Cell Biochemistry Martinsried


1. Goals
The biochemical analysis of viable unicellular organisms or plant cells is of increasing interest for environmental but also for biotechnological or medical purposes.

Bacteria, marine plankton but also isolated plant cells frequently exhibit a strong natural autofluorescence from chlorophyll or other pigments e.g. phycobiliproteins.

The concept for the flow cytometric determination of functional or constituent parameters is such cells is to determine autofluorescence above 600nm simultaneously with the fluorescences of functional or other biochemical stains below 600nm (Tab.2).

2. Practical Concepts
In case of UV-excitation (350-370nm), fluorescence emission from added functioanl dyes like:

INDO1 for Ca2+
ADB for intracellular pH and
OPT for intracellular glutathione and free protein SH-groups

is collected in fluorescence channels F1 and F2 between 390-440nm and 500-600nm while natural chlorophyll fluorescence is determined in fluorescence channel F3 in addition to forward (FSC) and sideward (SSC) light scatter signals.

In case of FITC-excitation (488nm), functional dye fluorescence of e.g:

DiOC6(3) for transmembrane potential
R123 mitochondrial potential
DHR sensitive H2O2/peroxidase activity
DCFH-DA H2O2/peroxidase
HE O2-general oxidation
R110 substrates cysteine + serine proteinases
EB DNA dead cells

is collected between 510-540nm and 540-580nm in fluorescence channels F1 and F2. Chlorophyll fluorescence is again collected in fluorescence channel F3.

Natural autofluorescence may also occur in fluorescence channels F1 or F2. In this case, the added fluorescent dyes due to their brightness should still give valuable information. The natural fluorescence of each cell cluster in an unstained control sample has to be subtracted from the observed fluorescence of the respective cell cluster in the stained sample.

For problems or comments, please contact:
G.Valet, E-mail: valet@vms.biochem.mpg.de, Max-Planck-Institut für Biochemie, Am Klopferspitz 18a, D-82152 Martinsried, Germany, Tel: +49/89/8578-2518, -2525, Fax: +49/89/8578-2563, INTERNET address: http://www.biochem.mpg.de/valet/cellbio.html
Last Update: Oct.24, 1996

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CD ROM Vol 2 was produced by staff at the Purdue University Cytometry Laboratories and distributed free of charge as an educational service to the cytometry community. If you have any comments please direct them to Dr. J. Paul Robinson, Professor & Director, PUCL, Purdue University, West Lafayette, IN 47907. Phone:(317) 494-0757; FAX (317) 494-0517; Web http://www.cyto.purdue.edu EMAIL robinson@flowcyt.cyto.purdue.edu