ライフサイエンスコーパス: oxidation

1 (low) BAP1 mutant UM cells employ fatty acid oxidation.

2 d oxygen activation, as well as on ascorbate oxidation.

3 vidence for the alternation of brain glucose oxidation.

4 wn to depolymerize actin filaments by direct oxidation.

5 ve effects on the enzymes in fatty acid beta-oxidation.

6 for both syntrophic propionate and butyrate oxidation.

7 PL) are the main substrates of lipolysis and oxidation.

8 tuted derivatives resist direct photoinduced oxidation.

9 which was attributed to inefficient As(III) oxidation.

10 ough disulfide bridges generated by cysteine oxidation.

11 ically via both chemical and electrochemical oxidation.

12 can increase the product's susceptibility to oxidation.

13 via telescoped B-to-Bi transmetallation and oxidation.

14 g highly unsaturated oils such as FO against oxidation.

15 t was driven by chemolithoautotrophic sulfur oxidation.

16 teraction of gas reactants and catalyzing CO oxidation.

17 antioxidant in reducing the rate of primary oxidation.

18 ital, which is well positioned for substrate oxidations.

19 brown fat thermogenic program and fatty acid oxidation, 2) stimulate uncoupling protein 1 (UCP1)-inde

20 product chemoselectivity make asymmetric C-H oxidation a generally unsolved problem for nonenzymatic

21 Endoplasmic reticulum omega-oxidation, a minor fatty acid degradation pathway known

22 Fatty acid oxidation activity and tricarboxylic acid (TCA) cycle me

23 1-desaturation of GAs, but was lacking the 3-oxidation activity.

24 1) alternative oxygen sources during pyrite oxidation and 2) secondary overprinting by microbial rec

25 erformed multiple reactions, including 1beta-oxidation and 9,11-desaturation of GAs, but was lacking

26 / emission 410 nm) as indicator of tyrosine oxidation and carbonyl content significantly increased a

27 orter lag times and faster rates of net H(2) oxidation and dark carbon dioxide (CO(2)) fixation than

28 monitoring of additional attributes, such as oxidation and deamidation at specific sites in parallel

29 th electron-rich aryl aldehyde, we enable an oxidation and deprotonation event, which generates a key

30 by the protection of membrane lipids against oxidation and superoxide radical anion scavenging activi

31 de evidence that redox reactions within beta-oxidation and the electron transport system serve as a b

32 the identified compounds and indicated lipid oxidation and the Maillard were the reaction pathways re

33 toward oxygen-sparing glycolysis and glucose oxidation and to increase cAMP levels is dependent on MT

34 n a one-pot reaction of sequential coupling, oxidation, and deprotection followed by a single precipi

35 hondrial membrane potential and flavoprotein oxidation, and prevented myocardial hypertrophy.

36 es involved in TAG hydrolysis and fatty acid oxidation, and that PA relieves AHL4-mediated suppressio

37 ic nitrogen inputs, knowledge of how ammonia oxidation (AO) in the ocean responds to warming is cruci

38 oxygen consumption and corresponding carbon oxidation are not necessarily confined to cell membranes

39 ) to nitric oxide (NO) conversion and phenol oxidation are of prime importance.

40 Cardiac glucose uptake and oxidation are reduced in diabetes despite hyperglycemia.

41 ith Fe and Cu are well precedented, Ni-based oxidations are frequently less common due to less-access

42 sively dependent on mitochondrial fatty acid oxidation as a consequence of mitochondrial calcium unip

43 xygenic phototrophy and atmospheric hydrogen oxidation as supplemental energy sources.

44 ity owing to peptidyl methionine and proline oxidation as well as acetaldehyde adduct formation on ly

45 e oxygen species, we hypothesized that SERCA oxidation at C674 would modulate the effects of reactive

46 patic lipogenesis and increased hepatic beta-oxidation at organ programming peak in early life (P21).

