ライフサイエンスコーパス: photooxidation

1 njunction with the multigeneration gas-phase photooxidation.

2 pheric epoxides in forming SOA from isoprene photooxidation.

3 aerosol (SOA) from alpha-pinene and toluene photooxidation.

4 al one-electron oxidant, riboflavin-mediated photooxidation.

5 ding was consistent with a process involving photooxidation.

6 obal as well as tissue-specific responses to photooxidation.

7 ptacene derivative 4 especially resistant to photooxidation.

8 ontinuously generated H2O(2) or A2E-mediated photooxidation.

9 genic volatile organic compounds to aromatic photooxidation.

10 ulated A2E and were irradiated to induce A2E photooxidation.

11 n part, for cellular damage ensuing from A2E photooxidation.

12 ned through controlled chemical oxidation or photooxidation.

13 bed light energy and protect themselves from photooxidation.

14 gands and protected the nanocrystal from any photooxidation.

15 e fluorophore eosin followed by fluorescence photooxidation.

16 photooxidation mechanisms in later stages of photooxidation.

17 trum which is due to formation of P700+ upon photooxidation.

18 at early stages of methylene blue-sensitized photooxidation.

19 acellular injection with Lucifer Yellow, and photooxidation.

20 e that all samples undergo extensive partial photooxidation.

21 their protective effect against phytosterols photooxidation.

22 ion of ferrous iron-loaded Dps following DNA photooxidation, a W52A Dps mutant was significantly defi

23 f DOM in both the dark and in the light, but photooxidation accelerates the production of water-solub

24 Exposure to H2O(2) or A2E-mediated photooxidation also resulted in a twofold to threefold i

25 ses that alter DOM molecular weight, such as photooxidation and biological degradation.

26 We have characterized the photooxidation and dark decay of the redox-active access

27 emonstrated that petroleum readily undergoes photooxidation and generates water-soluble oxygen-contai

28 The mechanistic link between tryptophan photooxidation and inactivation of phosphatase may have

29 nes, often suffer from poor stability due to photooxidation and oligomerization, which are linked to

30 Here, the photooxidation and ozonolysis of isoprene were examined

31 ds are photosensitive compounds that undergo photooxidation and photodegradation when irradiated with

32 f chiral NPs and clusters, followed by their photooxidation and self-assembly into nanoribbons with s

33 aracterized by the application of controlled photooxidation and spontaneous desorption mass spectrome

34 nts, particulate products from heterogeneous photooxidation and the associated degradation mechanisms

35 SI cyclic electron transport by in vivo P700 photooxidation and the dark relaxation kinetics of P700(

36 was detected during the initial stage of the photooxidation and was shown to be intermediate in the f

37 es are consistent with activation of PTH via photooxidation and with Lewis acid cocatalysts scavengin

38 c particles, making them more susceptible to photooxidation, and alter the Earth's radiative forcing.

39 was associated with A2E photoisomerization, photooxidation, and photodegradation.

40 led to PS I based on 77 K fluorescence, P700 photooxidation, and PS I electron transport light satura

41 apparent molecular weight following partial photooxidation, and there is molecular level evidence of

42 pper limits of the primary quantum yield for photooxidation are derived from the fs-MIR data, which i

43 y organic aerosol (SOA) formed from isoprene photooxidation are investigated in environmental chamber

44 Also, catalysts for aqueous photooxidations are made by reacting the initial catalys

45 compounds, we hypothesize biodegradation and photooxidation as main degradation processes for homohop

46 For all HS, irradiation caused photooxidation, as shown by decreasing electron donating

47 idation at 45 C and light-riboflavin induced photooxidation at 37 C.

48 at 45 degrees C and light-riboflavin induced photooxidation at 37 degrees C.

49 ette experiments, small rafts formed without photooxidation at high cholesterol concentrations.

50 0 microM MnCl2 noncompetitively inhibits DPC photooxidation at the high-affinity site, with a Ki of 1

51 es it significantly affect high-affinity DPC photooxidation), but it does decrease the binding affini

52 r CPC versus CPG in DNA, CPC decomposes with photooxidation by [Rh(phi)2(bpy)]3+, while CPG undergoes

53 II indicates inhibition of steady-state Mn2+ photooxidation by DPC, but allows for a single photooxid

54 d by the unusually strong inhibition of Mn2+ photooxidation by the linear uranyl cation (UO22+).

