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- W2553433893 abstract "Epigallocatechin gallate (EGCG) is the most abundant catechin found in the leaves of green tea, Camellia sinensis. In this study, novel epigallocatechin gallate-glucocides (EGCG-Gs) were synthesized by using dextransucrase from Leuconostoc mesenteroides B-1299CB4. Response surface methodology was adopted to optimize the conversion of EGCG to EGCG-Gs, resulting in a 91.43% conversion rate of EGCG. Each EGCG-G was purified using a C18 column. Of nine EGCG-Gs identified by nuclear magnetic resonance analysis, five EGCG-Gs (2 and 4-7) were novel compounds with yields of 2.2-22.6%. The water solubility of the five novel compounds ranged from 229.7 to 1878.5 mM. The 5'-OH group of EGCG-Gs expressed higher antioxidant activities than the 4'-OH group of EGCG-Gs. Furthermore, glucosylation at 7-OH group of EGCG-Gs was found to be responsible for maintaining tyrosinase inhibitory activity and increasing browning-resistant activities." @default.
- W2553433893 created "2016-11-30" @default.
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- W2553433893 date "2016-11-28" @default.
- W2553433893 modified "2023-10-16" @default.
- W2553433893 title "Functional Properties of Novel Epigallocatechin Gallate Glucosides Synthesized by Using Dextransucrase from <i>Leuconostoc mesenteroides</i> B-1299CB4" @default.
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- W2553433893 doi "https://doi.org/10.1021/acs.jafc.6b04236" @default.
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