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Dong, Wei-Wei,Zhao, Jinhua,Zhong, Fei-Liang,Zhu, Wen-Jing,Jiang, Jun,Wu, Songquan,Yang, Deok-Chun,Li, Donghao,Quan, Lin-Hu The Korean Society of Ginseng 2017 Journal of Ginseng Research Vol.41 No.4
Background: In general, after Panax ginseng is administered orally, intestinal microbes play a crucial role in its degradation and metabolization process. Studies on the metabolism of P. ginseng by microflora are important for obtaining a better understanding of their biological effects. Methods: In vitro biotransformation of P. ginseng extract by rat intestinal microflora was investigated at $37^{\circ}C$ for 24 h, and the simultaneous determination of the metabolites and metabolic profile of P. ginseng saponins by rat intestinal microflora was achieved using LC-MS/MS. Results: A total of seven ginsenosides were detected in the P. ginseng extract, including ginsenosides Rg1, Re, Rf, Rb1, Rc, Rb2, and Rd. In the transformed P. ginseng samples, considerable amounts of deglycosylated metabolite compound K and Rh1 were detected. In addition, minimal amounts of deglycosylated metabolites (ginsenosides Rg2, F1, F2, Rg3, and protopanaxatriol-type ginsenosides) and untransformed ginsenosides Re, Rg1, and Rd were detected at 24 h. The results indicated that the primary metabolites are compound K and Rh1, and the protopanaxadiol-type ginsenosides were more easily metabolized than protopanaxatriol-type ginsenosides. Conclusion: This is the first report of the identification and quantification of the metabolism and metabolic profile of P. ginseng extract in rat intestinal microflora using LC-MS/MS. The current study provided new insights for studying the metabolism and active metabolites of P. ginseng.
Hu, Qicheng,Kim, Seul-Gi,Shin, Dong-Wook,Kim, Tae-Sung,Nam, Ki-Bong,Kim, Mun Ja,Chun, Hwan-Chul,Yoo, Ji-Beom Elsevier 2017 Carbon Vol.113 No.-
<P>In this work, large-scale (120 x 120 mm) nanometer-thick graphite films (NGFs) were synthesized on polycrystalline Ni foils using a 'two-stage' chemical vapor deposition (CVD) process. An intermediate cooling process was included in the CVD process; this process affected the isothermal graphene growth, which is explained using a growth model. We mainly studied a graphite film with the thickness of similar to 40 nm and the good thickness uniformity was characterized by atomic force microscopy (AFM), Raman spectroscopy and extreme ultraviolet (EUV) mapping. The graphite formed on the Ni grain boundary was analyzed by transmission electron microscopy (TEM). The relationships between the thickness, optical and electrical properties of the NGF and growth temperature were also studied. (C) 2016 Elsevier Ltd. All rights reserved.</P>
Chun-Lian Liu,Xiao-Ping Hu,Wei-Dong Guo,Li Yang,Jie Dang,Hai-Yan Jiao 한국유방암학회 2013 Journal of breast cancer Vol.16 No.4
Purpose: Genetic variation in fibroblast growth factor receptor 2(FGFR2) is a newly described risk factor for breast cancer. Thisstudy aimed to evaluate the association of four single nucleotidepolymorphisms (SNPs) in FGFR2 with breast cancer in Han Chinesewomen. Methods: Two hundred three women with breastcancer and 200 breast cancer-free age-matched controls wereselected. Four SNPs (rs2981579, rs1219648, rs2420946, andrs2981582) and their haplotypes were analyzed to test for theirassociation with breast cancer susceptibility. The presence ofthe four FGFR2 SNPs was determined by polymerase chain reaction-restriction fragment length polymorphism analysis. Results:A statistically significant difference was observed in thefrequency of rs2981582 in the FGFR2 gene (p<0.05) betweencase and control groups. In subjects stratified by menopausalstatus, rs2981582 TT, rs2420946 AA, and rs1219648 CC weresignificantly associated with the risk of breast cancer in postmenopausalsubjects, but no significant associations betweenthese four SNPs and the risk of breast cancer were identified inpremenopausal subjects. Further, there was no significant associationbetween hormone receptor status (estrogen receptor andprogesterone receptor) and breast cancer risk. Six common (>3%) haplotypes were identified. Three of these haplotypes,CGTC (odds ratio [OR], 0.613; 95% confidence interval [CI],0.457-0.82; p=0.001), TGTC (OR, 6.561; 95% CI, 2.064-20.854;p<0.001), and CATC (OR, 12.645; 95% CI, 1.742-91.799; p=0.001) were significantly associated with breast cancer risk. Conclusion:Our findings indicated that the SNP rs2981582 and haplotypesCGTC, TGTC, and CATC in FGFR2 may be associatedwith an increased risk of breast cancer in Han Chinese women.
