ライフサイエンスコーパス: nitrate

1 uent resource concentrations (e.g., <100 muM nitrate).

2 y during anaerobic respiration with abundant nitrate.

3 unction in post-anthesis acquisition of soil nitrate.

4 m autoinhibition and no longer influenced by nitrate.

5 of soil water, electrical conductivity, and nitrate.

6 reby nonsymbiotic haemoglobin oxidizes NO to nitrate.

7 uniformity and distribution of soil water or nitrate.

8 g ploidy and cell-size depending on external nitrate.

9 HI-6 dimethanesulfonate and atropine methyl nitrate.

10 ive to wild type and is set by the amount of nitrate.

11 broblasts was restored by addition of ferric nitrate.

12 ), pptv) for NO(2) and 148 pptv for ammonium nitrate.

13 showing that ammonium uptake dominated over nitrate.

14 lso experienced a profound loss of inorganic nitrate.

15 acids are produced by precursors other than nitrate.

16 plant metabolites including carotenoids and nitrates.

17 ers were optimized namely; Ir, Ru, and Pd/Mg nitrates.

18 (TNBT) in which all four phenolic rings are nitrated, (6) cytoplasmic vesicles in vascular endotheli

19 However, nitrate ABC transporter genes were upregulated under UV

20 Inorganic nitrate, abundant in leafy green vegetables and beetroot

21 .5 module has a key role in regulating grain nitrate accumulation and seed vigour.

22 We hypothesized that maternal dietary nitrate administration would increase NO bioavailability

23 ads to significant enhancements in secondary nitrate aerosol, of which 50 to 60% is estimated to be o

24 timated 54 per cent decrease in N loading in nitrate-affected watersheds such as the Mississippi Rive

25 itration, which also occurs via diet-derived nitrating agents in the gastrointestinal tract.

26 pproximately 5 to 10 times greater than with nitrate alone.

27 furrows of 90 m, the uniformity of water and nitrate along the length of the border or furrow is weak

28 , however methanogenesis was not observed in nitrate-amended controls.

29 cs were employed to address the influence of nitrate, ammonium, and urea on cellular physiology and p

30 Tracing (15) N-labelled nitrate, ammonium, and urea through the metabolome revea

31 The growth is confined to the nitrate-ammonium transition zone (NATZ), a widespread ge

32 These systems contain ammonium sulfate (AS)/nitrate (AN) and C3-C5 dicarboxylic acids, namely, malon

33 y mixing 1 M ammonium sulfate (AS), ammonium nitrate (AN), sodium sulfate (SS), or sodium nitrate (SN

34 rocystins in cells grown on urea compared to nitrate and ammonium.

35 ental lead and molecular caffeine, from lead nitrate and caffeine residues, was generated, demonstrat

36 rt of picloram and several anions, including nitrate and chloride.

37 pe signatures of methane, carbon dioxide and nitrate and monitored microbial community composition of

38 of oral bacteria, and pH, lactate, glucose, nitrate and nitrite concentrations.

39 the zmnlp5 mutant seedlings accumulated less nitrate and nitrite in the root tissues and ammonium in

40 tential roles of these pathways, we analyzed nitrate and nitrite levels in components of the eye and

41 Nitrate and nitrite levels were higher in cornea than in

42 to explore the putative effects of inorganic nitrate and nitrite on mitochondrial function in skeleta

43 ponents, and also xanthine oxidoreductase, a nitrate and nitrite reductase, in cornea and sclera.

44 NirC, resulting in mRNA cross-regulation of nitrate and nitrite transporter genes.

45 addition, nitric oxide (NO) is produced from nitrate and nitrite, at least partially by NR, in nectar

46 competing for two shared resources, namely, nitrate and organic carbon (COD).

47 d uranium should be categorized similarly to nitrate and phosphate in that it originates in part from

48 ay a dual role in detoxification from silver nitrate and protection from pathogens for the bacterium

49 s Lake (Washington, USA), stimulated by both nitrate and sulfate addition.

50 how that strain EF1 cells respire oxygen and nitrate and that cells have higher growth rates, express

51 oncrystalline UO(2)(s) by chemical oxidants (nitrate and/or nitrite) or by Thiobacillus denitrificans

52 Among the nitrated and oxygenated polycyclic aromatic hydrocarbons

53 oxide emissions from large point sources and nitrates and EC emissions from mobile sources contribute

54 cally porous frameworks made from rare-earth nitrates and hexahydroxytriphenylene.

