ライフサイエンスコーパス: nitrite

1 nhibitory effects due to the accumulation of nitrite.

2 play no role in growth of the bacterium with nitrite.

3 trification in supplying both processes with nitrite.

4 -damo) oxidize methane and reduce nitrate to nitrite.

5 tase is proposed to mediate the reduction of nitrite.

6 colonized with both bacteria and received no nitrite.

7 oducts after addition of either particles or nitrite.

8 ase, and showed that cyanate was oxidized to nitrite.

9 -alkyl anilines is reported using tert-butyl nitrite.

10 ident with a peak in hzsA gene abundance and nitrite.

11 s that potentially avoids them competing for nitrite.

12 olled by the photolysis rates of nitrate and nitrite.

13 as compared with biofilms that contained no nitrite.

14 usages produced with reduced level of sodium nitrite.

15 ogenous redox molecules such as ascorbate or nitrite.

16 ation were not affected by acute infusion of nitrite.

17 ve abnormal urinalyses with pyuria and urine nitrites.

18 When nitrite (0.1-2 mg N/L) was spiked into effluent samples,

19 trite and 0.150 uL/g TP; T4: 50 mg of sodium nitrite, 0.075 uL/g TP and 0.075 uL/g PM; T5: 50 mg of s

20 The endogenous addition of nitrite (1 mM) considerably increased heme iron nitrosyl

21 Occurrence of detectible nitrite (14-352 mg kg(-1) fw) was most frequent in winte

22 ss graft patients treated with either sodium nitrite (30-min infusion of 10 mumol/min) or vehicle [0.

23 VO2 was not significantly different between NITRITE (6.1 +/- 1.8 mL 100 g(-1) min(-1) ) and SALINE (

24 the combination (termed AB569) of acidified nitrite (A-NO(2) (-)) and Na(2)-EDTA (disodium ethylened

25 zole with the reactive species produced when nitrite absorbed sunlight was affected by the presence o

26 Stable nitrite accumulation (77%) was achieved through high F:M

27 Stable nitrite shunt with nitrite accumulation ratio over 95% and excellent nitrog

28 n and nitrogen removal by inducing sustained nitrite accumulation via a single spike of nitrite to ae

29 reasing nitrate concentrations, with minimal nitrite accumulation, further demonstrated microbial act

30 uggests that they are an important source of nitrite across marine OMZ boundary layers.

31 More specifically, nitrite activates histidine kinase sensor VbrK through S

32 suggesting limited or no effects of nitrate/nitrite administrations in highly oxidative and highly p

33 enuate the corrosion in sewers using calcium nitrite-admixed concrete.

34 A negative correlation between the calcium nitrite admixture in concrete and the abundance of sulfi

35 e, together with control coupons that had no nitrite admixture, for 18 months.

36 he goal of this study was to examine whether nitrite affects S. mutans virulence during polymicrobial

37 crease exhaled NO concentration over inhaled nitrite alone in pigs exposed to alveolar hypoxia.

38 ttuce growth; however had distinct impact on nitrite, amino acid, organic acid, and soluble sugar con

39 /g TP and 0.075 uL/g PM; T5: 50 mg of sodium nitrite and 0.150 uL/g PM.

40 50 mg of sodium nitrite; T3: 50 mg of sodium nitrite and 0.150 uL/g TP; T4: 50 mg of sodium nitrite,

41 mmonium-oxidizing (anammox) bacteria convert nitrite and ammonium via nitric oxide (NO) and hydrazine

42 By using on-site-produced nitrite and ammonium, the proposed strategy is feasible

43 phosphodiesterase type 5 inhibitors, sodium nitrite and endothelin receptor antagonists.

44 TCNM-FP in a non-nitrified effluent with low nitrite and nitrate concentrations but increased the TCN

45 itrite infusion significantly increased both nitrite and nitrate concentrations in plasma.

46 FP) of wastewater effluents and the roles of nitrite and nitrate in this process.

47 mmals both enzymatically and by reduction of nitrite and nitrate ions.

