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Updated: Jan 21, 2026

DNA Stable-Isotope Probing DNA-SIP
Published on: August 2, 2010
Microbial Taxon-Specific Isotope Incorporation with DNA Quantitative Stable Isotope Probing
Brianna K Finley1, Michaela Hayer2, Rebecca L Mau3
1Department of Biological Sciences, Center for Ecosystem Science and Society, Northern Arizona University, Flagstaff, AZ, USA. bkf24@nau.edu.
Abstract:
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.
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