首页> 外文期刊>Frontiers of chemical science and engine >Construction of a CaHPO_4-PGUS1 hybrid nanoflower through protein-inorganic self-assembly, and its application in glycyrrhetinic acid 3-O-mono-β-D-glucuronide preparation
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Construction of a CaHPO_4-PGUS1 hybrid nanoflower through protein-inorganic self-assembly, and its application in glycyrrhetinic acid 3-O-mono-β-D-glucuronide preparation

机译:蛋白质-无机自组装技术构建CaHPO_4-PGUS1杂种纳米花及其在甘草次酸3-O-单-β-D-葡糖醛酸苷制备中的应用

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Glycyrrhetinic acid 3-O-mono-beta-d-glucuronide (GAMG), an important pharmaceutical intermediate and functional sweetener, has broad applications in the food and medical industries. A green and cost-effective method for its preparation is highly desired. Using site-directed mutagenesis, we previously obtained a variant of beta-glucuronidase from Aspergillus oryzae Li-3 (PGUS1), which can specifically transform glycyrrhizin (GL) into GAMG. In this study, a facile method was established to prepare a CaHPO4-PGUS1 hybrid nanoflower for enzyme immobilization, based on protein-inorganic hybrid self-assembly. Under optimal conditions, 1.2 mg of a CaHPO4-PGUS1 hybrid nanoflower precipitate with 71.2% immobilization efficiency, 35.60 mg center dot g(-1) loading capacity, and 118% relative activity was obtained. Confocal laser scanning microscope and scanning electron microscope results showed that the enzyme was encapsulated in the CaHPO4-PGUS1 hybrid nanoflower. Moreover, the thermostability of the CaHPO4-PGUS1 hybrid nanoflower at 55 degrees C was improved, and its half-life increased by 1.3 folds. Additionally, the CaHPO4-PGUS1 hybrid nanoflower was used for the preparation of GAMG through GL hydrolysis, with the conversion rate of 92% in 8 h, and after eight consecutive runs, it had 60% of its original activity.
机译:甘草次酸3-O-单-β-d-葡糖醛酸(GAMG)是一种重要的药物中间体和功能性甜味剂,在食品和医疗行业具有广泛的应用。迫切需要一种绿色且经济有效的制备方法。使用定点诱变,我们先前从米曲霉Li-3(PGUS1)中获得了一种β-葡萄糖醛酸酶的变体,该变体可以将甘草甜素(GL)特异性转化为GAMG。在这项研究中,建立了一种简便的方法来制备CaHPO4-PGUS1杂合纳米花,用于基于蛋白质-无机杂化自组装的酶固定化。在最佳条件下,获得1.2 mg的CaHPO4-PGUS1杂合纳米花沉淀物,其固定效率为71.2%,中心点g(-1)的负载量为35.60 mg,相对活性为118%。共聚焦激光扫描显微镜和扫描电子显微镜结果表明,该酶被包裹在CaHPO4-PGUS1杂种纳米花中。此外,CaHPO4-PGUS1杂合纳米花在55摄氏度时的热稳定性得到改善,其半衰期增加了1.3倍。此外,CaHPO4-PGUS1杂合纳米花用于通过GL水解制备GAMG,在8小时内的转化率为92%,并且连续运行八次后,其原始活性为60%。

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