Literature DB >> 18600656

Measurement of bacterial random motility and chemotaxis coefficients: I. Stopped-flow diffusion chamber assay.

R M Ford1, B R Phillips, J A Quinn, D A Lauffenburger.   

Abstract

Bacterial chemotaxis, the directed movement of a cell population in response to a chemical gradient, plays a critical role in the distribution and dynamic interaction of bacterial populations in nonmixed systems. Therefore, in order to make reliable predictions about the migratory behavior of bacteria within the environment, a quantitative characterization of the chemotactic response in terms of intrinsic cell properties is needed.The design of the stopped-flow diffusion chamber (SFDC) provides a well-characterized chemical gradient and reliable method for measuring bacterial migration behavior. During flow through the chamber, a step change in chemical concentration is imposed on a uniform suspension of bacteria. Once flow is stopped, diffusion causes a transient chemical gradient to develop, and bacteria respond by forming a band of high cell density which travels toward higher concentrations of the attractant. Changes in bacterial spatial distributions observed through light scattering are recorded on photomicrographs during a 10-min period. Computer-aided image analysis converts absorbance of the photographic negatives to a digital representation of bacterial density profiles. A mathematical model (part II) is used to quantitatively characterize these observations in terms of intrinsic cell parameters: a chemotactic sensitivity coefficient, chi(0), from the aggregate cell density accumulated in the band and a random motility coefficient, mu, from population dispersion in the absence of a chemical gradient.Using the SFDC assay and an individual-cell-based mathematical model, we successfully determined values for both of these population parameters for Escherichia coli K12 responding to fucose. The values obtained were mu = 1.1 +/- 0. 4 x 10(-5) cm(2)/s and chi(o) = 8 +/- 3 +/- 10(-5) cm(2)/s. We have demonstrated a method capable of determining these parameter values from the now validated mathematical model which will be useful for predicting bacterial migration in application systems.

Entities:  

Year:  1991        PMID: 18600656     DOI: 10.1002/bit.260370707

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  18 in total

1.  Quantification of chemotaxis to naphthalene by Pseudomonas putida G7.

Authors:  R B Marx; M D Aitken
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

2.  A sensitive, versatile microfluidic assay for bacterial chemotaxis.

Authors:  Hanbin Mao; Paul S Cremer; Michael D Manson
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-18       Impact factor: 11.205

3.  Stochastic models for cell motion and taxis.

Authors:  Edward L Ionides; Kathy S Fang; R Rivkah Isseroff; George F Oster
Journal:  J Math Biol       Date:  2003-08-06       Impact factor: 2.259

4.  Cell balance equation for chemotactic bacteria with a biphasic tumbling frequency.

Authors:  Kevin C Chen; Roseanne M Ford; Peter T Cummings
Journal:  J Math Biol       Date:  2003-06-12       Impact factor: 2.259

5.  Collective bacterial dynamics revealed using a three-dimensional population-scale defocused particle tracking technique.

Authors:  Mingming Wu; John W Roberts; Sue Kim; Donald L Koch; Matthew P DeLisa
Journal:  Appl Environ Microbiol       Date:  2006-07       Impact factor: 4.792

6.  Continuous-flow capillary assay for measuring bacterial chemotaxis.

Authors:  Aaron M J Law; Michael D Aitken
Journal:  Appl Environ Microbiol       Date:  2005-06       Impact factor: 4.792

7.  Experimental verification of the behavioral foundation of bacterial transport parameters using microfluidics.

Authors:  Tanvir Ahmed; Roman Stocker
Journal:  Biophys J       Date:  2008-07-25       Impact factor: 4.033

8.  Analysis of chemotactic bacterial distributions in population migration assays using a mathematical model applicable to steep or shallow attractant gradients.

Authors:  R M Ford; D A Lauffenburger
Journal:  Bull Math Biol       Date:  1991       Impact factor: 1.758

9.  Stopped-flow chamber and image analysis system for quantitative characterization of bacterial population migration: Motility and chemotaxis ofEscherichia coli K12 to fucose.

Authors:  R M Ford; B R Phillips; J A Quinn; D A Lauffenburger
Journal:  Microb Ecol       Date:  1991-12       Impact factor: 4.552

10.  Quantitative analysis of transverse bacterial migration induced by chemotaxis in a packed column with structured physical heterogeneity.

Authors:  Meng Wang; Roseanne M Ford
Journal:  Environ Sci Technol       Date:  2010-01-15       Impact factor: 9.028

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