ライフサイエンスコーパス: nitrate

1 fide, methane and ammonium at the expense of nitrate.

2 mical decomposition to nitric oxide (NO) and nitrate.

3 be the primary response to perturbation with nitrate.

4 ymph proteins, dextran particles, and silver nitrate.

5 th before and after addition of ammonium and nitrate.

6 irm the counterintuitive Lewis pi-acidity of nitrate.

7 sses, which occur if a water sample contains nitrate.

8 evidence of nitrification of the ammonium to nitrate.

9 ters, they can also act in the net uptake of nitrate.

10 1.1 and independently of NLP7 in response to nitrate.

11 dant in low DO with the capability to reduce nitrate.

12 er that did overrule the negative effects of nitrate.

13 ern U.S. includes contributions from organic nitrates.

14 e also causes higher indoor exposure to fine nitrates.

15 nadolol and acute nonresponders with nadolol+nitrates.

16 catalytic nitration process was developed to nitrate 4-Me-DL-Trp.

17 Dietary nitrate, abundant in green leafy vegetables and beetroot

18 and 470 mg N/L/d, respectively, without any nitrate accumulation.

19 nths (55.6% versus 81.8%; P=0.33) and use of nitrates after 12 months.

20 ne (Tyr) by adding a nitro group (-NO2) with nitrating agents.

21 The stabilizing effect on indoor nitrate also causes higher indoor exposure to fine nitra

22 y measured dissolved nitrogen species (i.e., nitrate, ammonium, and dissolved organic nitrogen) were

23 At-NPF6.3 imports and senses nitrate and is regulated by phosphorylation at Thr-101 (

24 A1, and physically interact under continuous nitrate and N-starvation conditions.

25 xide reductase, one contained genes for both nitrate and nitric oxide reductase, and one had nitrate

26 nse to environmental signals such as oxygen, nitrate and nitric oxide.

27 It can reduce nitrate and nitrite as alternative electron acceptors to

28 ress conditions and, consequently, for using nitrate and nitrite as nitrogen sources.

29 rate and nitric oxide reductase, and one had nitrate and nitrite reductase.

30 metabolic responses to nitrate or NO and how nitrate and nitrite reduction are coordinated with the r

31 Although nitrate and nitrite reduction are tightly regulated in r

32 is regulation in which NrfS-NrfR coordinates nitrate and nitrite reduction to minimize toxicity due t

33 Nitrate and nitrite transport across biological membrane

34 independent of sediment depth and available nitrate and nitrite.

35 mperature (and associated properties such as nitrate and oxygen) propagates into estuaries through fa

36 inly derived from transportation of upstream nitrate and point sources from cities.

37 sis from a mixture of graphene oxide, copper nitrate and uric acid, followed by thermal annealing at

38 chlorination was observed after 15 days when nitrate and water were added together with labile organi

39 Dissolved oxygen (DO), nitrate, and dissolved organic carbon (DOC) were measure

40 to explain the concentration profiles of DO, nitrate, and DOC.

41 a global role in regulating the response to nitrate, and HcpR2 regulates the response to nitrosative

42 ption of inorganic anions (bromide, nitrite, nitrate, and iodide) to multiwalled carbon nanotubes.

43 and total concentrations of aqueous uranium, nitrate, and sulfate species in groundwater together wit

44 eostatic process, i.e., its oxidation to the nitrate anion.

45 ng studies indicate that oxygen derived from nitrate appears in the acetoxylation product, the transf

46 The rise in Subantarctic surface nitrate appears to have had both early deglacial and lat

47 rast, negligible N2 O was produced following nitrate application to either AMF treatment.

48 ng pharmacological preparations of inorganic nitrate are lacking.

49 Organic nitrates are commonly used in the treatment of cardiovas

50 Nitrates are rapidly absorbed from mucous membranes, the

51 TCP20 and NLP6&7-dependent up-regulation of nitrate assimilation and signaling genes and down-regula

52 e responses to nitrate availability, linking nitrate assimilation and signaling with cell-cycle progr

53 acid transporters but found no evidence of a nitrate assimilation system, in agreement with the N pre

54 rs NLP6 and NLP7, which act as activators of nitrate assimilatory genes, bind to adjacent sites in th

55 s along with increased expression of several nitrate assimilatory genes.

