Technical considerations for the use of 15N-DNA stable-isotope probing for functional microbial activity in soils

被引:45
作者
Cadisch, G [1 ]
Espana, M
Causey, R
Richter, M
Shaw, E
Morgan, JAW
Rahn, C
Bending, GD
机构
[1] Univ Hohenheim, Inst Plant Prod & Agroecol Trop & Subtrop 380A, D-70593 Stuttgart, Germany
[2] Univ London Imperial Coll Sci & Technol, Dept Agr Sci, Wye TN25 5AH, England
[3] Natl Inst Agr Res CENIAP, Maracay, Venezuela
[4] Univ Warwick, Warwick HRI, Warwick CV35 9EF, England
关键词
D O I
10.1002/rcm.1908
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 C-13 substrates while here we evaluate feasibility and limitations of N-15-DNA stable-isotope probing (SIP) using labelled and unlabelled pure microbial cultures or soil extracts. Our results showed that N-15-DNA probing is feasible for cultures as well as soil samples. Limitations of N-15-DNA-SIP are (a) the need for relatively large quantities of DNA to visualise bands (although molecular resolution is much higher) and (b) N-15-DNA enrichment needed to ideally be > 50 at%; however, this requirement can be lowered to approx. 40 atom% N-15 with pure cultures using a modified CsCl centrifugation method (140Kg for 69h). These advances in N-15-DNA-SIP methodology open new opportunities to trace active microbial populations utilising specific N substrates in situ. Copyright © 2005 John Wiley & Sons, Ltd.
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页码:1424 / 1428
页数:5
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