Extracellular DNA is abundant and important for microcolony strength in mixed microbial biofilms

被引:147
作者
Dominiak, Dominik Marek [1 ]
Nielsen, Jeppe Lund [1 ]
Nielsen, Per Halkjaer [1 ]
机构
[1] Univ Aalborg, Dept Biotechnol Chem & Environm Engn, Aalborg, Denmark
关键词
POLYPHOSPHATE-ACCUMULATING ORGANISMS; WATER TREATMENT PROCESSES; GREEN NONSULFUR BACTERIA; ACTIVATED-SLUDGE FLOCS; PSEUDOMONAS-AERUGINOSA; RIBOSOMAL-RNA; UNSATURATED BIOFILMS; NITRIFYING BACTERIA; MARINE-SEDIMENTS; TREATMENT PLANTS;
D O I
10.1111/j.1462-2920.2010.02375.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
P>A new approach for quantification of extracellular DNA (eDNA) in mixed biofilms at microscale resolution was developed and combined with other staining techniques to assess the origin, abundance and role of eDNA in activated sludge biofilms. Most eDNA was found in close proximity to living cells in microcolonies, suggesting that most of it originated from an active secretion or alternatively, by lysis of a sub-population of cells. When the staining was combined with fluorescence in situ hybridization for identification of the microorganisms, it was found that the eDNA content varied among the different probe-defined species. The highest amount of eDNA was found in and around the microcolonies of denitrifiers belonging to the genera Curvibacter and Thauera, the ammonium-oxidizing Nitrosomonas and the nitrite-oxidizing Nitrospira. Other floc-formers also produced eDNA, although in lower amounts. The total eDNA content in activated sludge varied from 4 to 52 mg per gram volatile suspended solids in different wastewater treatment plants. Very high local concentrations within some microcolonies were found with up to approximately 300 mg of eDNA per g of organic matter. DNase digestion of activated sludge led to general floc disintegration and disruption of the microcolonies with high eDNA content, implying that eDNA was an important structural component in activated sludge biofilms.
引用
收藏
页码:710 / 721
页数:12
相关论文
共 61 条
[1]   The isotope array, a new tool that employs substrate-mediated labeling of rRNA for determination of microbial community structure and function [J].
Adamczyk, J ;
Hesselsoe, M ;
Iversen, N ;
Horn, M ;
Lehner, A ;
Nielsen, PH ;
Schloter, M ;
Roslev, P ;
Wagner, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (11) :6875-6887
[2]   A characterization of DNA release in Pseudomonas aeruginosa cultures and biofilms [J].
Allesen-Holm, M ;
Barken, KB ;
Yang, L ;
Klausen, M ;
Webb, JS ;
Kjelleberg, S ;
Molin, S ;
Givskov, M ;
Tolker-Nielsen, T .
MOLECULAR MICROBIOLOGY, 2006, 59 (04) :1114-1128
[3]  
Amann R. I., 1995, MOL MICROBIAL ECOLOG, V3, P1
[4]  
[Anonymous], 1994, STANDARD METHODS EXA, V16th
[5]  
Björnsson L, 2002, MICROBIOL-SGM, V148, P2309, DOI 10.1099/00221287-148-8-2309
[6]   Bacterial extracellular DNA forming a defined network-like structure [J].
Boeckelmann, Uta ;
Janke, Andrea ;
Kuhn, Ramona ;
Neu, Thomas R. ;
Wecke, Joerg ;
Lawrence, John R. ;
Szewzyk, Ulrich .
FEMS MICROBIOLOGY LETTERS, 2006, 262 (01) :31-38
[7]   Gravitational Drainage of Compressible Organic Materials [J].
Christensen, Morten Lykkegaard ;
Dominiak, Dominik Marek ;
Nielsen, Per Halkjaer ;
Keiding, Kristian ;
Sedin, Maria .
AICHE JOURNAL, 2010, 56 (12) :3099-3108
[8]   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
[9]   Glycogen-accumulating organisms in laboratory-scale and full-scale wastewater treatment processes [J].
Crocetti, GR ;
Banfield, JF ;
Keller, J ;
Bond, PL ;
Blackall, LL .
MICROBIOLOGY-SGM, 2002, 148 :3353-3364
[10]   Novel Nitrospira-like bacteria as dominant nitrite-oxidizers in biofilms from wastewater treatment plants:: diversity and in situ physiology [J].
Daims, H ;
Nielsen, PH ;
Nielsen, JL ;
Juretschko, S ;
Wagner, M .
WATER SCIENCE AND TECHNOLOGY, 2000, 41 (4-5) :85-90