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1 of incubation for ammonia-oxidizing bacteria Nitrosomonas and Nitrosospira, unlike archaea and comamm
2 harp contrast, the low-potential heme in the Nitrosomonas enzyme already is in the "activated" state
3                                    Since the Nitrosomonas enzyme is in the active state, the structur
4 oxide (NO) and N2 O at low cell densities of Nitrosomonas europaea (AOB) and Nitrosopumilus maritimus
5                                              Nitrosomonas europaea (ATCC 19718) is a gram-negative ob
6 ly studied model ammonia oxidizing bacteria, Nitrosomonas europaea (ATCC19718), to three IC availabil
7 ogical treatment, model nitrifying organisms Nitrosomonas europaea and Nitrobacter winogradskyi were
8 solated from the ammonia-oxidizing bacterium Nitrosomonas europaea and the methane-oxidizing bacteriu
9                     The nitrifying bacterium Nitrosomonas europaea can obtain all its carbon for grow
10        Hydroxylamine oxidoreductase (HAO) of Nitrosomonas europaea catalyzes the four-electron oxidat
11 O) from the autotrophic nitrifying bacterium Nitrosomonas europaea catalyzes the oxidation of NH(2)OH
12 O) from the autotrophic nitrifying bacterium Nitrosomonas europaea catalyzes the oxidation of NH2OH t
13 he enzyme cytochrome (cyt) P460 from the AOB Nitrosomonas europaea converts hydroxylamine (NH2OH) qua
14                     Notably, the enzyme from Nitrosomonas europaea does not require prereduction.
15 f the fully oxidized di-heme peroxidase from Nitrosomonas europaea has been solved to a resolution of
16              The ammonia-oxidizing bacterium Nitrosomonas europaea has been widely recognized as an i
17                                              Nitrosomonas europaea has two copies of the operon encod
18                        Cytochrome c-552 from Nitrosomonas europaea is a 9.1-kDa monoheme protein that
19 etraheme cytochrome c(554) (cyt c(554)) from Nitrosomonas europaea is an essential electron transfer
20 etraheme cytochrome c(554) (cyt c(554)) from Nitrosomonas europaea is believed to function as an elec
21                         The monooxygenase of Nitrosomonas europaea is encoded by two nearly identical
22  Here the cytochrome c peroxidase (CcP) from Nitrosomonas europaea is examined using the technique of
23 hemolithotrophic ammonia-oxidizing bacterium Nitrosomonas europaea is known to be highly resistant to
24                                     Although Nitrosomonas europaea lacks measurable alpha-ketoglutara
25      Populations of the beta-proteobacterial Nitrosomonas europaea lineage were abundant at the initi
26 eling approaches have been used to elucidate Nitrosomonas europaea metabolism at a pathway level.
27      Hydroxylamine oxidoreductase (HAO) from Nitrosomonas europaea normally catalyzes oxidation of NH
28                                              Nitrosomonas europaea participates in the biogeochemical
29       We have modeled RhAG on the homologous Nitrosomonas europaea Rh50 protein and shown that these
30                               Mutagenesis of Nitrosomonas europaea was achieved by electroporation an
31      The structure of a bacterial RhAG (from Nitrosomonas europaea) has been solved and its gas chann
32                   Nitrifying bacteria (i.e., Nitrosomonas europaea) were much more susceptible than n
33 m citrate silver nanoparticles (AgNP) toward Nitrosomonas europaea, a model ammonia oxidizing bacteri
34                        In the present study, Nitrosomonas europaea, a model ammonia oxidizing bacteri
35                                           In Nitrosomonas europaea, ammonia monooxygenase (AMO) and h
36  hydroxylamine oxidoreductase structure from Nitrosomonas europaea, both in the presence and absence
37 a type C two-domain multicopper oxidase from Nitrosomonas europaea, has been determined to 1.9 A reso
38  the ammonia-oxidizing autotrophic bacterium Nitrosomonas europaea, is shown to be a homo-oligomer of
39 OH was measurable in the incubation media of Nitrosomonas europaea, Nitrosospira multiformis, Nitroso
40 the pure culture ammonia-oxidizing bacteria, Nitrosomonas europaea, was shown to increase monochloram
41 o the nitrite-responsive repressor NsrR from Nitrosomonas europaea, we propose that the yjeB gene of
42               The heme of cytochrome P460 of Nitrosomonas europaea, which is covalently crosslinked t
43 ers AmtB from Escherichia coli and Rh50 from Nitrosomonas europaea.
44 tinobacteria and in the beta-proteobacterium Nitrosomonas europaea.
45 d obtained previously using pure cultures of Nitrosomonas europaea.
46 er aerobic conditions in the model nitrifier Nitrosomonas europaea.
47 lithoautotrophic ammonia-oxidizing bacterium Nitrosomonas europaea.
48 rvation of chemolithoheterotrophic growth of Nitrosomonas europaea.
49 ated and characterized from the periplasm of Nitrosomonas europaea.
50 apsulatus and ammonia monooxygenase (AMO) of Nitrosomonas europaea.
51  present in multiple copies in the genome of Nitrosomonas europaea.
52 solated from the ammonia oxidizing bacterium Nitrosomonas europaea.
53           Under long-term low DO conditions, Nitrosomonas europaea/eutropha remained as the dominant
54 eme c-type cytochrome, cytochrome P460, from Nitrosomonas europea.
55 e sequences close to those of, respectively, Nitrosomonas eutropha and Nitrobacter hamburgensis that
56 rization of ammonia oxidizing bacteria (AOB) Nitrosomonas eutropha D23, an environmental microbe that
57 ily Nitrososphaeraceae) and Nitrosospira and Nitrosomonas (family Nitrosomonadaceae).
58 group were distributed across the bay, while Nitrosomonas group B phylotypes were absent from low sal
59  AOB phylotypes predominantly from the known Nitrosomonas group were distributed across the bay, whil
60 cle) selected for FA- and FNA-resistant AOB (Nitrosomonas IWT514) and against NOB, stabilizing nitrit
61 were lower in abundance (0.37 +/- 0.03%) and Nitrosomonas-like ammonia oxidizers were even lower (0.1
62 surface area-to-volume ratio compared to the Nitrosomonas-like AOB clusters, which maintained a porou
63  the dominant ammonia-oxidizing organism was Nitrosomonas oligotropha; however, these populations dec
64 bundance within the AOP decreased because of Nitrosomonas proliferation.
65  for FA-tolerant ammonia-oxidizing bacteria (Nitrosomonas sp. NM107) and NOB (Nitrobacter sp.).
66 he canonical subclass of peroxidases and the Nitrosomonas subclass of enzymes, respectively.
67 hin Methanosarcina, Pseudomonas, Bartonella, Nitrosomonas, Thermotoga, and Aquifex showed a strong pr
68 ming dominated by Accumulibacter Acc-SG3 and Nitrosomonas ureae.
69                                     Multiple Nitrosomonas variants (betaproteobacterial ammonia oxidi
70 pira over canonical ammonia oxidizers (i.e., Nitrosomonas) was attributed to the low residual ammoniu