The regulation of plaque urease activity by urea, ammonia and arginine
was examined using microcosm dental plaques cultured in a multi-plaqu
e 'artificial mouth' from the mixed oral microbiota. The plaques were
supplied periodically with sucrose and continuously (3.6 ml/h/plaque)
with a mucin containing medium (BMM) supplemented either with urea at
concentrations found in saliva, or with arginine, or ammonia. Urease l
evels in plaque range from 400 to 1500 nmol NH3/min/mg plaque protein.
In the absence of urea supplementation, microcosm plaque urease level
s were usually less than 100 nmol NH3/min/mg protein. They decreased a
fter 2 to 3 wks growth and were not restored by subsequent urea applic
ation. BMM containing 1, 5 and 20 mmol/l urea throughout growth produc
ed a proportional increase in urease levels initially, similar to thos
e observed in plaques in vivo. Subsequently, urease levels decreased a
s the plaques aged. BMM supplemented with arginine (1 mmol/l) or ammon
ia (2 mmol/l) reduced urease levels. The high urease levels found in s
upragingival plaque can be explained by the availability of urea at co
ncentrations secreted in saliva. Ammonia and arginine lowered plaque u
rease levels.