48 c environment, the absorption of sunlight by nitrite and nitrate leads to the transformation of trace

49 In addition to gaseous NO/NO(2), nitrite and nitrate were also detected in water, with th

50 es analyzed by HPIEC-SCD that were devoid of nitrite and nitrate were subjected to HRMS using a Q-exa

51 Since both nitrite and nitric oxide are proposed oxidants in denitr

52 ogenates from normal placentas, and that NO, nitrite and nitrosothiols react with placental homogenat

53 Exogenous NO, nitrite and nitrosothiols react with placental homogenat

54 Findings indicate that nitrate, nitrite and nitrosothiols, but not NO or iron nitrosyl s

55 vironments reduction of both ammonia-derived nitrite and NO could lead to nitrous oxide (N(2)O) produ

56 These studies establish that nitrite and NO perform multiple functions during plant h

57 eye components via tears and then reduced to nitrite and NO, thereby being an important source of NO

58 likely as a consequence of its reduction to nitrite and NO.

59 horylation status did not differ between the nitrite and saline groups.

60 e in vivo to generate nitric oxide (NO) from nitrite and that this formation is increased in the pres

61 colorimetric reaction that occurred between nitrite and the added Griess reagent.

62 creased generation of nitric oxide (NO) from nitrite and vascular relaxation in vitro.

63 directly and indirectly through provision of nitrite and, after further oxidation, nitrate to denitri

64 ng compounds (for example, nitrates, amines, nitrites and nitrogen oxides) that are typically present

65 is produced in vivo during the reduction of nitrites and participate in NO homeostasis.

66 igher flow rates released significantly more nitrites and SEAP into perfusion effluent, and SC cells

67 emoval of dissolved nitrogen (i.e., nitrate, nitrite, and ammonia) and organic carbon, the formate-to

68 he presence of the photosensitizers nitrate, nitrite, and humic acid.

69 There were measurable levels of ammonium, nitrite, and nitrate during free chlorine application, a

70 rs, including amino acids, vitamins, oxygen, nitrite, and sulfate.

71 nants when relatively high concentrations of nitrite are present (e.g., in surface waters receiving r

72 t the pathogen V. parahaemolyticus perceives nitrite as a host-derived signal and responds by downreg

73 demonstrated that this novel use of calcium nitrite as an admixture in concrete is a promising strat

74 Concrete coupons with calcium nitrite as an admixture were exposed in a sewer manhole,

75 es biofilms with S. parasanguinis containing nitrite as compared with biofilms that contained no nitr

76 1a), this report illustrates NO release from nitrite at copper(II) following a proton-coupled electro

77 tric oxide (NO) is produced from nitrate and nitrite, at least partially by NR, in nectaries and nect

78 tion of nitrite oxidation resulted in higher nitrite availability for DNRA, anammox, and nitrite-depe

79 leading to more acidic conditions and lower nitrite availability in healthy individuals.

80 pH impacted the removal rates of nitrate and nitrite but not that of total dissolved nitrogen or form

81 meat samples, were analysed for nitrate and nitrite by an optimised RP-HPLC technique with isocratic

82 Oxidation of ammonia to nitrite by bacteria and archaea is responsible for globa

83 Under anaerobic conditions, production of nitrite by nitrate-reducing microorganisms and enzymatic

84 he salutary metabolic effects of nitrate and nitrite can be ascribed to nitrite-derived formation of

85 Nitrite can maintain ATP generation under hypoxia by cou

86 solved oxygen (DO) and associated variables (nitrite, chlorophyll, and ammonium) with depth and betwe

87 convective O(2) delivery, an elevated plasma nitrite concentration affects neither muscle force, nor

88 tential applications to routinely screen the nitrite concentration of meat products and ensure food s

89 Nitrite concentration was determined by monitoring the c

90 The higher the nitrite concentration, the greater the increase in the T

91 ary nitrate supplementation increases plasma nitrite concentration, which provides an oxygen-independ

92 reported positive effects of elevated plasma nitrite concentrations are presumably mediated by the in

93 Interestingly, high salivary nitrite concentrations have been associated with a decre

94 Winter and summer nitrate/nitrite concentrations in 11 salad vegetables were surve

95 ometry, as well as indirectly by determining nitrite concentrations in cell incubation media.

