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1  of incoming DIN, whereas the Dry Basin only denitrified 1%.
2 ical nosZ occur in Bacteria and Archaea that denitrify (44% of genomes), do not possess other denitri
3                 The Wet Basin was capable of denitrifying 58% of incoming DIN, whereas the Dry Basin
4 s shifted to a net N sink, either storing or denitrifying ~8 kg of N ha(-1) year(-1).
5 characteristics and potential nitrifying and denitrifying activities (PNA and PDA), which are key in
6     Nitrogen removal by using the synergy of denitrifying anaerobic methane oxidation (DAMO) and anae
7 in situ hybridization analysis revealed that denitrifying anaerobic methane oxidation (DAMO) archaea,
8                                              Denitrifying anaerobic methane oxidation (DAMO) can miti
9  removal by using the synergy of anammox and denitrifying anaerobic methane oxidation (DAMO) microorg
10                                              Denitrifying anaerobic methane oxidation (N-DAMO) has th
11                            Nitrate-dependent denitrifying anaerobic methane oxidizing archaea (n-damo
12 e gene clusters, underscoring its ability to denitrify and to fix CO2 while coupled to As(III) oxidat
13  anammox rates and quantify the abundance of denitrifying and anammox bacteria in the OMZ regions of
14 nalyse the community composition of actively denitrifying and N2O-reducing microbial communities, we
15                             The diversity of denitrifying and nondenitrifying microorganisms with cap
16  model predicted substantial accumulation of denitrifying and sulfate-reducing bacteria, and U(IV) pr
17 erales and Leptolyngbya and the H2-oxidizing denitrifying autotroph Sulfuritalea.
18  indicate that the ano-cathodophilic biofilm denitrified autotrophically using the electrode (-200 to
19  in anaerobic ethylbenzene mineralization in denitrifying Azoarcus sp. strain EB1 is the oxidation of
20         To explore the relationships between denitrifying bacteria (DB) and sulfate-reducing bacteria
21                             The abundance of denitrifying bacteria (DB), assayed by the nirK and nirS
22 pes of each "primary" microbial group, i.e., denitrifying bacteria (DB), perchlorate-reducing bacteri
23 zobium etli, and Azospirillum lipoferum) and denitrifying bacteria (i.e., Pseudomonas stutzeri).
24 c constraints on the widely held belief that denitrifying bacteria account for a significant fraction
25                             The abundance of denitrifying bacteria always exceeded that of anammox ba
26 ed from the conversion of NO3(-) by cultured denitrifying bacteria and off-axis integrated cavity out
27 stinct groups of anaerobic bacteria, such as denitrifying bacteria and sulfate-reducing bacteria.
28  nitrous oxide, which is consumed by benthic denitrifying bacteria before it reaches the water column
29 tudy, we sought to understand the ecology of denitrifying bacteria by using next-generation sequencin
30                                         Many denitrifying bacteria can adjust to life in both oxic an
31                                              Denitrifying bacteria convert nitrate (NO(3) (-) ) to di
32                                              Denitrifying bacteria convert nitrate in soils to inert
33 e hypothesized that airway colonization with denitrifying bacteria could alter nitrogen balance in th
34 3)(-)-N reductases, which reflected that the denitrifying bacteria could channel their respiratory el
35 in which removal of bioavailable nitrogen by denitrifying bacteria ensures widespread selection for d
36                The diversity and activity of denitrifying bacteria found in association with the colo
37 chment and characterization of psychrophilic denitrifying bacteria from polar sediments, and two gene
38  the regulation of nitrous oxide emission by denitrifying bacteria in response to different environme
39 seous N emissions to the atmosphere owing to denitrifying bacteria in the soil.
40                                              Denitrifying bacteria metabolize nitrogen oxides through
41               These results demonstrate that denitrifying bacteria produce NO as a signal molecule to
42                                          The denitrifying bacteria protect themselves from the endoge
43 ning and dietary nitrate are likely to favor denitrifying bacteria such as Neisseria, which are linke
44 itrous oxide (N20) generated from nitrate by denitrifying bacteria that lack N2O-reductase activity.
45                                              Denitrifying bacteria use two entirely different enzymes
46 accumulation by intracellular metabolites in denitrifying bacteria using metabolomics and genome-base
47         The solid components are autotrophic denitrifying bacteria, autotrophic perchlorate-reducing
48                                           In denitrifying bacteria, nitric oxide (NO) is an electron
49 lasmic nitrate reductases have been found in denitrifying bacteria.
50 ances of N(2)O production-related genes than denitrifying bacteria.
51 advantage for scarce forms of N to anaerobic denitrifying bacteria.
52 erization was used to describe psychrophilic denitrifying bacterial communities in sediments of three
53 erns emerging from studies of nitrifying and denitrifying bacterial cultures.
