An exploratory effort to selectively detect the presence of a nitrifyi
ng bacterium, Nitrosomonas europaea, successfully demonstrated the fun
damental utility of an enzyme-based immunoassay protocol. The applied
polyclonal antibody test seemingly offered a marked improvement over t
he available analytical options, including plating, activity, and fluo
rescence immunoassay techniques. Following an initial purification ste
p to enhance overall specificity, this procedure had an apparent lower
limit of detection of similar to 5 x 10(6) cells per ml. Tests conduc
ted with activated sludge samples exhibited a distinct difference betw
een nitrifying and nonnitrifying mixed liquors, although the highest N
itrosomonas levels observed (i.e., at 1 to 2% of the overall viable ce
ll density) were relatively close to the latter detection boundary.