96 Modulating nitrite concentrations in the oral cavity could be a use

97 ercise-induced changes in muscle nitrate and nitrite concentrations in young healthy humans, under ba

98 In addition, fasting plasma nitrite concentrations increased after the modified diet

99 Increased plasma nitrite concentrations may have beneficial effects on sk

100 We found that baseline nitrate and nitrite concentrations were far higher in muscle than in

101 Lower saliva and plasma nitrite concentrations were found after using CHX, follo

102 supplemented with BRJ+ (P < 0.001), whereas nitrite concentrations were increased only in eNOS(-/-)

103 BP was measured; at GD18.5, maternal nitrate/nitrite concentrations, uterine artery (UtA) blood flow

104 BRJ- did not alter nitrate/nitrite concentrations.

105 teria, and pH, lactate, glucose, nitrate and nitrite concentrations.

106 Sodium ascorbate decreased residual nitrite considerably.

107 The lowest residual nitrite content and TBARS value were observed in treatme

108 a* value (redness) and an increased residual nitrite content in products that was still within the ra

109 min had an alkaline environment and a higher nitrite content than that at the other lengths of treatm

110 ganic peppermint (PM) on pH, color, residual nitrite content, lipid oxidation (TBARS value) and total

111 The study shows that the nitrate and nitrite contents of meat samples in Fiji were below the

112 ient in hcp is not able to grow with 200 muM nitrite, demonstrating that the sensitivity of the HcpR

113 nitrite availability for DNRA, anammox, and nitrite-dependent anaerobic methane oxidation.

114 Aerobic and nitrite-dependent methanotrophs make a living from oxidi

115 Mice were subjected to a nitrate/nitrite-depleted diet for 2 wk, then supplemented with s

116 ts of nitrate and nitrite can be ascribed to nitrite-derived formation of NO species and activation o

117 BCs and then deoxygenated in the presence of nitrite, export of NO bioactivity was detected as inhibi

118 al oxygen tension, but it is unclear whether nitrite exposure can delay fatigue development and impro

119 echanisms by which increased skeletal muscle nitrite exposure might be ergogenic and imply that this

120 Sodium nitrite failed to improve mitochondrial metabolic effici

121 similar to those of abiotic experiments with nitrite (from 1.15 x 10(-14) to 4.94 x 10(-13) mol m(-2)

122 gle mouse muscle fibres acutely treated with nitrite had a lower force and cytosolic calcium concentr

123 In addition to these functions, nitrite has been reported to influence mitochondrial str

124 de-producing oral commensal streptococci and nitrite has been shown to mediate the generation of reac

125 as sodium, potassium, calcium, chloride, and nitrite, has significant diagnostic value in detecting v

126 erference, we developed a bioassay to remove nitrite in HS samples using the denitrifying bacterium P

127 l method for extraction and determination of nitrite in meat and chicken products by vortex-assisted

128 ulace, the present study reports nitrate and nitrite in meat.

129 ice (uPAD) to determine the concentration of nitrite in pork and enhanced the limit of detection by a

130 The limit of detection of this device for nitrite in pork was determined to be 19.2 mg kg(-1) by a

131 uccessfully applied for the determination of nitrite in processed products.

132 tion and preconcentration of trace levels of nitrite in soil, sausage, water samples (tap, mineral, a

133 ior to infection with S. mutans and received nitrite in the drinking water, as compared with animals

134 e nitric oxide generation from benign sodium nitrite in the presence of modest electric fields.

