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Applied and Environmental Microbiology
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Research Article

Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa.

D G Davies, A M Chakrabarty, G G Geesey
D G Davies
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A M Chakrabarty
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G G Geesey
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ABSTRACT

Reporter gene technology was employed to detect the activity of an alginate promoter of Pseudomonas aeruginosa when the organism was grown as a biofilm on a Teflon mesh substratum and as planktonic cells in liquid medium. Alginate biosynthetic activity was determined with a mucoid cell line derived from a cystic fibrosis isolate and containing an alginate algC promoter fused to a lacZ reporter gene. Reporter activity was demonstrated with chromogenic and fluorogenic substrates for beta-galactosidase. Expression of algC was shown to be upregulated in biofilm cells compared with planktonic cells in liquid medium. Gene up-expression correlated with alginate biosynthesis as measured by Fourier transform infrared spectroscopy, uronic acid accumulation, and alginate-specific enzyme-linked immunosorbent assay. The algC promoter was shown to have maximum activity in planktonic cultures during the late lag and early log phases of the cell growth cycle. During a time course experiment, biofilm algC activity exceeded planktonic activity except during the period immediately following inoculation into fresh medium. In continuous-culture experiments, conversion of lacZ substrate was demonstrated microscopically in individual cells by epifluorescence microscopy.

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Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa.
D G Davies, A M Chakrabarty, G G Geesey
Applied and Environmental Microbiology Apr 1993, 59 (4) 1181-1186; DOI:

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Exopolysaccharide production in biofilms: substratum activation of alginate gene expression by Pseudomonas aeruginosa.
D G Davies, A M Chakrabarty, G G Geesey
Applied and Environmental Microbiology Apr 1993, 59 (4) 1181-1186; DOI:
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