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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.
Adams
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 (
lacZ rpoS+) and its isogenic
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.

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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