ライフサイエンスコーパス: nitrate reductase

1 This enhancement required a functional nitrate reductase.

2 tate had no influence on synthesis of either nitrate reductase.

3 ation, and thereby regulates the activity of nitrate reductase.

4 confirming that the NapA enzyme is the sole nitrate reductase.

5 low to support respiration by membrane-bound nitrate reductase.

6 the activities of both acid phosphatase and nitrate reductase.

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

8 , that is constitutive and not inducible for nitrate reductase.

9 ation of phosphoenolpyruvate carboxylase and nitrate reductase.

10 biosynthesis of a molybdopterin cofactor of nitrate reductase.

11 required by various molybdoenzymes, such as nitrate reductase.

12 at the first seven genes encode a functional nitrate reductase.

13 omponents as exemplified by incorporation of nitrate reductase.

14 produced NO, and this requires expression of nitrate reductase.

15 e aerobe, expresses two distinct respiratory nitrate reductases.

16 , such as the membrane-bound and periplasmic nitrate reductases.

17 ree of homology to prokaryotic dissimilatory nitrate reductases.

18 cteria readily reduce nitrate to nitrite via nitrate reductases.

19 y double mutations in NOA1 and either of the nitrate reductases.

20 . Typhimurium strains with defects in either nitrate reductase A (narG mutant) or the regulator induc

21 Escherichia coli nitrate reductase A (NarGHI) is a membrane-bound enzyme

22 The molybdenum atom of Escherichia coli nitrate reductase A (NarGHI) is coordinated by two PPT-d

23 Synthesis of active nitrate reductase A and the cytoplasmic, NADH-dependent

24 s with a second set of mutants revealed that nitrate reductase A couples more effectively with ubiqui

25 es present in Escherichia coli suggests that nitrate reductase A, encoded by the narGHI genes, is the

26 te of the only functional nitrate reductase, nitrate reductase A, is located in the cytoplasm, so nit

27 ocess, we knocked down the gene encoding for nitrate reductase, a key enzyme required for the assimil

28 we show that the native localization of the nitrate reductase, a major respiratory complex under ana

29 the biofilm state included those encoding a nitrate reductase, a nitrite reductase, and a nitric oxi

30 sence of protein FA, to enhance the level of nitrate reductase activation achieved on incubation with

31 lent cations among the CRP/FNR (fumarate and nitrate reductase activator protein) superfamily of regu

32 AMP receptor protein)- and FNR (fumarate and nitrate reductase activator protein)-dependent promoters

33 Increases in nitrate reductase activities after exposure of barley pl

34 oli which produced formate hydrogenlyase and nitrate reductase activities only when grown in medium w

35 efects in metabolism including a loss of all nitrate reductase activities, biofilm maturation, and vi

36 that the PA1006 protein is critical for all nitrate reductase activities, growth as a biofilm in a c

37 ures and hypoxic cultures yielded comparable nitrate reductase activities.

38 We also detected nitrate-inducible nitrate reductase activity (2 to 39 nmol min-1 mg-1) in

39 Nitrate reductase activity (NRA) associated with the mic

40 shown to moderately affect fermentation, but nitrate reductase activity and fnr are dispensable for f

41 berated from the membrane, NarGH retains its nitrate reductase activity and forms films on graphite a

42 produced a strain that had aerobic levels of nitrate reductase activity but failed to show hypoxic up

43 vity increased approximately 100-fold, while nitrate reductase activity decreased 10-fold in whole-ce

44 ing the loss of assimilatory and respiratory nitrate reductase activity in a mobA deletion mutant.