55 The stable isotopes of sulfate, nitrate, and phosphate are frequently used to study geob

56 We find that groundwater calcium, nitrate, and sulfate concentrations, soil pH, and clay c

57 le Nernstian slope for potassium-, calcium-, nitrate-, and carbonate-selective electrodes by combinin

58 uare pyramidal geometry with two coordinated nitrate anions.

59 Concentrations of aerosol nitrate are determined by difference relative to a paral

60 Nitrates are widely used as fertilizer and oxidizing age

61 P450 subfamily TxtE utilizes O(2) and NO to nitrate aromatic substrates such as L-tryptophan.

62 tes that mature coniferous trees assimilated nitrate as efficiently as ammonium from soils even at lo

63 Ammonium nitrate, as the mobile phase, and a suitable rinsing reg

64 VdAtf1 affects ammonium and nitrate assimilation in response to various nitrogen sou

65 id, downregulation of ammonium transport and nitrate assimilation, restriction of protein degradation

66 In contrast, calmodulin nitrated at Tyr-138 produced more nitric oxide and did s

67 ts from in vitro eNOS assays with calmodulin nitrated at Tyr-99 revealed that this nitration reduces

68 The production of N(2)O was driven by nitrate availability and N(2) generation increased in th

69 tiple physiological experiments that altered nitrate availability, salinity and temperature to create

70 Concentration of Nd (based on UV-vis) and nitrate (based on Raman) was chemometrically measured du

71 care bundle that included early intravenous nitrate boluses; management of precipitating factors, su

72 genetic code expansion to site-specifically nitrate calmodulin at its two tyrosine residues, we asse

73 artery disease, whereas supplementation with nitrate can improve submaximal exercise performance.

74 yclization in the presence of ceric ammonium nitrate (CAN) as the oxidant.

75 ction (NOR) approach is developed to produce nitrate catalyzed by ZnFe(x) Co(2-x) O(4) spinel oxides.

76 est palisade grass could be a more efficient nitrate catch crop than ruzigrass (the most extensively

77 clear to what extent mature conifers can use nitrate compared to ammonium under field conditions wher

78 Our data showing biological effects of non-nitrate components of BRJ have implications for both int

79 Overexpressing TaNAC2-5A increases grain nitrate concentration and seed vigour by directly bindin

80 of TaNRT2.5-3B increases seed vigour, grain nitrate concentration and yield, whereas RNA interferenc

81 DOC concentrations were larger than 33 mg/L, nitrate concentration did not show a significant effect

82 In the current study, we show that nitrate concentration is substantially greater in skelet

83 design for optimizing the conditions of pH, nitrate concentration, and dissolved organic carbon (DOC

84 ntly as ammonium from soils even at low soil nitrate concentration, in contrast to the results from h

85 They suggest that nitrate concentrations from agricultural lands will esca

86 regression trees (BRTs) were used to relate nitrate concentrations in base flow (n = 156) to explana

87 Due to low nitrate concentrations in offshore regions, anammox bact

88 ion significantly increased both nitrite and nitrate concentrations in plasma.

89 BRT model was developed to predict base flow nitrate concentrations in streams throughout the Chesape

90 Predictive models of base flow nitrate concentrations in streams will help identify whi

91 The lowest nitrate concentrations in the BRT model were associated

92 lfidic zones, but in coastal regions, higher nitrate concentrations probably promoted complete S-oxid

93 Nitrite +nitrate concentrations were >100 times the average while

94 The highest base flow nitrate concentrations were associated with intensive ag

95 Plasma nitrate concentrations were increased in both WT and eNO

96 ty-five weeks of dynamic methane, oxygen and nitrate concentrations.

97 in the riparian zone, is limiting base flow nitrate concentrations.

98 carbonate terrane, are critical for limiting nitrate concentrations.

99 T) and eNOS(-/-) mice were supplemented with nitrate-containing beetroot juice (BRJ+) from gestationa

100 Importantly, the effects of nitrate-containing BRJ were compared with both 'placebo'

101 erage low quarter distribution uniformity of nitrate content DU(lqN) was 79.04, and there was no sign

102 er, and the electrical conductivity (EC) and nitrate content gradually decreased with increasing soil

103 P5 cDNA fragment significantly increased the nitrate content in the root tissues compared with that o

104 There was a decreasing trend in soil EC and nitrate content with decreasing fertilizer rates.

105 k for soil water content and is moderate for nitrate content, based on the uniformity coefficient (CV

106 mine the distribution of soil water and soil nitrate content.

