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1 itrate reductase, a nitrite reductase, and a nitric oxide reductase.
2 ating expression and activity of nitrite and nitric oxide reductase.
3 talloproteins related to beta-lactamases and nitric oxide reductases.
4 ights regarding the mechanism of flavodiiron nitric oxide reductases.
5 lic active sites of heme-copper oxidases and nitric oxide reductases.
6 ible new insights regarding the mechanism of nitric oxide reductases.
7 active reduced active-site form of bacterial nitric oxide reductase, a heme/non-heme diiron(II) compl
8 Inactivation of norEF reduced nitrite and nitric oxide reductase activity and increased the sensit
9 nant D. vulgaris FprA shows robust anaerobic nitric oxide reductase activity in vitro and also protec
12 nzymes endowed with bona fide oxygen- and/or nitric-oxide reductase activity, although their substrat
13 ns often invoke a hyponitrite species, as in nitric oxide reductase and NOx reduction catalysis, litt
14 s are highly conserved in the cNOR family of nitric oxide reductases and have previously been implica
15 se, one contained genes for both nitrate and nitric oxide reductase, and one had nitrate and nitrite
17 copper-containing nitrite reductases, and a nitric oxide reductase are involved in the denitrificati
19 oxidases (dioxygen reductases) or scavenging nitric oxide reductases, but the questions of which of t
20 ) and the enzyme that reduces NO; the c-type nitric oxide reductase (cNOR), from the model soil bacte
21 Two classes of diiron proteins, flavodiiron nitric oxide reductases (FNORs) and the hemerythrin-like
23 The reduction of NO to N(2)O by flavodiiron nitric oxide reductases (FNORs) is related to the disrup
28 ite reductase) and norB (encoding a putative nitric oxide reductase) genes is repressed by the transc
30 pic expression of one of these genes, a P450 nitric oxide reductase homologue, was sufficient to incr
31 ncludes genes required for the expression of nitric oxide reductase in Rhodobacter sphaeroides 2.4.3
32 s D. vulgaris FprA functions as a scavenging nitric oxide reductase in vivo and that this activity pr
33 product shares significant identity with the nitric oxide reductases in Ralstonia eutropha and Synech
37 e and 4.2 K are presented for fully oxidized nitric oxide reductase (NOR) from Pseudomonas stutzeri.
38 structural and functional model of bacterial nitric oxide reductase (NOR) has been designed by introd
39 enhouse gas whose production is catalyzed by nitric oxide reductase (NOR) members of the heme-copper
41 reductase (Nir) to convert nitrite to NO and nitric oxide reductase (Nor) to convert NO to nitrous ox
43 al and functional model of a metalloprotein, nitric oxide reductase (NOR), by introducing three histi
46 ss NO detoxification mechanisms, such as the nitric oxide reductase (NorB) of Neisseria meningitidis
47 or barrier to understanding the mechanism of nitric oxide reductases (NORs) is the lack of a selectiv
48 sed toward this end, as bacterial and fungal nitric oxide reductases (NORs) produce N(2)O with differ
49 )N(beta) of N2O generated by purified fungal nitric oxide reductase (P450nor) from Histoplasma capsul
56 from strains such as 2.4.1, which likely use nitric oxide reductase to mitigate stress due to episodi
57 ncestor related to the NnrU (for nitrite and nitric oxide reductase U) gene required for bacterial de
58 th nitrate reductase, nitrite reductase, and nitric oxide reductase, which catalyze successive steps