Cultivation of denitrifying bacteria: Optimization of isolation conditions and diversity study

被引:233
作者
Heylen, K
Vanparys, B
Wittebolle, L
Verstraete, W
Boon, N
De Vos, P
机构
[1] Univ Ghent, Microbiol Lab, Dept Biochem Physiol & Microbiol, B-9000 Ghent, Belgium
[2] Univ Ghent, LabMET, B-9000 Ghent, Belgium
关键词
D O I
10.1128/AEM.72.4.2637-2643.2006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
An evolutionary algorithm was applied to study the complex interactions between medium parameters and their effects on the isolation of denitrifying bacteria, both in number and in diversity. Growth media with a pH of 7 and a nitrogen concentration of 3 mM, supplemented with 1 ml of vitamin solution but not with sodium chloride or riboflavin, were the most successful for the isolation of denitrifiers from activated sludge. The use of ethanol or succinate as a carbon source and a molar C/N ratio of 2.5, 20, or 25 were also favorable. After testing of 60 different medium parameter combinations and comparison with each other as well as with the standard medium Trypticase soy agar supplemented with nitrate, three growth media were highly suitable for the cultivation of denitrifying bacteria. All evaluated isolation conditions were used to study the cultivable denitrifier diversity of activated sludge from a municipal wastewater treatment plant. One hundred ninety-nine denitritiers were isolated, the majority of which belonged to the Betaproteobacteria (50.4%) and the Alphaproteobacteria (36.8%). Representatives of Gammaproteobacteria (5.6%), Epsilonproteabacteria (2%), and Firmicutes (4%) and one isolate of the Bacteroidetes were also found. This study revealed a much more diverse denitrifying community than that previously described in cultivation-dependent research on activated sludge.
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页码:2637 / 2643
页数:7
相关论文
共 38 条
[1]   Dechloromonas agitata gen. nov., sp nov and Dechlorosoma suillum gen. nov., sp nov., two novel environmentally dominant (per)chlorate-reducing bacteria and their phylogenetic position [J].
Achenbach, LA ;
Michaelidou, U ;
Bruce, RA ;
Fryman, J ;
Coates, JD .
INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY, 2001, 51 :527-533
[2]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[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]  
[Anonymous], 1990, USFCC NEWSL
[6]   Evolutionary algorithms and flow cytometry to examine the parameters influencing transconjugant formation [J].
Boon, N ;
Depuydt, S ;
Verstraete, W .
FEMS MICROBIOLOGY ECOLOGY, 2006, 55 (01) :17-27
[7]   Nitrite reductase genes (nirK and nirS) as functional markers to investigate diversity of denitrifying bacteria in Pacific northwest marine sediment communities [J].
Braker, G ;
Zhou, JZ ;
Wu, LY ;
Devol, AH ;
Tiedje, JM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (05) :2096-2104
[8]   16S rDNA analysis for characterization of denitrifying bacteria isolated from three agricultural soils [J].
Chèneby, D ;
Philippot, L ;
Hartmann, A ;
Hénault, C ;
Germon, JC .
FEMS MICROBIOLOGY ECOLOGY, 2000, 34 (02) :121-128
[9]  
DAVIES ZS, 2002, APPL ENVIRON MICROB, V66, P1435
[10]   16S rDNA sequence analysis of bacterial isolates from biodeteriorated mural paintings in the Servilia tomb (necropolis of Carmona, Seville, Spain) [J].
Heyrman, J ;
Swings, J .
SYSTEMATIC AND APPLIED MICROBIOLOGY, 2001, 24 (03) :417-422