55 s are based on the observations that (a) DPC photooxidation can be inhibited by Zn2+ and Co2+; (b) Zn

56 We conclude that Mn inhibition of DPC photooxidation can be used to identify Mn-binding sites

57 n (ORR1) pathway demonstrated altered P(700) photooxidation capacity, changes in spectral properties,

58 Moreover, its potential in photooxidation catalysis has also been demonstrated by s

59 oiding metal-dependent Fenton reactions when photooxidation causes disassembly of the iron-rich photo

60 Photooxidation commonly results in green-to-red photocon

61 all-trans-retinal, is unusually sensitive to photooxidation damage mediated by all-trans-retinal in v

62 provide a window to parse biodegradation and photooxidation during advanced stages of oil weathering.

63 Presumably, their photooxidation eliminates defects on the nanoparticle su

64 Results from a time-resolved alpha-pinene photooxidation experiment show that the 2-hydroxyterpeny

65 Here, photooxidation experiments for OS-related precursors und

66 Steady-state, preparative photooxidation experiments show that aryltrimethylstanna

67 and condensed organosulfur species formed in photooxidation experiments with SO2 are present in the S

68 In photooxidation experiments, long-range oxidative damage

69 ) in the t1/2, from 0.2 to 0.25 ms, of cyt f photooxidation, far less than anticipated (ca. 100-fold)

70 In contrast, photooxidation had little effect on the samples' electro

71 hese lipid-soluble compounds protect against photooxidation, harvest light for photosynthesis, and di

72 Stage I is dominated by photooxidation in a near-surface layer.

73 Rates of cytochrome f photooxidation in all strains were similar (t1/2 approxi

74 The action spectrum for photooxidation in full fat bovine milk was measured.

75 indicative of a contribution from lipofuscin photooxidation in RPE.

76 parametric survey on the kinetics of lateral photooxidation in structurally identical WS(2) and MoS(2

77 d its susceptibility to partial and complete photooxidation in surface waters is currently lacking.

78 Photooxidation in terms of off-flavors was measured by a

79 t electron donation by Mn2+ to YZ+; (d) Mn2+ photooxidation in the presence of DPC is not inhibited b

80 ndent manner in calf thymus DNA subjected to photooxidation in the presence of riboflavin.

81 photoredox catalyst for photoreductions and photooxidations in the presence of red light (lambda(max

82 st triphasic superhydrophobic sensitizer for photooxidations in water droplets.

83 yield of dGuo modifications from riboflavin photooxidation increased dramatically in the presence of

84 argely explained the differential effects of photooxidation induced at low temperature on thioredoxin

85 Rates of indirect photooxidation induced by (1)O(2) and (3)DOM* slightly d

86 /MS), to demonstrate that A2E also undergoes photooxidation-induced degradation and we have elucidate

87 y the content of carotenoids, very effective photooxidation inhibitors, is at high level in compariso

88 Isoprene photooxidation is a major driver of atmospheric chemistr

89 n2+ (but not Zn2+ or Co2+) inhibition of DPC photooxidation is accompanied by nondecaying fluorescenc

90 Photooxidation is an important abiotic transformation pa

91 In sunlight, Trp photooxidation is dominated by the reaction with excited

92 level on the dynamics of vesicles undergoing photooxidation is not trivial and thus carefully discuss

93 and H117Q, indicating that its efficiency of photooxidation is unchanged by the mutations.

94 It has long been appreciated that the photooxidation kinetics of amino acid (AA) residues in a

95 ce microscopy showed that, in the absence of photooxidation, large rafts did not form in giant unilam

96 was reduced by up to 94% with heterogeneous photooxidation, likely due to a significantly lower cyto

97 accumulation of hydroperoxides from Type II photooxidation may enhance Type I reactions.

98 We report here that inhibition of DPC photooxidation may involve two different types of high-a

99 Here, we report a water-accelerated photooxidation mechanism dominating the degradation kine

100 iles indicate a shift from Type II to Type I photooxidation mechanisms in later stages of photooxidat

101 ion by molecular oxygen though quenching and photooxidation mechanisms.

