Affiliation:
1. CEA/Cadarache, DSV, DEVM, Laboratoire de Bioénergétique Cellulaire, 13108 St. Paul lez Durance Cedex,1 and
2. Laboratoire de Cristallographie et Cristallogénèse des Protéines, Institut de Biologie Structurale JP Ebel CEA-CNRS, 38027 Grenoble Cedex 1,2 France
Abstract
ABSTRACT
Preliminary studies showed that the periplasmic nitrate reductase (Nap) of
Rhodobacter sphaeroides
and the membrane-bound nitrate reductases of
Escherichia coli
are able to reduce selenate and tellurite in vitro with benzyl viologen as an electron donor. In the present study, we found that this is a general feature of denitrifiers. Both the periplasmic and membrane-bound nitrate reductases of
Ralstonia eutropha, Paracoccus denitrificans
, and
Paracoccus pantotrophus
can utilize potassium selenate and potassium tellurite as electron acceptors. In order to characterize these reactions, the periplasmic nitrate reductase of
R. sphaeroides
f. sp.
denitrificans
IL106 was histidine tagged and purified. The
V
max
and
K
m
were determined for nitrate, tellurite, and selenate. For nitrate, values of 39 μmol · min
−1
· mg
−1
and 0.12 mM were obtained for
V
max
and
K
m
, respectively, whereas the
V
max
values for tellurite and selenate were 40- and 140-fold lower, respectively. These low activities can explain the observation that depletion of the nitrate reductase in
R. sphaeroides
does not modify the MIC of tellurite for this organism.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
178 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献