We have performed three different optical experiments to determine the mean size of the bacterial strain Streptococcus mutans 10449, a microorganism with dimensions comparable to the wavelength of the light used in our experiments. The three optical measurements give size values which are consistent with one another and favorably comparable to the consistency we found in identical measurements on a test system of polystyrene spheres of dimensions similar to the bacteria. Homodyne time correlation and power spectrum spectroscopy both depend on the coherence and monochromaticity of laser light for the determination of the mean diffusion coefficient of the scatterers. The Stokes-Einstein equation then relates the diffusion constant to the cell size. Differential light scattering relies for the interpretation of experimental data on the classical theoretical analysis of the angular distribution of scattered light from a scattering object. The three methods yield mean values for the radius of S. mutans 10499 of 0.324 +/- 0.006 mum, 0.0325 +/- 0.007 mum, and 0.315 +/- 0.009 mum, respectively. However, since intensity correlation spectroscopy provides a direct measure of polydispersity, it would appear to be the preferred single measurement technique for size determination.
Intensity fluctuation spectroscopy was used to study dextran-induced aggregation of Streptococcus mutans bacteria. Smoluchowski's theory of colloidal flocculation provided a consistent model of the agglutination process. Our experiments indicated that aggregation was inhibited by the negatively charged surfaces of the cells, while dextran polymers effectively bound organisms together. Our experimental data were consistent with the quantitative predictions of a polymer bridge model of agglutination.
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