107 if any such effect is related to their high nitrate content.

108 ling, and the regulatory networks underlying nitrate-controlled outputs in plants.

109 (2)(Hampd)(2)(PhCO(2))(4)}(+) units with six nitrate counterions to give the neutral cluster.

110 hus likely to both decrease DOM and increase nitrate delivery to the main stem Yenisei River, and ult

111 le for sulfate delta(34)S and delta(18)O and nitrate delta(15)N and delta(18)O, based on in-house and

112 ctor (MBfR) by coupling anammox with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO) m

113 ic ammonium oxidation (anammox) with nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO),

114 CVO and compared its gene expression during nitrate-dependent sulfide oxidation to the coastal sedim

115 microorganisms and enzymatically catalyzed, nitrate-dependent U(IV) oxidation are likely dual proces

116 Control mice received an equivalent dose of nitrate-depleted BRJ (BRJ-) or normal drinking water.

117 ining BRJ were compared with both 'placebo' (nitrate-depleted) BRJ as well as water to control for po

118 ected after sterile inflammation with silver nitrate despite levels of Saa1 and Saa2 being comparable

119 Nitrate did not enhance methane oxidation under oxygen l

120 ills containing the same amount of inorganic nitrate does not decrease ambulatory SBP in subjects wit

121 tem and further suggest that the addition of nitrate drives shifts in the dominant life-stage of the

122 dds of association were found between eating nitrated dry cured meat and other psychiatric disorders.

123 We found that a history of eating nitrated dry cured meat but not other meat or fish produ

124 Cerium(IV) ammonium nitrate efficiently promoted the formation of 2-deoxy S-

125 ETN derivatives using azide, nitramine, and nitrate ester functional groups.

126 classes, namely nitramines (RDX and HMX) and nitrate esters (pentaerythritol tetranitrate (PETN) and

127 e were associated with lower urinary nitrite/nitrate excretion and markedly increased urinary PGE(2)

128 surface vertical chemical contrasts regulate nitrate export patterns under different land use conditi

129 Altogether, our results show that nitrated fatty acids can be considered a valuable tool f

130 similar to that previously reported for non-nitrated fatty acids.

131 t to analyze the effect of pretreatment with nitrated food proteins on the immune response in a mouse

132 Wildfires increased concentrations of nitrate for a decade, while decreasing concentrations of

133 selects for migratory diatoms that can store nitrate for respiration in the absence of light.

134 Dietary inorganic nitrate, found in high concentration in green leafy vege

135 Leaching of nitrate from fertilisers diminishes nitrogen use efficie

136 Much of this nitrogen is derived as nitrate from groundwater that discharges to streams as b

137 frequently internally mixed with sulfate and nitrate, from multiphase chemical processing from elevat

138 an example, we consider the case of a copper nitrate gain medium generating ~ 5 x [Formula: see text]

139 We conclude nitrate generally controls cotyledon and leaf size by in

140 Simultaneously, after the addition of nitrate, genes associated with calcification and genes u

141 o group, -1.2 +/- 6.8 mm Hg in the potassium nitrate group, and -0.5 +/- 6.6 mm Hg in the leafy green

142 The study of plant responses to nitrate has gained considerable interest over the last 3

143 alculations to study the iodine acids-iodine nitrate [HIO(x) (x = 2 and 3)-IONO(2)] dynamics at the a

144 ation of a suite of isoprene-derived hydroxy nitrate (IHN) isomers during the OH-initiated oxidation

145 cetoxy)]iodobenzene, and ammonium cerium(IV) nitrate in acetonitrile.

146 ime quantification of non-refractory aerosol nitrate in ambient air is described.

147 nt air measurements of pON and total aerosol nitrate in Calgary are presented.

148 s for understanding and managing the fate of nitrate in ecosystems, which could also be applied more

149 sult in lower uptake efficiency of in-stream nitrate in recently burned watersheds.

150 fers can adapt to increasing availability of nitrate in soil, for example, under the context of globa

151 The model allergen ovalbumin (OVA) was nitrated in different nitration degrees, and the seconda

152 However, by retaining nitrates in anoxic conditions within the soil profile, S

153 tile range) of 27.0 (9-54) mg of intravenous nitrates in the first 4 hours vs 4.0 (2.0-6.0) mg in the

154 with transcriptional analysis, we found that nitrate increases glucose uptake and oxidative catabolis

155 d emphasize the importance of accounting for nitrate-independent effects of BRJ in study design and i

156 Our data show novel, nitrate-independent effects of BRJ to lower blood pressu

157 emented with either BRJ+ or BRJ-, indicating nitrate-independent effects of BRJ.