47 ly, followed by three site-selective allylic oxidations at C5, C10, and C13, which led to the two-pha

48 Anammox (anaerobic ammonium oxidation) bacteria are important for the nitrogen cycle

49 luated their catalytic activity in ascorbate oxidation based on redox cycling between Cu(I) and Cu(II

50 noxic incubations both showed active methane oxidation by a Methylobacter species, with anoxic rates

51 ng a similar obese phenotype, increasing FAO oxidation by deletion of ACC2 prevented HFD-induced card

52 mitochondrial energy production via glucose oxidation by depressing pyruvate dehydrogenase complex a

53 and chlorpyrifos showing an increase in its oxidation by increasing times, especially with chlorpyri

54 hrough in situ detection of specific protein oxidation by matrix-assisted laser desorption/ionization

55 Electrochemical alcohol oxidation by NiOOH has been understood since the 1970s t

56 provides an effective strategy against MXene oxidation by restricting the interaction of water molecu

57 geneous solutions, while heterogeneous water oxidation by the same catalyst leads exclusively to oxyg

58 e removal from produced water relying on the oxidation by unactivated peroxymonosulfate.

59 ally rescued pyruvate and palmitoylcarnitine oxidation capacities, implicating dysregulation of CoA-d

60 thane monooxygenase, the predominant methane oxidation catalyst in nature.

61 i(OH)(2) has been widely studied as methanol oxidation catalyst, the initial process of oxidizing Ni(

62 Here we report a new approach to oxidation catalysts for total oxidation of hydrocarbons

63 The need for active and stable oxidation catalysts is driven by the demands in producti

64 the current mechanistic understanding of DMS oxidation chemistry and geostationary satellite cloud im

65 Analysis of volatile oxidation compounds can be an alternative method for p-a

66 developing a model for the biological water oxidation cycle.

67 The rate constants for tyrosine oxidation decreased by 125-fold with three added proline

68 Optical properties suggest that permanganate oxidation decreased DOM aromaticity (decreased SUVA-254)

69 can undergo various chemical reactions e.g., oxidation, dehydrogenation, dehydration and polymerisati

70 These results further resolve oxidation-driven structural perturbation of CaM, with im

71 ss cake (called "helpers") to minimize lipid oxidation during acid/alkaline pH-shift protein isolatio

72 ormula: see text]/[Formula: see text] Pyrite oxidation during chemical weathering on land consumes [F

73 ems a promising tool for inhibition of lipid oxidation during pH-shift processing of sensitive fish b

74 lates lipid mobilization and fatty acid beta-oxidation during seed germination and seedling establish

75 loped to simulate incomplete bromide (Br(-)) oxidation during short prechlorination periods because i

76 This rapid and extensive dark oxidation elevates the importance of nocturnal chemistry

77 The lag phase before lipid oxidation enters the exponential phase reciprocally shor

78 on via clipping, deamidation, isomerization, oxidation, etc.

79 an atmosphere immediately prior to the Great Oxidation Event.

80 This enzymatic silane oxidation extends nature's impressive catalytic repertoi

81 Increased fatty acid oxidation (FAO) has long been considered a culprit in th

82 ocess through directly activating fatty acid oxidation (FAO) in the ground-state ESCs.

83 D36, accumulated lipids, and used fatty acid oxidation (FAO) instead of glycolysis for energy.

84 Fatty acid oxidation (FAO) is a key bioenergetic pathway often dysr

85 lymph gland, we demonstrate that Fatty Acid Oxidation (FAO) is essential for the differentiation of

86 ing oxidative phosphorylation and fatty acid oxidation (FAO) with substantial accumulation of acyl-ca

87 ypoxia-inducible factors (HIFs), reducing FA oxidation (FAO).

