β-Galactosidase enzymes catalyze the hydrolysis of terminal non-reducing β-D-galactose residues in β-galactosides. These enzymes are important in producing lactose-free dairy products, reducing the lactose content of whey in dairy products, and for production of galactooligosaccharides (GOS) as prebiotic additives to infant formula. To use β-galactosidases in industrial settings, enzyme immobilization procedures are used to enhance their activity and stability and to minimize enzyme quantities and cost. In this study, recombinant Bifidobacterium adolescentis β-galactosidase BgaC was immobilized in calcium alginate and gelatin cross-linked with glutaraldehyde. The kinetic parameters and stability properties of immobilized BgaC were characterized in comparison with free soluble enzyme. The K(M) for immobilized BgaC using ortho-nitrophenyl-β-galactoside (ONPG) was 810â±â220 μM and the K(M) of free BgaC was 2500â±â3 μM. The k(cat) and k(cat/)K(M) of immobilized BgaC were 802 s(-1) and 990 s(-1) mM(-1), respectively, compared to k(cat) and k(cat/)K(M) values of 209 s(-1) and 84 s(-1) mM(-1), respectively, for free BgaC. Immobilized BgaC β-galactosidase was active at all tested pH (pH 4-10), while the free enzyme had decreased activity at pHâ<â5.5 andâ>â8.0. The immobilized enzyme had optimum activity at 40 °C, while the free enzyme was most active at 37 °C. In addition, immobilization enhanced acidic pH and temperature stability compared to the free enzyme. Reutilization of the BgaC beads was assessed and the enzyme maintained 69% activity after 12 rounds of reutilization. Therefore, the enhanced performance properties of immobilized BgaC make it a promising candidate for industrial applications. KEY POINTS: ⢠Bifidobacterium adolescentis β-galactosidase BgaC was successfully immobilized ⢠Immobilized BgaC has enhanced enzymatic activity and stability and allows recycling ⢠Sustained activity of immobilized BgaC is advantageous for industrial applications.
Immobilized β-galactosidase BgaC from Bifidobacterium adolescentis retains stability and activity during repeated cycles of use.
来自青春双歧杆菌的固定化β-半乳糖苷酶BgaC在重复使用循环中保持稳定性和活性
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作者:Mulualem Daniel Mehabie, Dwan Orla, Kilcoyne Michelle, O'Byrne Conor, Boyd Aoife
| 期刊: | Applied Microbiology and Biotechnology | 影响因子: | 4.300 |
| 时间: | 2025 | 起止号: | 2025 Jul 30; 109(1):174 |
| doi: | 10.1007/s00253-025-13564-5 | 研究方向: | 微生物学 |
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