158 RJ as well as water to control for potential nitrate-independent effects.

159 Nitrate induces LGO gene expression as early as 3 days a

160 Mechanistically, we determined that nitrate induces these phenotypic changes in primary adip

161 A wheat nitrate-inducible NAC transcription factor, TaNAC2, play

162 in blood and is elevated further by dietary nitrate ingestion in human volunteers.

163 ) is intercepted by NO(2) to form the iodine nitrate (IONO(2)).

164 These results suggest that nitrate ions are concentrated in the lacrimal glands by

165 cies, while nitrogen atoms are oxidized into nitrate ions.

166 Nitrate is a nitrogen nutrient that can act as a potent

167 Nitrate is the main source of N available to plants in a

168 ion, the oxidation of ammonia via nitrite to nitrate, is a key process in marine nitrogen (N) cycling

169 to pollution from reactive solutes, such as nitrate, is determined by the interplay between hydrolog

170 n(III)-peroxynitrite species that is able to nitrate l-Trp efficiently.

171 implications and would lead to increases in nitrate leaching (+30%), nitrous oxide emissions (+30%),

172 ruzigrass (Brachiaria ruziziensis) affected nitrate leaching and retention, measured via chemical br

173 across Europe are potentially vulnerable to nitrate leaching for at least one-third of the year.

174 produced by palisade grass, subtly decreased nitrate leaching potential through increased complexity

175 a meta-analysis of tropical field studies of nitrate leaching, nitrous oxide emissions, nitric oxide

176 The addition of nitrate led to significant changes in transcript abundan

177 s raised ascorbate concentration and reduced nitrate levels in treated plants.

178 o enhance the electrolyte stability, lithium nitrate (LiNO(3) ) and 1,1,2,2-tetrafuoroethyl-2',2',2'-

179 arger roots in ruzigrass and maize increased nitrate loss through enhanced solute flow bypassing the

180 The nitrate-mediated enhancement of glucose uptake and catab

181 -regulated genes, and anaerobic respiration, nitrate metabolism and aromatic amino acid biosynthesis

182 nitrogen (N(2)) in arable soils include high nitrate, moisture and plants; we investigate how differe

183 Additionally, a greater level of available nitrate-N (52-57 and 225 mg kg(-1) in mineral and organi

184 reduce N(2)O production and maintain greater nitrate-N levels in flooded soil.

185 unsustained conversion of refractory sodium nitrate (NaNO(3)) was observed at the inlet temperature

186 itrate (pON) (at 350 degrees C) and ammonium nitrate (NH(4)NO(3)) aerosol (at 540 degrees C) to nitro

187 In the light, nitrate + nitrate (NO(x)) was significantly elevated and

188 Stable isotopic composition of atmospheric nitrate (nitric acid (HNO(3)) + particulate nitrate (pNO

189 Findings indicate that nitrate, nitrite and nitrosothiols, but not NO or iron n

190 results suggesting limited or no effects of nitrate/nitrite administrations in highly oxidative and

191 ternal SBP was measured; at GD18.5, maternal nitrate/nitrite concentrations, uterine artery (UtA) blo

192 BRJ- did not alter nitrate/nitrite concentrations.

193 udied the relationship between dissimilatory nitrate/nitrite reduction to ammonium (DNRA) and diel ve

194 ng of nitric oxide (NO) and the reduction of nitrate/nitrite regulate important mechanisms that contr

195 Mice were subjected to a nitrate/nitrite-depleted diet for 2 wk, then supplemente

196 train F2 to nitrous nitrogen (NO(2)(-)N) and nitrate nitrogen (NO(3)(-)N) in saline conditions were i

197 ation (+74%), bringing tropical agricultural nitrate, nitrous oxide, and ammonia losses in line with

198 are among the few eukaryotes known to store nitrate (NO(3) (-) ) and to use it as an electron accept

199 pathways, denitrification and dissimilatory nitrate (NO(3) (-) ) reduction to ammonium (DNRA), deter

200 prefer to take up ammonium (NH(4) (+) ) over nitrate (NO(3) (-) ).

