Affiliation:
1. Department of Soil and Environmental Sciences, University of California, Riverside, California 92521, 1 and Pacific Southwest Forest and Range Experiment Station, Forest Service, U.S. Department of Agriculture, Riverside, California 925072
Abstract
A series of
15
N isotope tracer experiments showed that
Nitrosomonas europaea
produces nitrous oxide only under oxygen-limiting conditions and that the labeled N from nitrite, but not nitrate, is incorporated into nitrous oxide, indicating the presence of the “denitrifying enzyme” nitrite reductase. A kinetic analysis of the
m/z
44, 45, and 46 nitrous oxide produced by washed cell suspensions of
N. europaea
when incubated with 4 mM ammonium (99%
14
N) and 0.4 mM nitrite (99%
15
N) was performed. No labeled nitrite was reduced to ammonium. All labeled material added was accounted for as either nitrite or nitrous oxide. The hypothesis that nitrous oxide is produced directly from nitrification was rejected since (i) it does not allow for the large amounts of double-labeled (
m/z
46) nitrous oxide observed; (ii) the observed patterns of
m/z
44, 45, and 46 nitrous oxide were completely consistent with a kinetic analysis based on denitrification as the sole mechanism of nitrous oxide production but not with a kinetic analysis based on both mechanisms; (iii) the asymptotic ratio of
m/z
45 to
m/z
46 nitrous oxide was consistent with denitrification kinetics but inconsistent with nitrification kinetics, which predicted no limit to
m/z
45 production. It is concluded that
N. europaea
is a denitrifier which, under conditions of oxygen stress, uses nitrite as a terminal electron acceptor and produces nitrous oxide.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
577 articles.
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