56 cpk32 triple mutants to define comprehensive nitrate-associated regulatory and developmental programs

57 d" was below 15mgkg(-1) (expressed as sodium nitrate at 12% of moisture).

58 emical performance recovered upon removal of nitrate at 3.7 mg C/mg N but did not at 1.8 mg C/mg N.

59 Here, we investigated the impact of nitrate at different C/N ratios of 1.8, 3.7, and 7.4 mg

60 ncrease in Betaproteobacteria in response to nitrate at low C/N ratios and no significant changes at

61 bed calcium channel blockers and long-acting nitrates at discharge (DM versus not: 27.9% versus 20.9%

62 hic trend constrains the onset of widespread nitrate availability associated with ocean oxygenation.

63 n phenotypes with fewer lateral roots at low nitrate availability, but the opposite was true in low p

64 ghts into how plants coordinate responses to nitrate availability, linking nitrate assimilation and s

65 ly reported role in regulating the switch to nitrate-based respiration during low-oxygen growth, saNO

66 ide polyphenols, oligosaccharides, fiber and nitrate (beet juice), which may induce a prebiotic-like

67 for the effective complexation of chloride, nitrate, bicarbonate and sulfate anions via hydrogen bon

68 Structural predictions identified a nitrate binding His (H362) in NPF6.6 but not in NPF6.4.

69 cy is often limited due to the production of nitrate by the Anammox reaction and the sensitivity to t

70 Ceric ammonium nitrate (CAN) or Ce(IV) (NH4 )2 (NO3 )6 is often used in

71 with a trend towards reduced affinity of the nitrated chemokine for its cognate receptor CCR2b.

72 The nitrated chemokine was unable to induce transendothelial

73 factors, including levels of soil moisture, nitrate, chloride, and labile organic carbon, influenced

74 different potassium salts (acetate, iodide, nitrate, chloride, dihydrophosphate, perchlorate) showed

75 alibration curve was generated that gave the nitrate concentration at each pixel in the chemical imag

76 These data suggest a reduced summer surface nitrate concentration in both the Antarctic and Subantar

77 For quantification of the nitrate concentration in the rhizosphere of experimental

78 a new constraint on the controls of surface nitrate concentration in this region and allow us to qua

79 ron recycling rates, seasonal variability in nitrate concentration on and off the equator can be expl

80 t and the fungi, Laccaria bicolor, where the nitrate concentration was five times higher near mycorrh

81 fluence nitrite production and find that pH, nitrate concentration, and the presence of an (*)OH scav

82 ues were independent of equilibrium time and nitrate concentration.

83 ly be modeled using zero-order kinetics when nitrate concentrations are >2 mg-N L(-1).

84 Nitrate concentrations in rivers draining Leverett Glaci

85 els were tested for their ability to predict nitrate concentrations in the experimental columns.

86 Nitrate concentrations varied by 4.4 muM (+/-0.2 muM) ov

87 Marked changes in nitrate concentrations were observed when discharge bega

88 a range of measured flow rates and influent nitrate concentrations with an artificial stormwater mat

89 ite to that of the dissolved oxygen (DO) and nitrate concentrations.

90 termined using varying equilibrium times and nitrate concentrations.

91 compounds in the presence of Ce(IV) ammonium nitrate constitutes the first example of a multicomponen

92 Here we show that nitrate consumption in these waters cannot be fueled sol

93 Rather, a substantial fraction of nitrate consumption must be supported by the recycling o

94 ntify the degree and temporal variability of nitrate consumption.

95 tection was used for determining nitrite and nitrate content of sugar by-products included in feed ma

96 BRE with highly reduced amounts of salts and nitrate content.

97 The rise of marine nitrate could have allowed for the rapid diversification

98 Nitrate-coupled CPK signalling phosphorylates conserved

99 nal-scale estimates and observed groundwater nitrate data.

100 was shown that the use of either ammonium or nitrate determined how copper was distributed within the

101 Interestingly, competition for nitrate did not lead to exclusion of one particular grou

102 egligible interference from oxygen, nitrite, nitrate, dopamine and ascorbic acid and retained 86% of

103 ter recharge containing (fertilizer-derived) nitrate drives the redox shift from originally reducing

104 1 and Gammaproteobacteria KI89A clades while nitrate enriched Gammaproteobacteria SAR86, SAR92 and OM

105 upled to reductions of sulfate, nitrite, and nitrate, evidence that AOM is coupled with extracellular

106 ategy that provides an interval of no or low nitrate exposure during each 24-h period.

