Sustainable 3D-printed β-galactosidase immobilization coupled with continuous-flow reactor for efficient lactose-free milk production

•Layer-by-layer self-assembly simplified the process of carrier modification.•Genipin was able to covalently immobilize β-Gal with 92.87% immobilization efficiency.•Flow reactor increased substrate mass transfer for 96.06% lactose hydrolysis.•3D printed PLA carriers enabled easy recycling and saved...

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Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2024-02, Vol.481, p.148557, Article 148557
Hauptverfasser: Shao, Yun, Gan, Ni, Gao, Bingbing, He, Bingfang
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Sprache:eng
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Zusammenfassung:•Layer-by-layer self-assembly simplified the process of carrier modification.•Genipin was able to covalently immobilize β-Gal with 92.87% immobilization efficiency.•Flow reactor increased substrate mass transfer for 96.06% lactose hydrolysis.•3D printed PLA carriers enabled easy recycling and saved production costs.•PLA-HPGG galactose-free inhibition enabled on-demand production of low and lactose-free milk. The production of low-lactose and lactose-free milk remains a critical challenge. Novel enzyme immobilization integrated with the flow reactor that could be applied to hydrolyze milk with cost-effectiveness, facilitation, and safety is highly expected. Here, we present a novel continuous-flow bioreactor loaded with β-galactosidase (β-Gal) covalently immobilized 3D-printed scaffolds for the production of lactose-free milk. 3D-printed polylactic acid (PLA) scaffolds modified by self-assembly of polyethyleneimine and sodium hyaluronate layers are rapidly branched with functional groups, followed by covalent immobilization of β-Gal using genipin as the cross-linker. The use of genipin allows efficient and stable immobilization of the enzyme (92.87 % immobilization efficiency), and the immobilized enzyme retains 90.53 % activity after 6th repeated use. Moreover, the 3D-printed scaffolds integrated into the flow reactor perturbed the fluids in the different reactors through directional channels, which improved the internal mass transfer to achieve high catalytic activity (94.20 % lactose hydrolysis efficiency). The lactose residues of milk reacted in the β-Gal flow reactor for 6 and 12 h were 1.87 g dL-1 and 0.38 g dL-1, which fully met the requirements of the national food safety standards for low-lactose and lactose-free milk. Due to the high efficiency of enzyme immobilization and the stable catalytic activity of the reactor, it has a broad application prospect for the production of low-lactose and lactose-free milk and other biocatalytic fields.
ISSN:1385-8947
1873-3212
DOI:10.1016/j.cej.2024.148557