88 wn and beige adipocytes uncouples fatty acid oxidation from ATP generation in mitochondria and promot

89 om high to low F:M-C:N recovered the nitrite oxidation function, with an increase in Nitrobacter as t

90 piration that accelerating flux through beta-oxidation generates a corresponding increase in mitochon

91 with phosphonate or pyridyl sites for water oxidation, gives surfaces with a 5:1 chromophore to cata

92 of Hg(I) and Hg(II) leads to insufficient Hg oxidation globally.

93 Therefore, changes in pathways of lipid oxidation, glycolysis, and mitochondrial oxidative phosp

94 For any degree of oxidation, GO does not disperse in PVA as a thermodynami

95 intrinsic GQD fluorescence by 31.5% for low-oxidation GQDs and enables aqueous dispersion of otherwi

96 strongly to no-oxidation GQDs, weakly to low-oxidation GQDs, and not at all for heavily oxidized GQDs

97 ssDNA is determined to adsorb strongly to no-oxidation GQDs, weakly to low-oxidation GQDs, and not at

98 aqueous dispersion of otherwise insoluble no-oxidation GQDs.

99 AG catabolism and downstream fatty acid beta-oxidation have not been characterised in diatoms.

100 are colloidally stable and resistant to bulk oxidation in air.

101 Tryptophan oxidation in biology has been recently implicated in a v

102 lating the expression of genes in fatty acid oxidation in humanized livers through its interaction wi

103 betaOHB oxidation in mitochondria boosts the synthesis of cytoso

104 ospholipids or by oxPLs generated during HDL oxidation in plasma by the physiologically relevant MPO-

105 The ability to switch fuels for oxidation in response to changes in macronutrient compos

106 associated with mitochondria and fatty acid oxidation in RYR1 mutants when compared with WT controls

107 The results show that O(3) oxidation in the dark diminishes light absorption of woo

108 c acid alters markers of impaired fatty acid oxidation in the liver.

109 Treatment with 3P10 reverses excessive lipid oxidation in tumor-bearing mice and prevents cancer cach

110 enetics in Salmonella enterica Cerro 87, and oxidation-induced abasic sites in DNA from E. coli treat

111 Oxidation induction time (OIT) using differential scanni

112 When atmospheric oxidation is dominated by OH, OFR conditions can often b

113 ously reported finding that protein cysteine oxidation is increased during mitosis relative to other

114 eostasis and proliferation even when glucose oxidation is increased.

115 Lipid oxidation is one of the major quality issues of wholegra

116 demonstrate in vitro and in cells that Fes1 oxidation is reversible and is regulated by the cytoplas

117 When pK(a)(LAC-MeCN) >> 0, the oxidation is reversible when there is no gross change in

118 ic acid (SRFA) on Cu(II) reduction and Cu(I) oxidation kinetics at pH 8.2.

119 l as a reducing agent followed by subsequent oxidation leads to a great variety of polycyclic nitroge

120 crobial count, chemical stability (pH, lipid oxidation, lipolysis), and optical properties.

121 alternative to the industrial anthraquinone oxidation method, as it allows decentralized H(2)O(2) pr

122 trategically combines chemical and enzymatic oxidation methods.

123 nitrite/nitrate-dependent anaerobic methane oxidation (n-DAMO) microorganisms, at a temperature as l

124 talyze the regioselective and stereospecific oxidation of 2-arachidonoyl-lysophosphatidylcholine (2-A

125 A low-temperature, protecting-group-free oxidation of 2-substituted anilines has been developed t

126 resolved quantification of the EGF-dependent oxidation of 4200 cysteine sites in A431 cells.

127 own to improve activity for electrocatalytic oxidation of 5-hydroxymethylfurfural (HMF), as an exampl

128 ranslocation (TET) dioxygenases catalyze the oxidation of 5-methylcytosine (5mC), the central epigene

129 dical intermediates are formed by the direct oxidation of a B-B bond between a boron cluster cage and

130 thesis of an indigoid "semi-Nindigo" (2) via oxidation of a diindolopyrrole (1).

