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首页> 外文期刊>The Journal of General and Applied Microbiology >Efficient and direct identification of fructose fermenting and non-fermenting bacteria from calf gut microbiota using stable isotope probing and modified T-RFLP
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Efficient and direct identification of fructose fermenting and non-fermenting bacteria from calf gut microbiota using stable isotope probing and modified T-RFLP

机译:使用稳定的同位素探测和改良的T-RFLP可以直接识别小牛肠道菌群中的果糖发酵菌和非发酵菌

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摘要

The aim of this study was the development of an efficient method to identify the prebiotics-as-similating-bacteria in gut microbiota using DNA-stable isotope probing (DNA-SIP) technology. For efficient probing of microbiota with stable isotopes, a small-scale repeated batch culture using a low-carbon-source-containing medium was developed. Fecal samples from cattle were inoculated and [U-~(13)C]-fructose was applied to the culture after 24 h stabilization. Organic acid production, pH value of the period and the total diversity of microorganisms of the culture were successfully maintained during the chasing period. DNA samples were extracted from the culture and were subjected to isopycnic centrifugation and fractionation in order to separate fructose fermenters from non-fermenters. T-RFLP (Terminal Restriction Fragment Length Polymorphism) and the modified T-RFLP of each fraction suggested that Streptococcus bow's was the most dominant fructose fermenter in this culture. In addition, we improved the modified T-RFLP method and successfully identified Lactobacillus vitulinus and Megasphaella eldenii as minor fructose-fermenters and several species of Clostridium cluster IV as non-fermenters. From these results we concluded that the methods shown here provide a means for assessing the importance of individual prebiotics on gut microbiota.
机译:这项研究的目的是开发一种有效的方法,以利用DNA稳定同位素探测(DNA-SIP)技术鉴定肠道菌群中的益生元作为同化细菌。为了用稳定的同位素有效地探测微生物群,开发了使用含低碳源的培养基进行的小规模重复分批培养。接种牛粪便样品,并在稳定24小时后将[U-〜(13)C]果糖应用于培养物中。在追赶期间成功地维持了有机酸的产生,该时期的pH值和培养物中微生物的总多样性。从培养物中提取DNA样品,并进行等温离心和分级分离,以将果糖发酵罐与非发酵罐分开。 T-RFLP(末端限制性片段长度多态性)和每个部分的修饰T-RFLP表明,链球菌弓是这种培养物中最主要的果糖发酵罐。此外,我们改进了改良的T-RFLP方法,并成功地确定了小分子果糖发酵剂为玻璃乳杆菌和Eldenii大球藻,非发酵剂为梭状芽孢杆菌IV类。根据这些结果,我们得出结论,此处显示的方法为评估各个益生元对肠道菌群的重要性提供了一种方法。

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