ライフサイエンスコーパス: electron transport

1 or II (no change in isolated photosynthetic electron transport).

2 rks, extreme event statistics, to physics of electron transport.

3 iate (formate or H2)-dependent inter-species electron transport.

4 liminating the ohmic heating associated with electron transport.

5 ta-carboxysome biogenesis and photosynthetic electron transport.

6 both of which are central players in cyclic electron transport.

7 e low luminal pH generated by photosynthetic electron transport.

8 abolism during the blockage of mitochondrial electron transport.

9 s lattice thermal conductivity more than the electron transport.

10 g of how the structure of DNA determines its electron transport.

11 contribute to this novel mode of biological electron transport.

12 rvesting sunlight to fuel the photosynthetic electron transport.

13 ntimycin A, which both inhibit mitochondrial electron transport.

14 research on the regulation of photosynthetic electron transport.

15 h targets will produce highly structured hot electron transport.

16 contact resistance and energetic barrier for electron transport.

17 eir thylakoids exhibited a decreased rate of electron transport.

18 or carbon cloth (CC)) to facilitate mass and electron transport.

19 o induce superconductivity, as well as probe electron transport.

20 g to render the channelized pathways for the electron transport.

21 which is evidenced by the enhanced hole and electron transport abilities of the active layer.

22 Exploring long-range electron transport across protein assemblies is a centra

23 The electron-transport activation energy and the Coulomb blo

24 of the mitochondrial proteome, modulation of electron transport, activation of biogenesis or mitophag

25 r WSe2 is degraded more severely relative to electron transport after helium ion irradiation.

26 sed on a polymer that supports both hole and electron transport along its backbone when doped through

27 d their products including the components of electron transport and 16S mt-rRNA, similar to the pheno

28 ong-term cyclelife, benefiting from promoted electron transport and a shortened Na(+) diffusion lengt

29 tein cytochrome c (cyt c) plays key roles in electron transport and apoptosis, switching function by

30 ing microbes via inhibition of intracellular electron transport and consumption is an important reaso

31 gle and interface surfaces that had improved electron transport and diffusion compared with currently

32 ; inactivation of mitochondrial Src inhibits electron transport and increases reactive oxygen species

33 thesis that favor either diffusion-dependent electron transport and photoprotection or protein repair

34 lls has implications for diffusion-dependent electron transport and photoprotective energy-dependent

35 ons between cyclic and noncyclic alternative electron transport and that an excess capacity for alter

36 cells, rely on AIF to maintain mitochondrial electron transport and that metabolic, rather than apopt

37 ein nanostructures for transmembrane ion and electron transport and the mechanistic understanding und

38 mechanisms (cyclic and noncyclic alternative electron transport), and regulation of Rubisco activity

39 hibition of net assimilation, photosynthetic electron transport, and isoprene emission rates, but DOA

40 cycle, glycolysis, TCA cycle, mitochondrial electron transport, and starch and sucrose metabolisms w

41 m has no measurable effect on photosynthetic electron transport around PSI or on accumulation of prot

42 A nanostructuring approach that enables electron transport as well as phonon transport to be man

43 er, there is still no clear understanding of electron transport, as reported values span over three o

44 observations and demonstrate a beam-like hot electron transport at initial time-scales that may be at

45 tochondrial defects that include inefficient electron transport between complex I and ubiquinone.

46 However, the biochemical mechanisms for electron transport between these H2 /formate-generating

47 s on the quantum efficiency of PSI and PSII, electron transport, biomass, and seed yield in Arabidops

48 This paper further demonstrates enhanced electron transport by close to an order of magnitude in

49 response to the reduction of photosynthetic electron transport by high light treatments.

