This material was originally published in the Purdue Cytometry CD-ROM Series
.

Flow Cytometry and Microbiology

 

Analysis of marine picoplankton by flow cytometry.

Dominique Marie, Daniel Vaulot, Frederic Partensky and Stephan Jacquet
Station Biologique
Centre National de la Recherche Scientifique
et Universite Pierre et Marie Curie
Place Georges Tessier
BP 74, F-29680 Roscoff, France

email: marie@sb-roscoff.fr


Data Examples
 

Figure 1: Typical right-angle light scatter (RALS) vs. red fluorescence plot of an unstained, live culture of the oceanic photosynthetic prokaryote Prochlorococcus sp. (Proc) clone MED4 (size = 0.6 um). Fluorescent microspheres (0.95 um beads) were added to the samples to calibrate the system.

 

Figure 2: DNA fluorescence (green) vs. chlorophyll fluorescence (red) plot of a culture of the oceanic photosynthetic prokaryote Prochlorococcus sp. (Proc) clone MED4 after fixing with 0.1% glutaraldehyde and staining with the DNA-specific dye SYBR Green I (Molecular Probes, Inc.). Determining DNA distribution in Prochlorococcus cells (Proc) and enumerating contaminant bacteria (Bact) was possible with this stain. The insert shows the DNA distribution of the Prochlorococcus population on a linear scale.

 

Figure 3: Right-angle light scatter (RALS) vs. red fluorescence plot of an unstained, live sample of phytoplankton taken at 95 m in the Equatorial Pacific. This dot plot shows the distribution of Prochlorococcus (Proc, size= 0.6 um, most abundant autotrophic population), the Synechococcus cyanobacteria (Syn, size= 1 um) and the picoeukaryotes (Euk, size = 2 um). Fluorescent microspheres (0.95 um beads) were added to the samples in order to calibrate the system.

 

Figure 4: Orange vs. red fluorescence plot of unstained, live samples of phytoplankton taken at 95 m in the Equatorial Pacific. This multiparameter approach allows discrimination between Prochlorococcus (Proc), picoeukaryotes (Euks) and the phycoerythrin-containing Synechococcus (Syn).

 

Figure 5: DNA fluorescence (green) vs. chlorophyll fluorescence (red) plot of a natural sample collected in the Equatorial Pacific at 95 m depth after fixation and staining with the DNA-specific dye SYBR Green I (Molecular Probes, Inc.). With this stain, determining DNA distribution in Prochlorococcus cells (Proc) and enumerating heterotrophic bacteria (Bact) was possible. Heterotrophic bacteria and Prochlorococcus largely outnumbered (ca. 100X) Synechococcus and picoeukaryotes (not visible on the graph). Fluorescent microspheres were added to the samples in order to calibrate the system.

 

Figure 6: DNA fluorescence (green) vs chlorophyll fluorescence (red) density plot that corresponds to Figure 5.

 

Figure 7: Right-angle light scatter (RALS) vs. green fluorescence plot of a natural sample collected in the Equatorial Pacific at 95 m depth after fixation and staining with the DNA-specific dye SYBR Green I (Molecular Probes, Inc.). Using this method, at least two populations of heterotrophic bacteria (Bact-I and Bact-II) can be discriminated based on observations previously made by Li et al (Limnol. Oceanogr. 1995, 40:1485-1495).

 

Figure 8: RALS vs green fluorescence density plot that corresponds to Figure 7.


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