RNA isolation from soil for bacterial community and functional analysis: evaluation of different extraction and soil conservation protocols

被引:69
作者
Sessitsch, A [1 ]
Gyamfi, S [1 ]
Stralis-Pavese, N [1 ]
Weilharter, A [1 ]
Pfeifer, U [1 ]
机构
[1] ARC Seibersdorf Res GMBH, Div Life & Environm Sci, A-2444 Seibersdorf, Austria
关键词
RNA; soil; 16S rRNA; T-RFLP analysis;
D O I
10.1016/S0167-7012(02)00065-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The impact of three different RNA isolation methods on the community analysis of metabolically active bacteria was determined by reverse transcription (RT) and PCR amplification of 165 rRNA genes and subsequent terminal restriction fragment length polymorphism (T-RFLP) analysis. Furthermore, soil samples were stored at different conditions in order to evaluate the effect of soil conservation methods on the outcome of the population analysis. The quality of mRNA was assessed by reverse transcription and PCR amplification of cubacterial glutamine synthetase genes. Our results indicated that the community composition as well as the abundance of individual members were affected by the kind of RNA isolation method. Furthermore, the extraction method influenced the recovery of mRNA. Lyophilization, storage at - 20 degreesC as well as storage in glycerol stocks at - 80 degreesC proved to be equally appropriate for the storage of soils and subsequent RNA isolation. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:171 / 179
页数:9
相关论文
共 31 条
[1]   Molecular microbial diversity of an agricultural soil in Wisconsin [J].
Borneman, J ;
Skroch, PW ;
OSullivan, KM ;
Palus, JA ;
Rumjanek, NG ;
Jansen, JL ;
Nienhuis, J ;
Triplett, EW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (06) :1935-1943
[2]  
Chang S. J., 1993, Plant Molecular Biology Reporter, V11, P113, DOI 10.1007/BF02670468
[3]   Extraction of ribosomal RNA and genomic DNA from soil for studying the diversity of the indigenous bacterial community. [J].
Duarte, GF ;
Rosado, AS ;
Seldin, L ;
Keijzer-Wolters, AC ;
van Elsas, JD .
JOURNAL OF MICROBIOLOGICAL METHODS, 1998, 32 (01) :21-29
[4]   Analysis of bacterial communities in the rhizosphere of chrysanthemum via denaturing gradient gel electrophoresis of PCR-amplified 16S rRNA as well as DNA fragments coding for 16S rRNA [J].
Duineveld, BM ;
Kowalchuk, GA ;
Keijzer, A ;
van Elsas, JD ;
van Veen, JA .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (01) :172-178
[5]  
Dunbar J, 1999, APPL ENVIRON MICROB, V65, P1662
[6]   Phylogenetic specificity and reproducibility and new method for analysis of terminal restriction fragment profiles of 16S rRNA genes from bacterial communities [J].
Dunbar, J ;
Ticknor, LO ;
Kuske, CR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (01) :190-197
[7]   ISOLATION AND DIRECT COMPLETE NUCLEOTIDE DETERMINATION OF ENTIRE GENES - CHARACTERIZATION OF A GENE CODING FOR 16S-RIBOSOMAL RNA [J].
EDWARDS, U ;
ROGALL, T ;
BLOCKER, H ;
EMDE, M ;
BOTTGER, EC .
NUCLEIC ACIDS RESEARCH, 1989, 17 (19) :7843-7853
[8]  
Felske A, 1998, APPL ENVIRON MICROB, V64, P871
[9]   Direct ribosome isolation from soil to extract bacterial rRNA for community analysis [J].
Felske, A ;
Engelen, B ;
Nubel, U ;
Backhaus, H .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (11) :4162-4167
[10]   Ribosome analysis reveals prominent activity of an uncultured member of the class Actinobacteria in grassland soils [J].
Felske, A ;
Rheims, H ;
Wolterink, A ;
Stackebrandt, E ;
Akkermans, ADL .
MICROBIOLOGY-UK, 1997, 143 :2983-2989