50 Herein, ionic liquids facilitated electron transport by two-fold without any interfacial b

51 icroscopy (STM) break junction technique and electron transport calculations are carried out on such

52 dizing microorganisms inducing long-distance electron transport, can delay the onset of euxinia in co

53 The results show that photo-activated electron transport cannot be described by a superpositio

54 respiration (P CI , P CI+II ; P = 0.008) and electron transport capacity (E CI+II ; P = 0.01) increas

55 ves led to a more heterogenous saturation of electron transport capacity and lowered its CO2 concentr

56 distribution of light absorption relative to electron transport capacity in sun- and shade-grown sunf

57 Electron transport capacity was also greater in Loda tha

58 ation of proteins involved in photosynthetic electron transport, carbon fixation, oxidative stress pr

59 f about 50-60 ns makes this dyad a potential electron-transporting catalyst to carry out energy-deman

60 Electron transport chain (ETC) activity generates an ele

61 A decline in electron transport chain (ETC) activity is associated wi

62 cations of Krebs cycle components as well as electron transport chain (ETC) alterations.

63 ae morphology, fusion in TM cells configures electron transport chain (ETC) complex associations favo

64 ns with the mRNAs encoding the mitochondrial electron transport chain (ETC) complex I as well as hund

65 as well as significantly decreased (40%-50%) electron transport chain (ETC) complex I, II, IV, V, and

66 abundance of mitochondria and high levels of electron transport chain (ETC) complexes within these mi

67 The Mycobacterium tuberculosis (Mtb) electron transport chain (ETC) has received significant

68 hondria undergo fragmentation in response to electron transport chain (ETC) poisons and mitochondrial

69 ction through the coupled integration of the electron transport chain (ETC) with oxidative phosphoryl

70 evealed that among components of the aerobic electron transport chain (ETC), only genes involved in t

71 of respiratory quiescence by remodeling the electron transport chain (ETC).

72 (TCA) cycle, and ATP synthesis powered by an electron transport chain (ETC); instead, they produce AT

73 n is associated with a dramatic reduction in electron transport chain abundance.

74 Inhibition of complex I of the mitochondrial electron transport chain activated AMPK and inhibited Kv

75 Biochemically mutant mice showed impaired electron transport chain activity and accumulated autoph

76 n a reduction in mitochondrial RNAs, reduced electron transport chain activity, and reduced ATP level

77 ion in mitochondria, including modulation of electron transport chain activity.

78 IMM constriction requires electron transport chain activity.

79 s the activity of both complex II/III of the electron transport chain and ATP synthase.

80 capacity and efficiency of the mitochondrial electron transport chain and ATP synthesis.

81 synthesis while maintaining a redox-balanced electron transport chain and avoiding excessive reactive

82 ylococcus aureus typically lack a functional electron transport chain and cannot produce virulence fa

83 is critically dependent on the mitochondrial electron transport chain and oxidative phosphorylation m

84 itochondria including the citric acid cycle, electron transport chain and ROS production and scavengi

85 Recently, complex II of the electron transport chain appears to be more important th

86 SIRT3 rescued the IR-induced blockade of the electron transport chain at the level of complex III, at

87 bility of our method by assembling a minimal electron transport chain capable of adenosine triphospha

88 Moreover, electron transport chain complex (I, V) decrease in FECD

89 trium and cervix function, and mitochondrial electron transport chain complex enzymatic activities we

90 s of riboflavin, downstream metabolites, and electron transport chain complex I activity.

91 Electron transport chain complex I and complex II activi

92 d skeletal muscle mitochondrial respiration, electron transport chain complex I dysfunction, as well

93 ration rate that is likely due to defects in electron transport chain complex I.

94 Electron transport chain complexes are downregulated, po

95 Mitochondrial electron transport chain complexes are organized into su

96 e process of dismantling their mitochondrial electron transport chain complexes as they adapt to anae

97 drial mass and differential contributions of electron transport chain complexes I and II to respirati

98 ngly, although subunits of the mitochondrial electron transport chain complexes were reduced at the p

99 Furthermore, assembled, electron transport chain complexes were significantly mo

100 he enzymatic activities of the mitochondrial electron transport chain complexes.

101 re we show a role for the dysfunction of the electron transport chain component cytochrome c oxidase

102 ndicated that Pitx2 activated genes encoding electron transport chain components and reactive oxygen

103 ive capacity and abundant expression of both electron transport chain components and uncoupling prote

104 nt TCP/TRiC/CCT chaperonin and mitochondrial electron transport chain components.

