Department of Biotechnology, Delft University of Technology, Julianalaan 67, Delft, 2628 BC, The Netherlands.
AMB Express. 2014 Apr 12;4:35. doi: 10.1186/s13568-014-0035-x. eCollection 2014.
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.
确定单个生物质浓度是深入了解厌氧消化过程和混合微生物转化的关键步骤。了解单个生物质浓度可以计算生物质特异性转化率,这是厌氧消化模型的基础。目前为止,只有少数尝试用于确定产甲烷微生物生态系统中单个生物质浓度的绝对定量,这限制了生物质特异性转化率的计算和模型验证。本研究提出了一种通过将天然 qPCR 信号(循环阈值,Ct)与单个生物质浓度(mg 干物质/L)相关联来直接确定产甲烷微生物群落中单个生物质浓度的定量 PCR(qPCR)方法。与现有方法不同,所提出的方法避免了通常用于将基因拷贝数或细胞浓度转换为实际生物质浓度的易错转换因子。新开发的方法经过评估,适用于脱硫弧菌 G11 和产甲烷八叠球菌 JF1 的定义共培养物中单个生物质浓度的测定。所得校准曲线显示出高精度,表明该新方法非常适合任何需要单个生物质浓度知识的工程应用。