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Applied and Environmental Microbiology, July 1999, p. 2847-2852, Vol. 65, No. 7
Department of Environmental Sciences and
Engineering, School of Public Health, The University of North
Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7400
Received 6 August 1998/Accepted 15 April 1999
The capillary assay was used to quantify the chemotactic response
of Pseudomonas putida G7 to naphthalene. Experiments were conducted in which the cell concentration in the assay chamber, the
naphthalene concentration in the capillary, or the incubation time was
varied. Data from these experiments were evaluated with a model that
accounted for the effect of diffusion on the distribution of substrate
and the transport of cells from the chamber through the capillary
orifice. By fitting a numerical solution of this model to the data, it
was possible to determine the chemotactic sensitivity coefficient,
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Copyright © 1999, American Society for Microbiology. All rights reserved.
Quantification of Chemotaxis to Naphthalene by
Pseudomonas putida G7
0. The mean of the best-fit values for
0
from the three types of experiments was 7.2 × 10
5
cm2/s. A less computationally intensive model based on
earlier approaches that ignore cell transport in the chamber resulted
in
0 values that were approximately three times higher.
The models evaluated in the present study could simulate the results of
capillary assays only at low chamber cell concentrations, for which the
effect of consumption on the distribution of substrate was negligible. Results from this work suggest that it is possible to use the capillary
assay to quantify taxis towards environmentally relevant chemoeffectors
that have low aqueous solubility.
*
Corresponding author. Mailing address: Department of
Environmental Sciences and Engineering, CB #7400, Rosenau Hall, School of Public Health, The University of North Carolina, Chapel Hill, NC
27599-7400. Phone: (919) 966-3860. Fax: (919) 966-7911. E-mail: rmarx{at}emailunc.edu.
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