105 The mitochondrial electron transport chain consists of individual protein

106 Our results show that mitochondrial electron transport chain defect initiates a retrograde s

107 s of AIF in fibroblasts led to mitochondrial electron transport chain defects and loss of proliferati

108 id metabolism, as well as the first complete electron transport chain described for a member of the C

109 aging theories and implicates mitochondrial electron transport chain dysfunction with subsequent inc

110 I represses genes critical for mitochondrial electron transport chain enzyme activity, oxidative stre

111 me is essential for processing heme into the electron transport chain for use as an electron acceptor

112 anding of the structural organization of the electron transport chain from the original idea of a com

113 types, while copy number alterations in the electron transport chain gene SCO2, fatty acid uptake (C

114 tion, we explored whether restoration of the electron transport chain in this organism also affected

115 Redox cycling, mitochondrial DNA damage and electron transport chain inhibition have been identified

116 Electron transport chain inhibition is the main pathway

117 the actual rates observed in the absence of electron transport chain inhibitors, so maximum capaciti

118 ons were observed in proteins throughout the electron transport chain membrane complexes, ATP synthas

119 model of the reactions in the photosynthetic electron transport chain of C3 species.

120 serves as the last enzyme in the respiratory electron transport chain of eukaryotic mitochondria.

121 dase, the terminal enzyme in the respiratory electron transport chain of mitochondria, from hippocamp

122 ndrial architecture, increased expression of electron transport chain proteins, and depletion of fat

123 man AML, treatment with ddC decreased mtDNA, electron transport chain proteins, and induced tumor reg

124 T cells by interfering with the formation of electron transport chain respiratory supercomplexes.

125 Two atypical mitochondrial electron transport chain subunits (Ndufa4l2 and Cox4i2)

126 way, ion channels and atypical mitochondrial electron transport chain subunits.

127 iological data suggest that Aer monitors the electron transport chain through the redox state of its

128 Inhibition of complex I of the mitochondrial electron transport chain using phenformin activated AMPK

129 that can be transferred to the mitochondrial electron transport chain via the electron transfer flavo

130 nction with an uncoupler or interrupting the electron transport chain with cyanide (CN(-)) alters ER

131 pecies (ROS) generated as by-products of the electron transport chain within mitochondria significant

132 ochrome c oxidoreductase (complex III of the electron transport chain).

133 te dehydrogenase activity (complex II of the electron transport chain); 3) increase catalase activity

134 RNA, blocks the assembly of complex I in the electron transport chain, and causes an arrest in embryo

135 ired for the tricarboxylic acid (TCA) cycle, electron transport chain, and oxidative phosphorylation,

136 ation is given by phosphorylation subsystem, electron transport chain, and substrate dehydrogenation

137 oxidase, xanthine oxidase, the mitochondrial electron transport chain, and uncoupled endothelial nitr

138 ich are involved in energy generation by the electron transport chain, detoxification of host immune

139 Campylobacter jejuni harbors a branched electron transport chain, enabling respiration with diff

140 PINK1, as well as chemical inhibition of the electron transport chain, impaired lysosomal activity an

141 e methods severely disrupt the mitochondrial electron transport chain, mtDNA-depleted cells still mai

142 RT5-treated membrane proteins pointed to the electron transport chain, particularly Complex I, as bei

143 lso known as complex II of the mitochondrial electron transport chain, providing support for the bifu

144 are critical components of the mitochondrial electron transport chain, we hypothesized that reduced r

145 on ferredoxin reduced by the photosynthetic electron transport chain, which fuels reducing power to

146 ation, electrons leak from the mitochondrial electron transport chain, which is captured by molecular

147 r genes, all components of the mitochondrial electron transport chain, which show significant loss of

148 to water without involving cytochrome-linked electron transport chain.

149 by slowing respiration at the mitochondrial electron transport chain.

