Synthesis and characterization of hydroquinone glucoside using Leuconostoc mesenteroides dextransucrase
| Autor: | Jin-Ha Lee, Jin Kang, Eun-Seong Seo, Doman Kim, Ghahyun J. Kim, Go-Eun Kim |
|---|---|
| Rok vydání: | 2009 |
| Předmět: |
Sucrose
biology Hydroquinone Silica gel Stereochemistry Butanol Bioengineering biology.organism_classification Applied Microbiology and Biotechnology Biochemistry Dextransucrase chemistry.chemical_compound Column chromatography chemistry Glucoside Leuconostoc mesenteroides Biotechnology Nuclear chemistry |
| Zdroj: | Enzyme and Microbial Technology. 45:355-360 |
| ISSN: | 0141-0229 |
| DOI: | 10.1016/j.enzmictec.2009.07.011 |
| Popis: | We synthesized a hydroquinone glucoside (HG) as a potential skin-whitening agent using Leuconostoc mesenteroides (B-1299CB BF563) dextransucrase with hydroquinone (HQ) as an acceptor and sucrose as a donor. The product was purified using butanol partitioning and silica gel column chromatography. The structure of the purified HG was determined by nuclear magnetic resonance and the ionic product was observed at m / z 295 (C12, H16, O7 Na) + . HG was identified as 4-hydroxyphenyl-α- d -glucopyranoside. The optimum condition of HG synthesis, determined using a response surface methodology, was 450 mM HQ, 215 mM sucrose, and 0.55 U/mL dextransucrase; the final HG produced was 544 mg/L. The IC 50 of diphenylpicryl-hydrazyl scavenging activity was 3.85 mM indicating a higher antioxidant activity compared to β-arbutin (IC 50 = 6.04 mM). HG-mediated inhibition of lipid peroxidation was 3.51% that of HQ (100%) and much higher than that of β-arbutin (0.81% of HQ). In addition the IC 50 value of nitrite-scavenging activity was 14.76 mM showing a superior scavenging activity to that of β-arbutin (IC 50 = 27.09 mM). |
| Databáze: | OpenAIRE |
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