Characterization of the metabolism of 5-hydroxymethylfurfural by human intestinal microflora using ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry

化学 色谱法 细菌 人类粪便 葡萄糖醛酸化 代谢物 新陈代谢 质谱法 微生物代谢 大肠杆菌 生物化学 代谢途径 生物 微粒体 遗传学 基因
作者
Min Zhao,Jun Xu,Dawei Qian,Jianming Guo,Shu Jiang,Erxin Shang,Jin‐Ao Duan,Leyue Du
出处
期刊:Analytical Methods [Royal Society of Chemistry]
卷期号:6 (11): 3826-3826 被引量:9
标识
DOI:10.1039/c4ay00596a
摘要

5-Hydroxymethylfurfural (5-HMF), isolated from a wide range of heat-processed foods and medicines, exhibits a variety of pharmacological activities and biological effects. The human intestinal microbiota might have an important impact on drug metabolism and ultimately on the drug oral bioavailability. However, the interactions of this active compound with intestinal bacteria are not clear. In this work, different pure bacteria from human feces were isolated and used to investigate their conversion capability of 5-HMF compared with the mixed intestinal bacteria. The ultra-performance liquid chromatography/quadrupole-time-of-flight mass spectrometry (UPLC-Q-TOF/MS) technique combined with the Metabolynx™ software was applied to analyze 5-HMF and its metabolites. Compared with blank samples, the parent compound and three metabolites were detected and tentatively identified based on the characteristics of their protonated ions. The metabolites were produced by three main metabolic pathways including methylation, acetylation and glucuronidation. 5-HMF could be converted to its methylated product (M1) by the majority of the isolated intestinal bacteria and the mixed intestinal bacteria. However, acetylated 5-HMF (M2) was obtained from the minor bacterial samples like Bacteroides sp. 45 and glucuronidated 5-HMF (M3) was detected only in the sample of Escherichia sp. 88. The metabolic routes and metabolites of 5-HMF produced by human intestinal bacteria were reported for the first time. This study will be very helpful for further investigation of the pharmacokinetic research of 5-HMF in vivo.

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