45 We measured reduced viologen-dependent nitrate reductase activity in a series of strains with c

46 Consistent with our hypothesis, nitrate reductase activity in colonized plants was twice

47 This indicates that nitrate reductase activity in M. tuberculosis is due to

48 Mycobacterium tuberculosis induces nitrate reductase activity in response to decreasing oxy

49 The buzz mutant also showed increased nitrate reductase activity in the shoots under low nitra

50 The narG mutant showed no nitrate reductase activity in whole culture or in cell-f

51 In this hypoxic state, nitrate reductase activity is strongly induced.

52 All eight lines had detectable nitrate reductase activity ranging from 7% to 150% of wi

53 ized that colonized plants would have higher nitrate reductase activity than uncolonized plants becau

54 phenotype in line with a severe reduction in nitrate reductase activity that may be due to the overac

55 subsequently express methyl viologen-linked nitrate reductase activity under aerobic conditions with

56 previous studies had demonstrated that high nitrate reductase activity under substrate-limiting cond

57 The napF operon-encoded nitrate reductase activity was not sensitive to azide, a

58 rains have lost hydrogen sulfide production, nitrate reductase activity, and gas production from gluc

59 elated with enhanced nitrate content, higher nitrate reductase activity, and sustained ammonium conte

60 re or assimilate nitrate and did not express nitrate reductase activity, confirming that the NapA enz

61 reported appearance of a respiratory type of nitrate reductase activity, the increase in glycine dehy

62 5, neither of which contained any detectable nitrate reductase activity, were selected for complement

63 trate reduction requires exogenous microbial nitrate reductase activity, which is unlikely to be achi

64 erepressed and expresses very high levels of nitrate reductase activity.

65 yanide was a noncompetitive inhibitor of the nitrate reductase activity.

66 the Wood-Ljungdahl pathway genes and repress nitrate reductase activity.

67 60 and AMC364 lack methyl viologen-supported nitrate reductase activity.

68 ron catalyst inspired by the active sites of nitrate reductase and (per)chlorate reductase enzymes.

69 which are predicted to encode a periplasmic nitrate reductase and eight encode proteins homologous t

70 e cofactors of many metalloenzymes including nitrate reductase and Mo-nitrogenase.

71 ose oxidase and galactose oxidase deactivate nitrate reductase and must be quenched for biosensor app

72 Both membrane nitrate reductase and nitrite reductase enzyme complexes

73 nitrate or nitrite at 15 degreesC, although nitrate reductase and nitrite reductase were still activ

74 we generated knockouts of the genes encoding nitrate reductase and nitrite reductase, resulting in st

75 n of reduction equivalent, and activities of nitrate reductase and nitrite reductase.

76 lates 3-hydroxy-3-methylglutaryl-Coenzyme A, nitrate reductase and sucrose phosphate synthase in vitr

77 A fluorometric assay using nitrate reductase and the NADPH regenerating system was

78 K, which delivers nitrate to the respiratory nitrate reductase and transfers the product, nitrite, to

79 x, generating substitution of the silacidin, nitrate reductase and urease genes by a resistance casse

80 y both cytosolic (Nar) and periplasmic (Nap) nitrate reductases and fractionates the stable isotopes

81 , together with nasBC (encoding assimilatory nitrate reductase) and nasF (required for nitrite reduct

82 and catalase, and lack of motility, oxidase, nitrate reductase, and gelatinase.

83 sponding enrichment in molecular chaperones, nitrate reductases, and a heat-shock protein.

84 strains defective in the two membrane-bound nitrate reductases, and also defective in either ubiquin

85 It is well established that assimilatory nitrate reductase (ANR) activity in soil is inhibited by

86 ry effect of ammonium (NH4+) on assimilatory nitrate reductase (ANR) activity in soil is not due to N

87 NarG nitrate reductases are observed to typically have an (18

88 ed sites in sulfite oxidase and assimilatory nitrate reductase as deduced from crystallography (sulfi

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

90 are critical for controlling the activity of nitrate reductase, as the formation of polar assemblies

91 stant Staphylococcus aureus in </=6 h: (i) a nitrate reductase assay and (ii) a resazurin microplate