107 Nitrated fatty acids are endogenously present in human a

108 We also show that in nitrate-fed mice there is reduced systemic leukocyte rol

109 wheat cultivation, with the use of ammonium nitrate fertilizer alone accounting for around 40%.

110 transcription of nirK and nirS genes during nitrate flux, suggesting that denitrification to N2 and

111 riethanolamine (TEA) solution as nitrite and nitrate for delta(15)N analysis using the denitrifier me

112 roscopy (DRIFTS) results show the absence of nitrate formation on catalyst.

113 t provide evidence for its role in cold-pool nitrate formation.

114 Rs) are increasingly being applied to remove nitrate from runoff.

115 peaking transports dissolved oxygen (DO) and nitrate from the vadose zone into the alluvial aquifer.

116 es more rapidly and in higher yield than non-nitrated furans.

117 e responses to environmental fluctuations in nitrate have been identified; however, little is known a

118 underlying genes regulating the response to nitrate have yet to be characterized.

119 systematic study of Cu(NO3)2.2.5 H2O (copper nitrate hemipentahydrate, CN), an alternating Heisenberg

120 The decomposition of nitrate, if formed, is an endothermic event.

121 Exposure to oxygen and nitrate impacted the community structure, but did not su

122 vices were evaluated by the determination of nitrate in a soil slurry containing zinc particles for t

123 3D printing and applied for the analysis of nitrate in soil.

124 om 0 to 60 ppm, covering the normal range of nitrate in soil.

125 the evaluation of the content of nitrite and nitrate in sugar by-products.

126 Nitrate in the lower reaches was mainly derived from tra

127 2000, we quantify the peak global storage of nitrate in the vadose zone as 605-1814 Teragrams (Tg).

128 site of human hemopexin, which was similarly nitrated in rabbit and rat hemopexins.

129 he distribution of nutrients, in particular, nitrate, in the rhizosphere.

130 ncentrations of solutes such as chloride and nitrate increase quickly in a gaining reach.

131 Moreover, nitrate increased circulating growth hormone levels in h

132 e show that during incubations with elevated nitrate, increased N2O fluxes are not mediated by direct

133 Inorganic nitrate increases exercise efficiency, tolerance, and pe

134 n lateral root GSA in Arabidopsis: while low nitrate induces less vertical lateral root GSA, phosphat

135 We found that nitrate induces PGC1alpha expression and a switch toward

136 Nitrate induces physiological responses that mimic exerc

137 Nitrate induces the release of exercise/PGC1alpha-depend

138 bantarctic iron fertilization and increasing nitrate input from the surface Antarctic Zone, respectiv

139 reducing toward oxidizing environments, when nitrate input has consumed the reducing capacity of the

140 Higher vegetable nitrate intake (per SD) also was associated with a lower

141 modeling to examine the association between nitrate intake and ASVD mortality before and after adjus

142 Nitrate intake from vegetables was calculated by use of

143 ed HR: 0.87 (95% CI: 0.78, 0.97), P = 0.011].Nitrate intake from vegetables was inversely associated

144 ective was to investigate the association of nitrate intake from vegetables with ASVD mortality.A tot

145 The mean +/- SD vegetable nitrate intake was 67.0 +/- 29.2 mg/d.

146 Each SD higher vegetable nitrate intake was associated with a lower risk of ASVD

147 e to transform ammonium sulfate and ammonium nitrate into (MEA)2SO4 and (MEA)NO3.

148 chetii, caused near depletion of the surface nitrate inventory and a decline in dissolved inorganic c

149 -shaped outer-sphere lanthanide chloride and nitrate ion clusters in hydrocarbon solutions formed dur

150 re the dominant forms of cobalt species with nitrate ions.

151 Nitrate is a constituent of different wastewaters and ca

152 One major limitation of the use of nitrates is the development of tolerance.

153 Nitrate isotope measurements provide a new constraint on

154 potentially be responsible for the shift of nitrate isotope signature.

155 This demonstrated that nitrate isotopes of delta(15)NNO3 and delta(18)ONO3 do n

156 The spatial variation of ammonium and nitrate isotopes show that nitrification is a key proces

157 ne (1) the dose-response effect of potassium nitrate (KNO3) on exercise capacity; (2) the population-

158 Using estimates of groundwater depth and nitrate leaching for 1900-2000, we quantify the peak glo

159 , projected based on current temperature and nitrate levels as well as those forecast for the future.