54 erobic mineralization of ethylbenzene by the denitrifying bacterium Azoarcus sp. strain EB1 was recen
55 hat active benzylsuccinate synthase from the denitrifying bacterium Azoarcus sp. strain T harbors an
56 ion were studied in Azoarcus sp. strain T, a denitrifying bacterium capable of mineralizing m-xylene
57  Anaerobic assays conducted with strain T, a denitrifying bacterium capable of mineralizing toluene t
58 ylosoxidans, an opportunistic pathogen and a denitrifying bacterium of importance in the nitrogen cyc
59 rk, impact of pH on the proteome of the soil denitrifying bacterium Paracoccus denitrificans PD1222 w
60                    Here, we show that in the denitrifying bacterium Paracoccus denitrificans, NarJ se
61 ay to remove nitrite in HS samples using the denitrifying bacterium Pseudomonas nitroreducens.
62 he structural genes for NO reductase, in the denitrifying bacterium Rhodobacter sphaeroides 2.4.3, we
63 ole freshwater or saltwater samples with the denitrifying bacterium Stenotrophomonas nitritireducens,
64 athway was discovered in a cholesterol-grown denitrifying bacterium Sterolibacterium (S.) denitrifica
65                              A salt-tolerant denitrifying bacterium strain F2 was isolated from seawa
66 own not to be formed by Thauera aromatica, a denitrifying bacterium that degrades benzoate by a pathw
67 nzoyl coenzyme A reductase isolated from the denitrifying bacterium Thauera aromatica.
68                                          The denitrifying bacterium Thauera sp. MZ1T, a common member
69 ation of ethylbenzene were investigated in a denitrifying bacterium, strain EB1.
70  of production/consumption were obtained for denitrifying batch cultures under four conditions: initi
71 e (N(2) O) has previously been documented in denitrifying biological phosphorus (P) removal bioproces
72 ed metagenomics and metatranscriptomics to a denitrifying bioprocess enriched in as-yet-uncultivated
73 assess the feasibility of employing woodchip denitrifying bioreactors to treat legacy N derived from
74 ling analysis shows that at COD:N of 4:1 the denitrifying cells slowly generate electron equivalents
75 by Thiobacillus denitrificans, a widespread, denitrifying, chemolithoautotrophic model bacterium.
76          The dynamics of denitrification and denitrifying communities are thought to be altered by la
77 standing of the distribution and dynamics of denitrifying communities in San Francisco Bay, and provi
78 abolite dynamics from metagenomes, designing denitrifying communities, and discovering how genome evo
79 ta from batch experiments with heterotrophic denitrifying communities, where reduction of mixtures of
80 erm fertilization suggests resilience of the denitrifying communities.
81 ed ammonia oxidation rates; (ii) changed the denitrifying community and increased nitrous oxide produ
82 ysis did not identify notable variability in denitrifying community composition across sites.
83 nd), which is considerably higher than under denitrifying conditions (delta(15)N(bulk)(N2O) 2.4 to -1
84  a soil microcosm experiment conducted under denitrifying conditions and performed Illumina amplicon
85 levels decreased and was not repressed under denitrifying conditions as observed in another Rhodobact
86  Genes upregulated (ca. 4- to 95-fold) under denitrifying conditions included nar, nir, and nor genes
87  null mutant strain was unable to grow under denitrifying conditions on either toluene or m-xylene, w
88 bilized chromium reduced under predominantly denitrifying conditions was mobilized at low concentrati
89 in EB1 mineralized ethylbenzene to CO2 under denitrifying conditions, as demonstrated by conversion o
90 gnature: When cells grow anaerobically under denitrifying conditions, NOR dominates; when cells exper
91 ation and CO2 fixation) under aerobic versus denitrifying conditions, we conducted whole-genome, cDNA
92 relative flux of NO3(-) production under net denitrifying conditions, whether catalyzed aerobically o
93 uring metabolic switches between aerobic and denitrifying conditions.
94 for assimilation of aromatic compounds under denitrifying conditions.
95 dation in paddy soils under both aerobic and denitrifying conditions.
96 rs at the field-scale also for predominantly denitrifying conditions.
97  naturally during growth on nitrate or under denitrifying conditions.
98 tion were assessed with a methanol-utilizing denitrifying culture both prior to and after its exposur
99  N2O reduction rates of a methanol-utilizing denitrifying culture under various carbon and nitrogen o
100                            Here, we report a denitrifying Denitratisoma sp. strain DHT3 capable of ca
101 ein identity to the characterized EmtAB from denitrifying Denitratisoma spp., known for methylating e
102 humid croplands, where the nitrate cannot be denitrified due to the presence of oxygen and lack of ca
103 cularly the electron-storing capacity of the denitrifying electroactive biofilms (EABs) on the cathod
104 ome c) and the synthesis and activity of key denitrifying enzymes.
105 , which enables us to predict the ability to denitrify for additional foraminiferal species.
106          This suggests that the cell size of denitrifying foraminifera is not limited by O(2) but rat
107         We infer the last common ancestor of denitrifying foraminifera, which enables us to predict t
108 nce of an intracellular NO(3) (-) storage in denitrifying foraminifera.
109 (-) removal was supported by the presence of denitrifying genes (nirS and nirK) within the biomat.
