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Quantitative monitoring of a hydrogen-producing Clostridium butyricum strain from a continuous-flow, mixed culture bioreactor employing real-time PCR

机译:使用实时PCR对连续流混合培养生物反应器中产氢丁酸梭菌菌株的定量监测

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A quantitative real-time PCR (qrt-PCR) method was developed for quantification of a hydrogen-producing Clostridium butyricum strain. The strain was the main hydrogen producer in a mixed culture bioreactor that was operated on a continuous-flow mode for 156 days. The qrt-PCR target was a segment of 16S rDNA, which was amplified from DNA extracted from bioreactor samples. The amplified target was quantified by measuring lanthanide fluorescence in a time-resolved manner. The linear range of this qrt-PCR assay was 10~2 -10~7 bacterial genomes. The results showed substantial variation (over two orders of magnitude) in the quantity of the target 16S rDNA of C. butyricum during the continuous-flow operation. Hydrogen production rate and butyrate concentration also varied with time. The method is applicable to any selected species in bioreactors and provides valuable insight into bioprocess performance and microbial community structure in complex dynamic systems.
机译:建立了定量实时PCR(qrt-PCR)方法,用于定量产氢丁酸梭菌菌株。该菌株是混合培养生物反应器中主要的氢气产生者,该反应器以连续流模式运行156天。 qrt-PCR靶标是16S rDNA的一个片段,该片段从从生物反应器样品中提取的DNA中扩增而来。通过以时间分辨的方式测量镧系元素荧光来定量扩增的靶标。此qrt-PCR测定的线性范围是10〜2 -10〜7个细菌基因组。结果表明,在连续流操作过程中,丁酸梭菌的目标16S rDNA的数量存在很大的变化(超过两个数量级)。制氢率和丁酸盐浓度也随时间变化。该方法适用于生物反应器中的任何选定物种,并提供了对复杂动态系统中生物过程性能和微生物群落结构的宝贵见解。

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