High bacterial diversity of a waste gas-degrading community in an industrial biofilter as shown by a 16S rDNA clone library

被引:69
作者
Friedrich, U [1 ]
Prior, K [1 ]
Altendorf, K [1 ]
Lipski, A [1 ]
机构
[1] Univ Osnabruck, Fachbereich Biol Chem, Abt Mikrobiol, D-49069 Osnabruck, Germany
关键词
D O I
10.1046/j.1462-2920.2002.00349.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The bacterial diversity of an industrial biofilter used for waste gas abatement in an animal-rendering plant was investigated. A 16S rDNA clone library was generated and 444 clones were screened using computer-aided amplified ribosomal DNA restriction analysis (ARDRA). Of the screened clones, 60.8% showed unique ARDRA patterns and the remaining 174 clones were clustered into 65 groups. Almost full-length 16S rDNA sequences of 106 clones were determined and 90.5% of the clones were affiliated with the two phyla Proteobacteria and Bacteroidetes. Alpha-, Beta-, and Gammaproteobacteria accounted for 22.1, 17.6 and 18.6% respectively. Minor portions were affiliated with the Actinobacteria (2.0%), Firmicutes and Verrucomicrobia (both 1.0%), and the Deltaproteobacteria and Thermomicrobia (each 0.5%). Only six out of the 106 16S rDNA sequences exhibited similarities of more than 97% to classified bacterial species indicating that a substantial fraction of the clone sequences were derived from unknown taxa. It was also evaluated whether a database containing 281 computer-simulated bacterial rDNA fragment patterns generated from published reference sequences can be used for identification purposes. The data analysis demonstrated that this was possible only for a small number of clones, which were closely related to described bacterial strains. Rarefaction analysis of ARDRA clusters demonstrated that the 444 clones screened are insufficient to describe the entire diversity of the clone library.
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页码:721 / 734
页数:14
相关论文
共 55 条
[1]   Polyphasic classification of Proteobacteria isolated from biofilters [J].
Ahrens, A ;
Lipski, A ;
Klatte, S ;
Busse, HJ ;
Auling, G ;
Altendorf, K .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 1997, 20 (02) :255-267
[2]   Direct proof for the presence and expression of two 5% different 16S rRNA genes in individual cells of Haloarcula marismortui [J].
Amann, G ;
Stetter, KO ;
Llobet-Brossa, E ;
Amann, R ;
Antón, J .
EXTREMOPHILES, 2000, 4 (06) :373-376
[3]   PHYLOGENETIC IDENTIFICATION AND IN-SITU DETECTION OF INDIVIDUAL MICROBIAL-CELLS WITHOUT CULTIVATION [J].
AMANN, RI ;
LUDWIG, W ;
SCHLEIFER, KH .
MICROBIOLOGICAL REVIEWS, 1995, 59 (01) :143-169
[4]   CHEMOTAXONOMIC DIFFERENTIATION OF CORYNEFORM BACTERIA ISOLATED FROM BIOFILTERS [J].
BENDINGER, B ;
KROPPENSTEDT, RM ;
KLATTE, S ;
ALTENDORF, K .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (03) :474-486
[5]   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
[6]   Effect of PCR template concentration on the composition and distribution of total community 16S rDNA clone libraries [J].
Chandler, DP ;
Fredrickson, JK ;
Brockman, FJ .
MOLECULAR ECOLOGY, 1997, 6 (05) :475-482
[7]   INTRASPECIFIC VARIATION IN SMALL-SUBUNIT RIBOSOMAL-RNA SEQUENCES IN GENBANK - WHY SINGLE SEQUENCES MAY NOT ADEQUATELY REPRESENT PROKARYOTIC TAXA [J].
CLAYTON, RA ;
SUTTON, G ;
HINKLE, PS ;
BULT, C ;
FIELDS, C .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1995, 45 (03) :595-599
[8]   BACTERIAL GENOMICS [J].
COLE, ST ;
SAINTGIRONS, I .
FEMS MICROBIOLOGY REVIEWS, 1994, 14 (02) :139-160
[9]   Identification of polyphosphate-accumulating organisms and design of 16S rRNA-directed probes for their detection and quantitation [J].
Crocetti, GR ;
Hugenholtz, P ;
Bond, PL ;
Schuler, A ;
Keller, J ;
Jenkins, D ;
Blackall, LL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (03) :1175-1182
[10]  
Devinny JS., 1999, BIOFILTRATION AIR PO