Evolving perspectives of biofilm structure

被引:121
作者
Stoodley, P
Boyle, JD
DeBeer, D
Lappin-Scott, HM
机构
[1] Univ Exeter, Sch Biol Sci, Environm Microbiol Res Grp, Exeter EX4 4PS, Devon, England
[2] Univ Exeter, Sch Engn, Exeter EX4 4QF, Devon, England
[3] Max Planck Inst Marine Microbiol, D-28359 Bremen, Germany
基金
美国国家科学基金会;
关键词
biofilm; confocal scanning laser microscopy; drag; hydrodynamics; mass transfer; structure;
D O I
10.1080/08927019909378398
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
The application of confocal scanning laser microscopy (CSLM) to biofilm research has provided detailed new information on the structural complexity of fully hydrated living biofilms. Biofilms studied by CSLM are widely reported to be heterogeneous and consist of micro-colonies or cell clusters (aggregates of microbial cells in an extracellular polysaccharide matrix) separated by interstitial voids and channels. CSLM combined with molecular probing can identify the distribution of individual species within biofilms, while CSLM combined with microelectrodes and particle tracking has demonstrated the significance of structural heterogeneity on mass transfer in biofilms. In this review the contribution that CSLM has made towards the development of conceptual and mathematical biofilm models over the last decade is discussed. The significance of biofilm structural heterogeneity to understanding of mass transfer processes in biofilm systems and the fundamental significance of hydrodynamics in shaping biofilm structure are also discussed. Finally, some of the recent findings which suggest that biofilm structure may be controlled in part by cell signalling, quorum sensing mechanisms, are briefly discussed.
引用
收藏
页码:75 / +
页数:20
相关论文
共 88 条
[1]   IDENTIFICATION OF INDIVIDUAL PROKARYOTIC CELLS BY USING ENZYME-LABELED, RIBOSOMAL-RNA-TARGETED OLIGONUCLEOTIDE PROBES [J].
AMANN, RI ;
ZARDA, B ;
STAHL, DA ;
SCHLEIFER, KH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (09) :3007-3011
[2]  
ATKINSON B, 1967, T I CHEM ENG-LOND, V45, P257
[3]   SENSITIVITY OF BIOFILMS TO ANTIMICROBIAL AGENTS [J].
BROWN, MRW ;
GILBERT, P .
JOURNAL OF APPLIED BACTERIOLOGY, 1993, 74 :S87-S97
[4]   EARLY FOULING BIOFILM FORMATION IN A TURBULENT-FLOW SYSTEM - OVERALL KINETICS [J].
BRYERS, J ;
CHARACKLIS, W .
WATER RESEARCH, 1981, 15 (04) :483-491
[5]  
Bryers JD, 1998, BIOTECHNOL BIOENG, V60, P462, DOI 10.1002/(SICI)1097-0290(19981120)60:4<462::AID-BIT8>3.0.CO
[6]  
2-K
[7]  
CALDWELL DE, 1992, ADV MICROB ECOL, V12, P1
[8]   ANALYSIS OF BIOFILM FORMATION USING 2D VS 3D DIGITAL IMAGING [J].
CALDWELL, DE ;
KORBER, DR ;
LAWRENCE, JR .
JOURNAL OF APPLIED BACTERIOLOGY, 1993, 74 :S52-S66
[9]  
Characklis W.G., 1990, BIOFILMS, P195
[10]  
Christensen BB, 1998, APPL ENVIRON MICROB, V64, P2247