Lin-Hu Quan,Jin-Ying Piao,Jin-Woo Min,Ho-Bin Kim,Sang-Rae Kim,Dong-Uk Yang,Deok Chun Yang 고려인삼학회 2011 Journal of Ginseng Research Vol.35 No.3
Ginsenoside Rb<sub>1</sub>is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb<sub>1</sub> was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F<sub>2</sub> and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30℃. Under optimal conditions, ginsenoside Rb<sub>1</sub> was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by high-performance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb<sub>1</sub>→gypenoside XVII and ginsenoside Rd→ginsenoside F<sub>2</sub>→compound K.
Lin-Hu Quan,Jin-Ying Piao,Jin-Woo Min,Ho-Bin Kim,Sang-Rae Kim,Dong-Uk Yang,Deok Chun Yang 고려인삼학회 2011 Journal of Ginseng Research Vol.35 No.3
Ginsenoside Rb_1is the main component in ginsenosides. It is a protopanaxadiol-type ginsenoside that has a dammarane-type triterpenoid as an aglycone. In this study, ginsenoside Rb_1 was transformed into gypenoside XVII, ginsenoside Rd, ginsenoside F_2 and compound K by glycosidase from Leuconostoc mesenteroides DC102. The optimum time for the conversion was about 72 h at a constant pH of 6.0 to 8.0 and the optimum temperature was about 30°C. Under optimal conditions, ginsenoside Rb_1was decomposed and converted into compound K by 72 h post-reaction (99%). The enzymatic reaction was analyzed by highperformance liquid chromatography, suggesting the transformation pathway: ginsenoside Rb_1→ gypenoside XVII and ginsenoside Rd→ginsenoside F_2→compound K.
Quan, Lin-Hu,Min, Jin-Woo,Yang, Dong-Uk,Kim, Yeon-Ju,Yang, Deok-Chun Springer International 2012 Applied microbiology and biotechnology Vol.94 No.2
<P>Microbacterium esteraromaticum was isolated from ginseng field. The beta-glucosidase gene (bgp1) from M. esteraromaticum was cloned and expressed in Escherichia coli BL21 (DE3). The bgp1 gene consists of 2,496 bp encoding 831 amino acids which have homology to the glycosyl hydrolase family 3 protein domain. The recombinant beta-glucosidase enzyme (Bgp1) was purified and characterized. The molecular mass of purified Bgp1 was 87.5 kDa, as determined by SDS-PAGE. Using 0.1 mg ml(-1) enzyme in 20 mM sodium phosphate buffer at 37A degrees C and pH 7.0, 1.0 mg ml(-1) ginsenoside Rb1 was transformed into 0.444 mg ml(-1) ginsenoside Rg3 within 6 h. The Bgp1 sequentially hydrolyzed the outer and inner glucose attached to the C-20 position of ginsenosides Rb1. Bgp1 hydrolyzed the ginsenoside Rb1 along the following pathway: Rb1 -> aEuro parts per thousand Rd -> aEuro parts per thousand 20(S)-Rg3. This is the first report of the biotransformation of ginsenoside Rb1 to ginsenoside 20(S)-Rg3 using the recombinant beta-glucosidase.</P>
Quan, Lin-Hu,Min, Jin-Woo,Sathiyamoorthy, Subramaniyam,Yang, Dong-Uk,Kim, Yeon-Ju,Yang, Deok-Chun Kluwer Academic Publishers 2012 Biotechnology letters. Vol.34 No.5
<P>Ginsenosides Re and Rg1 were transformed by recombinant 관-glucosidase (Bgp1) to ginsenosides Rg2 and Rh1, respectively. The bgp1 gene consists of 2,496??bp encoding 831 amino acids which have homology to the glycosyl hydrolase families 3 protein domain. Using 0.1??mg enzyme ml(-1) in 20??mM sodium phosphate buffer at 37°C and pH 7.0, the glucose moiety attached to the C-20 position of ginsenosides Re and Rg1, was removed: 1??mg ginsenoside Re ml(-1) was transformed into 0.83??mg Rg2??ml(-1) (100% molar conversion) after 2.5??h and 1??mg ginsenoside Rg1??ml(-1) was transformed into 0.6??mg ginsenoside Rh1??ml(-1) (78% molar conversion) in 15??min. Using Bgp1 enzyme, almost all initial ginsenosides Re and Rg1 were converted completely to ginsenosides Rg2 and Rh1. This is the first report of the conversion of ginsenoside Re to ginsenoside Rg2 and ginsenoside Rg1 to ginsenoside Rh1 using the recombinant 관-glucosidase.</P>