Cargando…

Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent

Gallic acid glycoside was enzymatically synthesized by using dextransucrase and sucrose from gallic acid. After purification by butanol partitioning and preparative HPLC, gallic acid glucoside was detected at m/z 355 (C(13), H(16), O(10), Na)(+) by matrix-assisted laser desorption ionization time-of...

Descripción completa

Detalles Bibliográficos
Autores principales: Nam, Seung-Hee, Park, Jeongjin, Jun, Woojin, Kim, Doman, Ko, Jin-A, Abd El-Aty, A. M., Choi, Jin Young, Kim, Do-Ik, Yang, Kwang-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741567/
https://www.ncbi.nlm.nih.gov/pubmed/29273963
http://dx.doi.org/10.1186/s13568-017-0523-x
_version_ 1783288202448076800
author Nam, Seung-Hee
Park, Jeongjin
Jun, Woojin
Kim, Doman
Ko, Jin-A
Abd El-Aty, A. M.
Choi, Jin Young
Kim, Do-Ik
Yang, Kwang-Yeol
author_facet Nam, Seung-Hee
Park, Jeongjin
Jun, Woojin
Kim, Doman
Ko, Jin-A
Abd El-Aty, A. M.
Choi, Jin Young
Kim, Do-Ik
Yang, Kwang-Yeol
author_sort Nam, Seung-Hee
collection PubMed
description Gallic acid glycoside was enzymatically synthesized by using dextransucrase and sucrose from gallic acid. After purification by butanol partitioning and preparative HPLC, gallic acid glucoside was detected at m/z 355 (C(13), H(16), O(10), Na)(+) by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The yield of gallic acid glucoside was found to be 35.7% (114 mM) by response surface methodology using a reaction mixture of 319 mM gallic acid, 355 mM sucrose, and 930 mU/mL dextransucrase. The gallic acid glucoside obtained showed 31% higher anti-lipid peroxidation and stronger inhibition (Ki = 1.23 mM) against tyrosinase than that shown by gallic acid (Ki = 1.98 mM). In UVB-irradiated human fibroblast cells, gallic acid glucoside lowered matrix metalloproteinase-1 levels and increased the collagen content, which was indicative of a stronger anti-aging effect than that of gallic acid or arbutin. These results indicated that gallic acid glucoside is likely a superior cosmetic ingredient with skin-whitening and anti-aging functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13568-017-0523-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5741567
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-57415672018-01-23 Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent Nam, Seung-Hee Park, Jeongjin Jun, Woojin Kim, Doman Ko, Jin-A Abd El-Aty, A. M. Choi, Jin Young Kim, Do-Ik Yang, Kwang-Yeol AMB Express Original Article Gallic acid glycoside was enzymatically synthesized by using dextransucrase and sucrose from gallic acid. After purification by butanol partitioning and preparative HPLC, gallic acid glucoside was detected at m/z 355 (C(13), H(16), O(10), Na)(+) by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. The yield of gallic acid glucoside was found to be 35.7% (114 mM) by response surface methodology using a reaction mixture of 319 mM gallic acid, 355 mM sucrose, and 930 mU/mL dextransucrase. The gallic acid glucoside obtained showed 31% higher anti-lipid peroxidation and stronger inhibition (Ki = 1.23 mM) against tyrosinase than that shown by gallic acid (Ki = 1.98 mM). In UVB-irradiated human fibroblast cells, gallic acid glucoside lowered matrix metalloproteinase-1 levels and increased the collagen content, which was indicative of a stronger anti-aging effect than that of gallic acid or arbutin. These results indicated that gallic acid glucoside is likely a superior cosmetic ingredient with skin-whitening and anti-aging functions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13568-017-0523-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-12-22 /pmc/articles/PMC5741567/ /pubmed/29273963 http://dx.doi.org/10.1186/s13568-017-0523-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Nam, Seung-Hee
Park, Jeongjin
Jun, Woojin
Kim, Doman
Ko, Jin-A
Abd El-Aty, A. M.
Choi, Jin Young
Kim, Do-Ik
Yang, Kwang-Yeol
Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title_full Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title_fullStr Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title_full_unstemmed Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title_short Transglycosylation of gallic acid by using Leuconostoc glucansucrase and its characterization as a functional cosmetic agent
title_sort transglycosylation of gallic acid by using leuconostoc glucansucrase and its characterization as a functional cosmetic agent
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741567/
https://www.ncbi.nlm.nih.gov/pubmed/29273963
http://dx.doi.org/10.1186/s13568-017-0523-x
work_keys_str_mv AT namseunghee transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT parkjeongjin transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT junwoojin transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT kimdoman transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT kojina transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT abdelatyam transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT choijinyoung transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT kimdoik transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent
AT yangkwangyeol transglycosylationofgallicacidbyusingleuconostocglucansucraseanditscharacterizationasafunctionalcosmeticagent