Insights in the recalcitrance of theasinensin a to human gut microbial degradation

Jean Paul Vincken*, Zhibin Liu, Wouter J.C. De Bruijn, Mark G. Sanders, Sisi Wang, Marieke E. Bruins

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Due to low bioavailability of dietary phenolic compounds in small intestine, their metabolism by gut microbiota is gaining increasing attention. The microbial metabolism of theasinensin A (TSA), a bioactive catechin dimer found in black tea, has not been studied yet. Here, TSA was extracted and purified for in vitro fermentation by human fecal microbiota, and epigallocatechin gallate (EGCG) and procyanidin B2 (PCB2) were used for comparison. Despite the similarity in their flavan-3-ol skeletons, metabolic fate of TSA was distinctively different. After degalloylation, its core biphenyl-2,2',3,3',4,4'-hexaol structure remained intact during fermentation. Conversely, EGCG and PCB2 were promptly degraded into a series of hydroxylated phenylcarboxylic acids. Computational analyses comparing TSA and PCB2 revealed that TSA's stronger interflavanic bond and more compact stereoconfiguration might underlie its lower fermentability. These insights in the recalcitrance of theasinensins to degradation by human gut microbiota are of key importance for a comprehensive understanding of its health benefits.

Original languageEnglish
Pages (from-to)2477–2484
JournalJournal of Agricultural and Food Chemistry
Volume69
Issue number8
DOIs
Publication statusPublished - 23 Feb 2021

Keywords

  • Bond dissociation enthalpy
  • Gut microbiota
  • Microbial degradation
  • Theasinensins
  • UHPLC-Q-Orbitrap-MS

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