150 tion of reactive oxygen species (ROS) by the electron transport chain.

151 rial respiration due to lack of NADH for the electron transport chain.

152 participating in redox reactions within the electron transport chain.

153 t characterized complex of the mitochondrial electron transport chain.

154 rough complex I and II, respectively, of the electron transport chain.

155 bition of Complex I within the mitochondrial electron transport chain.

156 fer of electrons to O2 via the mitochondrial electron transport chain.

157 lectron leak occurring at complex III of the electron transport chain.

158 of cytochrome c oxidase in the mitochondrial electron transport chain.

159 lates with the redox state of photosynthetic electron transport chain.

160 inant, physiologically relevant state of the electron transport chain.

161 rease in expression of genes involved in the electron transport chain.

162 y and nanomolar potency as complex II of the electron transport chain.

163 buildup of energy metabolites that feed the electron transport chain.

164 of a reduction signal in the photosynthetic electron transport chain.

165 dogenous superoxide (O2(*-)) produced in the electron transport chain.

166 e Krebs cycle and is located upstream of the electron transport chain.

167 ctors, mitochondrial ribosomal proteins, and electron-transport chain subunits.

168 Therefore, the lack of functional electron transport chains in SCV S. aureus and wild-type

169 ed genes and highlighted re-modelling of the electron transport chains.

170 (II)Phthalocyanines were linked to different electron-transport chains featuring pairs of electron ac

171 boxylation rate and 23% lower photosynthetic electron transport compared with the highest g NIL.

172 teractions with the fumarate reductase (Frd) electron transport complex.

173 prolonged ischemia/reperfusion also damages electron transport complexes, we investigated whether su

174 te and appears to be losing cytochrome-based electron transport (complexes III and IV).

175 er hormone-mediated pathways, photosynthetic electron transport components, sugar, amino acid, and ce

176 switch to a more reduced state when reverse electron transport conditions are in place.

177 on of ABA or the inhibitor of photosynthetic electron transport, DCMU, abolishes the MAMP-induced chl

178 t to the development of light-harvesting and electron-transport devices.

179 Water plays a vital role in electron transport energetics by electrowetting the cofa

180 ir prominent role in mediating extracellular electron transport (ET), but one of their key fundamenta

181 We investigated the solid-state electron transport (ETp) across a self-assembled monolay

182 n from temperature-independent to -dependent electron transport, ETp, was reported at approximately 4

183 issue, where it generates heat by uncoupling electron transport from ATP production.

184 avoprotein ferrodoxin reductase required for electron transport from NADPH to cytochrome P450.

185 pport their role as bound redox cofactors in electron transport from nanowires to metal oxides.

186 tates from light harvesting with the rate of electron transport from water to carbon dioxide.

187 Photosynthetic electron transport function and protein levels of Fe-dep

188 The uncoupling of complex II's electron transport function from its succinate dehydroge

189 gger oxidative bacterial death by disrupting electron transport, generating superoxide anion and inac

190 d expression of chloroplast and mitochondria electron transport genes in p5cs1-4 These results show t

191 uction components, including Krebs cycle and electron transport genes, decreased by 43% +/- 5% (mean

192 sites, good wetting behavior, and effective electron transport, giving rise to greatly enhanced perf

193 However, uniform electron transport has not yet been achieved across the

194 ent component of total linear photosynthetic electron transport in 21% O2 This O2-dependent component

195 of photoprotective processes in chloroplast electron transport in leaves under canopy solar radiatio

196 s especially important for processes such as electron transport in metabolism and signal propagation

197 Cytochrome c (cyt c), required for electron transport in mitochondria, possesses a covalent

198 ility of magnetite to be used for long range electron transport in soils and sediments.