102 Upon irradiation in a photooxidation microcosm, thin films of the asphalt bind

103 Yet, the photooxidation must compete with photoreductive Fe-N bon

104 onal antibody, YX1-40H10, that catalyzes the photooxidation of (+)-2 into the nonpsychoactive compoun

105 a large disparity in driving force favoring photooxidation of (1)MMb relative to photoreduction (del

106 lly, SO-PCN shows catalytic activity towards photooxidation of 1,5-dihydroxynaphthalene.

107 lluminator (wavelength of 365 nm) results in photooxidation of 1-thioglycerol (TG) mediated by Os-PVP

108 dienenitrile oxide (7a), was observed during photooxidation of 1a, whereas transformations of the nit

109 and found to be catalytically active for the photooxidation of 2-chloroethyl ethyl sulfide (CEES, a c

110 A new product, CO(2), was observed in the photooxidation of 2-H,N1-H imidazoles, but not in 2-subs

111 MW 226 OSs is tentatively explained through photooxidation of 3-Z-hexenal in the gas phase, resultin

112 The sand- and ash-catalyzed heterogeneous photooxidation of 6:2 FTOH resulted in the rapid product

113 nce context, products of riboflavin-mediated photooxidation of 8-oxodG were highly sequence dependent

114 n source, dihydroacridine, demonstrated that photooxidation of 9,10-dihydroacridine was necessary for

115 nellol through the Schenck-ene reaction, and photooxidation of a diene.

116 surface-bound, oxide-based procedure for the photooxidation of a family of aromatic hydrocarbons by a

117 In proximity labeling, photooxidation of a ligand-conjugated singlet oxygen gen

118 The photooxidation of a mustard-gas simulant, 2-chloroethyl

119 The mechanism of the photooxidation of a number of asymmetrically substituted

120 ust bind at its effector site so that stable photooxidation of a second Mn2+ ion can occur, forming t

121 The photooxidation of a series of aldoxime ethers was studie

122 oncomitant with double bond migration during photooxidation of a sulfide is reported.

123 light-triggered redox cascade culminating in photooxidation of a yet unknown substrate or binding par

124 e complex mixture of products resulting from photooxidation of A2E might include a range of fragments

125 ctrum leads to singlet oxygen production and photooxidation of A2E.

126 an uncommon example of active site-directed photooxidation of an enzyme by singlet oxygen.

127 lavoproteins, the reverse process (i.e., the photooxidation of anionic flavin radicals) can also occu

128 The mechanism of the photooxidation of aromatic azides containing a substitue

129 We suggest that products of the photooxidation of bis-retinoid lipofuscin pigments in RP

130 e oxidative stress produced by laser-induced photooxidation of cardiac myocytes in vitro.

131 e playing a far more significant role in the photooxidation of CDOM than has been previously recogniz

132 shear stress in assembled ribbons caused by photooxidation of CdS.

133 The initiation stage of the photooxidation of CdSe nanocrystals themselves increased

134 escence quenching is attributed to the rapid photooxidation of ChlZ, and the slow phase is attributed

135 ndings implicating toxic agents resulting in photooxidation of cholesterol in the etiology of age-rel

136 Herein, we report a selective photooxidation of commodity postconsumer polyolefins to

137 The photooxidation of compounds in petroleum, following expo

138 condary organic aerosol (SOA), formed in the photooxidation of diesel fuel, biodiesel fuel, and 20% b

139 ugh dissolved free AAs are well studied, the photooxidation of dissolved combined AAs (DCAAs) remains

140 t defences might counteract the UVA-mediated photooxidation of DNA 6-TG at this intermediate step and

141 No oxidative damage was found upon photooxidation of DNA/RNA duplexes containing tethered m

142 We synthesized uroporphomethene by photooxidation of enzymatically generated uroporphyrinog

143 f [2Fe-2S] and [4Fe-4S] clusters through the photooxidation of ferrous ions and the photolysis of org

144 The photooxidation of FnY356 within the alpha/beta subunit i

145 n, a phenomenon recently established for the photooxidation of freely dissolved tryptophan.

146 that can catalyze the challenging catalytic photooxidation of H(2)O into four protons, four electron

147 )-39-Cc at low ionic strength leads to rapid photooxidation of heme c, followed by intracomplex elect

148 te that also requires a carboxyl ligand; (d) photooxidation of high-affinity DPC by YZ* with a KM of

149 iginated from anthropogenic sources, such as photooxidation of hydrocarbons present in diesel and bio

150 iimine) compounds were prepared to study the photooxidation of iodide.

