Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger

Abstract Background Aspergillus niger ATCC 20611 is an industrially important fructooligosaccharides (FOS) producer since it produces the β-fructofuranosidase with superior transglycosylation activity, which is responsible for the conversion of sucrose to FOS accompanied by the by-product (glucose)...

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Main Authors: Xiufen Wan, Lu Wang, Jingjing Chang, Jing Zhang, Zhiyun Zhang, Kewen Li, Guilian Sun, Caixia Liu, Yaohua Zhong
Format: Article
Language:English
Published: BMC 2024-03-01
Series:Microbial Cell Factories
Subjects:
Online Access:https://doi.org/10.1186/s12934-024-02353-w
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author Xiufen Wan
Lu Wang
Jingjing Chang
Jing Zhang
Zhiyun Zhang
Kewen Li
Guilian Sun
Caixia Liu
Yaohua Zhong
author_facet Xiufen Wan
Lu Wang
Jingjing Chang
Jing Zhang
Zhiyun Zhang
Kewen Li
Guilian Sun
Caixia Liu
Yaohua Zhong
author_sort Xiufen Wan
collection DOAJ
description Abstract Background Aspergillus niger ATCC 20611 is an industrially important fructooligosaccharides (FOS) producer since it produces the β-fructofuranosidase with superior transglycosylation activity, which is responsible for the conversion of sucrose to FOS accompanied by the by-product (glucose) generation. This study aims to consume glucose to enhance the content of FOS by heterologously expressing glucose oxidase and peroxidase in engineered A. niger. Results Glucose oxidase was successfully expressed and co-localized with β-fructofuranosidase in mycelia. These mycelia were applied to synthesis of FOS, which possessed an increased purity of 60.63% from 52.07%. Furthermore, peroxidase was expressed in A. niger and reached 7.70 U/g, which could remove the potential inhibitor of glucose oxidase to facilitate the FOS synthesis. Finally, the glucose oxidase-expressing strain and the peroxidase-expressing strain were jointly used to synthesize FOS, which content achieved 71.00%. Conclusions This strategy allows for obtaining high-content FOS by the multiple enzymes expressed in the industrial fungus, avoiding additional purification processes used in the production of oligosaccharides. This study not only facilitated the high-purity FOS synthesis, but also demonstrated the potential of A. niger ATCC 20611 as an enzyme-producing cell factory.
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spelling doaj.art-ccf0faabd65b4933bbdc1cacfe9cc26b2024-03-10T12:24:50ZengBMCMicrobial Cell Factories1475-28592024-03-0123111310.1186/s12934-024-02353-wEffective synthesis of high-content fructooligosaccharides in engineered Aspergillus nigerXiufen Wan0Lu Wang1Jingjing Chang2Jing Zhang3Zhiyun Zhang4Kewen Li5Guilian Sun6Caixia Liu7Yaohua Zhong8State Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong UniversityState Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong UniversityState Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong UniversityState Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong UniversityShandong Academy of Pharmaceutical SciencesBaolingbao Biology Co., LtdBaolingbao Biology Co., LtdShandong Academy of Pharmaceutical SciencesState Key Laboratory of Microbial Technology, Institute of Microbial Technology, Shandong UniversityAbstract Background Aspergillus niger ATCC 20611 is an industrially important fructooligosaccharides (FOS) producer since it produces the β-fructofuranosidase with superior transglycosylation activity, which is responsible for the conversion of sucrose to FOS accompanied by the by-product (glucose) generation. This study aims to consume glucose to enhance the content of FOS by heterologously expressing glucose oxidase and peroxidase in engineered A. niger. Results Glucose oxidase was successfully expressed and co-localized with β-fructofuranosidase in mycelia. These mycelia were applied to synthesis of FOS, which possessed an increased purity of 60.63% from 52.07%. Furthermore, peroxidase was expressed in A. niger and reached 7.70 U/g, which could remove the potential inhibitor of glucose oxidase to facilitate the FOS synthesis. Finally, the glucose oxidase-expressing strain and the peroxidase-expressing strain were jointly used to synthesize FOS, which content achieved 71.00%. Conclusions This strategy allows for obtaining high-content FOS by the multiple enzymes expressed in the industrial fungus, avoiding additional purification processes used in the production of oligosaccharides. This study not only facilitated the high-purity FOS synthesis, but also demonstrated the potential of A. niger ATCC 20611 as an enzyme-producing cell factory.https://doi.org/10.1186/s12934-024-02353-wFructooligosaccharidesAspergillus nigerHeterologous expressionβ-fructofuranosidaseGlucose oxidasePeroxidase
spellingShingle Xiufen Wan
Lu Wang
Jingjing Chang
Jing Zhang
Zhiyun Zhang
Kewen Li
Guilian Sun
Caixia Liu
Yaohua Zhong
Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
Microbial Cell Factories
Fructooligosaccharides
Aspergillus niger
Heterologous expression
β-fructofuranosidase
Glucose oxidase
Peroxidase
title Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
title_full Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
title_fullStr Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
title_full_unstemmed Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
title_short Effective synthesis of high-content fructooligosaccharides in engineered Aspergillus niger
title_sort effective synthesis of high content fructooligosaccharides in engineered aspergillus niger
topic Fructooligosaccharides
Aspergillus niger
Heterologous expression
β-fructofuranosidase
Glucose oxidase
Peroxidase
url https://doi.org/10.1186/s12934-024-02353-w
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