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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2017
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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 |
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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 |
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