135 utant seedlings accumulated less nitrate and nitrite in the root tissues and ammonium in the shoot ti

136 This undersizing caused accumulation of nitrite in the system when liquid was circled in a quasi

137 of sodium, potassium, calcium, chloride, and nitrite in urine, accurately quantified using a smartpho

138 steps, the aerobic oxidation of ammonia and nitrite, in a single organism.

139 ius model, we evaluated the effects of acute nitrite infusion on muscle force and skeletal muscle oxi

140 Nitrite infusion significantly increased both nitrite an

141 a (but normal convective O(2) delivery) with nitrite infusion.

142 mbined infusion of acetazolamide with sodium nitrite inhalation did not further increase exhaled NO c

143 that the combination of S. parasanguinis and nitrite inhibited S. mutans growth and biofilm formation

144 developed to determine the concentration of nitrite ion (the nitrogen compound that possess higher t

145 y nontrained personnel to not only determine nitrite ion concentration but also to automatically send

146 ne database, allowing a worldwide mapping of nitrite ion concentration.

147 nitrogen cycle disruption, these systems for nitrite ion screening will suddenly become a standard gl

148 hermal lysis of nitro-explosives to generate nitrite ions.

149 on wanes in the succeeding 3 h of hypoxia as nitrite is metabolized and excreted.

150 er is constructed between a graphitic carbon nitrite layer (g-C(3) N(4) ) and carbon cloth (CC), enab

151 color changes, textural properties, residual nitrite level and lipid oxidation).

152 The residual nitrite level increased with the addition of quinoa so t

153 of DBD-CP was optimized based on the pH and nitrite level of the plasma-treated water (PTW).

154 s of these pathways, we analyzed nitrate and nitrite levels in components of the eye and lacrimal gla

155 ation and postharvest storage on nitrate and nitrite levels in lettuce, rocket and spinach.

156 Nitrate and nitrite levels were higher in cornea than in other eye p

157 UV/vis spectropotentiometry showed that nitrite-loaded Shewanella oneidensis ccNiR is reduced in

158 tures - particularly subsurface ammonium and nitrite maxima.

159 l OAB urinary biomarkers including ATP, ACh, nitrite, MCP-1 and IL-5 and participants' confounders, a

160 Pore water nitrite, methane and oxygen were key factors influencing

161 Here, we show that host-derived nitrite modifies the activity of a bacterial histidine k

162 Nitrite +nitrate concentrations were >100 times the aver

163 kout mice were associated with lower urinary nitrite/nitrate excretion and markedly increased urinary

164 age-specific diversifications of NOSs and NO/nitrite/nitrate sensors from the common ancestor of Meta

165 ng soluble guanylate cyclases as putative NO/nitrite/nitrate sensors.

166 ssociated with a significant increase in the nitrite/nitrate, IL-6 and TNF-alpha levels, iNOS express

167 film reactor (MBfR) by coupling anammox with nitrite/nitrate-dependent anaerobic methane oxidation (n

168 anaerobic ammonium oxidation (anammox) with nitrite/nitrate-dependent anaerobic methane oxidation (n

169 ctroscopy (OES), whereas hydrogen peroxides, nitrites, nitrates, and pH were measured in PAB.

170 reduction of nitrate to dinitrogen gas over nitrite, nitric oxide, and nitrous oxide.

171 During contractions, sodium nitrite (NITRITE) or sodium chloride (SALINE) was infuse

172 -) ) supplementation, which increases plasma nitrite (NO(2) (-) ) concentration, has been reported to

173 rigins of and analytical tools for detecting nitrite (NO(2) (-)), nitrate (NO(3) (-)), nitrosyl-metal

174 plied bleach via aqueous reactions involving nitrite (NO(2)(-)) and ammonia (NH(3)), respectively.

175 -SCD) was validated for the determination of nitrite (NO(2)(-)) and nitrate (NO(3)(-)) in the edible

176 dicate oxygen isotopic equilibration between nitrite (NO(2)(-)) and water, and kinetic isotope effect

177 n the exclusive action of the acid (H(+)) or nitrite (NO(2)(-)) counterparts.

