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首页> 外文期刊>Journal of applied microbiology >Evaluation of 16s rRNA and cellular fatty acid profiles as markers of human intestinal bacterial growth in the chemostat
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Evaluation of 16s rRNA and cellular fatty acid profiles as markers of human intestinal bacterial growth in the chemostat

机译:评价16s rRNA和细胞脂肪酸谱作为人在恒化器中肠道细菌生长的标志

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摘要

Chemostats were used to study the effects of carbon and nitrogen limitation and specific growth rate on 16S rRNA synthesis and cellular fatty acid (CFA) profiles in four human intestinal bacteria (Bacteroides thetaiotaomicron, Bifidobacterium adolescentis, Clostridium bifermentans and Cl. difficile). Cellular fatty acid synthesis varied with dilution rate and nutrient availability in different species, but these cellular constituents were relatively stable phenotypic characteristics in Bact. thetaiotaomicron, where branched chain and hydroxy CFA were good taxonomic markers. Conversely, CFA in the Gram-positive bacteria varied markedly with changes in growth environment. For example, in chemostats, cyclopropane CFA were only synthesized in Cl.bifermentans and Cl. difficile under N-limited conditions. Similarly, Dimethyl acetal (DMA) fatty acids in Bif. adolescentis were primarily produced during N-limited growth, and this was inversely related to dilution rate. At low growth rates, 16S rRNA concentrations (#mu#g rRNA per ml culture) correlated with viable bacterial counts, but were more closely related to specific growth rate when expressed sa a function of cell mass (#mu#g rRNA per mg dry weight bacteria). However,this did not reveal differences in bacterial population size and rRNA concentration in C-limited cultures. Thus, at low dilution rates, C limitation strongly reduced rRNA synthesis in Cl. bifermentans, despite viable cell counts being similar to those in N-limited cultures. These results indicate that, while 16S rRNA is a useful indicator of microbial activity, cell growth rate does not necessarily relate to rRNA concentration under all nutritional conditions. Consequently, bowel habit and diet will affect both CFA and rRNA content in bacteria isolated from intestinal samples, and this should be taken into consideration when interpreting such data measurements.
机译:恒化器用于研究碳和氮限制以及特定生长速率对四种人体肠道细菌(拟杆菌,亚双歧杆菌,双歧梭状芽胞杆菌和艰难梭菌)的16S rRNA合成和细胞脂肪酸(CFA)谱的影响。不同物种中细胞脂肪酸合成随稀释率和养分利用率的变化而变化,但这些细胞成分在细菌中具有相对稳定的表型特征。 thetaiotaomicron,其中支链和羟基CFA是良好的分类标记。相反,革兰氏阳性细菌中的CFA随生长环境的变化而显着变化。例如,在化学恒温器中,仅在双歧双歧杆菌和双歧杆菌中合成环丙烷CFA。在N限制条件下艰难。同样,Bif中的二甲基乙缩醛(DMA)脂肪酸。青春期主要在N限制生长期间产生,这与稀释率成反比。在低生长速率下,16S rRNA浓度(每毫升培养物#mu#g rRNA)与活细菌数相关,但当表达为细胞质量的函数时(每毫克干重#mu#g rRNA)与特异性生长速率更紧密相关。重细菌)。然而,这并没有揭示出限碳培养物中细菌种群大小和rRNA浓度的差异。因此,在低稀释率下,C限制会大大降低Cl中的rRNA合成。 Bifermentans,尽管活细胞计数与N限制培养中的相似。这些结果表明,尽管16S rRNA是微生物活性的有用指标,但细胞生长速率并不一定与所有营养条件下的rRNA浓度有关。因此,排便习惯和饮食习惯将影响从肠道样本中分离出的细菌中的CFA和rRNA含量,在解释此类数据测量值时应考虑到这一点。

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