151 Laboratory studies indicate that the photooxidation of iodine produces iodine oxides (I(x)O(y

152 Atmospheres from the photooxidation of isoprene and 1,3-pentadiene also induc

153 Atmospheric photooxidation of isoprene is an important source of sec

154 Isoprene epoxydiols (IEPOX), formed from the photooxidation of isoprene under low-NO(x) conditions, h

155 by mixtures of Fe(2+) and SOA generated from photooxidation of isoprene, a-terpineol, and toluene.

156 reactions of biogenic SOA generated by (*)OH photooxidation of isoprene, B-pinene, a-terpineol, and d

157 reactions of biogenic SOA generated by (*)OH photooxidation of isoprene, beta-pinene, alpha-terpineol

158 constituents derived from MAE to those from photooxidation of isoprene, methacrolein, and MPAN under

159 ation and addition reactions in OA formed by photooxidation of isoprene.

160 Moreover, photooxidation of L-tryptophan mediated by TCP-C60 films

161 These results show that photooxidation of low levels of NH3 on TiO2 surfaces rep

162 that does not require carboxyl residues; (e) photooxidation of low-affinity DPC with a KM = 1200 micr

163 d glutamate residues in MSP are perturbed by photooxidation of manganese during the S1 to S2 transiti

164 nodic steps have a PEC nature and are due to photooxidation of MeOH by the NPs at the electrode surfa

165 We use photooxidation of MeOH by TiO2 NPs as a model system of

166 Studies on the photooxidation of methyl-substituted aromatic hydrocarbo

167 Photooxidation of methylene blue-NP41-bound nerves, foll

168 ght-driven charge separations coupled to the photooxidation of Mn(2+) in order to form the first stab

169 The first step, the binding and photooxidation of Mn(2+) to Mn(3+), is specifically stim

170 th increased accessibility (or affinity) and photooxidation of Mn2+ at one or both of the two binding

171 Initial binding and photooxidation of Mn2+ to the apoprotein is critically d

172 otooxidation by DPC, but allows for a single photooxidation of Mn2+.

173 cles are more likely to be produced from the photooxidation of molecular iodine.

174 ty of the composition of SOA formed from the photooxidation of MPAN to that formed from isoprene and

175 been investigated for the first time for the photooxidation of n-dodecane (C12H26) in the presence of

176 These net reactions represent the photooxidation of NADH to NAD+.

177 y organic aerosol (SOA) prepared by high-NOx photooxidation of naphthalene (NAP SOA).

178 tion was measured for SOA generated from the photooxidation of naphthalene in the presence of iron su

179 itrate radicals are obtained by one-electron photooxidation of nitrate anions and are very reactive t

180 During direct photooxidation of organic carbon (OC) alone, the PAH(eve

181 Second, we discuss processes involving the photooxidation of organic species, either directly or vi

182 l/proximal damage ratios were compared after photooxidation of otherwise identical Rh-tethered assemb

183 In this paper, we report that photooxidation of P(700) in cyanobacterial PSI perturbs

184 (2)H exchange experiments, we conclude that photooxidation of P(700) perturbs internal or bound wate

185 -induced FTIR difference spectroscopy of the photooxidation of P700 has been combined with site-direc

186 that persist following photoinduced CS drive photooxidation of PDI(-*) components of [SWNT((*+)n)]-(P

187 In order to prevent the photooxidation of phytosterols, a new type of Pickering

188 unction of PSI is sensitized by a reversible photooxidation of primary electron donor P700, which lau

189 We show experimentally that the photooxidation of rhodochrosite in suspension with light

190 ls, and leads to very good stability against photooxidation of Si nanowires in solar water-reduction

191 We report the photooxidation of siderite (FeCO3) by UV radiation to pr

192 ated quantum yield for the reaction suggests photooxidation of siderite would have been a significant

193 The photooxidation of sulfinate salts yields the much more s

194 Exposing wine to light can cause photooxidation of tartaric acid to form glyoxylic acid,

195 In addition, partial photooxidation of the (FS)U residue to 5-fluorouridine w

196 studies revealed that fullerenes promote the photooxidation of the 1,3-dithiolylidene bond.

