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Updated: Aug 18, 2026

DNA Stable-Isotope Probing (DNA-SIP)
Published on: August 2, 2010
Technical considerations for the use of 15N-DNA stable-isotope probing for functional microbial activity in soils
Georg Cadisch1, Mingrelia Espana, Rachel Causey
1Institute of Plant Production and Agroecology in the Tropics and Subtropics (380a), University of Hohenheim, 70593 Stuttgart, Germany. cadisch@uni-hohenheim.de
Abstract:
Stable-isotope DNA probing is a culture-independent technique that may provide a link between function and phylogeny of active microorganisms. The technique has been used in association with 13C substrates while here we evaluate feasibility and limitations of 15N-DNA stable-isotope probing (SIP) using labelled and unlabelled pure microbial cultures or soil extracts. Our results showed that (15)N-DNA probing is feasible for cultures as well as soil samples. Limitations of 15N-DNA-SIP are (a) the need for relatively large quantities of DNA to visualise bands (although molecular resolution is much higher) and (b) 15N-DNA enrichment needed to ideally be >50 at%; however, this requirement can be lowered to approx. 40 atom% 15N with pure cultures using a modified CsCl centrifugation method (140K g for 69 h). These advances in 15N-DNA-SIP methodology open new opportunities to trace active microbial populations utilising specific N substrates in situ.

