Analysis of tyrosinase binders from Glycyrrhiza uralensis root: Evaluation and comparison of tyrosinase immobilized magnetic fishing-HPLC and reverse ultrafiltration-HPLC
Abstract
Tyrosinase inhibitors play an important role in cosmetic products, food supplements and medicinal industries. In this study, a new facile method based on tyrosinase immobilized magnetic fishing (IMF) coupled with high performance liquid chromatography-diode array detector-tandem mass spectrometry (HPLC-DAD-MS/MS) was developed to screen and identify tyrosinase binders from Glycyrrhiza uralensis root. Experiments were carried out to select optimal immobilization and incubation conditions. The activity of immobilized tyrosinase retained 76.3% after ten consecutive cycles, and remained over 95% when stored at 4°C for about two months. Eleven tyrosinase binders, including original compounds and transformation products were successfully screened and characterized from G. uralensis root, while dihydrodaidzein and pratensein were reported for the first time. Compared with ultrafiltration-HPLC assay, IMF-HPLC displayed many attractive advantages, including convenient solid-liquid separation ability, good stability, high reusability and activity, which indicated that IMF-HPLC had a broad applicability. The results indicated that IMF-HPLC method is a facile, effective and reproductive way to screen and identify active components from complex mixtures.
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Secondary metabolites of G. uralensis root including liquiritin apioside, neolicuroside, liquiritigenin, licorice saponin G2, chrysoeriol, dihydrodaidzein, formononetin, glycyrrhisoflavanone, glycyrrhizinic acid, licoarylcoumarin, and pratensein inhibit tyrosinase activity.
“Secondary metabolites of G. uralensis root such as liquiritin apioside, neolicuroside, liquiritigenin, licorice saponin G2, chrysoeriol, dihydrodaidzein, formononetin, glycyrrhisoflavanone, glycyrrhizinic acid, licoarylcoumarin, and pratensein showed the capacity to inhibit tyrosinase activity [45].”
From Licorice (Glycyrrhiza glabra, G. uralensis, and G. inflata) and Their Constituents as Active Cosmeceutical Ingredients (2022) · cites this paper as [45]
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Cerulli, A., Masullo, M., Montoro, P., & Piacente, S. (2022) · Cosmetics · doi:10.3390/cosmetics9010007 · Cited by 83 · see citing works
Profiling of Tyrosinase Inhibitors in Mango Leaves for a Sustainable Agro-Industry
Shi, F., Xie, L., Lin, Q., Tong, C., Fu, Q., Xu, J., Xiao, J., & Shi, S. (2020) · Food Chemistry · doi:10.1016/j.foodchem.2019.126042 · Cited by 47 · see citing works
Self-citation
- Authors
- Liu, L., Shi, S., Chen, X., & Peng, M.
- Affiliations
- Central South University (CN)
- Jishou University (CN)
- Corresponding author
- Shi, Shuyun
- Chen, Xiaoqing
- Venue
- Journal of Chromatography B
- Publisher
- Elsevier BV
- Published
- 2013-08
- Volume
- 932
- Pages
- 19-25
- ISSN
- 1570-0232 (ISSN-L)
- OpenAlex
- W2067664537
- Cited by
- 33
- References
- 0
- Citations by year
- 2026: 1 · 2024: 4 · 2023: 1 · 2022: 3 · 2021: 4 · 2020: 1 · 2019: 4 · 2018: 2 · 2016: 5 · 2015: 3 · 2014: 3 · 2013: 2
- FWCI
- 4.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Chromatography B (publishedVersion)
- PubMed (publishedVersion)
- Journal of Chromatography A
- Topics
- Physical Sciences › Chemistry › Analytical Chemistry › Chromatography in Natural Products
- Health Sciences › Medicine › Complementary and alternative medicine › Traditional Chinese Medicine Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioactive natural compounds
- Keywords
- tyrosinase inhibitors, dihydrodaidzein, enzyme immobilization, enzyme reusability, degradation intermediates
- MeSH terms
- Agaricales, Chromatography, High Pressure Liquid, Enzyme Inhibitors, Enzymes, Immobilized, Plant Extracts, Monophenol Monooxygenase, Ultrafiltration, Plant Roots, Glycyrrhiza uralensis, Tandem Mass Spectrometry, Magnetite Nanoparticles
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