197 In addition, we studied sensitized photooxidation of the dipyrrinone subunit by singlet oxy

198 ion capacity via the photodriven binding and photooxidation of the free inorganic cofactors within th

199 face of the nanocrystal, which initiated the photooxidation of the ligands and protected the nanocrys

200 ligands on the surface of nanocrystals, the photooxidation of the nanocrystals, and the precipitatio

201 Photooxidation of the oxazole moiety in 1 gave enigmimid

202 The photooxidation of the redox-active accessory chlorophyll

203 t is proposed that MSP regulates the binding/photooxidation of the second Mn2+ of the photoligation s

204 able of catalyzing the otherwise inefficient photooxidation of thiols to the key thiyl radical interm

205 Photooxidation of this triene forms a cyclopropanone and

206 osition from alpha-pinene ozonolysis and the photooxidation of toluene and acetylene by OH.

207 ting from the ozonolysis of alpha-pinene and photooxidation of toluene, redispersed soil dust samples

208 duced increase of the fluorescence: a prompt photooxidation of tryptophan moieties or a fast prolifer

209 Our data further suggest that direct photooxidation of tryptophan residues within the protein

210 Here we examine the photooxidation of two kinetically fast electron hole tra

211 Photooxidation of volatile organic compounds (VOCs) prod

212 oxides have been extensively studied for the photooxidation of water, their utilization for photoredu

213 e that utilizes solar energy to catalyze the photooxidation of water.

214 Photooxidations of anthraquinone-modified DNA assemblies

215 Many similarities exist between the photooxidations of imidazole and guanosine in organic so

216 l/methyl fragmentation selectivities for the photooxidations of phenyltrimethylstannane and (4-methyl

217 ments, the observed clay and humic-dependent photooxidation pathways of tetracycline and the differin

218 s the surface functional molecules of the UV photooxidation patterned polymer to direct the nucleatio

219 Among such processes are photoisomerization, photooxidation/photoreduction, breaking and making of co

220 substituted pentacenes are most resistant to photooxidation, possess relatively small HOMO-LUMO gaps

221 Evidence that ATR dimer undergoes a photooxidation process involving the addition of oxygens

222 lipid oxidation in food through a sensitized-photooxidation process, which involves the participation

223 tion of which was directly correlated to the photooxidation process.

224 The photooxidation processes of tryptophan (Trp) in the pres

225 ts potential as a competitive ROS species in photooxidation processes.

226 Importantly, photooxidation produces a relationship between the (1)O2

227 However, photooxidation produces residual dot and rod domains wit

228 itioning and particle-phase reactions of the photooxidation product glyoxal.

229 The compound 3-methyleneoxindole (MOI), a photooxidation product of the plant auxin indole-3-aceti

230 se effects of A2E accumulation, with the A2E photooxidation products being damaging intermediates.

231 The photooxidation products of 1,3,5-trimethylbenzene and NO

232 The photooxidation products of a mixture of alpha-pinene (in

233 The authors previously reported that photooxidation products of A2E can activate complement.

234 velopment and to a role in the metabolism of photooxidation products of cholesterol in the retina.

235 f C5-epoxydiols, second-generation gas-phase photooxidation products of isoprene.

236 Photooxidation products resulting from volatile organic

237 Rather, the dissolved organic photooxidation products stimulated significantly more mi

238 vity of soluble Fe(III) toward known benzene photooxidation products that include fumaric (trans-bute

239 The main photooxidation products were 1-hexene, CO, vinyl alcohol

240 genicity of emitted VOCs should consider VOC photooxidation products, especially dienes with terminal

241 thelium that were irradiated to generate A2E photooxidation products.

242 acetonitrile, with no formation of secondary photooxidation products.

243 ne and cysteine sulfinic acid were the major photooxidation products.

244 leate methyl esters and was used to generate photooxidation profiles for the photosensitizers methyle

245 Our results suggest that the photooxidation properties of the GFP chromophore in an a

246 f alpha2 in facilitating PT during beta-Y356 photooxidation; PT occurs by way of readily exchangeable

247 Furthermore, the photooxidation rate of bacitracin A with (1)O2 decreased

248 The kinetic of a photooxidation reaction of benzo(a)pyrene (BaP) carried

249 t His245 is oxidized to aspartate during the photooxidation reaction was supported by the extremely l

250 nel to UV radiation, which induced a surface photooxidation reaction, resulting in the production of

251 ion of acetaldehyde, which reverses the EtOH photooxidation reaction.

