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Isolation of catechin-converting human intestinal bacteria.

机译:分离儿茶素的人肠道细菌的分离。

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Aims: To isolate and characterize bacteria from the human intestine that are involved in the conversion of catechins, a class of bioactive polyphenols abundant in the human diet. Methods and Results: Two bacterial strains, rK3 and aK2, were isolated from an epicatechin-converting human faecal suspension. The isolates catalysed individual steps in the degradation of (-)-epicatechin and (+)-catechin. Based on their phenotypic characteristics and 16S rRNA gene sequences, the isolates were identified as Eggerthella lenta and Flavonifractor plautii (formerly Clostridium orbiscindens). Eggerthella lenta rK3 reductively cleaved the heterocyclic C-ring of both (-)-epicatechin and (+)-catechin giving rise to 1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl)propan-2-ol. The conversion of catechin proceeded five times faster than that of epicatechin. Higher (epi)catechin concentrations led to an accelerated formation of the ring fission product without affecting the growth of Eg. lenta rK3. Flavonifractor plautii aK2 further converted 1-(3,4-dihydroxyphenyl)-3-(2,4,6-trihydroxyphenyl)propan-2-ol to 5-(3,4-dihydroxyphenyl)- gamma -valerolactone and 4-hydroxy-5-(3,4-dihydroxyphenyl)valeric acid. Flavonifractor plautii DSM 6740 catalysed the identical reaction indicating it is not strain specific. Conclusions: The conversion of dietary catechins by the isolated Eg. lenta and F. plautii strains in the human intestine may affect their bioavailability. Significance and Impact of the Study: The majority of catechin metabolites are generated by the intestinal microbiota. The identification of catechin-converting gut bacteria therefore contributes to the elucidation of the bioactivation and the health effects of catechins.
机译:目的:从人肠中分离和表征参与儿茶素转化的细菌,儿茶素是人类饮食中丰富的一类生物活性多酚。方法和结果:从转化表儿茶素的人类粪便悬液中分离出两个细菌菌株rK3和aK2。分离物催化(-)-表儿茶素和(+)-儿茶素降解的各个步骤。根据它们的表型特征和16S rRNA基因序列,分离物被鉴定为兰氏鼠疫杆菌和黄藻分枝杆菌(以前称为梭状梭状芽孢杆菌)。 Eggerthella lenta rK3还原裂解(-)-表儿茶素和(+)-儿茶素的杂环C环,生成1-(3,4-二羟基苯基)-3-(2,4, 6-三羟苯基)丙-2-醇。儿茶素的转化速度比表儿茶素快五倍。较高的表儿茶素浓度导致环裂变产物的加速形成,而不会影响Eg的生长。 lenta rK3。 Flavonifractor plautii aK2进一步将1-(3,4-二羟基苯基)-3-(2,4,6-三羟基苯基)丙-2-醇转化为5-(3,4-二羟基苯基)-γ -戊内酯和4-羟基-5-(3,4-二羟基苯基)戊酸。 Flavonifractor plautii DSM 6740催化了相同的反应,表明该反应不是菌株特异性的。结论:分离出的 Eg可转化饮食中的儿茶素。 lenta 和 F。人肠中的plautii菌株可能会影响其生物利用度。研究的意义和影响:儿茶素的大部分代谢产物是由肠道菌群产生的。因此,识别儿茶素的肠道细菌有助于阐明儿茶素的生物活性和健康影响。

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