ライフサイエンスコーパス: oxidase

1 endothelial cell protein expression of NADPH oxidase.

2 ermease, and arsH encoding the ArsH MAs(III) oxidase.

3 tegy to inhibit assembly of neutrophil NADPH oxidase.

4 lpha-amylase, alpha-glucosidase and xanthine oxidase.

5 MO-1, as a protein that inhibits BLI-3/NADPH oxidase.

6 rresponding to a bacteroid-specific terminal oxidase.

7 th nitrating nitrite/myeloperoxidase/glucose oxidase.

8 peptide that blocks the activity of NAD(P)H oxidase.

9 on membrane to immobilize the enzyme glucose oxidase.

10 ial for host defense via the phagocyte NAPDH oxidase.

11 zed by 1-aminocyclopropane-1-carboxylic acid oxidase.

12 ECM) components and high expression of lysyl oxidases.

13 is highly selective over LOX and other amine oxidases.

14 A. flavus derived FADGDH and of two glucose oxidases.

15 c FeS enzymes such as aconitase and aldehyde oxidases.

16 e mono- and trinuclear Cu sites of bilirubin oxidases.

17 ldehyde dehydrogenases but never to aldehyde oxidases.

18 ion and deacetylimination catalyzed by lysyl oxidases.

19 ROS originate from mitochondria and NADPH oxidases.

20 expression of 28 transcripts [e.g., acyl-CoA oxidase 1 (ACOX1) and FAT atypical cadherin 1 (FAT1)], w

21 hat CS exposure modulates expression of Dual oxidase 1 (Duox-1), a NADPH oxidases known to generate H

22 ndidate glycoproteins identified (cytochrome oxidase 2 (COX2) and NADH:ubiquinone oxidoreductase core

23 forming stably functional complex with NADPH oxidase 2 (Nox2).

24 nicotinamide adenine dinucleotide phosphate-oxidase 2 and inducible nitric oxide synthase and enhanc

25 /+) ECs and was suppressed by PI3K and NADPH oxidase 2 inhibitors.

26 vealed that OsKO2, which encodes ent-kaurene oxidase 2 of the gibberellin biosynthesis pathway, is do

27 amide adenine dinucleotide phosphate (NADPH) oxidase-2 (NOX-2) expression.

28 he omega-6 lipid products of cytochrome P450 oxidase 2C promote neovascularization in both the retina

29 NADPH oxidase 4 (NOX4) enzyme, which catalyzes the reduction o

30 High-glucose increases NADPH oxidase 4 (NOX4) expression, reactive oxygen species gen

31 h reduced oxidative stress and reduced NAPDH oxidase 4 (NOX4) in glomeruli of diabetic eNOS(-/-) mice

32 d hindlimb that only in the brain does NADPH oxidase 4 (NOX4) lead to ischemic damage.

33 Here we discover that NAD(P)H oxidase 4 (NOX4), an enzyme known to catalyse the oxidat

34 tive oxygen species-generating enzyme, NADPH oxidase 4 (Nox4), regulates a number of physiological an

35 oxide resulting from the activation of NADPH oxidase 4 (NOX4).

36 r-1alpha (HIF-1alpha), downstream of NAD(P)H oxidase-4 (NOX4)-derived reactive oxygen species (ROS).

37 levels of Bax, cleaved caspase-3, and NADPH oxidase-4 expression and reactive oxygen species (ROS) g

38 the effects of the 40% increase in monoamine oxidase A (MAO-A) levels that occurs during PPB, a dieta

39 We report that monoamine oxidase A (MAOA) is a clinically and functionally import

40 ifferentiation factor-3 (GDF3) and monoamine oxidase A (MAOA) that is known to degrade noradrenaline.

41 In a screening for potential monoamine oxidase A and B inhibition ciproxifan showed efficacy on

42 Inhibiting xanthine oxidase, a major reactive oxygen species (ROS) contribut

43 SSPs, aryl-alcohol oxidases (AAO) and the intracellular aryl-alcohol dehydr

44 ity of 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), the enzyme catalysing the final step of e

45 tors (ERF-VII) that, together with plant Cys oxidases, act as an oxygen-sensing mechanism.