199 elevated levels of proteins associated with electron transport, indicates greater investment in leaf

200 enzymatic activities including mitochondrial electron transport, iron mobilization, and peptide hormo

201 Electron transport is conventionally determined by the m

202 Mitochondrial electron transport is essential for oxidative phosphoryl

203 We hypothesize that the loss of electron transport is inducing feedback inhibition of me

204 and that an excess capacity for alternative electron transport is required to ensure adequate redox

205 1,5-bisphosphate) carboxylation (Vcmax ) and electron transport (Jmax ) at each treatment's respectiv

206 of Rubisco (Vcmax ), and the maximum rate of electron transport (Jmax )), leaf mass, nitrogen (N) and

207 carboxylation (Vcmax ), the maximum rate of electron transport (Jmax ), the maximum rate of phosphoe

208 The high photoconductivity of the TiO2 electron transport layer leads to improved efficiency fo

209 le silane-functionalized and doped fullerene electron transport layer, the perovskite devices deliver

210 d by using a defective TiO2 thin film as the electron transport layer.

211 llinity and the emergent perovskite/hole (or electron) transport layer on device performance and phot

212 ls incorporating the post-treated TiO2 :TOPD electron-transport layer achieve the highest efficiency

213 igh crystallinity, the relatively thick SnO2 electron-transporting layer ( approximately 120 nm) prov

214 demonstrated to serve as a stable and robust electron-transporting layer for high-performance perovsk

215 mesoporous titanium dioxide (mp-TiO2) as an electron-transporting layer.

216 rb characteristics are accomplished by novel electron transport layers (ETLs) and engineered quantum

217 (x) and n-type ZnO nanoparticles as hole and electron transport layers, respectively, and shows impro

218 Electron-transport layers doped in this manner are used

219 fluorescence, P700 photooxidation, and PS I electron transport light saturation experiments.

220 To become an efficient electron transport material for organic photovoltaics an

221 ability, strong catalytic activity and is an electron transport material in organic solar cells.

222 ow-temperature, solution-processable organic electron-transporting material (ETM) is successfully dev

223 omising building blocks for the synthesis of electron transport materials.

224 for functionalization of building blocks for electron transport materials.

225 nt diffusion lengths of holes and electrons, electron transporting materials (ETMs) used in PSCs play

226 successfully shown to function as efficient electron-transporting materials (ETMs) for perovskite so

227 nd hPDI3-Pyr-hPDI3 (2) are used as efficient electron-transporting materials (ETMs) in inverted plana

228 ut also for the early evolution of microbial electron transport mechanisms.

229 delivered succinate bypasses CI and supports electron transport, membrane potential and ATP productio

230 als showed that several proteins involved in electron transport, mitochondrial dynamics, and mitochon

231 mework, including magnetization dynamics and electron transport model, has been developed for analyzi

232 hole-transporting P3HT, (ii) semicrystalline electron-transporting N2200, (iii) low-crystallinity hol

233 ing balance between the rate of light-driven electron transport occurring in photosystem I (PSI) and

234 ength, a transition from coherent to hopping electron transport occurs, enabling observation of redox

235 ee dyes highlight the suitable properties of electron-transport of the BTBT as the pi-bridge in organ

236 de evidence that Weyl nodes act as sinks for electron transport on the surface of these materials.

237 gs may prove valuable for the development of electron transporting organic semiconductors and for the

238 the wood vessels, which deliver directional electron transport parallel to the alignment direction.

239 dated is linked to lithium-ion diffusion and electron-transport paths across both spatial and tempora

240 reinhardtii to determine the integration of electron transport pathways critical for maintaining act

241 he mitochondrial translation and respiratory electron transport pathways to be significantly downregu

242 tes contain genes involved in photosynthetic electron transport (PET) [12-18] as well as central carb

243 chitectures to study charge accumulation and electron transport phenomena.

244 nolayers and nanostructured films of a model electron-transporting polymer.

245 s demonstrate the potential for manipulating electron transport processes to increase crop productivi

246 c devices that use single molecules, yet its electron transport properties have not been fully elucid

247 These electron transport properties have potential for the dev

248 We investigate the low temperature electron transport properties of manganese doped lead su

249 reason for the enhanced PEC properties, the electron transport properties of the photoelectrodes wer

250 rk in the 3D architecture provides excellent electron transport properties, and its hierarchical poro

251 nd powerful way of analyzing their catalytic electron transport properties.