92 Our results were confirmed with the nitrate reductase assay and genomic sequencing.

93 nitrogen cycle and human health, taxonomy of nitrate reductases, assimilatory and dissimilatory nitra

94 to nitrite was accomplished using NADPH and nitrate reductase, (b) excess NADPH, proteins, and inter

95 The construction and characterization of a nitrate reductase-based amperometric electrode for deter

96 Plasma NO3- was reduced to NO2- by nitrate reductase before determination of NO2- concentra

97 lack nitrate reductase Z and the periplasmic nitrate reductase, but express all combinations of narK

98 tein, NarJ, which is not present in purified nitrate reductase, but is required for biogenesis of the

99 nd conclude that 14-3-3 most likely inhibits nitrate reductase by inducing a conformational change th

100 have been found to regulate the plant enzyme nitrate reductase by reversible phosphoserine binding.

101 , alpha, beta, and gamma, of the respiratory nitrate reductase complex in Escherichia coli.

102 ssion of genes coding for the membrane-bound nitrate reductase complex is responsive to CF sputum nit

103 taining bacteriochlorophyll and assimilative nitrate reductase constituted <1% of the sampled bacteri

104 Two of these nitrate reductase-deficient cell lines, nia 3 and nia 25

105 tant with the napA gene encoding periplasmic nitrate reductase deleted could not respire or assimilat

106 eletion mutations in genes encoding membrane nitrate reductase (Delta narGH) and nitrite reductase (D

107 bunit of R. solanacearum's sole assimilatory nitrate reductase, did not grow on nitrate as a sole nit

108 te sensor-response regulator and in membrane nitrate reductase displayed altered motility and biofilm

109 The P. aerophilum nitrate reductase distinguishes itself from nitrate redu

110 ochrome c reductase fragment of spinach NADH-nitrate reductase (EC 1.6.6.1), consisting of the contig

111 al inactivation of the aerobically expressed nitrate reductase eliminated aerobic nitrate reduction,

112 operon and a periplasmic cytochrome c-linked nitrate reductase encoded by the napFDAGHBC operon.

113 Periplasmic nitrate reductase, encoded by the napFDAGHBC operon, fun

114 Also required are respiratory nitrate reductase, encoded by the narGHJI operon, and mo

115 Two distinct nitrate reductases, encoded by narGHI and nasBC, functio

116 The S. Typhimurium genome contains three nitrate reductases, encoded by the narGHI, narZYV, and n

117 sses two membrane-bound proton-translocating nitrate reductases, encoded by the narGHJI and narZYWV o

118 rifier whose genome contains two periplasmic nitrate reductase-encoding gene clusters.

119 Eight of these were further analyzed for nitrate reductase enzyme activity and nitrate reductase

120 r nitrite and electron transport through the nitrate reductase enzyme in narK mutants reveals that Na

121 , and skin commensal bacteria can synthesize nitrate reductase enzyme.

122 trate reduction among different forms of the nitrate reductase enzyme.

123 coli synthesizes two biochemically distinct nitrate reductase enzymes, a membrane-bound enzyme encod

124 ertion of the M. tuberculosis narGHJI into a nitrate reductase Escherichia coli mutant allowed anaero

125 ate reduction by two assimilatory eukaryotic nitrate reductase (eukNR) enzymes.

126 should include microbial, amine precursor or nitrate reductase expression data to provide further mec

127 nts was counteracted by azide, which induced nitrate reductase expression only if the transcriptional

128 while ORF4 codes for a putative fumarate and nitrate reductase (FNR)-type transcription factor, relat

129 metal molybdenum (Mo), which is required by nitrate reductase for denitrification and dissimilatory

130 study constitutes the first description of a nitrate reductase from a hyperthermophilic archaeon.

