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

被引:47
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
相关论文
共 13 条
[1]  
Birnie GD, 1978, CENTRIFUGAL SEPARATI, P169
[2]   Use of stable-isotope probing, full-cycle rRNA analysis, and fluorescence in situ hybridization-microautoradiography to study a methanol-fed denitrifying microbial community [J].
Ginige, MP ;
Hugenholtz, P ;
Daims, H ;
Wagner, M ;
Keller, J ;
Blackall, LL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (01) :588-596
[3]  
HEWITT EJ, 1952, SAND WATER CULTURE M
[4]   Analysis of methanotrophic bacteria in Movile Cave by stable isotope probing [J].
Hutchens, E ;
Radajewski, S ;
Dumont, MG ;
McDonald, IR ;
Murrell, JC .
ENVIRONMENTAL MICROBIOLOGY, 2004, 6 (02) :111-120
[5]   Enhanced sensitivity of DNA- and rRNA-based stable isotope probing by fractionation and quantitative analysis of isopycnic centrifugation gradients [J].
Lueders, T ;
Manefield, M ;
Friedrich, MW .
ENVIRONMENTAL MICROBIOLOGY, 2004, 6 (01) :73-78
[6]   Technical considerations for RNA-based stable isotope probing: an approach to associating microbial diversity with microbial community function [J].
Manefield, M ;
Whiteley, AS ;
Ostle, N ;
Ineson, P ;
Bailey, MJ .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (23) :2179-2183
[7]   RNA stable isotope probing, a novel means of linking microbial community function to Phylogeny [J].
Manefield, M ;
Whiteley, AS ;
Griffiths, RI ;
Bailey, MJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (11) :5367-5373
[8]   Stable-isotope probing of nucleic acids: a window to the function of uncultured microorganisms [J].
Radajewski, S ;
McDonald, IR ;
Murrell, JC .
CURRENT OPINION IN BIOTECHNOLOGY, 2003, 14 (03) :296-302
[9]   Stable-isotope probing as a tool in microbial ecology [J].
Radajewski, S ;
Ineson, P ;
Parekh, NR ;
Murrell, JC .
NATURE, 2000, 403 (6770) :646-649
[10]   Identification of active methylotroph populations in an acidic forest soil by stableisotope probing [J].
Radajewski, S ;
Webster, G ;
Reay, DS ;
Morris, SA ;
Ineson, P ;
Nedwell, DB ;
Prosser, JI ;
Murrell, JC .
MICROBIOLOGY-SGM, 2002, 148 :2331-2342