[KSCI] Korea Science Citation Index Service

http://dx.doi.org/10.1016/j.jgr.2016.12.009

Rare ginsenoside Ia synthesized from F1 by cloning and overexpression of the UDP-glycosyltransferase gene from Bacillus subtilis: synthesis, characterization, and in vitro melanogenesis inhibition activity in BL6B16 cells

Wang, Dan-Dan (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)
Jin, Yan (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)
Wang, Chao (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)
Kim, Yeon-Ju (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)
Perez, Zuly Elizabeth Jimenez (Graduate School of Biotechnology, College of Life Science, Kyung Hee University)
Baek, Nam In (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)
Mathiyalagan, Ramya (Graduate School of Biotechnology, College of Life Science, Kyung Hee University)
Markus, Josua (Graduate School of Biotechnology, College of Life Science, Kyung Hee University)
Yang, Deok-Chun (Department of Oriental Medicinal Biotechnology, Ginseng Bank, College of Life Science, Kyung Hee University)

Publication Information

Journal of Ginseng Research / v.42, no.1, 2018 , pp. 42-49 More about this Journal

Abstract

Background: Ginsenoside F1 has been described to possess skin-whitening effects on humans. We aimed to synthesize a new ginsenoside derivative from F1 and investigate its cytotoxicity and melanogenesis inhibitory activity in B16BL6 cells using recombinant glycosyltransferase enzyme. Glycosylation has the advantage of synthesizing rare chemical compounds from common compounds with great ease. Methods: UDP-glycosyltransferase (BSGT1) gene from Bacillus subtilis was selected for cloning. The recombinant glycosyltransferase enzyme was purified, characterized, and utilized to enzymatically transform F1 into its derivative. The new product was characterized by NMR techniques and evaluated by MTT, melanin count, and tyrosinase inhibition assay. Results: The new derivative was identified as (20S)- $3{\beta},6{\alpha},12{\beta}$ ,20-tetrahydroxydammar-24-ene-20-O- ${\beta}$ -D-glucopyranosyl-3-O- ${\beta}$ -D-glucopyranoside(ginsenoside Ia), which possesses an additional glucose linked into the C-3 position of substrate F1. Ia had been previously reported; however, no in vitro biological activity was further examined. This study focused on the mass production of arduous ginsenoside Ia from accessible F1 and its inhibitory effect of melanogenesis in B16BL6 cells. Ia showed greater inhibition of melanin and tyrosinase at $100{\mu}mol/L$ than F1 and arbutin. These results suggested that Ia decreased cellular melanin synthesis in B16BL6 cells through downregulation of tyrosinase activity. Conclusion: To our knowledge, this is the first study to report on the mass production of rare ginsenoside Ia from F1 using recombinant UDP-glycosyltransferase isolated from B. subtillis and its superior melanogenesis inhibitory activity in B16BL6 cells as compared to its precursor. In brief, ginsenoside Ia can be applied for further study in cosmetics.

Keywords

UDP-glycosyltransferase; ginsenoside F1; melanogenesis; ginsenoside Ia; B16BL6 cell line;

Citations & Related Records

Times Cited By KSCI : 3 (Citation Analysis)

Reference
Cited By KSCI

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