252 Four sequential photooxidation reactions are required for oxygen product

253 Four sequential photooxidation reactions are required to generate oxygen

254 Four sequential photooxidation reactions are required to generate oxygen

255 d to reveal mechanistic details for enhanced photooxidation reactions in general.

256 advantage of the catalytic nature of type II photooxidation reactions.

257 of biological processes, is known to undergo photooxidation reactions.

258 also leached from roads and highways through photooxidation reactions.

259 e separated species were passed through a UV photooxidation reactor which decomposed the organic spec

260 cells to H(2)O(2), paraquat, or A2E-mediated photooxidation resulted in increased expression and secr

261 Because photooxidation results in peroxidation at lipid double b

262 ctivity of the composite electrode for water photooxidation results, at least in part, from reduced r

263 cted, we hypothesize that biodegradation and photooxidation share responsibility for the accumulation

264 This abrupt shift in isoprene photooxidation, sparked by human activities, speaks to o

265 The 20-30 ps trapping component and P(700) photooxidation spectra derived from data on the 100 ps s

266 tyrin and resveratrol, exhibited the highest photooxidation stability.

267 As with other photooxidation systems, experiments performed without se

268 of cyt f, displayed net rates of cytochrome photooxidation that were slightly faster than those in t

269 , the most fundamental property underpinning photooxidation, the electron detachment energy, has only

270 Because water is a possible product of dry photooxidation, these results highlight the need for enc

271 of H2O2, .OH, and triplet HS decreased with photooxidation, thus demonstrating selective destruction

272 rgoing direct photoionization and sensitized photooxidation to form radical cation species, which the

273 e presence of sunlight, and requires days of photooxidation to reach the levels observed in the atmos

274 und to be especially effective in catalyzing photooxidation (typically 3%).

275 ecular reaction rate constants, showing slow photooxidation under environmental conditions.

276 A similar result is apparent with photooxidation using a DNA-tethered anthraquinone.

277 tor the oxidation of DNA-bound Dps after DNA photooxidation using an intercalating ruthenium photooxi

278 However, formulas most susceptible to photooxidation vary depending on the initial DOM composi

279 Photooxidation was accompanied by decreases in specific

280 But if photooxidation was allowed to proceed, large rafts were

281 ormation of several spectral features due to photooxidation was attributed to ketones, carboxylic aci

282 F(B)-less complexes, a normal level of P700 photooxidation was detected accompanied by a high yield

283 Our knowledge on the mechanism of water photooxidation was greatly advanced by high-resolution s

284 y indicated that the initiation stage of the photooxidation was not caused by the chemical oxidation

285 Isoprene photooxidation was separated from SOM production by usin

286 SOM production from isoprene photooxidation was studied under hydroperoxyl-dominant c

287 Thus, photooxidation was the cause of raft enlargement during

288 ids, and PAHs indicated that evaporation and photooxidation were major processes contributing to dilb

289 photodegradation arises from edge-initiated photooxidation, wherein oxidative attack is powered by p

290 otoelectrocatalytic activity toward methanol photooxidation which is observed following electrochemic

291 protect the tree against photoinibition and photooxidation, which allows a more efficient recovery o

292 the relationship between DOM composition and photooxidation, which has important implications for car

293 ne-electron oxidation by riboflavin-mediated photooxidation, which is consistent with the predominanc

294 Chamber photooxidation with a midexperiment aldehyde injection c

295 studied in a phospholipid membrane model of photooxidation with a new isotope dilution gas chromatog

296 conjugates leads to lambda(irr) independent photooxidation with a quantum yield of ~4% in aerated pH

297 A) photocross-linking and peptide (melittin) photooxidation with incorporation of molecular oxygen.

298 Indeed, strategies for how to potentiate photooxidations with additives remain highly underexplor

299 lectron injection induces Mn(II) --> Mn(III) photooxidation, with a half-time for regeneration of the

300 HF result only in photochemical thinning or photooxidation, without a significant influence on quant