131 We used V. carteri nitrate reductase gene (nitA) regulatory sequences to co

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

133 A cloned Arabidopsis thaliana nitrate reductase gene Nia 2 was introduced into each of

134 A 1.8-kb promoter fragment from the nitrate reductase gene NIA1 was identified that acts as

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

136 ase under the control of the promoter of the nitrate reductase gene, or was encoded on an episome rep

137 In addition, the narH (nitrate reductase) gene frequency, identified using the

138 gions, designated as NP1 and NP2, of the two nitrate reductase genes NR1 and NR2, respectively, are s

139 ranscription of the two Arabidopsis thaliana nitrate reductase genes.

140 uctural genes, except for single cis-QTL for nitrate reductase, Glu dehydrogenase, and shikimate dehy

141 h a 14-3-3-binding phosphopeptide, including nitrate reductase, glyceraldehyde- 3-phosphate dehydroge

142 uminex, and No2-/No3- was measured using the nitrate reductase/Griess assay.

143 hen incubated at 100 degrees C, the purified nitrate reductase had a half-life of 1.5 h.

144 synthase-type enzyme and from nitrite using nitrate reductase has been demonstrated previously.

145 Hypotheses that nitrate reductase has direct or indirect roles in nitrat

146 ons, the napF operon, encoding a periplasmic nitrate reductase, has unique features with respect to i

147 Both membrane-bound and periplasmic nitrate reductases have been found in denitrifying bacte

148 The electrode consisted of nitrate reductase held by dialysis membrane onto a Nafio

149 ntial expression of nitrate transporter (and nitrate reductase in all three mutants).

150 nces appear to be related to the activity of nitrate reductase in cells and to the possible expressio

151 Yet the role of periplasmic nitrate reductase in denitrification has not been clearl

152 Low expression of membrane-bound nitrate reductase in narK mutants was counteracted by az

153 To analyze the function of the periplasmic nitrate reductase in Pseudomonas sp. strain G-179, the n

154 is is consistent with a role for the aerobic nitrate reductase in redox homeostasis.

155 s of acid phosphatase, cysteine protease and nitrate reductase in sap samples from epidermal and meso

156 propose that they should be designated nap (nitrate reductase in the periplasm) genes.

157 These results suggest that the periplasmic nitrate reductase in this strain plays a primary role in

158 thways, we conclude that the NO(2)-dependent nitrate reductase-independent pathway is crucial for NO

159 loroplasts and nitrite reductase, but not by nitrate reductase, indicated that N(2)O produced by leav

160 at position 543 (Ser543) promotes binding to nitrate reductase inhibitor protein (NIP).

161 ese findings suggest that the membrane-bound nitrate reductase is critical for P. aeruginosa anaerobi

162 al analysis revealed that the membrane-bound nitrate reductase is essential for P. aeruginosa anaerob

163 Since nitrate reductase is likely responsible for NO productio

164 These results show that one of the nitrate reductases is specific for respiration and denit

165 ra crassa, the expression of the nit-3 gene (nitrate reductase) is dependent upon nitrogen derepressi

166 gulated structural gene nit-3, which encodes nitrate reductase, is dependent upon a synergistic inter

167 uctase1 (NR1) and NR2 (genes that encode two nitrate reductase isoforms) was greatly reduced in the n

168 The activity of the more slowly migrating nitrate reductase isozyme (NR1) was induced by NO3- in g

169 Four isogenic lines with different nitrate reductase isozyme combinations were used to dete

170 r all four genotypes indicating that neither nitrate reductase isozyme has a direct role in nitrate u

171 ld type indicating that the NADH and NAD(P)H nitrate reductase isozymes are responsible for most of t

172 Both nitrate reductase isozymes were induced by nitrate and w

173 L.) has NADH-specific and NAD(P)H-bispecific nitrate reductase isozymes.

174 These results indicate that periplasmic nitrate reductase, like fumarate reductase, can function

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

176 ctor (MoCo) biosynthesis proteins as well as nitrate reductase maturation factor NarJ and component N

177 on of other cytoplasmic molybdenum-dependent nitrate reductases may be phylogenetically widespread as

178 ed for nitrate reductase enzyme activity and nitrate reductase mRNA production.

