose is shown. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00253-021-11411-x. Springer Berlin Heidelberg 2021-06-30 2021 /pmc/articles/PMC8285329/ /pubmed/34189615 http://dx.doi.org/10.1007/s00253-021-11411-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biotechnological Products and Process Engineering
Kruschitz, Andreas
Peinsipp, Linda
Pfeiffer, Martin
Nidetzky, Bernd
Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title_full Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title_fullStr Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title_full_unstemmed Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title_short Continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
title_sort continuous process technology for glucoside production from sucrose using a whole cell-derived solid catalyst of sucrose phosphorylase
topic Biotechnological Products and Process Engineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8285329/
https://www.ncbi.nlm.nih.gov/pubmed/34189615
http://dx.doi.org/10.1007/s00253-021-11411-x
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