131 = cyclic (alkyl)(amino)carbene], prepared by oxidation of a zero-valent beryllium complex with 2,2,6,

132 ochemical mediators for the electrocatalytic oxidation of alcohols by an iridium amido dihyride compl

133 re the hydroxylation of heterocycles and the oxidation of aldehydes to their corresponding carboxylic

134 The oxidation of alkyl thiols to disulfides has been achieve

135 ntrations of gaseous species formed from the oxidation of alpha-pinene was explored.

136 work comprising a core domain catalyzing the oxidation of amines with an auxiliary domain for substra

137 llenges of designing molecular catalysts for oxidation of ammonia and highlights recent key contribut

138 l radical cation formed through one-electron oxidation of an N-heterocyclic carbene-carbodiimide (NHC

139 st identically to Au disk electrodes for the oxidation of an outer-sphere redox couple (ferrocene met

140 rise to an ideal platform for the selective oxidation of anthracene.

141 Although oxidation of aromatics by these radicals has been studie

142 ld peak current increase for electrochemical oxidation of ascorbic acid, which resulted in a highly s

143 tions on the time-dependent plasma-supported oxidation of benzyl alcohol, benzaldehyde and phenol in

144 (2) as oxidant, up to ~300 turnovers for the oxidation of benzylic C-H bonds were obtained.

145 With surfactant micelles, oxidation of BODIPY(665/676) was observed.

146 osmotic energy conversion and reveal how the oxidation of BP influences power generation.

147 re effective in preventing the AAPH-mediated oxidation of Caco-2 cells, low-density lipoprotein and d

148 Here we report selective electrochemical oxidation of CH(4) to methyl bisulfate (CH(3)OSO(3)H) at

149 We discuss the idea that oxidation of conserved cysteine residues and partial unf

150 s intermediate is formed concurrently to the oxidation of CoOOH to CoO(2).

151 Oxidation of dissolved manganese ions results in high-va

152 biased sufficiently positive for concurrent oxidation of DmFc and oxalate (C(2)O(4)(2-)), blip-type

153 termediates in the process of DsbB catalyzed oxidation of DsbA.

154 The straightforward oxidation of electron-rich arenes, namely, phenols, naph

155 ate also induced autophagy and promoted beta-oxidation of fatty acids and stimulated gene expression

156 ulator of cellular metabolism by suppressing oxidation of fatty acids, and thus adapts the cells to a

157 ved energy metabolism through increased beta-oxidation of fatty acids.

158 uctive deposition of rhodium or platinum and oxidation of Fe(2+) from magnetite (Fe(3)O(4)).

159 and reproducible approach to the successful oxidation of fullerenes (oxC(60)) and the formation of h

160 the presence of [Ga(arene)(n) ](+) salts on oxidation of Ga metal with AgOTf in arene solvents.

161 east in part by increasing the mitochondrial oxidation of glucose and glutamine carbons to support th

162 nicity was abolished by chemical (periodate) oxidation of gTSSA-I glycosylation but retained after he

163 sformation allows for the efficient benzylic oxidation of heteroarenes to afford heterocyclic styrene

164 ew approach to oxidation catalysts for total oxidation of hydrocarbons (e.g., propane) by surface oxy

165 hydrogen peroxide generated by XO catalysed oxidation of hypoxanthine, and PAO catalysed oxidation o

166 species have been proposed to facilitate the oxidation of inert C-H bonds, reactions that are unknown

167 ocatalytic activity-specifically the electro-oxidation of iodide at polycrystalline platinum-reveals

168 In contrast, secondary photo-oxidation of isobutanal to propane dominates at lower te

169 ration process and hence for the release and oxidation of its redox content during the collision onto

170 an be induced to form fibrillar filaments by oxidation of its two cysteine residues, generating an in

171 rgetics arose from Meyerhof's experiments on oxidation of lactate in isolated muscles recovering from

