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Microbial Taxon-Specific Isotope Incorporation with DNA Quantitative Stable Isotope Probing.

Authors :
Finley BK
Hayer M
Mau RL
Purcell AM
Koch BJ
van Gestel NC
Schwartz E
Hungate BA
Source :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2019; Vol. 2046, pp. 137-149.
Publication Year :
2019

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.

Details

Language :
English
ISSN :
1940-6029
Volume :
2046
Database :
MEDLINE
Journal :
Methods in molecular biology (Clifton, N.J.)
Publication Type :
Academic Journal
Accession number :
31407302
Full Text :
https://doi.org/10.1007/978-1-4939-9721-3_11