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Absolute Quantification of Individual Biomass Concentrations in a Methanogenic Coculture

机译:产甲烷共培养物中单个生物质浓度的绝对定量

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摘要

Identification of individual biomass concentrations is a crucial step towards an improved understanding of anaerobic digestion processes and mixed microbial conversions in general. The knowledge of individual biomass concentrations allows for the calculation of biomass specific conversion rates which form the basis of anaerobic digestion models. Only few attempts addressed the absolute quantification of individual biomass concentrations in methanogenic microbial ecosystems which has so far impaired the calculation of biomass specific conversion rates and thus model validation. This study proposes a quantitative PCR (qPCR) approach for the direct determination of individual biomass concentrations in methanogenic microbial associations by correlating the native qPCR signal (cycle threshold, Ct) to individual biomass concentrations (mg dry matter/L). Unlike existing methods, the proposed approach circumvents error-prone conversion factors that are typically used to convert gene copy numbers or cell concentrations into actual biomass concentrations. The newly developed method was assessed and deemed suitable for the determination of individual biomass concentrations in a defined coculture of Desulfovibrio sp. G11 and Methanospirillum hungatei JF1. The obtained calibration curves showed high accuracy, indicating that the new approach is well suited for any engineering applications where the knowledge of individual biomass concentrations is required.
机译:一般而言,鉴定单个生物质浓度是改善对厌氧消化过程和混合微生物转化的理解的关键步骤。单个生物质浓度的知识允许计算生物质比转化率,这构成了厌氧消化模型的基础。只有很少的尝试解决了产甲烷微生物生态系统中单个生物质浓度的绝对定量问题,到目前为止,这已经损害了生物质比转化率的计算并因此影响了模型验证。这项研究提出了一种定量PCR(qPCR)方法,通过将天然qPCR信号(循环阈值,Ct)与单个生物质浓度(mg干物质/ L)相关联,直接确定产甲烷微生物协会中单个生物质的浓度。与现有方法不同,所提出的方法规避了易于出错的转换因子,该因子通常用于将基因拷贝数或细胞浓度转换为实际的生物质浓度。对新开发的方法进行了评估,并认为它适合于确定的Desulfovibrio sp。共培养物中单个生物量的浓度。 G11和Methanospirillum hungatei JF1。所获得的校准曲线显示出较高的准确性,表明该新方法非常适合需要了解单个生物质浓度的任何工程应用。

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