Using flow cytometry for counting natural planktonic bacteria and understanding the structure of planktonic bacterial communities

被引:702
作者
Gasol, JM
Del Giorgio, PA
机构
[1] CSIC, Inst Ciencias Mar, Dept Biol Marina & Oceanog, E-08039 Barcelona, Spain
[2] Univ Maryland, Hern Point Lab, Ctr Environm Sci, Cambridge, MD 21613 USA
关键词
heterotrophic and phototrophic bacteria; flow cytometry; counting bacteria; active bacteria;
D O I
10.3989/scimar.2000.64n2197
中图分类号
Q17 [水生生物学];
学科分类号
071004 ;
摘要
Flow cytometry is rapidly becoming a routine methodology in aquatic microbial ecology. The combination of simple to use bench-top flow cytometers and highly fluorescent nucleic acid stains allows fast and easy determination of microbe abundance in the plankton of lakes and oceans. The different dyes and protocols used to stain and count planktonic bacteria as well as the equipment in use are reviewed, with special attention to some of the problems encountered in daily routine practice such as Fixation, staining and absolute counting. One of the main advantages of flow cytometry over epifluorescence microscopy is the ability to obtain cell-specific measurements in large numbers of cells with limited effort. We discuss how this characteristic has been used for differentiating photosynthetic from non-photosynthetic prokaryotes, for measuring bacterial cell size and nucleic acid content, and for estimating the relative activity and physiological state of each cell. We also describe how some of the flow cytometrically obtained data can be used to characterize the role of microbes on carbon cycling in the aquatic environment and we prospect the likely avenues of progress in the study of planktonic prokaryotes through the use of flow cytometry.
引用
收藏
页码:197 / 224
页数:28
相关论文
共 232 条
[81]   LONG-TERM PRESERVATION OF PICOPHYTOPLANKTON FOR COUNTING BY FLUORESCENCE MICROSCOPY [J].
HALL, JA .
BRITISH PHYCOLOGICAL JOURNAL, 1991, 26 (02) :169-174
[82]  
HAUGLAND RP, 1994, METHOD CELL BIOL, V42, P641
[83]  
Haugland RP., 1999, HDB FLUORESCENT PROB
[84]  
HELDAL M, 1994, J MICROBIOL METH, V20, P255
[85]   Coexistence of phycoerythrin and a chlorophyll a/b antenna in a marine prokaryote [J].
Hess, WR ;
Partensky, F ;
vanderStaay, GWM ;
GarciaFernandez, JM ;
Borner, T ;
Vaulot, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (20) :11126-11130
[86]   FLOW CYTOMETRIC DETERMINATIONS OF CELLULAR SUBSTANCES IN ALGAE, BACTERIA, MOLDS AND YEASTS [J].
HUTTER, KJ ;
EIPEL, HE .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY, 1978, 44 (3-4) :269-282
[87]   SYTO16 labelling and flow cytometry of Mycobacterium avium [J].
Ibrahim, P ;
Whiteley, AS ;
Barer, MR .
LETTERS IN APPLIED MICROBIOLOGY, 1997, 25 (06) :437-441
[88]   RAPID DETECTION OF LEGIONELLA-PNEUMOPHILA BY FLOW-CYTOMETRY [J].
INGRAM, M ;
CLEARY, TJ ;
PRICE, BJ ;
PRICE, RL ;
CASTRO, A .
CYTOMETRY, 1982, 3 (02) :134-137
[89]  
Jacobsen CN, 1997, J MICROBIOL METH, V28, P35
[90]  
Jacquet S, 1998, LIMNOL OCEANOGR, V43, P1916