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Appl. Environ. Microbiol., Jun 1997, 2281-2286, Vol 63, No. 6
SE Batchelor, M Cooper, SR Chhabra, LA Glover, GS Stewart, P Williams and JI Prosser
The speed of recovery of cell suspensions and biofilm populations of the
ammonia oxidizer Nitrosomonas europaea, following starvation was
determined. Stationary-phase cells, washed and resuspended in ammoniumfree
inorganic medium, were starved for periods of up to 42 days, after which
the medium was supplemented with ammonium and subsequent growth was
monitored by measuring nitrite concentration changes. Cultures exhibited a
lag phase prior to exponential nitrite production, which increased from
8.72 h (no starvation) to 153 h after starvation for 42 days. Biofilm
populations of N. europaea colonizing sand or soil particles in
continuous-flow, fixed column reactors were starved by continuous supply of
ammonium-free medium. Following resupply of ammonium, starved biofilms
exhibited no lag phase prior to nitrite production, even after starvation
for 43.2 days, although there was evidence of cell loss during starvation.
Biofilm formation will therefore provide a significant ecological advantage
for ammonia oxidizers in natural environments in which the substrate supply
is intermittent. Cell density-dependent phenomena in a number of gram-
negative bacteria are mediated by N-acyl homoserine lactones (AHL),
including N-(3-oxohexanoyl)-L-homoserine lactone (OHHL). Addition of both
ammonium and OHHL to cell suspensions starved for 28 days decreased the lag
phase in a concentration-dependent manner from 53.4 h to a minimum of 10.8
h. AHL production by N. europaea was detected by using a luxR-luxAB AHL
reporter system. The results suggest that rapid recovery of high-density
biofilm populations may be due to production and accumulation of OHHL to
levels not possible in relatively low- density cell suspensions.
Copyright © 1997, American Society for Microbiology
Cell density-regulated recovery of starved biofilm populations of ammonia-oxidizing bacteria
Department of Molecular and Cell Biology, University of Aberdeen, Foresterhill, United Kingdom.
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