Bioconversion of Ginsenoside Rb1 to Compound K using Leuconostoc lactis DC201
1
조회
0
다운로드
1
인용
0
참고문헌
키워드
초록
Ginseng (Panax ginseng) is frequently used in Asian countries as a traditional medicine. The major components of ginseng are ginsenosides. Among these, ginsenoside compound K has been reported to prevent the formation of malignancy and metastasis of cancer by blocking the formation of tumor and suppressing the invasion of cancer cells. In this study, ginsenoside Rb1 was converted into compound K, via secreted β-glucosidase enzyme from the Leuconostoc lactis DC201 isolated, which was extracted from Kimchi. The strain DC201 was suspended and cultured in MRS broth at 37℃. Subsequently, the residue from the cultured broth supernatant was precipitated with EtOH and then dissolved in 20 mM sodium phosphate buffer (pH 6.0) to obtain an enzyme liquid. Meanwhile, the crude enzyme solution was mixed with ginsenoside Rb1 at a ratio of 1:4 (v/v).The reaction was carried out at 30℃ and 190 rpm for 72 hours, and then analyzed by TLC and HPLC. The result showed that ginsenoside Rb1 was transformed into compound K after 72 hours post reaction.
Abstract
Ginseng (Panax ginseng) is frequently used in Asian countries as a traditional medicine. The major components of ginseng are ginsenosides. Among these, ginsenoside compound K has been reported to prevent the formation of malignancy and metastasis of cancer by blocking the formation of tumor and suppressing the invasion of cancer cells. In this study, ginsenoside Rb1 was converted into compound K, via secreted β-glucosidase enzyme from the Leuconostoc lactis DC201 isolated, which was extracted from Kimchi. The strain DC201 was suspended and cultured in MRS broth at 37℃. Subsequently, the residue from the cultured broth supernatant was precipitated with EtOH and then dissolved in 20 mM sodium phosphate buffer (pH 6.0) to obtain an enzyme liquid. Meanwhile, the crude enzyme solution was mixed with ginsenoside Rb1 at a ratio of 1:4 (v/v).The reaction was carried out at 30℃ and 190 rpm for 72 hours, and then analyzed by TLC and HPLC. The result showed that ginsenoside Rb1 was transformed into compound K after 72 hours post reaction.
참고문헌 (20)
- Chi, H., "Transformation of ginsenosides Rb1 and Re from Panax ginseng by food microorganisms", Biotechnol Lett, 27(11), pp.765~771 (2005)
- Chi, H., "Transformation of ginsenosides Rb2 and Rc from Panax ginseng by food microorganisms", Biol. Pharm. Bull, 28(11), pp.2102~2105 (2005)
- Hall, T.A., "BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95", 98, Nucleic Acids Symp. Ser, pp.1999, 41[DOI]
- Hasegawa, H., "Main ginseng saponin metabolites formed by intestinal bacteria", Planta Med, 62, pp.453~457 (1995)
- Karikura, M., "Studies on absorption, distribution, excretion and metabolism of ginseng saponins. VII. Comparison of the decomposition modes of ginsenoside-Rb1 and Rb2 in the digestive tract of rats", Chem. Pharm. Bull. Tokyo, Japan, 39(9), pp.2357~2361 (1991)
- 김명금, "Sphingopyxis granuli sp. nov., a b-Glucosidase-Producing Bacterium in the Family Sphingomonadaceae in a-4 Subclass of the Proteobacteria", The Journal of Microbiology, 43(2), pp.152~157 (2005), 한국미생물학회
- Kim, S. D, "Production of the convertible enzyme of ginsenoside Rb1 by Rhizopus japonicus", Korean J. Mycology, 17(1), pp.31~34 (1989)
- Kimura, M., "The Neutral Theory of Molecular Evolution" (1983), Cambridge University Press
- Lee, S.J., "Antitumor activity of a novel ginseng saponin metabolite in human pulmonary adenocarcinoma cells resistant to cisplatin", Cancer Letters, 144(1), pp.39~43 (1999)
- Odashima S., "Control of phenotypic expression of cultured B16 melanoma cells by plant glycosides", Cancer Res, 45, pp.2781~2784 (1985)
- Park, S.Y., "Purification and characterization of ginsenoside Rb1-metabolizing beta-glucosidase from Fusobacterium K-60, a human intestinal anaerobic bacterium", Biosci Biotechnol Biochem, 65(5), pp.1163~1169 (2001)
- Saha, B.C., "Production, purification, and characterization of a highly glucose-tolerant novel β-glucosidase from Candida peltata", Appl. Environ. Microbiol, 62, pp.3165~3170 (1996)
- Saitou, N., "The neighbor-joining method: a new method for reconstructing phylogenetic trees", Mol. Biol. Evol, 4, pp.406~425 (1987)
- Ji-Eun Shin, "Cytotoxicity of Compound K (IH-901) and Ginsenoside Rh2, MainBiotransformants of Ginseng Saponins by Bifidobacteria,against Some Tumor Cells", Journal of Ginseng Research, 27(3), pp.7~134 (2003), 고려인삼학회
- Takino, Y., "Studies on the pharmacodynamics of ginsenoside-Rg1, -Rb1 and-Rb2 in rats", YakugakuZasshi, 114(8), pp.550~564 (1994)
- Thompson, J.D., "The CLUSTAL_X windows interface: flexible trategies for multiple sequence alignment aided by quality analysis tools", Nucleic Acids Res, 25, pp.4876~4882 (1997)
- 전림호, "Lactobacillus brevis LH8이 생산하는 효소에 의한 Ginsenoside Rd의 Compound K로의 전환", Journal of Ginseng Research, 32(3), pp.226~231 (2008), 고려인삼학회
- Weisburg, W.G., "16S ribosomal DNA amplification for phylogenetic study", J. Bacteriol, 173, pp.697~703 (1991)
- Yang, S., "Characterization of a thermo stable extacellular β-glucosidase with activities of exoglucanase and transglycosylation from Paecilomyces thermophila", J. Agric. Food Chem, 56, pp.602~608 (2008)
- Zhou, W., "Studies on the preparation, crystal structure and bioactivity of ginsenoside compound K", J. Asian Natural Products Res, 8(6), pp.519~527 (2006)