110 hile modest when compared to the presence of denitrifying genes, a higher abundance of the anammox-sp
111          Microvirgula aerodenitrificans is a denitrifying Gram-negative organism first described by P
112 rocosm demonstrated that both nitrifying and denitrifying groups, responsible for controlling NO(3)(-
113 e separately capable of supporting anaerobic denitrifying growth but with growth defects that are par
114 c' levels were highest during photosynthetic denitrifying growth conditions.
115 biological mineralization were combined in a denitrifying H(2)-based membrane biofilm reactor to remo
116  vibrational data on bioengineered models of denitrifying heme-nonheme NO reductases support a simila
117 tal wetlands have the capacity to retain and denitrify large quantities of reactive nitrogen (N), mak
118 te and nitric oxide are proposed oxidants in denitrifying methane oxidation, the oxidative reactivity
119 e vertical distribution and the abundance of denitrifying methanotrophs related to Candidatus Methylo
120                         Through linkage to a denitrifying MFC, the MFC system improved the removal of
121 reased because of organic consumption in the denitrifying MFC.
122         These data imply that nitrifying and denitrifying microbes had already evolved by the late Ar
123 dy suggests that the direct effect of CO2 on denitrifying microbes via inhibition of intracellular el
124 ared riparian zone for supporting a putative denitrifying microbial community using 16S rRNA sequenci
125 simultaneous photosynthetic, nitrifying, and denitrifying microbial transcription spanning nine bacte
126 -assembled genomes revealed that many of the denitrifying microorganisms also have a genotypic abilit
127 ing effects of acidity on N(2)O EFs and soil denitrifying microorganisms, we show that soil pH predom
128  into bioavailable forms of carbon that fuel denitrifying microorganisms.
129 , next to nitrous oxide (N2O) reductase from denitrifying microorganisms.
130 e (NO(3)(-)) concentrations, but that <1% of denitrified N is converted to N(2)O.
131                              The fraction of denitrified N that escapes as N(2)O rather than N(2) (i.
132                                              Denitrifying NO reductases are transmembrane protein com
133 ogeochemical regimes characterized by either denitrifying or fermentative conditions (as indicated by
134 ith nitrate (r(s) = 0.4) and the presence of denitrifying organisms (Rhodacyclaceae).
135                                         Many denitrifying organisms contain the norEF gene cluster, w
136                                              Denitrifying organisms use nitrate as a terminal electro
137                                           In denitrifying organisms with copper containing dissimilat
138 stewater, and it further suggests a putative denitrifying PAO niche for Accumulibacter clade IA.
139 olution isotopic measurements, we found that denitrifying pathways dominated N(2)O emissions during a
140 A consumption on N2O accumulation during the denitrifying phosphorus removal process for the first ti
141                                            A denitrifying phosphorus removal process undergoes freque
142  all potential N2O accumulation steps in the denitrifying phosphorus removal process.
143  nitrous oxide (N2O) accumulation during the denitrifying phosphorus removal process.
144 2O production obtained from four independent denitrifying phosphorus removal study reports with diffe
145 y low N2O reduction rate by using PHA during denitrifying phosphorus removal.
146  nitric oxide (NO), and N2O consecutively by denitrifying polyphosphate accumulating organisms (DPAOs
147 g bioprocess enriched in as-yet-uncultivated denitrifying polyphosphate accumulating organisms (PAOs)
148                    Here, we demonstrate that denitrifying polyphosphate-accumulating organism (PAO) e
149 ochrome c' from an overexpressing variant of denitrifying R. sphaeroides 2.4.3 was investigated by pr
150                    Source characteristics of denitrified samples were reconstructed from dissolved-ga
151 nal potential and activity of nitrifying and denitrifying soil microbes to NO(y) emissions from soils
152                                  On balance, denitrifying spring bioreactors add a valuable complianc
153                                   We compare denitrifying spring bioreactors with conventional agricu
154                      Our work with the model denitrifying strain Paracoccus denitrificans further sho
155                                              Denitrifying strains Thauera aromatica and "Aromatoleum
156                 Ozone loss is amplified in a denitrified stratosphere, so the effects of falling temp
157                                          The denitrifying sulfur (S) conversion-associated enhanced b
158 ic trajectories >1, characteristic of marine denitrifying systems, arise predominantly under elevated
159 the dominant NO3(-) producing term in marine denitrifying systems, as stoichiometric constraints indi
160 ies, and harbored increased copiotrophic and denitrifying taxa (Marinomonas, Pontibacterium, Aliirose
161 ting particles have significant potential to denitrify the lower stratosphere.
162 ropropane (2-NP), a rat hepatocarcinogen, is denitrified to nitrite and acetone by rat liver microsom
163 ormed during anaerobic, in vitro assays with denitrifying, toluene-mineralizing strain T, we now repo
164       Cytochrome c' is a heme protein from a denitrifying variant of Rhodobacter sphaeroides which ma
165 des the copper-type nitrite reductase from a denitrifying variant of Rhodobacter sphaeroides, strain
166 e copper-containing nitrite reductase from a denitrifying variant of Rhodobacter sphaeroides.
167                        While the capacity to denitrify was ubiquitous across sites, denitrification g
168 rey on pathogens and bacteria that assist to denitrify water.
169                                              Denitrifying woodchip bioreactors (WBRs) are increasingl

 
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