ライフサイエンスコーパス: photooxidation

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

2 ding was consistent with a process involving photooxidation.

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

4 ptacene derivative 4 especially resistant to photooxidation.

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

6 genic volatile organic compounds to aromatic photooxidation.

7 ulated A2E and were irradiated to induce A2E photooxidation.

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

9 ned through controlled chemical oxidation or photooxidation.

10 gands and protected the nanocrystal from any photooxidation.

11 e fluorophore eosin followed by fluorescence photooxidation.

12 photooxidation mechanisms in later stages of photooxidation.

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

14 at early stages of methylene blue-sensitized photooxidation.

15 acellular injection with Lucifer Yellow, and photooxidation.

16 njunction with the multigeneration gas-phase photooxidation.

17 pheric epoxides in forming SOA from isoprene photooxidation.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

38 0 microM MnCl2 noncompetitively inhibits DPC photooxidation at the high-affinity site, with a Ki of 1

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

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

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

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

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

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

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

46 Photooxidation commonly results in green-to-red photocon

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

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

49 Presumably, their photooxidation eliminates defects on the nanoparticle su

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

51 Steady-state, preparative photooxidation experiments show that aryltrimethylstanna

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

53 In photooxidation experiments, long-range oxidative damage

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

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

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

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

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

59 indicative of a contribution from lipofuscin photooxidation in RPE.

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

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

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

63 st triphasic superhydrophobic sensitizer for photooxidations in water droplets.

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

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

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

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

68 Isoprene photooxidation is a major driver of atmospheric chemistr

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

70 Photooxidation is an important abiotic transformation pa

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

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

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

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

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

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

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

78 ion by molecular oxygen though quenching and photooxidation mechanisms.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

93 The photooxidation of a series of aldoxime ethers was studie

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

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

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

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

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

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

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

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

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

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

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

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

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

107 The photooxidation of compounds in petroleum, following expo

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

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

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

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

112 We synthesized uroporphomethene by photooxidation of enzymatically generated uroporphyrinog

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

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

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

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

117 )-39-Cc at low ionic strength leads to rapid photooxidation of heme c, followed by intracomplex elect

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

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

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

121 Atmospheric photooxidation of isoprene is an important source of sec

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

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

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

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

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

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

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

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

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

131 Studies on the photooxidation of methyl-substituted aromatic hydrocarbo

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 The photooxidation of sulfinate salts yields the much more s

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

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

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

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

158 The photooxidation of the redox-active accessory chlorophyll

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

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

161 Photooxidation of this triene forms a cyclopropanone and

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

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

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

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

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

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

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

169 Photooxidations of anthraquinone-modified DNA assemblies

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

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

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

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

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

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

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

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

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

179 However, photooxidation produces residual dot and rod domains wit

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

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

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

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

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

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

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

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

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

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

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

191 thelium that were irradiated to generate A2E photooxidation products.

192 acetonitrile, with no formation of secondary photooxidation products.

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

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

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

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

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

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

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

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

201 Four sequential photooxidation reactions are required for oxygen product

202 Four sequential photooxidation reactions are required to generate oxygen

203 Four sequential photooxidation reactions are required to generate oxygen

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

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

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

207 Because photooxidation results in peroxidation at lipid double b

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

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

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

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

212 As with other photooxidation systems, experiments performed without se

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

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

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

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

217 Photooxidation was accompanied by decreases in specific

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

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

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

221 Isoprene photooxidation was separated from SOM production by usin

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

223 Thus, photooxidation was the cause of raft enlargement during

224 otoelectrocatalytic activity toward methanol photooxidation which is observed following electrochemic

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

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

227 Chamber photooxidation with a midexperiment aldehyde injection c

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

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

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

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

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