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Immobilization of infant fecal microbiota and utilization in an in vitro colonic fermentation model

机译:婴儿粪便微生物群的固定化及其在体外结肠发酵模型中的利用

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Bacteria isolated from infant feces were immobilized in polysaccharide gel beads (2.5% gellan gum, 0.25% xanthan gum) using a two-phase dispersion process. A 52-day continuous culture was carried out in a single-stage chemostat containing precolonized beads and fed with a medium formulated to approximate the composition of infant chyme. Different dilution rates and pH conditions were tested to simulate the proximal (PCS), transverse (TCS), and distal (DCS) colons. Immobilization preserved all nine bacterial groups tested with survival rates between 3 and 56%. After I week fermentation, beads were highly colonized with all populations tested (excepted Staphylococcus spp. present in low numbers), which remained stable throughout the 7.5 weeks of fermentation, with variations below I log unit. However, free-cell populations in the circulating liquid medium, produced by immobilized cell growth, cell-release activity from gel beads, and free-cell growth, were altered considerably by culture conditions. Compared to the stabilization period, PCS was characterized by a considerable and rapid increase in Bifidobacterium spp. concentrations (7.4 to 9.6 log CFU/mL), whereas Bifidobacterium spp., Lactobacillus spp., and Clostridium spp. concentrations decreased and Staphylococcus spp. and coliforms increased during TCS and DCS. Under pseudo-steady-state conditions, the community structure developed in the chemostat reflected the relative proportions of viable bacterial numbers and metabolites generally encountered in infant feces. This work showed that a complex microbiota such as infant fecal bacteria can be immobilized and used in a continuous in vitro intestinal fermentation model to reproduce the high bacterial concentration and bacterial diversity of the feces inoculum, at least at the genera level, with a high stability during long-term experiment.
机译:使用两阶段分散工艺,将从婴儿粪便中分离出的细菌固定在多糖凝胶珠(2.5%吉兰糖胶,0.25%黄原胶)中。在包含预定殖珠子的单级恒化器中进行52天连续培养,并喂以配制为近似婴儿食糜成分的培养基。测试了不同的稀释率和pH条件,以模拟近端(PCS),横向(TCS)和远端(DCS)结肠。固定化保存了测试的所有九个细菌组,存活率在3%到56%之间。 I周发酵后,珠子在所有测试种群中高度定居(除了葡萄球菌属菌种数量很少),在整个7.5周的发酵过程中保持稳定,变化低于I log单位。但是,循环的液体培养基中由固定化细胞生长,凝胶珠的细胞释放活性和游离细胞生长产生的游离细胞数量,由于培养条件而发生了很大变化。与稳定期相比,PCS的特征是双歧杆菌属物种迅速大量增加。浓度(7.4至9.6 log CFU / mL),而双歧杆菌属,乳杆菌属和梭状芽胞杆菌。浓度下降和葡萄球菌属。在TCS和DCS期间大肠菌群增加。在伪稳态条件下,化学恒温器中形成的群落结构反映了婴儿粪便中通常遇到的存活细菌数量和代谢产物的相对比例。这项工作表明,可以固定复杂的微生物群,例如婴儿粪便细菌,并将其用于连续的体外肠道发酵模型中,以至少在属水平上以高稳定性重现粪便接种物的高细菌浓度和细菌多样性。在长期实验中。

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