160 The control group was treated with nadolol+nitrates+ligation.

161 n increased in the order bromide < nitrite < nitrate < iodide.

162 Nitrates may be beneficial in heart failure with preserv

163 conversion of 3-indoxylphosphate and silver nitrate, metallic silver is determined by anodic strippi

164 er the antiinflammatory effects of inorganic nitrate might prove useful in ameliorating atherosclerot

165 found for two related series of thorium (Th)-nitrate molecular compounds obtained by evaporating acid

166 eographic trends for violations of the 10 mg nitrate-N L(-1) MCL in the conterminous U.S.

167 aters because phytoplankton growth fueled by nitrate (new production) is limited by iron.

168 d when hemopexin was incubated in vitro with nitrating nitrite/myeloperoxidase/glucose oxidase.

169 s closest to the seabird colonies had higher nitrate + nitrite concentrations compared to more distan

170 f the (15)N abundances and concentrations of nitrate, nitrite, and ammonium in aqueous solutions with

171 a nitrate/proton symporter while NarK2 is a nitrate/nitrite antiporter.

172 g that, while these proteins are most likely nitrate/nitrite antiporters, they can also act in the ne

173 unctions, ranging from net nitrate uptake to nitrate/nitrite exchange.

174 biological processes, such as narU (encoding nitrate/nitrite transporter), ompX (encoding outer membr

175 Nitrate (NO3(-)) and nitrite (NO2(-)) are known to be ca

176 luble, but may be mobilized upon exposure to nitrate (NO3(-)) and oxygen (O2), which become elevated

177 g bedrock and superficial geologies, N2O and nitrate (NO3(-)) concentrations were analyzed in 651 riv

178 CT), its impact on water quality, especially nitrate (NO3(-)) loss remain controversial.

179 sitive prenatal windows for the influence of nitrate (NO3(-)) on child asthma, accounting for effect

180 Photolysis of nitrate (NO3(-)) produces reactive nitrogen and oxygen s

181 Recent evidence demonstrates that inorganic nitrate (NO3(-)) through sequential chemical reduction i

182 r superior competitive ability for dissolved nitrate (NO3(-)).

183 e ice age, the increase in Antarctic surface nitrate occurred through the deglaciation and continued

184 for the formation of O=N-O-O intermediate or nitrate on single supported Pd atoms.

185 ling route, namely photolysis of particulate nitrate, on the modeling of NOx abundance and O3 formati

186 ic acid (COOH) approximately hydroxyl (OH) > nitrate (ONO2) > carbonyl (CO) approximately ester (COO)

187 uplicate 20 liter polycarbonate carboys with nitrate or ammonium, tracking planktonic carbon fixation

188 tic and RNA-seq data, metabolic responses to nitrate or NO and how nitrate and nitrite reduction are

189 strate availability, the global responses to nitrate or NO were largely regulated independently.

190 aerobes enabling the community to adjust to nitrate or oxygen pulses.

191 Nitrated organic intermediates are formed under catalyti

192 r, decayed to radicals that hydroxylated and nitrated other active-site residues (Trp(52), Trp(396),

193 esent the discovery of a tonoplast localized nitrate/peptide family (NPF) transporter from Catharanth

194 Nitrate persists in eastern equatorial Pacific surface w

195 i(NO2(-))) of (1.1 +/- 0.2)% (313 nm, 50 muM nitrate, pH >/= 5), which is at the upper end of past me

196 At a nearshore station, nitrate, phosphate, and silicate concentrations reached

197 .03-6.24, and 0.24-45.5 mmol m(-2) d(-1) for nitrate, phosphate, and silicate, respectively, along th

198 in barley (Hordeum vulgare) under suboptimal nitrate, phosphorus, and potassium availability.

199 d plant growth by up to 52%, 73%, and 41% in nitrate-, phosphorus-, and potassium-limiting conditions

200 ts the need for the inclusion of particulate nitrate photolysis in future models for O3 and for the p

201 is often considered a very minor channel in nitrate photolysis, but our results indicate it is as im

202 plants the family has diverged to recognize nitrate, plant defense compounds, and hormones.

203 anced total plant N pools and decreased soil nitrate pools, largely through higher root biomass, and

204 ations are increasing, indicating persistent nitrate problems in drinking water.