172 bon ink or fumed silica can compete with the oxidation of mediators by mitochondria, yielding an over

173 ropose an adverse outcome pathway, where the oxidation of metabolic and regulatory Fe-S centers of pr

174 sent in the methanol produced in the partial oxidation of methane to methanol over Cu-SSZ-13 in a con

175 Selective partial oxidation of methane to methanol suffers from low effici

176 an zero for a given complex [MHL(n)](+), the oxidation of MHL(n) is irreversible due to proton loss f

177 xpressed a complete pathway for the terminal oxidation of n-alkanes including two alkane monooxygenas

178 ode was found active toward the voltammetric oxidation of OCl(-), with OCl(-) showing a characteristi

179 However, the over-oxidation of oxygen at highly charged states aggravates

180 We find that oxidation of phenolic compounds contributes the majority

181 refore, our results demonstrate irreversible oxidation of pollen proteins during SI and provide evide

182 of an electrochemically driven photochemical oxidation of primary and secondary aliphatic alcohols us

183 rmo catalysis are achieved via the catalytic oxidation of propane (C(3) H(8) ) over a Pt/TiO(2) -WO(3

184 tion at relatively low potentials by electro-oxidation of pyrrole, aniline, phenol, or 3,4-ethylenedi

185 This paper reports the oxidation of Remazol black B dye by employing iron ions

186 (ADHs) or retinol dehydrogenases (RDHs); and oxidation of retinaldehyde into RA by aldehyde dehydroge

187 esis of RA requires two enzymatic reactions: oxidation of retinol into retinaldehyde by alcohol dehyd

188 Rho activity across the spermatheca through oxidation of RHO-1 C20.

189 oxidation of hypoxanthine, and PAO catalysed oxidation of spermine, was coupled to horseradish peroxi

190 This activity supports continued oxidation of substrates within the tricarboxylic acid (T

191 or of dehydro-isoascorbic acid (DIA), on the oxidation of sulfhydryl groups (-SH) to disulfide bonds

192 have observed that reversible, low-potential oxidation of the active center leads to the protection a

193 nd a reversible protection against excessive oxidation of the catalytic cysteines in Cd-MsrB through

194 ated to correlate with the initial degree of oxidation of the Cu surface prior to the exposure to neg

195 s dissolved in liquid electrolyte to conduct oxidation of the fuel or reduction of the oxidant, typic

196 equency on mtDNA can be indirectly caused by oxidation of the mitochondrial replicase.

197 totic arrest is required for ROS buildup and oxidation of the nucleotide pool.

198 local peroxynitrite formation and subsequent oxidation of the regulatory protein AKAP150 at cysteine

199 revealed little or no charge separation and oxidation of the special pair, P700.

200 Compared to metal-free oxidation of the substrates, which is caused by reactive

201 sis by coupling the reduction of GalA to the oxidation of the sugar alcohol sorbitol that has a highe

202 In addition, the photosensitized oxidation of the sulfonamide antibiotic sulfadiazine (SD

203 NNT serves a specific role in mitigating the oxidation of these critical protein cofactors.

204 show how a small chemical modification, the oxidation of two cysteine thiols to a disulfide bond, du

205 ored the ET distance dependence for the CPET oxidation of tyrosine in a model system.

206 Serpentinization is the hydration and oxidation of ultramafic rock, which occurs as oceanic li

207 ) is able to promote the heterogeneous photo-oxidation of various primary amines with conversion effi

208 To test the effect of C674 oxidation on apoptosis in vivo, SERCA knock-in mice were

209 n mimic the functional effects of methionine oxidation on CaM's regulation of the calcium release cha

210 side and subsequently terminated by H(2)O(2) oxidation on the anodic membrane side, is crucial for (1

211 nic polysulfide, produced from either H(2) S oxidation or from L-cysteine metabolism.

