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高速逆流色谱在生物合成产物制备分离中的适用性:以糖基化产物为例。

The applicability of high-speed counter-current chromatography for preparative separation of biosynthesis products: Glycosylation products as example.

机构信息

Key Laboratory of Biodiversity Formation Mechanism and Comprehensive Utilization of Qinghai-Tibetan Plateau in Qinghai Province, Academy of Plateau Science and Sustainability, School of Life Science, Qinghai Normal University, Xining, P. R. China.

Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, P. R. China.

出版信息

J Sep Sci. 2021 Dec;44(24):4368-4375. doi: 10.1002/jssc.202100544. Epub 2021 Nov 1.

Abstract

Biosynthesis is a promising way to manufacture desired products, however, the purification of its final products is a tough work due to the huge amount of reaction matrix. Liquid stationary phase of high-speed counter-current chromatography could easily avoid the commonly disadvantages that occurred in traditional column chromatography in the field of biosynthesized products purification. This characteristic makes high-speed counter-current chromatography particularly applicable for final products separation in biosynthesis. In this study, the glycosylation products of Silybin B by one-pot glycosylation were successfully purified by high-speed counter-current chromatography to show the applicability of high-speed counter-current chromatography for preparative separation of biosynthesis products. An optimized n-hexane/ethyl acetate/methanol/water (2:5:2:3, v/v/v/v) system was applied in this study. As a result, four Silybin B glycosylation products, including 7 mg of Silybin B-5-O-β-D-glucoside (SG-1), 12 mg of Silybin B-3-O-β-D-glucoside (SG-2), 10 mg of Silybin B-7-O-β-D-glucoside (SG-3), and 24 mg of Silybin B-20-O-β-D-glucoside (SG-4), were simultaneously separated from 200 mg of glycosylation crude products, with the purity of 89.3, 95.2, 96.4, and 97.5%, respectively. Their structures were identified by spectroscopic analysis.

摘要

生物合成是制造所需产品的一种很有前途的方法,然而,由于反应基质的巨大数量,其最终产品的纯化是一项艰巨的工作。高速逆流色谱的液相固定相可以很容易地避免传统柱色谱在生物合成产物纯化领域中常见的缺点。这一特点使得高速逆流色谱特别适用于生物合成中最终产物的分离。在本研究中,通过一锅法糖基化成功地对水飞蓟宾 B 的糖基化产物进行了高速逆流色谱纯化,以展示高速逆流色谱在生物合成产物的制备分离中的适用性。本研究采用优化的正己烷/乙酸乙酯/甲醇/水(2:5:2:3,v/v/v/v)体系。结果,从 200mg 糖基化粗产物中同时分离出了四种水飞蓟宾 B 的糖基化产物,包括 7mg 的水飞蓟宾 B-5-O-β-D-葡萄糖苷(SG-1)、12mg 的水飞蓟宾 B-3-O-β-D-葡萄糖苷(SG-2)、10mg 的水飞蓟宾 B-7-O-β-D-葡萄糖苷(SG-3)和 24mg 的水飞蓟宾 B-20-O-β-D-葡萄糖苷(SG-4),其纯度分别为 89.3%、95.2%、96.4%和 97.5%。通过光谱分析鉴定了它们的结构。

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