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BIOTRANSFORMATION OF GINSENOSIDE Rb_1 INTO F-2 AND COMPOUND K BY BACTERIUM Sphingomonas sp. BG 25

机译:人参鞘脂单胞菌将人参皂甙Rb_1生物转化为F-2和化合物K。 BG 25

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摘要

Triterpenoid saponins and ginsenosides, the majority of which contain protopanaxadiol or protopanaxatriol as the aglycon, are important biologically active compounds of Panax ginseng C. A. Meyer. One of the principal ginsenosides, Rb_1 (1), has β-sophorose and β-gentiobiose residues in the C-3 and C-20 positions, respectively, of 20(S)-protopanaxadiol. The minor ginsenoside F-2 (2) with glucose residues on C-3 and C-20 and compound K (3) with only one glucose on C-20 have structures close to that of Rb_1 and are practically absent in ginseng roots [1]. Saponins 2 and 3 have broader spectra of biological activity than Rb_1. For example, compound K inhibits growth of cultivated melanoma B16-B6, hepatocellular carcinoma Hep-G2, and lung carcinoma 95-D cells whereas F-2 induces apoptosis of breast cancer stem cells [1, 2].
机译:三萜类皂苷和人参皂苷是人参的重要生物活性化合物,其中大多数都含有前托那沙糖醇或前托那沙三醇作为糖苷配基。一种主要的人参皂甙Rb_1(1)在20(S)-原托那沙糖醇的C-3和C-20位置分别具有β-槐糖和β-龙胆二糖残基。人参皂甙F-2(2)在C-3和C-20上具有葡萄糖残基,而化合物K(3)在C-20上仅具有一个葡萄糖,其结构与Rb_1接近,实际上在人参根中不存在[1]。 ]。皂苷2和3具有比Rb_1更大的生物活性谱。例如,化合物K抑制培养的黑素瘤B16-B6,肝细胞癌Hep-G2和肺癌95-D细胞的生长,而F-2诱导乳腺癌干细胞的凋亡[1、2]。

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