178 s of NO generation by nitrate (NO(3)(-)) and nitrite (NO(2)(-)) ions reduction has received much less

179 ing intracellular electron acceptors such as nitrite (NO(2)(-)) or nitric oxide (NO).

180 ce, the transition-metal-mediated routes for nitrite (NO(2)(-)) to nitric oxide (NO) conversion and p

181 However, the presence of nitrite (NO(2)(-)), a central intermediate of the N-cycl

182 Hydroxylamine (NH(2)OH) and nitrite (NO(2)(-)), intermediates during the nitritation

183 ene significantly upregulated in response to nitrite (NO(2)) and that this regulation is dependent on

184 Boosting this nitrate-nitrite-NO pathway results in attenuation of NADPH oxida

185 Dietary nitrate fuels a nitrate-nitrite-NO signaling pathway, which prevented many featu

186 he putative effects of inorganic nitrate and nitrite on mitochondrial function in skeletal muscle.

187 O(2)(s) by chemical oxidants (nitrate and/or nitrite) or by Thiobacillus denitrificans, a widespread,

188 During contractions, sodium nitrite (NITRITE) or sodium chloride (SALINE) was infused into th

189 hen supplemented with sodium nitrate, sodium nitrite, or sodium chloride (1 g/L) in drinking water ad

190 at it would be necessary to incorporate less nitrites, or it might even be unnecessary, contributing

191 ratory complexes I-V and the machineries for nitrite oxidation and carbon fixation via the reductive

192 Although oceanic ammonia and nitrite oxidation are balanced, ammonia-oxidizing archae

193 back from high to low F:M-C:N recovered the nitrite oxidation function, with an increase in Nitrobac

194 Ammonia and nitrite oxidation genes were expressed through the entir

195 ospira sublineage I OTU was found to perform nitrite oxidation in full-scale domestic wastewater trea

196 res with cobalamin (vitamin B(12)) increased nitrite oxidation rates and stimulated a 33-fold increas

197 Results showed that sulfide: (i) decreased nitrite oxidation rates but increased ammonia oxidation

198 We infer that inhibition of nitrite oxidation resulted in higher nitrite availabilit

199 o nitrogen cycling (i.e., ammonia oxidation, nitrite oxidation, and denitrification), and carbon fixa

200 trification, anammox, ammonia oxidation, and nitrite oxidation, were examined across the oxycline, su

201 effective catalysis of nitrate reduction and nitrite oxidation, which results in high cathode areal c

202 teria of the genus Nitrobacter, cosmopolitan nitrite oxidizers that inhabit nutrient-rich freshwater,

203 no need to invoke yet undiscovered, abundant nitrite oxidizers to explain nitrification rates in the

204 zing archaea (AOA) vastly outnumber the main nitrite oxidizers, the bacterial Nitrospinae.

205 Stable suppression of nitrite oxidizing bacteria (NOB) is one of the major bot

206 Thus, nitrite oxidizing bacteria (NOB) may in fact thrive unde

207 However, under mainstream conditions, nitrite oxidizing bacteria (NOB) out-select anammox bact

208 A) and free nitrous acid (FNA) inhibition on nitrite-oxidizing bacteria (NOB).

209 ptides related to housekeeping proteins from nitrite-oxidizing microorganisms were detected, their ab

210 etaproteobacterial ammonia monooxygenase and nitrite oxidoreductase transcript abundances revealed th

211 e biofilm reactors (MBfRs) fed with nitrate, nitrite, oxygen at a relatively low rate, and oxygen at

212 Plasma nitrite (P = 0.01), S-nitrosothiols (P = 0.03) and total

213 are needed, OH and NO generation by organic-nitrite photolysis in the UVA range is preferable.

214 droxyl radical (.OH) produced by nitrate and nitrite photolysis oxidizes contaminants, absorption of

215 e to six decades of chl-a, Secchi depth, and nitrite plus nitrate (NO(2) + NO(3)) data to support tre

216 cteria (NOB) out-select anammox bacteria for nitrite produced by ammonium oxidizing bacteria (AOB).

