Measurement of local diffusion coefficients in biofilms by microinjection and confocal microscopy
Measurement of local diffusion coefficients in biofilms by microinjection and confocal microscopy
A new technique for the determination of local diffusion coefficients in biofilms is described. It is based on the microinjection of fluorescent dyes and quantitative analysis of the subsequent plume formation using confocal laser microscopy. The diffusion coefficients of fluorescein (MW 332), TRITC-IgG (MW 150000) and phycoerythrin (MW 240000) were measured in the cell clusters and interstitial voids of a heterogeneous biofilm. The diffusivities measured in the voids were close to the theoretical values in water. Fluorescein had the same diffusivity in cell clusters, voids, and sterile medium. TRITC-IgG did not diffuse in cell clusters, presumably due to binding to the cell cluster matrix. After treatment of the biofilm with bovine serum albumin, binding capacity decreased and the diffusion coefficient could be measured. The diffusivity of phycoerythrin in cell clusters was impeded by 41%, compared to interstitial voids. From the diffusion data of phycoerythrin it was further calculated that the cell cluster matrix had the characteristics of a gel with 0.6 nm thick fibers and pore diameters of 80 nm. (c) 1997 John Wiley & Sons, Inc.
151-158
de Beer, D.
dacf8ca7-27c7-4572-882a-7111159d10cc
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f
Lewandowski, Z.
1f3f2a52-af00-4d39-99b9-cb4a372959ce
20 January 1997
de Beer, D.
dacf8ca7-27c7-4572-882a-7111159d10cc
Stoodley, P.
08614665-92a9-4466-806e-20c6daeb483f
Lewandowski, Z.
1f3f2a52-af00-4d39-99b9-cb4a372959ce
Abstract
A new technique for the determination of local diffusion coefficients in biofilms is described. It is based on the microinjection of fluorescent dyes and quantitative analysis of the subsequent plume formation using confocal laser microscopy. The diffusion coefficients of fluorescein (MW 332), TRITC-IgG (MW 150000) and phycoerythrin (MW 240000) were measured in the cell clusters and interstitial voids of a heterogeneous biofilm. The diffusivities measured in the voids were close to the theoretical values in water. Fluorescein had the same diffusivity in cell clusters, voids, and sterile medium. TRITC-IgG did not diffuse in cell clusters, presumably due to binding to the cell cluster matrix. After treatment of the biofilm with bovine serum albumin, binding capacity decreased and the diffusion coefficient could be measured. The diffusivity of phycoerythrin in cell clusters was impeded by 41%, compared to interstitial voids. From the diffusion data of phycoerythrin it was further calculated that the cell cluster matrix had the characteristics of a gel with 0.6 nm thick fibers and pore diameters of 80 nm. (c) 1997 John Wiley & Sons, Inc.
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Published date: 20 January 1997
Organisations:
Engineering Mats & Surface Engineerg Gp
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Local EPrints ID: 157467
URI: http://eprints.soton.ac.uk/id/eprint/157467
ISSN: 0006-3592
PURE UUID: df9a441f-1fda-49e9-8859-f2804331cb82
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Date deposited: 15 Jun 2010 15:22
Last modified: 14 Mar 2024 02:55
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Author:
D. de Beer
Author:
Z. Lewandowski
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