Biochemical Characterization of a Novel, Glucose-Tolerant β-Glucosidase from <i>Jiangella ureilytica</i> KC603, and Determination of Resveratrol Production Capacity from Polydatin
APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, cilt.197, sa.8, ss.5104-5130, 2025 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 197 Sayı: 8
- Basım Tarihi: 2025
- Doi Numarası: 10.1007/s12010-025-05272-7
- Dergi Adı: APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, PASCAL, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Compendex, EMBASE, Food Science & Technology Abstracts, MEDLINE, Pollution Abstracts, Veterinary Science Database
- Sayfa Sayıları: ss.5104-5130
- Karadeniz Teknik Üniversitesi Adresli: Evet
Özet
Beta-glucosidase, a ubiquitous enzyme, is responsible for catalyzing the hydrolysis of beta-glycosidic linkages present in polysaccharides and contributes significantly to several industrial sectors such as food, agriculture, and biofuel production. beta-glucosidases can convert polydatin to resveratrol through de-glycosylation. Resveratrol is important for human health and has potential applications in pharmacology. The preference of enzymatic conversion methods for resveratrol production improves the importance of beta-glucosidases. The glucose tolerance of beta-glucosidases also significantly impacts their applicability. Because the inhibition of many beta-glucosidase's activity by their reaction product, glucose, is a limiting factor for industrial applications. In this study, a robust beta-glucosidase was isolated from a novel-defined Jiangella ureilytica KC603 strain. The beta-glucosidase encoding gene (JurBglKC603) was cloned and expressed in E. coli BL21 (DE3) cells and a 50.1 kDa protein was purified using Ni-affinity column chromatography. The efficient polydatin deglycosylation capacity of JurBglKC603 was determined by Glucose Oxidase-Peroxidase (GOPOD) assay. JurBglKC603 exhibits remarkable resistance to glucose concentrations of up to 3 M. The enzyme remained active across a broad pH spectrum and was unaffected by most heavy metal ions, except for Hg2+. The kinetic parameters of JurBglKC603 were Km = 0.44 mM, Vmax = 26.87 U