217 We observed substantial and linear rates of nitrite production from urea and cyanate additions, whic

218 Since the nitrite production is self-supporting, no additional ong

219 Therefore, nitrite production is the bottleneck in mainstream anamm

220 Nitrite production reduced by 4-17 and 3-14 uM following

221 take and clearance, reactive oxygen species, nitrite production, autophagy, signaling, messenger RNA,

222 restored Nrf2/nNOSalpha expression and total nitrite production.

223 cytokine secretion, phagocytosis, or nitrate/nitrite production.

224 illary electrophoresis assays, we quantified nitrites (products of NO oxidation) and L-citrulline (co

225 demonstrate that commensal streptococci and nitrite provide protection against S. mutans pathogenesi

226 anged from 0.00 to 124 mg kg(-1) whereas the nitrite ranged from 0.00 to 164 mg kg(-1).

227 vement of nitrogen dioxide, which forms when nitrite reacts with hydroxyl radical.

228 ith l-3-aminoalanine and a polymer-supported nitrite reagent-mediated diazotization and cyclization o

229 any NO generation, whereas nebulized sodium nitrite reduces HPV by NO formation; however; combined i

230 A single nebulization of sodium nitrite reduces HPV, but this action wanes in the succee

231 OB and induced cross-feeding between AOB and nitrite reducing organisms.

232 tween the enzyme that produces NO; the cd(1) nitrite reductase (cd(1)NiR) and the enzyme that reduces

233 fer between the copper centers in the copper nitrite reductase (CuNiR) family of enzymes.

234 ossess atypical heme-binding sites, the NrfA nitrite reductase (CXXCK) and the SirA sulfite reductase

235 Cytochrome c nitrite reductase (NrfA) catalyzes the reduction of nitr

236 ZmNLP5 directly regulates the expression of nitrite reductase 1.1 (ZmNIR1.1) by binding to the nitra

237 ix, significantly increases copper-catalyzed nitrite reductase activity (CuNiR).

238 gns include those with carbonic anhydrase or nitrite reductase activity by incorporating a ZnHis(3) o

239 of our cupredoxin models, and enhancement of nitrite reductase activity up to 1000-fold.

240 We also report that CblC exhibits nitrite reductase activity, converting cob(I)alamin and

241 The newly described nitrite reductase and denitration activities of CblC ext

242 , including strains that are able to express nitrite reductase and grow in anaerobic environments, su

243 carbonic anhydrase as a nitrous anhydrase or nitrite reductase as a mechanism for its inhibition of H

244 We found that the robust activity of the nitrite reductase complex NirBD depended on expression o

245 function as either a nitrous anhydrase or a nitrite reductase in the lungs of pigs, and probably oth

246 ytic efficiency ( k(cat)/ K(M)) of native Cu nitrite reductase involve both substrate binding ( K(M))

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

248 llele encoding a highly efficient gonococcal nitrite reductase.

249 yi represents a new subclass of cytochrome c nitrite reductase.

250 cofactor in a conserved class of sulfite and nitrite reductases that catalyze the six-electron reduct

251 onditions of hypoxia and in the presence of "nitrite reductases" such as heme- and molybdenum-contain

252 electron configuration, can be generated by nitrite reduction at a copper(I) dichloride anion or by

253 psilon-nitrogen ligation allows for a better nitrite reduction catalyst, displaying 2 orders of magni

254 experiments previously showed that catalytic nitrite reduction to ammonia by S. oneidensis ccNiR requ

255 e relationship between dissimilatory nitrate/nitrite reduction to ammonium (DNRA) and diel vertical m

256 production; and (iii) induced dissimilatory nitrite reduction to ammonium (DNRA).

257 lowing only for methane oxidation coupled to nitrite-reduction.

