ライフサイエンスコーパス: electron transport

1 l regulatory element of plant photosynthetic electron transport.

2 electron-transport layer (ETL) for efficient electron transport.

3 on elongation is triggered by photosynthetic electron transport.

4 ms in a very large dynamic range to optimize electron transport.

5 stocyanin would jeopardize the efficiency of electron transport.

6 ences observed for absorbance, trapping, and electron transport.

7 rch synthesis in priming/regulating CBBC and electron transport.

8 0-fold faster than the rate-limiting step in electron transport.

9 xygen or nitrate reduction via long-distance electron transport.

10 ions, connectivity and QI in single-molecule electron transport.

11 ed to act as a shuttle dithiol/disulfide for electron transport.

12 eir thylakoids exhibited a decreased rate of electron transport.

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

14 research on the regulation of photosynthetic electron transport.

15 h targets will produce highly structured hot electron transport.

16 han the rate-limiting step in photosynthetic electron transport.

17 H) architecture that decouples gas, ion, and electron transport.

18 genes involved in mitochondrial function and electron transport.

19 duces NO into N(2)O using the photosynthetic electron transport.

20 so enhanced, indicating efficient long-range electron transport.

21 w that oxidative byproducts of mitochondrial electron transport(6,7) regulate the activity of dFB neu

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

23 wide bang gap of pristine oxide reduces its electron transport ability and photocatalytic activity.

24 interactions and magnetic fields may control electron transport across biotic-abiotic interfaces in b

25 chondrial fission, mitochondrial biogenesis, electron transport activities and cellular protection.

26 tus has a very high capacity for alternative electron transport (AET) measured as light-dependent oxy

27 , allows predicting a more favorable hole or electron transport already from screening the polymer fi

28 Therefore, electron transport also through non-Watson-Crick base-pa

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

30 Complex IV activity, improved mitochondrial electron transport and ATP synthesis, and restored cell

31 nnected HG framework can not only facilitate electron transport and CO(2) /Li(+) diffusion, but also

32 of BCP clustering from C(70), along with the electron transport and exciton blocking properties of th

33 Instead, tuning the rate of alternative electron transport and increasing the processing rates o

34 e mechanical deformation originates from the electron transport and ion intercalation in the redox ac

35 embrane potential that impairs mitochondrial electron transport and NAD(+) regeneration.

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

37 sites, 3D conductive pathways for efficient electron transport, and porous channels to facilitate el

38 egrals of 12.1-37.9 meV rationalizing the 3D electron transport, and relatively high mu(e) of 10(-4)

39 ble A(max) , maximum rates of carboxylation, electron transport, and Rubisco activity when compared w

40 ndicated that resources used for Rubisco and electron transport are reduced under both elevated tempe

41 ton gradients coupled to, and maintained by, electron transport are ubiquitous sources of chemiosmoti

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

43 sed expression of mitochondrial ribosome and electron transport-associated genes.

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

45 or with a nanoporous barrier to characterize electron transport between Shewanella oneidensis MR-1 an

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

47 chemical stability, non-toxicity, abundance, electron transport capability in many classes of optoele

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

49 Electron transport capacity was also greater in Loda tha

50 rticularly at the level of complex II of the electron transport chain (2.2-fold increase; P < 0.01).

51 lators of the respiratome; the mitochondrial electron transport chain (complexes I-IV) and the FoF1-A

52 ytosolic H(2)O(2) but leads to mitochondrial electron transport chain (ETC) activity.

53 l mass, membrane potential, respiration, and electron transport chain (ETC) activity.

54 is an electron carrier in the mitochondrial electron transport chain (ETC) and antioxidant.

55 al genes, thus enhancing the capacity of the electron transport chain (ETC) and restoring mitochondri

56 which phenazines abstract electrons from the electron transport chain (ETC) and thereby generate reac

57 Consistent with this, low electron transport chain (ETC) Complex I and Complex II

58 Assays of mitochondrial electron transport chain (ETC) complex I, IV, V activiti

59 myoblast cell lines display a severe loss of electron transport chain (ETC) complexes and exhibit com

60 thesis by interacting with components of the electron transport chain (ETC) complexes III, IV, and V,

61 We genetically disrupted electron transport chain (ETC) complexes in the intestin

62 ads to suppression and loss of mitochondrial electron transport chain (ETC) complexes.

63 ultiomic analysis revealed downregulation of electron transport chain (ETC) components in chRCC that

64 ed increases in mitochondrial mRNAs encoding electron transport chain (ETC) components.

65 lear encoded components of the mitochondrial electron transport chain (ETC) coordinated with an incre

66 Electron transport chain (ETC) defects occurring from mi

67 e the relative contribution of mitochondrial electron transport chain (ETC) derived H(2)O(2) versus c

68 ion changes, whereas biochemical analysis of electron transport chain (ETC) enzyme activities showed

69 MISTR proteins are associated with electron transport chain (ETC) factors and activated by

70 glycolysis and to transfer electrons to the electron transport chain (ETC) for fueling thermogenesis

71 that cancer cells become independent of the electron transport chain (ETC) for survival.

