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Applied and Environmental Microbiology, September 1999, p. 4285-4287, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Impact of rpoS Deletion on Escherichia coli Biofilms

Jennifer L. Adamsdagger and Robert J. C. McLean*

Department of Biology, Southwest Texas State University, San Marcos, Texas 78666-4616

Received 24 March 1999/Accepted 18 June 1999

Slow growth has been hypothesized to be an essential aspect of bacterial physiology within biofilms. In order to test this hypothesis, we employed two strains of Escherichia coli, ZK126 (Delta lacZ rpoS+) and its isogenic Delta rpoS derivative, ZK1000. These strains were grown at two rates (0.033 and 0.0083 h-1) in a glucose-limited chemostat which was coupled either to a modified Robbins device containing plugs of silicone rubber urinary catheter material or to a glass flow cell. The presence or absence of rpoS did not significantly affect planktonic growth of E. coli. In contrast, biofilm cell density in the rpoS mutant strain (ZK1000), as measured by determining the number of CFU per square centimeter, was reduced by 50% (P < 0.05). Deletion of rpoS caused differences in biofilm cell arrangement, as seen by scanning confocal laser microscopy. In reporter gene experiments, similar levels of rpoS expression were seen in chemostat-grown planktonic and biofilm populations at a growth rate of 0.033 h-1. Overall, these studies suggest that rpoS is important for biofilm physiology.


* Corresponding author. Mailing address: Department of Biology, Southwest Texas State University, 601 University Dr., San Marcos, TX 78666-4616. Phone: (512) 245-3365. Fax: (512) 245-8713. E-mail: RM12{at}swt.edu.

dagger Present address: Dynamac Corporation, Kennedy Space Center, FL 32899.


Applied and Environmental Microbiology, September 1999, p. 4285-4287, Vol. 65, No. 9
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



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