46 amide adenine dinucleotide phosphate (NADPH) oxidase activation because pretreatment of eosinophils w

47 LC on angiotensin II (Ang II)-induced NADPH oxidase activation in NRK-52E cells.

48 igher levels of Rac1-GTP, required for NADPH oxidase activation, than sham control kidneys, and genet

49 imulatory effect on catalase and glutathione oxidase activities induced by MCs was found on day 1, an

50 ocampal neurons via diverse effects on NADPH oxidase activity and dendritic spine morphology.

51 A significant decrease in both glucose oxidase activity and H2O2 production as well as defensin

52 her loss of memo-1 or increasing BLI-3/NADPH oxidase activity by overexpression is sufficient to incr

53 4 complete body maps, revealed by cytochrome-oxidase activity in layer 4 of 8 rodent and 1 lagomorph

54 rimary energy source for C. jejuni, inhibits oxidase activity in other bacteria.

55 Thus, the oxidase activity of AOC3 contributes to the development

56 rate 30-fold and 11-fold enhancements in the oxidase activity of Cu- and Fe-bound HCO mimics, respect

57 orbital of copper are central to its higher oxidase activity over iron.

58 la96Leu mutant showed a drastic reduction in oxidase activity using molecular oxygen as the electron

59 to ceCblC-bound cobalamin supports its thiol oxidase activity via a glutathionyl-cobalamin intermedia

60 uces ACC (1-aminocyclopropane-1-carboxylate) oxidase activity, ethylene production and respiration ra

61 rming that the current originates from NADPH oxidase activity.

62 re, IL-12-mediated protection required NADPH oxidase activity.

63 h an increase in F- actin assembly and NADPH oxidase activity.

64 echanism by which heme E degrees ' modulates oxidase activity.

65 Further, we discovered that Rv2466c lacks oxidase activity; rather, it receives electrons through

66 in (MMP-2) and unchanged expression of lysyl oxidase and a second metalloproteinase, MMP-9, in murine

67 tivity of mitochondrial enzymes cytochrome c oxidase and aconitase in differentiating NSC cultures ex

68 de dioxygenase (PDO), rhodanese, and sulfite oxidase and converts H2S to thiosulfate and sulfate.

69 dox enzymes for biosensors (i.e. cholesterol oxidase and glucose oxidase) are targeted.

70 ble silencing of the mRNA encoding glycolate oxidase and increased serum glycolate concentrations in

71 his study aimed to analyze the role of NADPH oxidase and inducible nitric oxide synthase (iNOS) in a

72 to the resistance of Mtuberculosis to NADPH oxidase and LC3 trafficking in vivo.

73 hat virus infection activates endosomal NOX2 oxidase and restricts TLR7 signaling, and that an endoso

74 Chemokine-controlled NADPH oxidases and metabolically controlled mitochondrial sour

75 l NKT cells were primarily produced by NADPH oxidases and not mitochondria.

76 of beta2-integrin-dependent adhesion, NADPH oxidase, and a subset of protein kinases.

77 furcating flavoproteins nitroreductase, NADH oxidase, and flavodoxin.

78 a biocathode made from laccase or bilirubin oxidase, and the anode is made from a zinc plate.

79 ea lion pups for Nissl substance, cytochrome oxidase, and vesicular glutamate transporters.

80 itrogenase, plant leghemoglobin, respiratory oxidases, and other Fe proteins in both organisms.

81 ave either high (PAO) or low (TAO) ascorbate oxidase (AO) activities relative to the wild type.

82 r, followed by the immobilization of alcohol oxidase (AOx) in an intermediate chitosan layer, along w

83 Aldehyde oxidase (AOX) is a metabolic enzyme catalyzing the oxida

84 Alternative oxidase (AOX) is a mitochondrial inner-membrane oxidase

85 Aldehyde oxidase (AOX) is a molibdo-flavoenzyme that has raised g

86 The cyanide-insensitive alternative oxidase (AOX) is a non-proton-pumping ubiquinol oxidase

87 de (H2O2) enzymatically generated by alcohol oxidase (AOx).