252 ITCC shows improved electron-transport properties and a high-lying lowest un

253 Emergent behaviour from electron-transport properties is routinely observed in s

254 and NDI-CPZs, a finding attributed to their electron-transport properties.

255 atrix we achieve dual control of phonon- and electron-transport properties.

256 approximately 120 nm) provides a respectable electron-transporting property to yield a promising powe

257 n which electrical contacts are made between electron transport proteins associated with the outer me

258 the relative abundance of key mitochondrial electron transport proteins in 263K-infected animals rel

259 The crowded electron transport proteins in the periplasm of the orga

260 e synergistic effect of the fast kinetics of electron transport provided by the free-standing structu

261 Here, the diurnal relationship between electron transport rate (ETR) and irradiance was measure

262 The strongest relationship expressed maximum electron transport rate (Jmax ) as a multivariate functi

263 xylation rate of Rubisco (Vmax), the maximum electron transport rate (Jmax) and the chlorophyll fluor

264 nsity was correlated to the maximum relative electron transport rate (rETRm).

265 eters maximum carboxylation rate and maximum electron transport rate at 25 degrees C (Vc,max.25 and J

266 lated to plant photosynthetic activity (i.e. electron transport rate).

267 ochemical parameters and the decrease in the electron transport rate.

268 a threshold light intensity, photosynthetic electron transport rates (water --> CO2) decrease in sta

269 pubescens significantly reduced the maximum electron transport rates and total biomass of U. europae

270 etraploids were also shown by more efficient electron transport rates of photosystems I and II.

271 , which can be used to correct apparent PSII electron transport rates to photons absorbed by PSII.

272 t b(6)/f supercomplex to regulate PSI cyclic electron transport rather than the regulation of state t

273 al biological relevance of the regulation of electron transport reactions within the photosynthetic c

274 classes, with varied functions that include electron transport, regulation of gene expression, subst

275 proteins, anti-stress/anti-disease protein, electron transport-related protein, and plant growth ass

276 related genomes favored those functional in electron transport, resulting in a host-beneficial purif

277 ence has implicated succinate-driven reverse electron transport (RET) through complex I as a major so

278 Succinate-driven reverse electron transport (RET) through complex I is hypothesiz

279 ce area, remarkable electron mobility, ready electron transport, sizeable band gaps and ease of hybri

280 ially compensated for by an increased cyclic electron transport, suggesting that in flowering plants,

281 Quantification of the proportion of total electron transport supporting photorespiration enabled e

282 noids that play key roles in the respiratory electron transport system of some prokaryotes by shuttli

283 ivergence across different components of the electron transport system.

284 s it is not caused by a direct effect on the electron transport system.

285 nd UQCR-14, a gene involved in mitochondrial electron transport, that has reduced expression in older

286 In terms of electron transport, the maximum extreme is given by carb

287 odified electrodes to explore spin-selective electron transport through hydrated duplex DNA.

288 unction depends on ROS production by reverse electron transport through mitochondrial complex I, and

289 ortant factors determining the efficiency of electron transport through organic conjugated molecules,

290 In electron transport through single nanometer scale magnet

291 evice in which there is interference between electron transport through the highest occupied molecula

292 metry suggest that the doped CPE facilitates electron transport to electrodes and reveal structure-fu

293 tions and appeared to play a role in reverse electron transport to generate NADH.

294 s paralleled by a gradual increase in cyclic electron transport to maintain ATP production.

295 arious hopping mechanisms, such as activated electron transport, variable range hopping, and Poole Fr

296 e can be reduced by long-range extracellular electron transport via Geobacter nanowires, and what mec

297 of a chain of amino acids with extraordinary electron transport, was helically wrapped around a semic

298 Fe deficiency first affected photosynthetic electron transport with concomitant reductions in carbon

299 respiratory activity influenced chloroplast electron transport with consequent overreduction of plas

300 ibbons are a promising platform for tailored electron transport, yet they suffer from low conductivit