179 ared in wild-type Columbia-0 (Col-0) and the nitrate reductase mutant nia1nia2.

180 Interestingly, the membrane nitrate reductase mutant was avirulent in C. elegans, wh

181 Nitrate reductase mutants were isolated from hNP 588 pro

182 ous oxide, we demonstrate that a periplasmic nitrate reductase, NAD(P)-linked and copper-containing n

183 occus pantotrophus can express a periplasmic nitrate reductase (Nap) during aerobic growth.

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

185 This result suggests that the periplasmic nitrate reductase (Nap) of S. gotlandica strain GD1(T) f

186 scherichia coli K-12, encoding a periplasmic nitrate reductase (Nap), encodes seven proteins.

187 ified into three distinct types--periplasmic nitrate reductase (Nap), respiratory nitrate reductase (

188 Periplasmic nitrate reductase NapA is a member of the DMSO reductase

189 t, a strain lacking a functional periplasmic nitrate reductase (napA mutant) exhibited a marked growt

190 atory arsenate reductase (arrA), periplasmic nitrate reductase (napA) and membrane-bound selenate red

191 xample the signal peptide of the periplasmic nitrate reductase (NapA) is bound by a cytoplasmic chape

192 Periplasmic nitrate reductase (NapABC enzyme) has been characterized

193 Periplasmic nitrate reductase (napFDAGHBC operon product) functions

194 plasmic nitrate reductase (Nap), respiratory nitrate reductase (Nar) and assimilatory nitrate reducta

195 copper, zinc superoxide dismutase (SOD1) and nitrate reductase (NaR) coimmobilized on carbon nanotube

196 for a reagentless nitrate biosensor based on nitrate reductase (NaR) from Escherichia coli could be a

197 NO), FNR also regulates genes, including the nitrate reductase (nar) operon, a major source of endoge

198 nitrate differently than the membrane-bound nitrate reductase (Nar), which is generally prevalent am

199 atalysis by eukaryotic molybdenum-containing nitrate reductase (NaR, EC 1.7.1.1-3) were investigated

200 chaperone for both the anaerobic respiratory nitrate reductase (NarG) and the assimilatory nitrate re

201 (tnaA), a tryptophan permease (tnaB), and a nitrate reductase (narG), as well as a natural drop in t

202 rification pathway employs inventory such as nitrate reductase NarGH serving M. denitrificans sp. nov

203 e-containing subunit NarI of the respiratory nitrate reductase NarGHI as proteins that interact with

204 coregulation of NasDEF with the respiratory nitrate reductase NarGHI during nitrate respiration.

205 compared with the highly similar respiratory nitrate reductase NarGHI, which has a relatively much lo

206 uctase family of enzymes, which includes the nitrate reductase NarGHI.

207 The expression of nitrate reductase (NarGHI) was examined using a narG-lip

208 and regulatory regions of the membrane-bound nitrate reductase narGHJI operon (Pnar) are fused to a g

209 er altered nitrate control of NarL-dependent nitrate reductase (narGHJI) and fumarate reductase (frdA

210 (star) mutants that constitutively activate nitrate reductase (narGHJI) gene expression and repress

211 m the structural genes of the membrane-bound nitrate reductase (narGHJI) in Paracoccus pantotrophus t

212 trimethylamine oxide reductase (dmsABC), and nitrate reductase (narGHJI), used during anaerobic respi

213 an anaerobic regulator, FNR, and respiratory nitrate reductase, NarGHJI.