88 As the H3R and monoamine oxidases are all capable of affecting neurotransmitter m

89 nicotinamide adenine dinucleotide phosphate oxidases are also inhibited.

90 Sulfite oxidases are metalloenzymes that oxidize sulfite to sulf

91 ensors (i.e. cholesterol oxidase and glucose oxidase) are targeted.

92 that identified high-affinity cytochrome bd oxidase as an essential bacterial gene product for mosqu

93 raldehyde with putrescine oxidase or diamine oxidase as catalysts.

94 he generation of superoxide anion from NADPH oxidase, as well as the amount of hydrogen peroxide and

95 2 and Cox10, a gene encoding a cytochrome IV oxidase assembly factor, prevented the metabolic shift i

96 ymatic fuel cell together with a multicopper oxidase at the cathode, or in a proton exchange membrane

97 artially restored in mice deficient in NADPH oxidase, Atg5, or Atg7, demonstrating that CpsA makes a

98 xidases with slight preference for monoamine oxidase B in both species.

99 The SB is composed of a glucose oxidase-based biosensor, a sentinel platinum sensor, a l

100 iously we showed that an effective bilirubin oxidase (BOD)-based biocathode using graphene oxide (GO)

101 ogether with the high assay versatility (any oxidase can be coupled with HRP-based color change react

102 h (SRCR) repeats, rather than the C-terminal oxidase catalytic domain, represent the major deacetylas

103 Cytochrome c oxidase (CcO) catalyzes the reduction of oxygen to water

104 Cytochrome c oxidase (CcO) is a transmembrane protein that uses the f

105 Proton pumping A-type cytochrome c oxidase (CcO) terminates the respiratory chains of mitoc

106 Cytochrome c oxidase (CcO), the terminal enzyme in the electron trans

107 itochondrial respiratory enzyme cytochrome c oxidase (CcO).

108 all-molecule activator of coproporphyrinogen oxidase (CgoX) from Gram-positive bacteria, an enzyme es

109 mes, acetylcholinesterase (AChE) and choline oxidase (ChO), on the surface of iron oxide nanoparticle

110 egregated projections to distinct cytochrome oxidase (CO) stripes in area V2: neurons in CO blob colu

111 lutamic acid decarboxylase (GAD), cytochrome oxidase (CO), and calretinin (CR).

112 Cholesterol oxidase (COase) is a bacterial enzyme catalyzing the fir

113 is but rather have a problem in cytochrome c oxidase complex (COX) assembly.

114 his defect in terms of assembly of the NADPH oxidase complex and subsequent ROS production.

115 se patients, carrying mutations in the NADPH oxidase complex or a MPO-deficient patient were examined

116 ression of cytosolic components of the NADPH oxidase complex.

117 that are required for assembly of the NADPH oxidase complex.

118 ast bc1 complex (complex III) and cytochrome oxidase (complex IV) are mosaics of core subunits encode

119 phil CXCR2, CD11b, and reduced NAD phosphate oxidase components (p22phox, p67phox, and gp91phox) were

120 us infection in CF and themselves affect key oxidase components in murine non-CF cells.

121 leading to reduced phosphorylation of NADPH oxidase components p47 (phox) and p40 (phox) in comparis

122 Eros is required for expression of the NADPH oxidase components, gp91phox and p22phox Consequently, E

123 assembly/activity, showed higher alternative oxidase content/activity, and displayed a growth retarda

124 NADPH oxidases contribute to LPS-induced reactive oxygen speci

125 Amine oxidase copper containing-3 (AOC3) is a cell-surface-exp

126 protein with essential roles in cytochrome c oxidase (COX) assembly and the regulation of copper home

127 Cytochrome c oxidase (COX) was initially purified more than 70 years

128 is required for the activity of cytochrome c oxidase (COX), the terminal electron-accepting complex o

129 n the assembly of mitochondrial cytochrome c oxidase (COX).

130 Coproporphyrinogen III oxidase (CPO) catalyzes the conversion of coproporphyrin

131 sibility that the alternate terminal bd-type oxidase (cytochrome bd oxidase) is capable of maintainin

132 dispersion of the class-enzyme D-amino acid oxidase (DAO) and L-amino acid oxidase (LAO) for selecti

133 rich food due to reduced activity of diamine oxidase (DAO).

