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利用从人参种植土壤细菌中分离的新型人参皂苷转化β-葡萄糖苷酶提高绞股蓝皂苷LXXV的产量及其抗癌特性

Enhanced Production of Gypenoside LXXV Using a Novel Ginsenoside-Transforming β-Glucosidase from Ginseng-Cultivating Soil Bacteria and Its Anti-Cancer Property.

作者信息

Cui Chang-Hao, Kim Da Jung, Jung Suk-Chae, Kim Sun-Chang, Im Wan-Taek

机构信息

Intelligent Synthetic Biology Center, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Korea.

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Korea.

出版信息

Molecules. 2017 May 19;22(5):844. doi: 10.3390/molecules22050844.

Abstract

Minor ginsenosides, such as compound K, Rg₃(), which can be produced by deglycosylation of ginsenosides Rb₁, showed strong anti-cancer effects. However, the anticancer effects of gypenoside LXXV, which is one of the deglycosylated shapes of ginsenoside Rb₁, is still unknown due to the rarity of its content in plants. Here, we cloned and characterized a novel ginsenoside-transforming β-glucosidase (BglG167b) derived from sp. Gsoil 167 which can efficiently hydrolyze gypenoside XVII into gypenoside LXXV, and applied it to the production of gypenoside LXXV at the gram-scale with high specificity. In addition, the anti-cancer activity of gypenoside LXXV was investigated against three cancer cell lines (HeLa, B16, and MDA-MB231) in vitro. Gypenoside LXXV significantly reduced cell viability, displaying an enhanced anti-cancer effect compared to gypenoside XVII and Rb₁. Taken together, this enzymatic method would be useful in the preparation of gypenoside LXXV for the functional food and pharmaceutical industries.

摘要

次要人参皂苷,如化合物K、Rg₃(),可通过人参皂苷Rb₁的去糖基化产生,具有很强的抗癌作用。然而,人参皂苷LXXV作为人参皂苷Rb₁的去糖基化形式之一,由于其在植物中的含量稀少,其抗癌作用仍不清楚。在此,我们克隆并鉴定了一种源自sp. Gsoil 167的新型人参皂苷转化β-葡萄糖苷酶(BglG167b),该酶可有效地将绞股蓝皂苷XVII水解为人参皂苷LXXV,并将其用于克级规模的人参皂苷LXXV的高特异性生产。此外,还研究了人参皂苷LXXV对三种癌细胞系(HeLa、B16和MDA-MB231)的体外抗癌活性。人参皂苷LXXV显著降低了细胞活力,与绞股蓝皂苷XVII和Rb₁相比,显示出增强的抗癌效果。综上所述,这种酶法在功能性食品和制药行业制备人参皂苷LXXV方面将具有实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2cd/6153937/bff602e8fa73/molecules-22-00844-g001.jpg

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