212 Soy flours were stable to lipid and protein oxidation over 250 days storage in chilled or ambient co

213 -10 production, shifting from the fatty acid oxidation pathway conventionally utilized for proinflamm

214 the very-long-chain fatty acid (VLCFA) beta-oxidation pathway in peroxisomes and leads to H(2)O(2) p

215 tase (SQOR), the first enzyme in the sulfide oxidation pathway.

216 sults provide a detailed understanding of CO oxidation pathways on systems where noble metals such as

217 tic investigations reveal multiple competing oxidation pathways that depend on substrate identity and

218 The oxidation peak currents of colorants were obtained by CV

219 is detected, which is owing to the reduction-oxidation phenomena of the NiO(x) membranes.

220 tives are highly fluorescent and feature low oxidation potentials.

221 for the design and operation of an advanced oxidation process (AOP) in water treatment.

222 Peroxymonosulfate (PMS)-based advanced oxidation processes generate highly reactive SO(4)(*-) a

223 The structural response to the oxidation processes is found to be different in Li(2)FeS

224 ealed that two isobaric isomers of a dimeric oxidation product were formed.

225 The absolute amount of oxidation products (per powder mass) increased with the

226 MS/MS methods to equally sample all isomeric oxidation products across their elution window, greatly

227 The characteristic oxidation products can provide valuable markers for the

228 a quantitative yield of dG and two-electron oxidation products of 8-oxodGuo.

229 ing method development time and reducing the oxidation products quantified in a single LC-MS/MS run.

230 between electrochemically generated isomeric oxidation products.

231 comparatively examined to determine primary oxidation products.

232 ated immunity via the generation of reactive oxidation products.

233 Understanding how PLA2 inhibits lipid oxidation promoted by hemoglobin (Hb) is important for i

234 redox-sensitive [2Fe-2S] cluster that, upon oxidation, promotes FBXL5 binding to IRP2 to effect its

235 to new approaches for improving the partial oxidation properties of copper zeolites.

236 cobalamin (vitamin B(12)) increased nitrite oxidation rates and stimulated a 33-fold increase of 2-m

237 s system is dedicated to in situ chromosomal oxidation rather than correcting OG incorporated by acce

238 pared a range of essential parameters for an oxidation reaction on platinum nanoparticles (NPs) confi

239 esults indicated that EVs markedly inhibited oxidation reaction, total volatile base nitrogen (TVBN),

240 wed for preequilibration before starting the oxidation reaction.

241 Oxidation reactions include molecular oxygen under solve

242 few representative examples of photoinduced oxidation reactions to focus on in this Perspective.

243 echanistic understanding of flavin-catalyzed oxidation reactions, in either the absence or presence o

244 tly enhance the kinetics of radical-mediated oxidation reactions-pollutant degradation in particular.

245 Reduction/oxidation (redox) changes in the glutathione pool (GSH),

246 Here, we quantified how oxidation-reduction (redox) conditions impact the fate o

247 tion metal L-edges to gain insights into the oxidation/reduction processes of positive and negative a

248 at hepatocytes displayed malfunctioning beta-oxidation, reflected by increased acylcarnitines (ACs) a

249 entally, the unique photoresponse induced by oxidation-related defects in 2D black phosphorus (BP) is

250 Our discovery of phosphorene cut upon oxidation represents a previously unknown mechanism for

251 ANAMMOX (anaerobic ammonium oxidation) represents an energy-efficient process for bi

252 ods for the incorporation of alcohols by C-H oxidation require the use of the alcohol component as a

253 arachidonic acid, followed by its enzymatic oxidation resulting in a vast array of eicosanoid produc

254 is using stability of proteins from rates of oxidation (SPROX) revealed a clemastine-induced thermody

255 However, at oxidation state IV, complex 2(+) becomes seven coordinat

256 ses in the nanometer order by modulating the oxidation state of a film of a conducting polymer, such

257 This signal implies an overall oxidation state of either Mn(III)(3)Mn(IV) or Mn(III)Mn(

258 ates that the semiquinonate is the preferred oxidation state of the dioxo ligand in this complex.

