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High-yield production and purification of prebiotic inulin-type fructooligosaccharides

Due to the health-promoting effects and functional properties of inulin-type fructooligosaccharides (I-FOS), the global market for I-FOS is constantly growing. Hence, there is a continuing demand for new, efficient biotechnological approaches for I-FOS production. In this work, crude inulosucrase In...

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Autores principales: Wienberg, Franziska, Hövels, Marcel, Deppenmeier, Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666576/
https://www.ncbi.nlm.nih.gov/pubmed/36380213
http://dx.doi.org/10.1186/s13568-022-01485-9
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author Wienberg, Franziska
Hövels, Marcel
Deppenmeier, Uwe
author_facet Wienberg, Franziska
Hövels, Marcel
Deppenmeier, Uwe
author_sort Wienberg, Franziska
collection PubMed
description Due to the health-promoting effects and functional properties of inulin-type fructooligosaccharides (I-FOS), the global market for I-FOS is constantly growing. Hence, there is a continuing demand for new, efficient biotechnological approaches for I-FOS production. In this work, crude inulosucrase InuGB-V3 from Lactobacillus gasseri DSM 20604 was used to synthesize I-FOS from sucrose. Supplementation with 1 mM CaCl(2), a pH of 3.5–5.5, and an incubation temperature of 40 °C were found to be optimal production parameters at which crude inulosucrase showed high conversion rates, low sucrose hydrolysis, and excellent stability over 4 days. The optimal process conditions were employed in cell-free bioconversion reactions. By elevating the substrate concentration from 570 to 800 g L(−1), the I-FOS concentration and the synthesis of products with a low degree of polymerization (DP) could be increased, while sucrose hydrolysis was decreased. Bioconversion of 800 g L(−1) sucrose for 20 h resulted in an I-FOS-rich syrup with an I-FOS concentration of 401 ± 7 g L(−1) and an I-FOS purity of 53 ± 1% [w/w]. I-FOS with a DP of 3–11 were synthesized, with 1,1-kestotetraose (DP4) being the predominant transfructosylation product. The high-calorie sugars glucose, sucrose, and fructose were removed from the generated I-FOS-rich syrup using activated charcoal. Thus, 81 ± 5% of the initially applied I-FOS were recovered with a purity of 89 ± 1%. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01485-9.
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spelling pubmed-96665762022-11-29 High-yield production and purification of prebiotic inulin-type fructooligosaccharides Wienberg, Franziska Hövels, Marcel Deppenmeier, Uwe AMB Express Original Article Due to the health-promoting effects and functional properties of inulin-type fructooligosaccharides (I-FOS), the global market for I-FOS is constantly growing. Hence, there is a continuing demand for new, efficient biotechnological approaches for I-FOS production. In this work, crude inulosucrase InuGB-V3 from Lactobacillus gasseri DSM 20604 was used to synthesize I-FOS from sucrose. Supplementation with 1 mM CaCl(2), a pH of 3.5–5.5, and an incubation temperature of 40 °C were found to be optimal production parameters at which crude inulosucrase showed high conversion rates, low sucrose hydrolysis, and excellent stability over 4 days. The optimal process conditions were employed in cell-free bioconversion reactions. By elevating the substrate concentration from 570 to 800 g L(−1), the I-FOS concentration and the synthesis of products with a low degree of polymerization (DP) could be increased, while sucrose hydrolysis was decreased. Bioconversion of 800 g L(−1) sucrose for 20 h resulted in an I-FOS-rich syrup with an I-FOS concentration of 401 ± 7 g L(−1) and an I-FOS purity of 53 ± 1% [w/w]. I-FOS with a DP of 3–11 were synthesized, with 1,1-kestotetraose (DP4) being the predominant transfructosylation product. The high-calorie sugars glucose, sucrose, and fructose were removed from the generated I-FOS-rich syrup using activated charcoal. Thus, 81 ± 5% of the initially applied I-FOS were recovered with a purity of 89 ± 1%. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13568-022-01485-9. Springer Berlin Heidelberg 2022-11-15 /pmc/articles/PMC9666576/ /pubmed/36380213 http://dx.doi.org/10.1186/s13568-022-01485-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Original Article
Wienberg, Franziska
Hövels, Marcel
Deppenmeier, Uwe
High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title_full High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title_fullStr High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title_full_unstemmed High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title_short High-yield production and purification of prebiotic inulin-type fructooligosaccharides
title_sort high-yield production and purification of prebiotic inulin-type fructooligosaccharides
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9666576/
https://www.ncbi.nlm.nih.gov/pubmed/36380213
http://dx.doi.org/10.1186/s13568-022-01485-9
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