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Utilization of major fucosylated and sialylated human milk oligosaccharides by isolated human gut microbes

机译:分离的人肠道微生物对主要岩藻糖基化和唾液酸化人乳寡糖的利用

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摘要

Human milk oligosaccharides (HMOS) are not digested in the proximal intestine. In distal intestine, HMOS collectively modify the microbiota, but the response of individual bacteria to individual components of the HMOS is not well defined. Here, each of 25 major isolates of the human intestinal microbiota was fed individual major fucosylated and sialylated HMOS in anaerobic culture. This allowed for an assessment of the influence of specific HMOS on the growth and metabolic products of individual microbiota bacteria. Most Bifidobacteria spp. and Bacteroides spp. grew, induced α-l-fucosidase activity, and produced abundant lactate or short-chain fatty acids (SCFAs) when fed 2′-fucosyllactose (2′-FL), 3-FL, and lactodifucotetraose (LDFT). Lactobacillus delbrueckii ATCC7830, Enterococcus faecalis ATCC19433, and Streptococcus thermophilus ATCC19258 exhibited slight growth, pH reduction, and lactate production when supplemented with 2′-FL or 3-FL, but not LDFT. Supplementation with 3′-sialyllactose (3′-SL) and 6′-SL promoted moderate growth of Bifidobacterium longum JCM7007, 7009, 7010, 7011, 1272, 11347, ATCC15708, Bacteroides vulgatus ATCC8482, and B. thetaiotaomicron ATCC29148; accordingly, these bacteria exhibited greater neuraminidase activity and produced copious lactate, SCFA, or both. Lactobacillus delbrueckii ATCC7830 also consumed 6′-SL. In contrast, Clostridium spp., L. rhamnosus ATCC53103, E. faecalis ATCC29200, Staphylococcus spp., Enterobacter spp., and Escherichia coli K12 did not consume milk oligosaccharides nor produce appreciable acidic fermentation products. Specific Bifidobacteria and Bacteroides differentially digest specific individual HMOS, with the major fucosylated milk oligosaccharides most strongly stimulating key species of mutualist symbionts. This suggests strategies for treating dysbiosis of the microbiota and associated inflammatory disorders.
机译:人乳寡糖(HMOS)在近端肠中不被消化。在远端肠中,HMOS共同修饰了微生物群,但单个细菌对HMOS单个成分的反应尚不明确。在这里,在厌氧培养中,分别给人肠道菌群的25个主要分离株分别喂食了主要的岩藻糖基化和唾液酸化HMOS。这可以评估特定HMOS对单个微生物群细菌的生长和代谢产物的影响。大多数双歧杆菌属。和拟杆菌属。当喂食2'-岩藻糖半乳糖(2'-FL),3-FL和乳二葡糖四糖(LDFT)时,其生长,诱导α-1-岩藻糖苷酶活性并产生大量的乳酸或短链脂肪酸(SCFA)。补充2'-FL或3-FL,但不添加LDFT时,德氏乳杆菌ATCC7830,粪肠球菌ATCC19433和嗜热链球菌ATCC19258表现出轻微的生长,pH降低和乳酸生成。补充3'-唾液酸乳糖(3'-SL)和6'-SL促进长双歧杆菌JCM7007、7009、7010、7011、1272、11347,ATCC15708,寻常小杆菌(Bacteroides vulgatus)ATCC8482和B. thetaiotaomicron ATCC29148的中等生长;因此,这些细菌表现出更大的神经氨酸酶活性并产生大量乳酸,SCFA或两者。德氏乳杆菌ATCC7830也消耗了6'-SL。相反,梭状芽胞杆菌属,鼠李糖乳杆菌ATCC53103,粪肠球菌ATCC29200,葡萄球菌属,肠杆菌属和大肠杆菌K12既不消耗牛奶寡糖也不产生明显的酸性发酵产物。特定的双歧杆菌和拟杆菌分别消化特定的HMOS,其中主要的岩藻糖基化牛奶寡糖最强烈地刺激了共生共生体的关键物种。这提出了治疗微生物菌群失调和相关炎性疾病的策略。

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