134 f the d-serine degrading enzyme d-amino acid oxidase (Dao1) in the hippocampus of cocaine-sired male

135 Muscle studies showed global cytochrome-c oxidase deficiency in all patients tested and severe, co

136 NADPH oxidase-deficient (gp91(phox) knockout [KO]), iNOS-defic

137 was increased in hIRECO EC as was Nox2 NADPH oxidase-dependent generation of superoxide, whereas insu

138 nicotinamide adenine dinucleotide phosphate) oxidase-dependent killing and, in turn, host susceptibil

139 that pneumolysin and streptococcal pyruvate oxidase-derived H2O2 production were required for cardio

140 E. coli mutants defective for cytochrome bd oxidase did not.

141 h larvae, activation of the epithelial NADPH oxidase Duox at the wound margin is required early durin

142 e, we demonstrate that ROS induced via NADPH oxidase during the early stages of L. amazonensis infect

143 Upon genetic deletion of the cytochrome bd oxidase-encoding genes cydAB, Q203 inhibited mycobacteri

144 y specific reference method based on lactate oxidase enzyme (correlation coefficient r > 0.9).

145 cell reaction also carried out in biology by oxidase enzymes, includes the critical O-O bond reductiv

146 nhibitors of ROS-producing respiratory burst oxidase enzymes.

147 d gene-1 (IL4I1), a secreted l-phenylalanine oxidase expressed by APCs, has been detected in B cells,

148 38] mg/L; P<0.01) and endothelial cell NADPH oxidase expression (P<0.05).

149 tions and also reverted the changes in NADPH oxidase expression triggered by Ang II.

150 , neutrophils with a genetic defect in NADPH oxidase fail to induce either actin and tubulin polymeri

151 (nicotinamide adenine dinucleotide phosphate oxidase) family includes seven unique members that are i

152 ensor which is based on fructosyl amino-acid oxidase (FAO) immobilized nitrogen-doped graphene/gold n

153 iggered interest in the terminal respiratory oxidases for antituberculosis drug development.

154 reatment with a silane derivative, bilirubin oxidase from Myrothecium verrucaria was immobilized onto

155 se from Corynascus thermophiles or bilirubin oxidase from Myrothecium verrucaria, were performed to o

156 f the molybdenum active site of the arsenite oxidase from the Alphaproteobacterium Rhizobium sp. NT-2

157 Proton transfer in cytochrome c oxidase from the cellular inside to the binuclear redox

158 In these 3 brothers strongly reduced NADPH oxidase function was found in granulocytes, leading to i

159 ne-based biosensors including screen-printed oxidase-functionalized graphene biosensor have been demo

160 or, horseradish peroxidase (HRP) and glucose oxidase (GOD) were electrodeposited within the hydrogel

161 hment of Azure A (Azu-A) mediator or glucose oxidase (GOx) enzyme.

162 three dimensional robust matrix for glucose oxidase (GOx) immobilization (PAA-rGO/VS-PANI/LuPc2/GOx-

163 Glucose oxidase (GOx) immobilized on the interface serves as the

164 Glucose oxidase (GOx) was immobilized on a modified indium tin o

165 of poly(toluidine blue O) (PTB) and glucose oxidase (GOx) with an electroanalytical microfluidic dev

166 Herein, inspired by the glucose oxidase (GOx)-assisted conversion of glucose into glucon

167 monolayer of covalently immobilized glucose oxidase (GOx).

168 amperometric glucose sensor based on glucose oxidase (GOx).

169 ierarchical self-assembly of GrO and glucose oxidase (GOx).

170 ticles separately containing Ex4 and glucose oxidase (GOx).

