PreprintCited by 4Enzyme Catalysis and ImmobilizationEnzyme Production and CharacterizationCarbohydrate Chemistry and Synthesis

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Thermostable D-Allulose 3-Epimerase for Long-Term Food-Compatible Continuous Production Systems

Open access
Cui, Jiawei, Li, Yan, Yan, Ming·2025·Applied Sciences

Preprint — published as 10.3390/app15137318

Abstract

D-allulose is a rare sugar with promising applications in food and health industries, owing to its low caloric value and multiple health benefits. In this study, we systematically investigated a thermostable D-allulose 3-epimerase (TcDAEase) from Thermogemmatispora carboxidivorans for food-compatible continuous production. The enzyme exhibited remarkable thermostability, with over 70% activity retained at 80 °C, and showed broad pH tolerance across the range of 8.0 to 13.0. Notably, TcDAEase exhibited high catalytic activity toward D-allulose and D-fructose even without addition of metal ions. Moreover, Food-grade Mg2+ was identified as enhancing enzyme activity by 14.3%, thus ensuring compliance with GRAS (Generally Recognized as Safe) standards for food applications. To improve industrial applicability, the enzyme was immobilized using a chitosan-diatomaceous earth (DE) matrix via a three-step adsorption–crosslinking–embedding strategy. The immobilized TcDAEase achieved 48.7% ± 2.4% activity recovery and retained 90.3% ± 1.5% activity over seven reaction cycles. Furthermore, continuous production of D-allulose was realized in a packed-bed reactor, operating stably at 60 °C, pH 8.0 and 5 mM Mg2+ for 150 days, producing 756 kg of D-allulose with a conversion yield exceeding 89.7% of the theoretical maximum. Overall, this study provides a feasible strategy for the continuous and efficient production of high value-added D-allulose in the food industry.

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Metadata

Authors
Cui, J., Li, Y., & Yan, M.
Affiliations
Nanjing Tech University (CN)
Venue
Applied Sciences
Publisher
MDPI AG
Published
2025-06-03
Volume
15
Issue
13
Pages
7318-7318
ISSN
2076-3417 (ISSN-L)
OpenAlex
W4411878489
Cited by
4
References
1
Citations by year
2026: 2 · 2025: 2
FWCI
1.21
Type
journal article
Language
en
Open access
Locations
  • Applied Sciences (publishedVersion, cc-by)
  • Preprints.org (acceptedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Guangdong Science and Technology Department (2022B0202120001)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Enzyme Catalysis and Immobilization
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Enzyme Production and Characterization
  • Physical Sciences › Chemistry › Organic Chemistry › Carbohydrate Chemistry and Synthesis
Keywords
D-allulose, D-allulose 3-epimerase, thermostable enzymes, rare sugars, enzyme immobilization, continuous production, fixed-bed reactor, food-grade enzymes, GRAS

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