Carbon steel (SAE 1018) samples were exposed to complex liquid media c
ontaining either the aerobic bacterium Pseudomonas fragi or the facult
ative anaerobe Escherichia coli DH5 alpha. Compared to sterile control
s, mass loss was consistently 2- to 10-fold lower in the presence of t
hese bacteria which produce a protective biofilm. Increasing the tempe
rature from 23 degrees C to 30 degrees C resulted in a 2- to 5-fold de
crease in corrosion inhibition with P. fragi whereas the same shift in
temperature resulted in a 2-fold increase in corrosion inhibition wit
h E. coli DH5 alpha. Corrosion observed with non-biofilm-forming Strep
tomyces lividans TK24 was similar to that observed in sterile media. A
dead biofilm, generated in situ by adding kanamycin to an established
biofilm, did not protect the metal (corrosion rates were comparable t
o those in the sterile control), and mass loss in cell-free, spent Lur
ia-Bertani (LB) medium was similar to that in sterile medium. Confocal
laser scanning microscopy analysis confirmed the presence of a biofil
m consisting of live and dead cells embedded in a sparse glycocalyx ma
trix. Mass-loss measurements were consistent with microscopic observat
ions of the metal surface after 2 weeks of exposure, indicating that u
niform corrosion occurred. The biofilm was also able to withstand mild
agitation (60 rpm), provided that sufficient time was given for its d
evelopment.