Scanning transmission X-ray, laser scanning, and transmission electron microscopy mapping of the exopolymeric matrix of microbial biofilms

被引:270
作者
Lawrence, JR
Swerhone, GDW
Leppard, GG
Araki, T
Zhang, X
West, MM
Hitchcock, AP
机构
[1] Natl Water Res Inst Branch, Saskatoon, SK S7N 3H5, Canada
[2] NWRI, Burlington, ON L7R 4A6, Canada
[3] McMaster Univ, Brockhouse Inst Mat Res, Hamilton, ON L8S 4M1, Canada
[4] McMaster Univ, Fac Hlth Sci, Hamilton, ON L8N 3Z5, Canada
关键词
D O I
10.1128/AEM.69.9.5543-5554.2003
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
Confocal laser scanning microscopy (CLSM), transmission electron microscopy (TEM), and soft X-ray scanning transmission X-ray microscopy (STXM) were used to map the distribution of macromolecular subcomponents (e.g., polysaccharides, proteins, lipids, and nucleic acids) of biofilm cells and matrix. The biotilms were developed from river water supplemented with methanol, and although they comprised a complex microbial community, the biotilms were dominated by heterotrophic bacteria. TEM provided the highest-resolution structural imaging, CLSM provided detailed compositional information when used in conjunction with molecular probes, and STXM provided compositional mapping of macromolecule distributions without the addition of probes. By examining exactly the same region of a sample with combinations of these techniques (STXM with CLSM and STXM with TEM), we demonstrate that this combination of multimicroscopy analysis can be used to create a detailed correlative map of biofilm structure and composition. We are using these correlative techniques to improve our understanding of the biochemical basis for biofilm organization and to assist studies intended to investigate and optimize biotilms for environmental remediation applications.
引用
收藏
页码:5543 / 5554
页数:12
相关论文
共 43 条
[1]  
Ade H., 2002, CHEM APPL SYNCHROTRO, P285
[2]  
Ade H., 1998, EXPT METHODS PHYS SC, V32, P225
[3]  
[Anonymous], ENV PARTICLES
[4]   Investigation of lotic microbial aggregates by a combined technique of fluorescent in situ hybridization and lectin-binding-analysis [J].
Böckelmann, U ;
Manz, W ;
Neu, TR ;
Szewzyk, U .
JOURNAL OF MICROBIOLOGICAL METHODS, 2002, 49 (01) :75-87
[5]  
COOKSEY KE, 1992, BIOFILMS SCI TECHNOL, V223, P137
[6]   MELAMINE RESINS AND THEIR APPLICATION IN ELECTRON-MICROSCOPY [J].
FROSCH, D ;
WESTPHAL, C .
ELECTRON MICROSCOPY REVIEWS, 1989, 2 (02) :231-255
[7]   Use of soft X-ray microscopy for analysis of early-stage biofilm formation [J].
Gilbert, ES ;
Khlebnikov, A ;
Meyer-Ilse, W ;
Keasling, JD .
WATER SCIENCE AND TECHNOLOGY, 1999, 39 (07) :269-272
[8]  
Glauert A.M., 1977, XRAY MICROANALYSIS E
[9]   EVALUATION OF FREEZE-SUBSTITUTION AND CONVENTIONAL EMBEDDING PROTOCOLS FOR ROUTINE ELECTRON-MICROSCOPIC PROCESSING OF EUBACTERIA [J].
GRAHAM, LL ;
BEVERIDGE, TJ .
JOURNAL OF BACTERIOLOGY, 1990, 172 (04) :2141-2149
[10]   MOLECULAR VISUALIZATION OF PECTIN AND DNA BY RUTHENIUM RED [J].
HANKE, DE ;
NORTHCOTE, DH .
BIOPOLYMERS, 1975, 14 (01) :1-17