Exploring the complexity of xylitol production in the fungal cell factory Aspergillus niger

Production of xylitol from agricultural by-products offers a promising approach for the circular bioeconomy. This study investigates the roles of transcription factors XlnR and CreA in xylitol production from wheat bran in Aspergillus niger by generating strains with a constitutively active XlnR (XlnR<sub>c</sub>, V756F mutation) and/or deletion of creA, in a previously generated xylitol-producing strain. The XlnR<sub>c</sub> mutation increased the initial rate of xylitol production but lowered the overall accumulation. Deletion of creA in this strain significantly improved both the onset and rate of xylitol production, indicating an inhibitory role of CreA in the PCP. These results demonstrate the complexity of metabolic engineering to generate fungal cell factories for valuable biochemicals, such as xylitol, as not only metabolic but also multiple gene regulation aspects need to be considered.

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Publication Details

Journal
Enzyme and Microbial Technology
Published
2024-11-23
DOI
https://doi.org/10.1016/j.enzmictec.2024.110550
Citations
4
Primary Topic
Biofuel production and bioconversion
Type
article
Field-Weighted Citation Impact
0.74

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article

Exploring the complexity of xylitol production in the fungal cell factory Aspergillus niger

Miia Mäkelä, Robert W. A. M. Kuijpers, Jiali Meng, Ronald P. de Vries et al.
4 citations
Enzyme and Microbial Technology
Biofuel production and bioconversion
0.74
article

Exploring the complexity of xylitol production in the fungal cell factory Aspergillus niger

Miia Mäkelä, Robert W. A. M. Kuijpers, Jiali Meng, Ronald P. de Vries, Astrid Müller
article en
4 citations

Abstract

Production of xylitol from agricultural by-products offers a promising approach for the circular bioeconomy. This study investigates the roles of transcription factors XlnR and CreA in xylitol production from wheat bran in Aspergillus niger by generating strains with a constitutively active XlnR (XlnR<sub>c</sub>, V756F mutation) and/or deletion of creA, in a previously generated xylitol-producing strain. The XlnR<sub>c</sub> mutation increased the initial rate of xylitol production but lowered the overall accumulation. Deletion of creA in this strain significantly improved both the onset and rate of xylitol production, indicating an inhibitory role of CreA in the PCP. These results demonstrate the complexity of metabolic engineering to generate fungal cell factories for valuable biochemicals, such as xylitol, as not only metabolic but also multiple gene regulation aspects need to be considered.

Enzyme and Microbial TechnologyVol. 183
Westerdijk Fungal Biodiversity Institute (NL), Aalto University (FI)
Academy of Finland, China Scholarship Council
Zero hunger
Openalex Percentile: Top 31%
Biofuel production and bioconversion
0.74
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Exploring the complexity of xylitol production in the fungal cell factory Aspergillus niger — Miia Mäkelä, Robert W. A. M. Kuijpers, et al. · Enzyme and Microbial Technology (2024) | TGRS Research Map | TGRS