The perfused biofilm fermenter was found to be unsuitable for the long
-term culture and growth rate control of Staphylococcus aureus and Pse
udomonas aeruginosa biofilms. In a simplified approach, biofilms of th
ese organisms were grown within Sorbarod filter plugs which were perfu
sed with culture medium. Pseudo-steady states were established which w
ere stable over several days at which the growth rate of the biofilm w
as reproducible, measurable and significantly slower than in broth cul
ture. Environmental scanning electron microscopy of dissected Sorbarod
s demonstrated an association of cells with the surfaces of individual
cellulose fibres, and growth characteristic of biofilms. Relatively h
igh cell numbers recovered from the Sorbarod model facilitated biochem
ical investigations of biofilm populations and cells released spontane
ously from them. SDS-PAGE demonstrated significant differences between
the protein profiles of biofilm and eluted populations, which include
, in Staph. aureus, the repression of a 48 kDa protein and increased e
xpression of a 21 kDa protein relative to planktonic controls cultured
at equivalent growth rates. The paper demonstrates the suitability of
the approach for the culture of biofilm samples which are suitable fo
r biochemical analysis.