171 The biosensor with diamine oxidase had the lowest measured concentration of 1mg/L o

172 The cbb3 oxidase has a high affinity for oxygen and is required f

173 A neutron diffraction study of cholesterol oxidase has revealed an unusual elongated main chain nit

174 Sulfite oxidases have been wired to electrode surfaces, but thei

175 Haem-copper oxidase (HCO) catalyses the natural reduction of oxygen

176 such as copper and iron, in the heme-copper oxidase (HCO) superfamily is critical to the enzymatic a

177 Human diamine oxidase (hDAO), required for histamine catabolism, has m

178 We used fructosyl amino acid oxidase, hexaammineruthenium(III) chloride as the electr

179 lower expression level of RESPIRATORY BURST OXIDASE HOMOLOG D (RbohD).

180 Transcripts encoding the Respiratory Burst Oxidase Homolog F, signaling components involved in ethy

181 The enzyme cocktail (glucose oxidase, horseradish peroxidase and potassium ferrocyani

182 on using a bienzymatic sensor phase (glucose oxidase/horseradish peroxidase) with ferrocyanide as ele

183 em I, cytochrome c (cyt c) and human sulfite oxidase (hSOX).

184 The related copper-containing amine oxidase human vascular adhesion protein-1 also exclusive

185 ata and mitochondrial DNA (mtDNA) cytochrome oxidase I (COI) and cytochrome b (Cyt b) gene markers, w

186 98-100% partial mitochondrial DNA Cytochrome Oxidase I (mtCOI) gene identity with the B. tabaci speci

187 genetic loci (16S rDNA, 28S rDNA, Cytochrome oxidase I and Cytochrome b).

188 and large-scale mitochondrial DNA cytochrome oxidase I barcoding has exposed many potential new crypt

189 locus, the barcode region in the cytochrome oxidase I mitochondrial gene, and analyzed representativ

190 levels of mitochondrial complex cytochrome c oxidase I/IV and lower ATP levels.

191 onse of the catalytic cycle of human sulfite oxidase immobilized on an electrode.

192 at -0.35V (vs pseudo-Ag/AgCl) using glucose oxidase immobilized on Pt-decorated graphite.

193 The active Mn oxidase in Bacillus sp. PL-12, Mnx, is a complex compose

194 ring CpcA-labelled cytochrome bd 1 ubiquinol oxidase in the cytoplasmic membrane show that CpcA-PEB a

195 ated NET release may arise in part via NADPH oxidase-independent mechanisms.

196 gonist, BzATP, and was attenuated by a NADPH oxidase inhibitor apocynin.

197 hich was normalized by a specific Nox2 NADPH oxidase inhibitor.

198 treatment with diphenylene iodonium, a NADPH oxidase inhibitor.

199 rbic peroxidases, peroxidases and polyphenol oxidases) involved in the antioxidant response in forty-

200 Consistent with cytochrome oxidase involvement, the glycolytic effect was enhanced

201 Q) of the redox center CuA from cytochrome c oxidase is attained by tuning the accessibility of a low

202 In air, the CydAB bd-type oxidase is essential for aerobic respiration and intrace

203 that the collagen cross-linking enzyme lysyl oxidase is expressed in all vascular cells and that in v

204 Our results indicate that NADPH oxidase is important to control A. actinomycetemcomitans

205 However, the assembly of this oxidase is poorly understood.

206 In contrast, the QoxAB aa 3-type oxidase is required neither for aerobic respiration in a

207 the electron flow through the cytochrome bd oxidase is sufficient to maintain respiration and ATP sy

208 Arsenite oxidase is thought to be an ancient enzyme, originating

209 re, we show that possession of both terminal oxidases is important in infection.

210 nate terminal bd-type oxidase (cytochrome bd oxidase) is capable of maintaining a membrane potential

211 atic source of reactive oxygen species, NOX2 oxidase, is activated by single stranded RNA and DNA vir

212 en species (ROS) produced by NADPH phagocyte oxidase isoform (NOX2) are critical for the elimination

213 entify an ATP-binding motif within the NADPH oxidase isoform, NOX4, and show that ATP directly binds

214 ve oxygen species derive from specific NADPH oxidase isoforms remains ill defined.

215 pression of Dual oxidase 1 (Duox-1), a NADPH oxidases known to generate H2O2.

216 D-amino acid oxidase (DAO) and L-amino acid oxidase (LAO) for selective "on the fly" biodetection of

217 , in turn, activates a Nox2-containing NADPH oxidase, leading to cerebrovascular oxidative stress.