214 duced genes, including those for respiratory nitrate reductase, narGHJI.B. subtilis has two distinct

215 ory nitrate reductase (Nar) and assimilatory nitrate reductase (Nas), they are defined by their cellu

216 itrate reductase (NarG) and the assimilatory nitrate reductase (NasC), the latter of which is active

217 Among tobacco transformants carrying a nitrate reductase (Nia) construct under the control of t

218 nse of NR2, but not NR1 or the gene encoding nitrate reductase (NiR), to light signals was impaired i

219 te assimilation, including the gene encoding nitrate reductase (NIT1), are subject to repression by a

220 as reporters Chlamydomonas genes that encode nitrate reductase (NITI) and arylsulfatase (ARS2) transc

221 The active site of the only functional nitrate reductase, nitrate reductase A, is located in th

222 nd nor genes (associated, respectively, with nitrate reductase, nitrite reductase, and nitric oxide r

223 s (e.g. those encoding nitrate transporters, nitrate reductase, nitrite reductase, ferredoxin reducta

224 Studies on the diurnal variations of nitrate reductase (NR) activity during the life cycle of

225 Nitrate reductase (NR) activity increased up to 14-fold

226 Although nitrate reductase (NR) activity increased with salinity,

227 experiments generally paralleled changes in nitrate reductase (NR) activity.

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

229 4-3-3 proteins bind to the hinge 1 region of nitrate reductase (NR) and inhibit its activity.

230 The nature of the association between nitrate reductase (NR) and membranes was examined.

231 state inhibition of the NO-generating enzyme nitrate reductase (NR) attenuates NO production in respo

232 The comparative induction of nitrate reductase (NR) by ambient NO3- and NO2- as a fun

233 The inactivation of phosphorylated nitrate reductase (NR) by the binding of 14-3-3 proteins

234 extremely low in alpha-DiT1 leaves, although nitrate reductase (NR) expression and activity remained

235 (NRs), the nucleotide sequences encoding 19 nitrate reductase (NR) genes from 16 species of fungi, a

236 Nitrate reductase (NR) in leaves is rapidly inactivated

237 Nitrate reductase (NR) is a complex molybdenum cofactor

238 Eukaryotic assimilatory nitrate reductase (NR) is a multi-domain protein that ca

239 reduction of nitrate to nitrite catalyzed by nitrate reductase (NR) is considered to be the rate-limi

240 Nitrate reductase (NR) is rapidly inactivated by phospho

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

242 Spinach leaf NADH:nitrate reductase (NR) responds to light/dark signals an

243 was capable of phosphorylating and rendering nitrate reductase (NR) sensitive to inhibition by 14-3-3

244 inhibited both glutamine synthetase (GS) and nitrate reductase (NR) was highly purified from cauliflo

245 inated phosphorylation and 14-3-3 binding of nitrate reductase (NR), 6-phosphofructo-2-kinase/fructos

246 , the major mechanism of NO synthesis is via NITRATE REDUCTASE (NR), an enzyme of nitrogen assimilati

247 Banding patterns of nitrate reductase (NR), nitrite reductase (NiR), and glu

248 milation in plants by tuning the activity of nitrate reductase (NR), the first and rate-limiting enzy

249 OH1)-mediated hydrogen peroxide (H2 O2 ) and NITRATE REDUCTASE (NR)-mediated nitric oxide (NO) in gua

250 A nitrate reductase (NR)-null mutant of Arabidopsis was co

251 to regulate the expression of genes encoding nitrate reductase (NR).

252 ation of inorganic nitrogen by knocking down nitrate reductase (NR).

