Finley Brianna K, Hayer Michaela, Mau Rebecca L, Purcell Alicia M, Koch Benjamin J, van Gestel Natasja C, Schwartz Egbert, Hungate Bruce A
Department of Biological Sciences, Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA.
Pathogen and Microbiome Institute, Northern Arizona University, Flagstaff, AZ, USA.
Methods Mol Biol. 2019;2046:137-149. doi: 10.1007/978-1-4939-9721-3_11.
Quantitative stable isotope probing (qSIP) measures rates of taxon-specific element assimilation in intact microbial communities, utilizing substrates labeled with a heavy isotope.The laboratory protocol for qSIP is nearly identical to that for conventional stable isotope probing, with two key additions: (1) in qSIP, qPCR measurements are conducted on each density fraction recovered after isopycnic separation, and (2) in qSIP, multiple density fractions are sequenced spanning the entire range of densities over which nucleic acids were recovered. qSIP goes beyond identifying taxa assimilating a substrate, as it also allows for measuring that assimilation for each taxon within a given microbial community. Here, we describe an analysis process necessary to determine atom fraction excess of a heavy stable isotope added to an environmental sample for a given taxon's DNA.
定量稳定同位素探测(qSIP)利用重同位素标记的底物来测量完整微生物群落中特定分类群元素同化的速率。qSIP的实验室方案与传统稳定同位素探测的方案几乎相同,有两个关键补充:(1)在qSIP中,对等密度分离后回收的每个密度级分进行qPCR测量,(2)在qSIP中,对回收核酸的整个密度范围内的多个密度级分进行测序。qSIP不仅能识别同化底物的分类群,还能测量给定微生物群落中每个分类群的同化情况。在此,我们描述了一个分析过程,该过程对于确定添加到环境样品中的重稳定同位素对于给定分类群DNA的原子分数过量是必要的。