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2 ical nosZ occur in Bacteria and Archaea that denitrify (44% of genomes), do not possess other denitri
6 in situ hybridization analysis revealed that denitrifying anaerobic methane oxidation (DAMO) archaea,
7 removal by using the synergy of anammox and denitrifying anaerobic methane oxidation (DAMO) microorg
8 e gene clusters, underscoring its ability to denitrify and to fix CO2 while coupled to As(III) oxidat
9 anammox rates and quantify the abundance of denitrifying and anammox bacteria in the OMZ regions of
10 nalyse the community composition of actively denitrifying and N2O-reducing microbial communities, we
12 model predicted substantial accumulation of denitrifying and sulfate-reducing bacteria, and U(IV) pr
14 indicate that the ano-cathodophilic biofilm denitrified autotrophically using the electrode (-200 to
15 in anaerobic ethylbenzene mineralization in denitrifying Azoarcus sp. strain EB1 is the oxidation of
18 pes of each "primary" microbial group, i.e., denitrifying bacteria (DB), perchlorate-reducing bacteri
20 c constraints on the widely held belief that denitrifying bacteria account for a significant fraction
22 ed from the conversion of NO3(-) by cultured denitrifying bacteria and off-axis integrated cavity out
23 stinct groups of anaerobic bacteria, such as denitrifying bacteria and sulfate-reducing bacteria.
24 nitrous oxide, which is consumed by benthic denitrifying bacteria before it reaches the water column
25 tudy, we sought to understand the ecology of denitrifying bacteria by using next-generation sequencin
29 e hypothesized that airway colonization with denitrifying bacteria could alter nitrogen balance in th
30 in which removal of bioavailable nitrogen by denitrifying bacteria ensures widespread selection for d
32 chment and characterization of psychrophilic denitrifying bacteria from polar sediments, and two gene
33 the regulation of nitrous oxide emission by denitrifying bacteria in response to different environme
38 itrous oxide (N20) generated from nitrate by denitrifying bacteria that lack N2O-reductase activity.
40 accumulation by intracellular metabolites in denitrifying bacteria using metabolomics and genome-base
43 erization was used to describe psychrophilic denitrifying bacterial communities in sediments of three
45 erobic mineralization of ethylbenzene by the denitrifying bacterium Azoarcus sp. strain EB1 was recen
46 hat active benzylsuccinate synthase from the denitrifying bacterium Azoarcus sp. strain T harbors an
47 ion were studied in Azoarcus sp. strain T, a denitrifying bacterium capable of mineralizing m-xylene
48 Anaerobic assays conducted with strain T, a denitrifying bacterium capable of mineralizing toluene t
49 he structural genes for NO reductase, in the denitrifying bacterium Rhodobacter sphaeroides 2.4.3, we
50 ole freshwater or saltwater samples with the denitrifying bacterium Stenotrophomonas nitritireducens,
51 own not to be formed by Thauera aromatica, a denitrifying bacterium that degrades benzoate by a pathw
54 of production/consumption were obtained for denitrifying batch cultures under four conditions: initi
55 ling analysis shows that at COD:N of 4:1 the denitrifying cells slowly generate electron equivalents
56 standing of the distribution and dynamics of denitrifying communities in San Francisco Bay, and provi
57 nd), which is considerably higher than under denitrifying conditions (delta(15)N(bulk)(N2O) 2.4 to -1
58 a soil microcosm experiment conducted under denitrifying conditions and performed Illumina amplicon
59 levels decreased and was not repressed under denitrifying conditions as observed in another Rhodobact
60 Genes upregulated (ca. 4- to 95-fold) under denitrifying conditions included nar, nir, and nor genes
61 null mutant strain was unable to grow under denitrifying conditions on either toluene or m-xylene, w
62 bilized chromium reduced under predominantly denitrifying conditions was mobilized at low concentrati
63 in EB1 mineralized ethylbenzene to CO2 under denitrifying conditions, as demonstrated by conversion o
64 ation and CO2 fixation) under aerobic versus denitrifying conditions, we conducted whole-genome, cDNA
65 relative flux of NO3(-) production under net denitrifying conditions, whether catalyzed aerobically o
69 tion were assessed with a methanol-utilizing denitrifying culture both prior to and after its exposur
70 N2O reduction rates of a methanol-utilizing denitrifying culture under various carbon and nitrogen o
71 humid croplands, where the nitrate cannot be denitrified due to the presence of oxygen and lack of ca
73 (-) removal was supported by the presence of denitrifying genes (nirS and nirK) within the biomat.
74 hile modest when compared to the presence of denitrifying genes, a higher abundance of the anammox-sp
76 e separately capable of supporting anaerobic denitrifying growth but with growth defects that are par
78 vibrational data on bioengineered models of denitrifying heme-nonheme NO reductases support a simila
79 tal wetlands have the capacity to retain and denitrify large quantities of reactive nitrogen (N), mak
80 e vertical distribution and the abundance of denitrifying methanotrophs related to Candidatus Methylo
84 dy suggests that the direct effect of CO2 on denitrifying microbes via inhibition of intracellular el
89 ogeochemical regimes characterized by either denitrifying or fermentative conditions (as indicated by
94 A consumption on N2O accumulation during the denitrifying phosphorus removal process for the first ti
98 2O production obtained from four independent denitrifying phosphorus removal study reports with diffe
100 nitric oxide (NO), and N2O consecutively by denitrifying polyphosphate accumulating organisms (DPAOs
102 ochrome c' from an overexpressing variant of denitrifying R. sphaeroides 2.4.3 was investigated by pr
107 ic trajectories >1, characteristic of marine denitrifying systems, arise predominantly under elevated
108 the dominant NO3(-) producing term in marine denitrifying systems, as stoichiometric constraints indi
110 ropropane (2-NP), a rat hepatocarcinogen, is denitrified to nitrite and acetone by rat liver microsom
111 ormed during anaerobic, in vitro assays with denitrifying, toluene-mineralizing strain T, we now repo
113 des the copper-type nitrite reductase from a denitrifying variant of Rhodobacter sphaeroides, strain
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