258 tric oxide (NO) and the reduction of nitrate/nitrite regulate important mechanisms that contribute to

259 Here, we present a prototype nitrate/nitrite sensor based on droplet microfluidics that in co

260 This study brings the mainstream nitrite shunt and PN/A one step closer to wide applicati

261 ion increased initially as the attainment of nitrite shunt but exhibited a declining trend during the

262 e major bottlenecks for achieving mainstream nitrite shunt or partial nitritation/anammox (PN/A).

263 over an extended time, leading to failure of nitrite shunt or PN/A.

264 Stable nitrite shunt with nitrite accumulation ratio over 95% a

265 In the presence of ~1 mg N/L of nitrite, sunlight irradiation for 8 h increased the TCNM

266 The nitrite-sunlight effect was also observed for four model

267 Neither sodium nitrate nor sodium nitrite supplementation altered mitochondrial coupling e

268 The nitrite supply challenge in mainstream anammox implement

269 tches were produced: T1: 100 mg/kg of sodium nitrite; T2: 50 mg of sodium nitrite; T3: 50 mg of sodiu

270 mg/kg of sodium nitrite; T2: 50 mg of sodium nitrite; T3: 50 mg of sodium nitrite and 0.150 uL/g TP;

271 cid, which is generated in situ from calcium nitrite that is added to the concrete.

272 d nitrite accumulation via a single spike of nitrite to aerobic digester operated at a natively low p

273 ermediate in the ccNiR-mediated reduction of nitrite to ammonia, whose degree of accumulation depends

274 electron reduction of sulfite to sulfide and nitrite to ammonia.

275 JGTA-S1 could not convert nitrate or nitrite to ammonium but harbors diazotrophic (N(2)-fixin

276 reductase (NrfA) catalyzes the reduction of nitrite to ammonium in the dissimilatory nitrate reducti

277 Nitrification, the oxidation of ammonia via nitrite to nitrate, is a key process in marine nitrogen

278 uctase activity, converting cob(I)alamin and nitrite to NOCbl.

279 otect the bacterial cytoplasm from excessive nitrite toxicity during anaerobic respiration with abund

280 ting in mRNA cross-regulation of nitrate and nitrite transporter genes.

281 significant expression of the active nitrate/nitrite transporter sialin in human skeletal muscle.

282 base pairing to repress the synthesis of the nitrite transporter, NirC, resulting in mRNA cross-regul

283 Microbial formate-nitrite transporter-type proteins (FNT) exhibit dual tra

284 Formate/nitrite transporters (FNTs) selectively transport monova

285 Nitrite treatment delayed fatigue development during rep

286 del with primary human hepatocyte spheroids, nitrite treatment reduced the degree of metabolically in

287 gestive tract even in conditions in which no nitrite was added to the model.

288 The estimated dietary intake of nitrate and nitrite was calculated from a 24-h diet recall study as

289 rk sausages produced with 50 mg/kg of sodium nitrite was investigated.

290 nitritation (i.e., conversion of ammonium to nitrite) was successfully achieved in the biotrickling f

291 Dissolution rates of UO(2)(s) with dissolved nitrite were approximately 5 to 10 times greater than wi

292 xhaled gas concentration from inhaled sodium nitrite were not increased by acetazolamide during alveo

293 ons, methanotrophs mainly oxidize ammonia to nitrite, whereas in hypoxic and anoxic environments redu

294 ion of NOCl that converts alcohol into alkyl nitrite, which in the presence of Fe(3+) ions and fluori

295 ral commensal bacteria may reduce nitrate to nitrite, which may subsequently be reduced to nitric oxi

296 (A6), an autotroph that oxidizes ammonium to nitrite while reducing ferric iron, were conducted in th

297 evance of augmented NO generation by CA from nitrite with acetazolamide in anaesthetized pigs during

298 can also be synthesized from the reaction of nitrite with an [LCu(II)Cu(I)](3+) synthon.

299 n quantify the concentrations of nitrate and nitrite within each droplet and provides high measuremen

300 detecting potassium, calcium, chloride, and nitrite within the whole physiological range of concentr