253 Recombinant Arabidopsis thaliana NADH:nitrate reductase (NR; EC 1.6.6.1) was produced in the m

254 des were based on sequences from Arabidopsis nitrate reductase (NR2) and the plasma membrane proton p

255 evolutionary mechanisms and relationships of nitrate reductases (NRs), the nucleotide sequences encod

256 The nitrate reductase of the hyperthermophilic archaeon Pyro

257 nitrate reductase distinguishes itself from nitrate reductases of mesophilic bacteria and archaea by

258 ed to determine the role of NADH and NAD(P)H nitrate reductases on nitrate transport and assimilation

259 uctase, narGHJI.B. subtilis has two distinct nitrate reductases, one for the assimilation of nitrate

260 tate levels of nitrate revealed that the two nitrate reductase operons are differentially expressed i

261 al that controls the expression of these two nitrate reductase operons in a differential and compleme

262 Mutants lacking either nitrate reductase or fumarate reductase also had major c

263 In support of this idea, mutants lacking nitrate reductase or fumarate reductase have extreme col

264 ochrome bd oxidase is more advantageous than nitrate reductase or fumarate reductase.

265 Strains lacking nitrate reductase outcompeted fumarate reductase mutants

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

267 Binding of 14-3-3 proteins to nitrate reductase phosphorylated on Ser543 (phospho-NR)

268 ilation through inhibition of phosphorylated nitrate reductase (pNR) in darkened leaves.

269 hO(-), 2-AdO(-), Pr(i)()O(-)), dissimilatory nitrate reductase (QR' = 2-AdS(-)), and formate dehydrog

270 ma 70-type promoter and an FNR (fumarate and nitrate reductase regulator protein) binding site, both

271 RP (cAMP receptor protein)/FNR (fumarate and nitrate reductase regulatory protein) family of transcri

272 genes, encoding nitrate/nitrite permease and nitrate reductase, respectively, were isolated from the

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

274 f the napFDAGHBC operon encoding periplasmic nitrate reductase results from synergistic transcription

275 ity to alpha- and beta-subunits of microbial nitrate reductase, selenate reductase, dimethyl sulfide

276 on of nitrate was developed using simplified nitrate reductase (SNaR) that was produced by genetic re

277 ory nitrate reduction, cellular locations of nitrate reductases, structural and redox chemistry are d

278 The MPT containing enzymes nitrate reductase, sulphite oxidase, and SN oxide reduct

279 ns still allow proper nitrogen repression of nitrate reductase synthesis.

280 he C-terminal domain of gp91(phox) on a corn nitrate reductase template suggests close proximity of t

281 Here we purify a nitrate reductase that specifically catalyzes the format

282 Unlike the membrane-bound nitrate reductase, the nitrate reduction activity in str

283 te-regulated genes (including those encoding nitrate reductase, the nitrate transporter NRT1, and glu

284 this strain are Mo-dependent enzymes, as is nitrate reductase; thus, transport of molybdate is impor

285 est that S. Typhimurium uses the periplasmic nitrate reductase to support its growth on the low nitra

286 lla cytochrome bd-II oxidase synergized with nitrate reductases to drive luminal expansion, and both

287 ess respiratory (Nar) and assimilatory (Nas) nitrate reductases to utilize this abundant respiratory

288 f the narGHJI operon encoding membrane-bound nitrate reductase under any growth condition tested.

289 Nitrate reductase utilizes a Moco but its activity was u

290 In contrast, when the anaerobic nitrate reductase was absent, aerobic nitrate reduction

291 The aerobic nitrate reductase was expressed but not utilized in liqu

292 te biosensor based on recombinant eukaryotic nitrate reductase was implemented in commercial screen-p

293 Notably, the expression of respiratory nitrate reductase was not affected by the carbon sources

294 Under anaerobic conditions the activity of nitrate reductase was reduced by only 50%, showing that

295 synthetic source of NO in tomato cotyledons, nitrate reductase was shown to be under strict control o

296 otype (Az12;Az70) which is deficient in both nitrate reductases, was only 13% of the wild type indica

297 ogenase 3 and several molybdoenzymes such as nitrate reductase were also increased.

298 The activities for fumarate and nitrate reductase were lower in ETRA-153, as were the le

299 ction focuses on the features of periplasmic nitrate reductase where the catalytic subunit of the Nap

300 n and use of four isogenic strains that lack nitrate reductase Z and the periplasmic nitrate reductas