Nitrification involves the sequential biological oxidation of reduced nitro
gen species such as ammonium-nitrogen (NH4+-N) to nitrite-nitrogen (NO2--N)
and nitrate-nitrogen (NO3--N). The adequacy of modeling NH4+-N to NO3--N o
xidation as one composite biochemical reaction was examined at different re
lative dynamics of NH4+-N to NO2--N and NO2--N to NO3--N oxidation. NH4+-N
to NO2--N oxidation and NO2--N to NO3--N oxidation by a mixed nitrifying co
nsortium were uncoupled using selective inhibitors allylthiourea and sodium
azide, The kinetic parameters of NH4+-N to NO2--N oxidation (q(max,ns) and
K-s,K-ns) and NO2--N to NO3--N oxidation (q(max,nb) and K-s,K-nb) were det
ermined by a rapid extant respirometric technique. The stoichiometric coeff
icients relating nitrogen removal, oxygen uptake and biomass synthesis were
derived from an electron balanced equation. NH4+-N to NO2--N oxidation was
not affected by NO2--N concentrations up to 100 mg NO2--N L-1. NO2--N to N
O3--N oxidation was noncompetitively inhibited by NH4+-N but was not inhibi
ted by NO3--N concentrations up to 250 mg NO3--N L-1. When NH4+-N to NO2--N
oxidation was the sole rate-limiting step, complete NH4+-N to NO3--N oxida
tion was adequately modeled as one composite process. However, when NH4+-N
to NO2--N oxidation and NO2--N to NO3--N oxidation were both rate limiting,
the estimated lumped kinetic parameter estimates describing NH4+-N to NO3-
-N oxidation were unrealistically high and correlated. These findings indic
ate that the use of single-step models to describe batch NH4+ oxidation yie
lds erroneous kinetic parameters when NH4+-to-NO2- oxidation is not the sol
e rate-limiting process throughout the assay. Under such circumstances, it
is necessary to quantify NH4+-N to NO2--N oxidation and NO2--N to NO3--N ox
idation, independently. (C) 2000 John Wiley & Sons, Inc. Biotechnol Bioeng
68: 396-406, 2000.