School of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore, 637551, Singapore.
School of Pharmacy, Jiangsu University, 301 Xuefu Road, Zhenjiang 212013, China.
Enzyme Microb Technol. 2019 Feb;121:51-58. doi: 10.1016/j.enzmictec.2018.12.002. Epub 2018 Dec 3.
Sagittatoside B, a rare secondary flavonol glycoside in Epimedii Folium, has much better in vivo bioactivities than its original glycoside epimedin B. Its preparation methods, such as acidic hydrolysis, are of low efficiency, and byproducts are generated. The objective of this study was to establish a novel catalysis system for convenient preparation of this compound based on recyclable and integrated biphase enzymatic hydrolysis. β-glucanase was selected from five commercial enzymes based on the best catalysis performance. After optimization of the conditions, the biphase system was constructed with propyl acetate and HAc-NaAc buffer (pH 4.5) (1:1, v/v) containing β-glucanase/epimedin B (1:2, w/w), and the hydrolysis was performed at 60 °C for 1 h. Consequently, epimedin B was completely hydrolyzed to sagittatoside B, and 95.7% of the product was transferred into the organic phase. Moreover, a high conversion ratio of 94.0% was achieved, even after the enzyme solution was used for six cycles. Additionally, the procedure was much simplified compared with conventional enzymatic hydrolysis. The newly proposed strategy is an efficient and promising approach for the preparation of sagittatoside B in industrial applications.
箭叶淫羊藿苷 B 是淫羊藿属植物中罕见的黄酮醇次级糖苷,其体内生物活性明显优于其原始糖苷淫羊藿苷 B。其制备方法如酸水解,效率低,且会产生副产物。本研究旨在建立一种基于可回收和集成两相酶水解的新型催化体系,方便制备该化合物。根据最佳催化性能,从五种商业酶中选择了β-葡聚糖酶。在优化条件后,将相转移β-葡聚糖酶/淫羊藿苷 B(1:2,w/w)的丙酸乙酯和 HAc-NaAc 缓冲液(pH 4.5)(1:1,v/v)构建成两相体系,并在 60°C 下反应 1 h。结果,淫羊藿苷 B 完全水解为箭叶淫羊藿苷 B,产物 95.7%转移到有机相中。此外,即使在酶溶液使用六次后,仍可达到 94.0%的高转化率。与传统的酶水解相比,该方法大大简化。该新提出的策略是一种在工业应用中制备箭叶淫羊藿苷 B 的有效且有前景的方法。