218 elating with a 10-fold upregulation of lysyl oxidase like-1 gene expression (P < 0.001).

219 Lysyl oxidase-like 2 (LOXL2) catalyses collagen cross-linking

220 nolics required the presence of active lysyl oxidase-like 2 (LOXL2), thereby limiting effects to fibr

221 To confirm oxidase-like activity of citrate-capped Pt NPs, their ac

222 result of collagen crosslinking by the lysyl oxidase (LOX) family of enzymes.

223 l-lactate biosensors employing l-lactate oxidase (LOx) have been developed mainly to measure l-la

224 Lysyl oxidase (LOX) remodels the tumour microenvironment by cr

225 hich is a monoamine metabolized by monoamine oxidase (MAO), exists widely in plants, animals, ferment

226 reductases (CREDs), hydrolases and monoamine oxidases (MAOs), providing a comprehensive overview of t

227 A multicopper oxidase (MCO) MnxG protein from marine Bacillus bacteria

228 l protein complex Mnx contains a multicopper oxidase (MCO) MnxG that, unusually, catalyzes the two-el

229 Mnx, is a complex composed of a multicopper oxidase (MCO), MnxG, and two accessory proteins, MnxE an

230 ve and inefficient Pt catalysts, multicopper oxidases (MCOs) have been envisioned because they provid

231 We show that SELENBP1 is a methanethiol oxidase (MTO), related to the MTO in methylotrophic bact

232 n kinase C inhibitor, DPI, a NADPH-dependent oxidase (NOX) inhibitor, GKT137831, a NOX1/4 inhibitor,

233 Previous studies implicate NADPH oxidase (Nox) proteins as important reactive oxygen spec

234 F3 is central in the activation of the NADPH oxidase (Nox)-2 component p40phox and the elevation of r

235 f reactive oxygen species derived from NADPH oxidase (NOX)-4 and mitochondrial sources.

236 ed that HDM-induced cellular injury is NADPH oxidase (NOX)-dependent, and apocynin, a NOX inhibitor,

237 sly demonstrated an important role for NADPH oxidase (NOX)-derived superoxide production during T1D p

238 the p47(phox) subunit of the phagocyte NADPH oxidase (NOX2), as the putative underlying causal varian

239 Furthermore, the NADPH oxidase NOX4 inhibits this transition and therefore supp

240 adenine dinucleotide phosphate reduced form oxidases (NOXs) in Mo-DC differentiation.

241 SHP2 oxidation requires NADPH oxidases (NOXs), and oxidized SHP2 co-localizes with pla

242 Cytochrome c oxidases of facultative members of the community were hi

243 rrelation between the number of cytochrome c oxidase operons and heterotrophic or diazotrophic capabi

244 tion to 4-aminobutyraldehyde with putrescine oxidase or diamine oxidase as catalysts.

245 r [(18)F]AV-1451, such as neuronal monoamine oxidase or neuromelanin.

246 Defects in mitochondrial cytochrome c oxidase or respiratory chain complex IV (CIV) assembly a

247 nisms, and pharmacologic inhibition of NADPH-oxidase partially impairs NET production.

248 monitored after the addition of NADP (NADPH) oxidase pathway modulators and inhibitors of Toll-like r

249 NADPH oxidase pathway modulators decreased ROS production but

250 itochondrial respiration via the alternative oxidase pathway.

251 The PLANT CYSTEINE OXIDASEs (PCOs) have been identified as catalysts of thi

252 n of channels on these devices using glucose oxidase, peroxidase, and 2,2'-azino-bis(3-ethylbenzothia

253 Pyranose oxidase (POx), which doesn't have electrically non-condu

254 nly by enzymatic browning through polyphenol oxidase (PPO) action.

255 esh and pulp colour by inhibiting polyphenol oxidase (PPO) activity of the both tissues.

256 from Garcinia mangostana rind, on polyphenol oxidase (PPO) activity was investigated.