259 charged complexes 1-4 in which the preferred oxidation state of the dioxo ligand is the uninegatively

260 c location may explain the regulation of the oxidation state on Pol delta activity, possibly useful d

261 and cellular metabolism, as well as a lower oxidation state that correlated with their enhanced prol

262 terising molecules in terms of their charge, oxidation state, and chirality via optoplasmonics.

263 hich contains uranium in the formal divalent oxidation state.

264 However, the origin of low-oxidation-state iron and the pathways responsible for it

265 However, the difficult access to their high oxidation states and the general labile character of the

266 heir modern counterparts, consistent with Fe-oxidation states measured on ancient igneous rocks.

267 3)-H bonds occurs via the sequence of nickel oxidation states Ni(I)-Ni(II)-Ni(I)-Ni(III) and of eleme

268 s on tetranuclear complexes mirroring the Mn oxidation states of the S(3) state remain rare.

269 mechanism over the Cu catalysts with various oxidation states was studied by using in situ surface-en

270 cur when the porphyrin units have fractional oxidation states.

271 tain binding site access to form high-valent oxidation states.

272 Here, we employed a sequential reduction and oxidation strategy to efficiently refold two high-yieldi

273 )O(3) layer, formed after an initial thermal oxidation, supports a wide range of metal and metal oxid

274 n pH, color, residual nitrite content, lipid oxidation (TBARS value) and total plate count (TPC) of c

275 owed a good correlation with the accelerated oxidation test.

276 importance of pathways for aromatic compound oxidation that do not result in ring hydroxylation, we i

277 Upon oxidation, the film expands nearly 30% in volume, and th

278 yl group deprotection of 16, phosphitylation/oxidation, then deprotection afforded 10, which was a fu

279 Exploiting the power of electrochemical oxidations, this method complements the existing organob

280 ibits exponential growth dependent on Mn(II) oxidation to a co-culture of two microbial species.

281 ter vapor, suggesting that spontaneous water oxidation to form H(2)O(2) from water microdroplets is a

282 tochrome P450 (CYP) enzymes and includes PCB oxidation to OH-metabolites, which often display a highe

283 that n-alkane degradation occurred via beta-oxidation to oxygenated transformation products with low

284 nduced radical bicyclization with late-stage oxidation to regenerate the aromatic terminator.

285 e most effective use of hydroxyl radicals in oxidation treatment scenarios.

286 In myoblasts, we find that impaired NADH oxidation upon electron transport chain (ETC) inhibition

287 can be controlled by changing the degree of oxidation, varying from fully aggregated over graphitic

288 Lipid oxidation was low (~30 mmol O(2)/kg lipid hydroperoxides

289 We observed previously that partial oxidation was responsible for increased TK(high) activit

290 Methane oxidation was strictly dependent on oxygen availability

291 The oxidation was successfully integrated into the trapping

292 Substrate oxidation was unchanged, and safety monitoring revealed

293 C4 to C12, reduced the secondary products of oxidation, when echium oil emulsions were prepared using

294 leavage products during the initial stage of oxidation whenever HO(*) or SO(4)(*-) is used for the tr

295 ted ManX stimulates the TCA cycle and carbon oxidation, while unphosphorylated PtsN stimulates potass

296 talyzed conditions in CH(2)Cl(2) followed by oxidation with DDQ (2,3-dichloro-5,6-dicyano-1,4-benzoqu

297 Chemical oxidation with hydroxyl radical (HO(*)) and sulfate radi

298 e formation of a Ti-formamidinate (4), while oxidation with S(8) yields a Ti-thioureate (5).

299 We now show that water oxidation with the cobalt-corrole CoBr(8) as electrocata

300 While aerobic oxidations with Fe and Cu are well precedented, Ni-based