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通过对柴胡皂苷的重组酶水解生产柴胡皂醇 F、柴胡皂醇 G、柴胡醇 F 和柴胡醇 G 及其抗癌作用。

Production of Prosaikogenin F, Prosaikogenin G, Saikogenin F and Saikogenin G by the Recombinant Enzymatic Hydrolysis of Saikosaponin and their Anti-Cancer Effect.

机构信息

Department of Biotechnology, Major in Applied Biotechnology, Hankyong National University, 327 Chungang-no, Anseong-si 17579, Gyeonggi-do, Korea.

AceEMzyme Co., Ltd., Academic Industry Cooperation, 327 Chungang-no, Anseong-si 17579, Gyeonggi-do, Korea.

出版信息

Molecules. 2022 May 19;27(10):3255. doi: 10.3390/molecules27103255.

DOI:10.3390/molecules27103255
PMID:35630731
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9145717/
Abstract

The saponins of L., saikosaponins, are the major components responsible for its pharmacological and biological activities. However, the anti-cancer effects of prosaikogenin and saikogenin, which are glycoside hydrolyzed saikosaponins, are still unknown due to its rarity in plants. In this study, we applied two recombinant glycoside hydrolases that exhibit glycoside cleavage activity with saikosaponins. The two enzymes, BglPm and BglLk, were cloned from and , and exhibited good activity between 30-37 °C and pH 6.5-7.0. Saikosaponin A and D were purified and obtained from the crude L. extract using preparative high performance liquid chromatography technique. Saikosaponin A and D were converted into saikogenin F via prosaikogenin F, and saikogenin G via prosaikogenin G using enzyme transformation with high β-glycosidase activity. The two saikogenin and two prosaikogenin compounds were purified using a silica column to obtain 78.1, 62.4, 8.3, and 7.5 mg of prosaikogenin F, prosaikogenin G, saikogenin F, and saikogenin G, respectively, each with 98% purity. The anti-cancer effect of the six highly purified saikosaponins was investigated in the human colon cancer cell line HCT 116. The results suggested that saikosaponins and prosaikogenins markedly inhibit the growth of the cancer cell line. Thus, this enzymatic technology could significantly improve the production of saponin metabolites of L.

摘要

党参中的甾体皂苷是其主要的药理和生物活性成分。然而,由于其在植物中较为罕见,糖苷水解后得到的原柴胡皂苷和柴胡皂苷的抗癌作用尚不清楚。在本研究中,我们应用了两种具有柴胡皂苷糖苷裂解活性的重组糖苷水解酶。这两种酶,BglPm 和 BglLk,分别从 和 中克隆得到,在 30-37°C 和 pH6.5-7.0 之间表现出良好的活性。柴胡皂苷 A 和 D 从粗党参提取物中通过制备高效液相色谱技术进行分离纯化得到。柴胡皂苷 A 和 D 分别通过具有高β-糖苷酶活性的酶转化为原柴胡皂苷 F 和柴胡皂苷 G。利用硅胶柱色谱法进一步分离纯化两种柴胡皂苷元和两种原柴胡皂苷元,得到 78.1、62.4、8.3 和 7.5mg 的原柴胡皂苷 F、原柴胡皂苷 G、柴胡皂苷 F 和柴胡皂苷 G,纯度均为 98%。研究了六种高度纯化的柴胡皂苷对人结肠癌细胞系 HCT 116 的抗癌作用。结果表明,柴胡皂苷和原柴胡皂苷显著抑制癌细胞系的生长。因此,这种酶促技术可以显著提高党参中皂苷代谢物的产量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/de9ae4f20a2f/molecules-27-03255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/36dfe6f8b228/molecules-27-03255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/6b7097a4839e/molecules-27-03255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/3fa68eb86399/molecules-27-03255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/69a447b63261/molecules-27-03255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/de9ae4f20a2f/molecules-27-03255-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/36dfe6f8b228/molecules-27-03255-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/6b7097a4839e/molecules-27-03255-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/3fa68eb86399/molecules-27-03255-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/69a447b63261/molecules-27-03255-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33c9/9145717/de9ae4f20a2f/molecules-27-03255-g005.jpg

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