257 Meanwhile, both the activity of polyphenol oxidase (PPO) and polyphenol peroxidase (POD) in fresh-c

258 SBA-3, and MCM-48) to immobilize polyphenol oxidase (PPO) at different pH has been tested.

259 Polyphenol oxidase (PPO) was extracted and characterized from ripe

260 Polyphenol oxidases (PPOs) such as tyrosinase and laccase catalyze

261 le for tissue browning are called polyphenol oxidases (PPOs).

262 sure and intrinsic factors such as the NADPH oxidases produce high levels of reactive oxygen species

263 amide adenine dinucleotide phosphate (NADPH) oxidases produce ROS locally in response to various stim

264 taining the DeltacpsA mutant recruited NADPH oxidase, produced ROS, associated with LC3, and matured

265 g membrane proteins, which include the NADPH oxidase proteins (NOX/DUOX).

266 lowed by direct phosphorylation of the NADPH oxidase RBOHD, resulting in elevated production of react

267 Consistently, PLC2 associates with the NADPH oxidase RBOHD, suggesting its potential regulation by PL

268 OS generated by the defense-associated NADPH oxidase, RBOHD.

269 oreover, CpsA was sufficient to impair NADPH oxidase recruitment to fungal particles that are normall

270 generates reactive oxygen species via NADPH oxidase, reducing the palmitoylation of receptor-associa

271 creased endothelial ROS production via NADPH oxidase signaling, up-regulated Nox4 expression, and pro

272 ific for spermine and spermidine and diamine oxidase specific for putrescine, were co-immobilized ont

273 In the present study, polyamine oxidase specific for spermine and spermidine and diamine

274 Semicarbazide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of primar

275 of 22 identical amino acids in cytochrome c oxidase subunit 1 and NADH dehydrogenase subunit 5.

276 region of the mitochondrial gene, cytochrome oxidase subunit I (COI), is highly variable among specie

277 uencing of genetic marker, COI (cytochrome c oxidase subunit I) and subsequent sequence data analysis

278 ibutes from its predicted ancestor, pyruvate oxidase, such as a ubiquinone-binding site and the requi

279 azonensis is impaired by inhibitors of NADPH oxidase, Syk, focal adhesion kinase, and proline-rich ty

280 dase (AOX) is a mitochondrial inner-membrane oxidase that accepts electrons directly from ubiquinol a

281 dase (AOX) is a non-proton-pumping ubiquinol oxidase that catalyzes the reduction of oxygen to water

282 onstrate that AMX-2 is the primary monoamine oxidase that metabolizes 5-HT in C. elegans, and we also

283 taining-3 (AOC3) is a cell-surface-expressed oxidase that regulates leukocyte extravasation.

284 raction between the two terminal respiratory oxidases that can be exploited for anti-TB drug developm

285 Conditional deletion of cytochrome c oxidase, the terminal enzyme in the respiratory electron

286 groups in the enzyme so as to attach glucose oxidase to the PL surface.

287 containing complex I, together with a quinol oxidase, to determine the kinetics of complex I catalysi

288 L. monocytogenes to switch between terminal oxidases under different oxygen conditions, providing ex

289 on assay, two sites (W160 and D112) of urate oxidase (Uox), a model therapeutic protein, were selecte

290 Exemplified with urate oxidase (UOx), the enzyme used for hyperuricemia treatme

291 One of the best-studied is vanillyl-alcohol oxidase (VAO) from the fungus Penicillium simplicissimum

292 centration for the biosensor with putrescine oxidase was 1mg/L.

293 3-induced activation of the neutrophil NADPH oxidase was abrogated by bacterium-derived proteolysis o

294 amount of superoxide anion produced by NADPH oxidase was measured by spectrophotometry through WST-1

295 monstrated that CrACX2 is a genuine acyl-CoA oxidase, which is responsible for the first step of the

296 asmic formate dehydrogenase and two terminal oxidases, which serve to metabolize formate and facilita

297 centration range for human and rat monoamine oxidases with slight preference for monoamine oxidase B

298 xanthine sensor using entrapment of xanthine oxidase (XO) enzyme in several nanostructures of tantalu

299 timate the phenolic composition and xanthine oxidase (XO) inhibitory activity of green coffee beans (

300 ment for direct electrochemistry of xanthine oxidase (XOD).