201 ently described pathways of NO generation by nitrate (NO(3)(-)) and nitrite (NO(2)(-)) ions reduction

202 with fertilizer production, post-application nitrate (NO(3)(-)) pollution of water bodies, and emissi

203 In the light, nitrate + nitrate (NO(x)) was significantly elevated and related t

204 Neither sodium nitrate nor sodium nitrite supplementation altered mitoc

205 molecular mechanisms governing the effect of nitrate on adipose tissue glucose metabolism and the con

206 direct photolysis both decompose the organic nitrates (ONs, representing bulk functionalities of NACs

207 We show that for a given anion (nitrate or chloride), the alkali cation has a notable im

208 JGTA-S1 could not convert nitrate or nitrite to ammonium but harbors diazotrophic

209 are facultative aerobes that can use either nitrate or oxygen as a terminal electron acceptor making

210 w-nitrate vegetables + nitrate pills (300 mg nitrate), or leafy green vegetables containing 300 mg ni

211 Nitrated organic compounds, particularly nitroaromatics,

212 Allergy-preventive treatment with OVA, nitrated OVA (nOVA), and maximally nitrated OVA (nOVAmax

213 with OVA, nitrated OVA (nOVA), and maximally nitrated OVA (nOVAmax) were performed before mice were i

214 Nitrated PAHs (NPAHs) are formed in combustion activitie

215 ase stabilization mechanism to form ammonium nitrate particles.

216 veral lines of evidence that a member of the nitrate/peptide transporter family is required for the a

217 es + placebo pills, low-nitrate vegetables + nitrate pills (300 mg nitrate), or leafy green vegetable

218 or leafy green vegetables containing 300 mg nitrate + placebo pills.

219 nitrate (nitric acid (HNO(3)) + particulate nitrate (pNO(3)(-))) provides a higher-order dimensional

220 quartz inlets to convert particulate organic nitrate (pON) (at 350 degrees C) and ammonium nitrate (N

221 elective reaction for sodium, using aluminum nitrate, potassium and ammonium fluoride in an acid medi

222 Research suggests that inorganic nitrate present in leafy green vegetables is converted i

223 Commercial nitrate production from nitrogen involves high-temperatu

224 Therefore, an alternative nitrate production method under ambient environment is o

225 Co(1.6) O(4) oxide demonstrates the highest nitrate production rate of 130+/-12 mumol h(-1) g(MO) (-

226 cript abundances, stable isotope probing and nitrate production.

227 and therefore could not produce homogenously nitrated protein.

228 Oral pretreatment with highly nitrated proteins induces a tolerogenic immune response

229 the activity of potential sulphide oxidizing nitrate reducers (Desulfobulbaceae, Acidiferrobacteracea

230 -reducing and methanogenic cultures, whereas nitrate-reducing cultures showed no SMX transformation.

231 aerobic conditions, production of nitrite by nitrate-reducing microorganisms and enzymatically cataly

232 nvolved in primary N assimilation, including nitrate reductase (NR) and alanine aminotransferase (Ala

233 ), also required for specific binding to the nitrate reductase (NR) promoter, NO production, and viru

234 ubunits, which evolved from the assimilatory nitrate reductase lineage.

235 homogenates possessed a measurable amount of nitrate reduction activity.

236 of functional genes related to assimilatory nitrate reduction in the emerged areas was higher than i

237 of functional genes related to dissimilatory nitrate reduction in the inundated areas was higher.

238 erotrophic denitrification and dissimilatory nitrate reduction to ammonium (DNRA) are two microbial p

239 of nitrite to ammonium in the dissimilatory nitrate reduction to ammonium (DNRA) pathway, a process

240 ic to some MAGs, including sulfur oxidation, nitrate reduction, and flagellar assembly.

241 Herein, we show that nitrate regulates vegetative growth by modulating cell s

242 phetamine and, for context, compared it with nitrate removal (denitrification and plant uptake).

243 Estimated nitrate removal was lower in the impacted creek, and hig

244 IFGEMs exhibited over 90% nitrate removal, as well as 50-70% total phosphorus remo

245 l communities, denitrification activity, and nitrate removal.

246 view provides an overview of key findings in nitrate research, spanning biochemistry, molecular genet

247 The balance between nitrate respiration pathways, denitrification and dissim

248 e reductase 1.1 (ZmNIR1.1) by binding to the nitrate-responsive cis-element at the 5' UTR of the gene

249 After a 2-wk run-in period on a nitrate-restricted diet the subjects were randomly assig

250 ifferences were observed between sulfate and nitrate salts.

251 iew of nitrate transport, local and systemic nitrate sensing/signaling, and the regulatory networks u

252 iring interactions with residues from NasR's nitrate-sensing NIT domain.