205 Mass balance analysis showed that nitrate produced by Anammox (122.2 mg N/L/d) was entirel

206 issolved oxygen (DO), ammonium, nitrite, and nitrate profiles within the biofilm and in the bulk, a 1

207 entation studies, using a mutant lacking the nitrate/proton symporter NasA from the assimilatory nitr

208 e pathway, support that NarK1 functions as a nitrate/proton symporter while NarK2 is a nitrate/nitrit

209 Nitrate radical (NO3) oxidation of biogenic volatile org

210 ate constants for nitrogen dioxide (NO2) and nitrate radicals (NO3) in the presence of the different

211 Nitrate recovery and isotope values were independent of

212 Sulfate reducers coexisted with facultative nitrate reducers or aerobes enabling the community to ad

213 h-dependent activity of fermenters, aerobes, nitrate reducers, sulfate reducers, and chemolithoautotr

214 ly inactive nitrate reductase, restoring its nitrate-reducing enzyme activity.

215 Here, we investigated a nitrate-reducing microbial community in a laboratory-sca

216 re we report that DnrF selectively repressed nitrate reductase (nap) genes, preventing further NO for

217 icated that two isolates held genes encoding nitrate reductase as the only dissimilatory N-oxide redu

218 assimilation, we generated a knockout in the nitrate reductase gene (NR-KO) of the model pennate diat

219 sites in the upstream promoter region of the nitrate reductase gene, NIA1, and physically interact un

220 /proton symporter NasA from the assimilatory nitrate reductase pathway, support that NarK1 functions

221 d to a heme-depleted, catalytically inactive nitrate reductase, restoring its nitrate-reducing enzyme

222 rom Arg but via conversion of nitrite by the nitrate reductase.

223 itrate transporter/sensor gene NRT1.1, while nitrate reduction and amino acid content were enhanced i

224 tion, as well as for anaerobic dissimilatory nitrate reduction and sulfate reduction, suggesting a si

225 at denitrification to N2 and not facultative nitrate reduction by Geobacter spp. might be the primary

226 cation and genes associated with respiratory nitrate reduction.

227 ained nitrifiers and heterotrophs capable of nitrate reduction.

228 We report here the identification of a nitrate regulatory mutant whose mutation mapped to the C

229 s master regulators that orchestrate primary nitrate responses.

230 In the mutant, induction of nitrate-responsive genes was inhibited independent of th

231 RATIONALE: Nitrate-rich beetroot juice has been shown to improve ex

232 Nitrate-rich vegetables lower blood pressure and improve

233 These results support the concept that nitrate-rich vegetables may reduce the risk of age-relat

234 n, however, whether increased consumption of nitrate-rich vegetables translates to a lower risk of at

235 reactors that can achieve decontamination of nitrate-rich water used for irrigation, irrigation with

236 Here we show that when the nitrate's charge is sufficiently dampened by resonating

237 his ancillary study of the NEAT-HFpEF trial (Nitrate's Effects on Activity Tolerance in HF With Prese

238 high-affinity nitrate transport activity and nitrate selectivity.

239 A nitrate-sensitized and targeted functional genomic scree

240 65 kDa protein encoded by CPSF30-L mediates nitrate signaling in part by regulating NRT1.1 expressio

241 n, thus adding an important component to the nitrate signaling network.

242 t the proportion of systems in violation for nitrate significantly increased from 0.28% to 0.42% of a

243 ds obtained by evaporating acidic aqueous Th-nitrate solutions in the presence of A(+) counterions.

244 l change of a picrate-selective electrode in nitrate solutions when determining the selectivity coeff

245 was a pH-dependent nonbiphasic high-affinity nitrate-specific transport protein.

246 N)Fe(O)(X)](+), whereas trifluoroacetate and nitrate stabilize the triplet state of the complex.

247 Both exercise and nitrate stimulated PGC1alpha-mediated gamma-aminobutyric

248 Estimates of nitrate storage are validated using basin-scale and nati

249 Nitrate storage per unit area is greatest in North Ameri

250 he nitrogen cycle do not explicitly consider nitrate stored in the vadose zone.