253 ific diversifications of NOSs and NO/nitrite/nitrate sensors from the common ancestor of Metazoa and

254 le guanylate cyclases as putative NO/nitrite/nitrate sensors.

255 molecular mechanism for how NasR couples its nitrate signal to RNA-binding activity, and generally sh

256 tructure in an "off" state in the absence of nitrate signal.

257 nitrate (AN), sodium sulfate (SS), or sodium nitrate (SN) solutions with 1 M phosphate buffer (PB) at

258 including secondary sulfate (SS), secondary nitrate (SN), biomass burning (BB), pyrolyzed organic ca

259 diet for 2 wk, then supplemented with sodium nitrate, sodium nitrite, or sodium chloride (1 g/L) in d

260 In situ FTIR showed the formation of surface nitrate species, which are considered to be key intermed

261 lating STXM neuromelanin imaging with silver nitrate-stained neuromelanin.

262 The nitrate storage efficiency (E(N)) was 65.47, and there w

263 ntrations of PM2.5 and its major components [nitrates, sulfates, elemental carbon (EC), and organic c

264 Finally, the latest evidence that nitrate supplementation improves vascular and therefore

265 the first to investigate effects of dietary nitrate supplementation in a pregnant animal model.

266 Dietary nitrate supplementation, from beetroot juice (BRJ), has

267 r the purported exercise benefits of dietary nitrate supplementation.

268 Finally, treatments that alter nitrate supply affect levels of hypoxic metabolites, nec

269 k secretion; however, alteration of vascular nitrate supply had no impact on Ala accumulation during

270 odiesterase (PDE) pathway, the evaluation of nitrates, synthetic natriuretic peptides (NP), and NP an

271 owth rates require the gas-particle ammonium nitrate system to be out of equilibrium in order to sust

272 transformation in ecosystems, produces soil nitrate that influences net primary productivity, while

273 ion of nitrite and, after further oxidation, nitrate to denitrifiers.

274 sts of the four-step sequential reduction of nitrate to dinitrogen gas over nitrite, nitric oxide, an

275 ingested, oral commensal bacteria may reduce nitrate to nitrite, which may subsequently be reduced to

276 nthine oxidoreductase-catalyzed reduction of nitrate to NO and independently of peroxisome proliferat

277 the feeding of meat preparations with added nitrate to rats resulted in hyperactivity reminiscent of

278 requires a partner protein TaNAR2.1 to give nitrate transport activity, and the transporter locates

279 Nitrate transport from aquifers to streams can take deca

280 ll plants were found to increase the rate of nitrate transport suggesting root systems increase the t

281 cuss how we have reached our current view of nitrate transport, local and systemic nitrate sensing/si

282 3 is also defective in chlorate (analogue of nitrate) transport and also shows reduced uptake of 15NO

283 candidate NarS that represents the 3' UTR of nitrate transporter NarK whose gene is silent during sta

284 ated gene was identified that is a NRT2-type nitrate transporter TaNRT2.5 with a key role in seed vig

285 lotting showed expression of sialin, a known nitrate transporter, in the lacrimal glands and other ey

286 imary adipocytes and white adipose tissue of nitrate-treated rats.

287 sues, ZmNLP5 was shown to rapidly respond to nitrate treatment.

288 ecific genomic loci functionally relevant to nitrate treatments.

289 e presence of wild-type T. denitrificans and nitrate, UO(2)(s) dissolution rates were similar to thos

290 Nitrate uptake (as uptake velocity) is strongly dependen

291 (3) (-) ) over 15 d to quantify ammonium and nitrate uptake and assimilation rates in four 40-yr-old

292 Thus, understanding how plants regulate nitrate uptake and metabolism is key for developing new

293 rols root growth and development, as well as nitrate uptake, but has no known role in determining yie

294 low-nitrate vegetables + placebo pills, low-nitrate vegetables + nitrate pills (300 mg nitrate), or

295 ollowing 3 interventions daily for 5 wk: low-nitrate vegetables + placebo pills, low-nitrate vegetabl

296 In addition to gaseous NO/NO(2), nitrite and nitrate were also detected in water, with the following

297 osphate, sulfate, bicarbonate, silicate, and nitrate) were selected due to their potential to compete

298 ly aerobic SUP05 are more active and respire nitrate when oxygen becomes available at low concentrati

299 rate constant of 10(10) M(-1) s(-1) forming nitrate, which migrates to the CD loop and unfurls the s

300 BCP-peroxy with NO produces bicyclic hydroxy nitrate with a branching ratio <0.2%, indicating efficie