251 Given the beneficial effects of dietary nitrate supplementation to date in non-pregnant humans a

252 In summary, we demonstrate that inorganic nitrate suppresses acute and chronic inflammation by tar

253 hat the vadose zone is an important store of nitrate that should be considered in future budgets for

254 In contrast to traditional organic nitrate therapies, an alternative strategy to restore NO

255 eries) and nonhemodynamic effects of organic nitrate therapy, via both nitric oxide-dependent and -in

256 5)NNO3 and delta(18)ONO3 during diffusion of nitrate through the DET gel was determined using varying

257 3 and for the photolysis rate of particulate nitrate to be quantified under variable atmospheric cond

258 non-crystalline U(IV) rapidly consume DO and nitrate to maintain anoxic conditions, yielding Fe(II) f

259 Conversion of nitrate to N2 by denitrification in sediments accounts f

260 ntaining zinc particles for the reduction of nitrate to nitrite using the Griess reagent.

261 In animal models of nitrate tolerance and angiotensin II-induced hypertensio

262 Only 1 method of preventing nitrate tolerance remains widely accepted: the use of a

263 ve been studied for use in the prevention of nitrate tolerance, none are currently recommended owing

264 in the spatial and temporal distributions of nitrate transformation in the Yellow River, the second-l

265 (Y370H) resulted in saturable high-affinity nitrate transport activity and nitrate selectivity.

266 NPF6.6, resulted in a similar high-affinity nitrate transport activity with increased Km, whereas eq

267 substrate specificity in plants and regulate nitrate transport affinity/selectivity using a conserved

268 ic Zones during the LGM, with little surface nitrate transport between them.

269 The fate of nitrate transported across groundwater-surface water int

270 Arabidopsis thaliana nitrate transporter 1/peptide transporter family (NPF) 6

271 nal concentrations, and a possible role as a nitrate transporter in the control of N-fixing nodule ac

272 By contrast, maize NPF6.4 was a low-affinity nitrate transporter with efflux activity.

273 mutant along with reduced expression of the nitrate transporter/sensor gene NRT1.1, while nitrate re

274 erization of a member of the Lotus japonicus nitrate transporter1/peptide transporter family, LjNPF8.

275 We show that dietary nitrate treatment, although having no effect upon total

276 hate diester, acetate, benzoate, perrhenate, nitrate, triflimide, perchlorate, hexafluorophosphate, h

277 pending on redox conditions is a result of a nitrate-triggered roll-front mobilization of geogenic ur

278 ransiently exposed the cultures to oxygen or nitrate twice daily and investigated the community respo

279 tyrosine nitration proceeded in vitro Three nitrated tyrosines reside in the heme-binding site of he

280 Nitrate uptake by plant cells requires both high- and lo

281 LjNPF8.6 achieves nitrate uptake in Xenopus laevis oocytes at both 0.5 and

282 e such different functions, ranging from net nitrate uptake to nitrate/nitrite exchange.

283 Nitrate uptake was decreased in the mutant along with re

284 The association between nitrate use and all-cause mortality and the composite of

285 ion >/=40%, we derived propensity scores for nitrate use using 52 baseline variables.

286 uctive pulmonary disease, diabetes mellitus, nitrate use, and elevated concentrations of glucose, N-t

287 e rapid diversification and proliferation of nitrate-using cyanobacteria and, potentially, eukaryotic

288 t significant NO can be derived from dietary nitrate, via the 'alternative NO pathway'.

289 y of nitroalkynes through the development of nitrated vinyl silyltriflate equivalents.

290 n the reaction of 4-OPA with AS and ammonium nitrate was greatly accelerated by evaporation of the so

291 In HFpEF, the use of nitrates was not associated with improvements in all-cau

292 rogenous concentrations and dual isotopes of nitrate were measured to ascertain the spatial and tempo

293 Nitrates were associated with worse composite outcome in

294 Interestingly, more than 95% of the nitrates were removed from the BRE after the three diafi

295 7; mean [SD] age, 76 [12] years; 46% women), nitrates were used in 17%, and the crude 1-year survival

296 report unique Ca(2+) signalling triggered by nitrate with live imaging of an ultrasensitive biosensor

297 The addition of nitrate with strong pi affinity nullified (IC50 = 2.2 mM

298 (15)N abundance is 7 mumol/L for nitrite and nitrate, with a relative standard deviation (RSD) of rep

299 The accumulation of nitrite and nitrate within the reactor, observed midway through the

300 to allow the organism to efficiently respire nitrate without the significant release of intermediates