72 aenorhabditis elegans, reduced mitochondrial electron transport chain (ETC) function during developme

73 The electron transport chain (ETC) functions at an elevated

74 le and negatively regulates transcription of electron transport chain (ETC) genes.

75 ng the following: mRNA and protein levels of electron transport chain (ETC) genes; mitochondrial dyna

76 s, we find that impaired NADH oxidation upon electron transport chain (ETC) inhibition depletes aspar

77 The mitochondrial electron transport chain (ETC) is necessary for tumour g

78 s a positive regulator of key genes encoding Electron Transport Chain (ETC) proteins and stimulates o

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

80 by hypoxia or by chemical inhibition of the electron transport chain (ETC), both of which are known

81 rotein, acting as an electron carrier in the electron transport chain (ETC), where it shuttles electr

82 f the heme and iron-sulfur cluster-dependent electron transport chain (ETC).

83 t c) plays a vital role in the mitochondrial electron transport chain (ETC).

84 es in the tricarboxylic acid (TCA) cycle and electron transport chain (ETC).

85 g bioenergetics and enzyme activities of the electron transport chain (ETC).

86 ase in mitochondrial encoded subunits of the electron transport chain (ETC).

87 es, respiration occurs via the mitochondrial electron transport chain (mETC) composed of several larg

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

89 ial ultrastructure, impaired respiration and electron transport chain activities, and persistent prot

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

91 sue of Cell, Bonnay et al. identify enhanced electron transport chain activity as a critical determin

92 cid oxidation, reduced complex I- associated electron transport chain activity, and ATP depletion.

93 AKAP1-RNA interactions reduces mitochondrial electron transport chain activity.

94 n because it encodes protein subunits of the electron transport chain and a full set of transfer and

95 oxide is known to inhibit complex IV of the electron transport chain and aconitase of the Krebs cycl

96 as a consequence of subunit function in the electron transport chain and citric acid cycle, respecti

97 lti-subunit complex III of the mitochondrial electron transport chain and is involved in the electron

98 ostharvest storage through the mitochondrial electron transport chain and NADPH oxidase, respectively

99 as an electron carrier in the mitochondrial electron transport chain and plays a key role in apoptos

100 produced at complex III of the mitochondrial electron transport chain and released into the intermemb

101 Relatedly, SDH sits at the crossroad of the electron transport chain and tricarboxylic acid (TCA) cy

102 hrome c (cyt c) is known for its role in the electron transport chain but transitions to a peroxidase

103 ation which reduced the effectiveness of the electron transport chain by lowering ATP and increasing

104 e found that inhibition of the mitochondrial electron transport chain causes paralysis as well as mus

105 that of control mice correlating with higher electron transport chain CcO activity in Ngb-H64Q-CCC-tr

106 e dehydrogenase A (SDHA), a key component of electron transport chain complex (ETC) II.

107 loss of mitochondrial respiration, decreased electron transport chain complex activity, and mitochond

108 ardial stunning resulting from mitochondrial electron transport chain complex I dysfunction.

109 The acetylation status of electron transport chain Complex I protein NDUFB8 was si

110 nduced reactive oxygen species generation at electron transport chain complex I.

111 ochondrial B-oxidation reduces mitochondrial electron transport chain complex II activity, contributi

112 nduces accumulation of misfolded subunits of electron transport chain complex II and complex V, resul

113 Mitochondrial cristae contain electron transport chain complexes and are distinct from

114 logy and altered expression of mitochondrial electron transport chain complexes and dynamics-regulati

115 The mitochondrial electron transport chain complexes are organized into su

116 respectively, with no significant change in electron transport chain complexes expression.

117 function, as it reflects the activity of the electron transport chain complexes working together.

118 dative phosphorylation (citrate synthase and electron transport chain complexes) markers and COX IV (

119 tochondrial oxygen consumption by inhibiting electron transport chain complexes.

120 spite no change in protein or mRNA levels of electron transport chain complexes.

121 ing ATP5A (ATP synthase F1 subunit alpha)-an electron transport chain component.

122 n center and its proper function requires an electron transport chain composed of NADH (or NADPH), cy

123 Our results suggest that the mitochondrial electron transport chain contributes to evofosfamide act

124 ium of cultured human cells with a defective electron transport chain decreased the extracellular lac

125 show that electrons enter the photosynthetic electron transport chain during EEU in the phototrophic

126 tem that allows precise perturbations of the electron transport chain for the understanding of the ca

127 d from electron pairs being passed along the electron transport chain from NADH to O(2) generates a m

128 ochrome-c-oxidase, COX) of the mitochondrial electron transport chain have been implicated in the pat

129 ranslation of most protein components of the electron transport chain in lymphoma cells, and many of

130 f the two photosystems of the photosynthetic electron transport chain in the chloroplasts of plants a

131 of their life cycle involves an alternative electron transport chain in which rhodoquinone (RQ) is r

132 rdiolipin content, preserved activity of the electron transport chain including mitochondrial complex

133 of mtDNA-encoded genes is impaired, and the electron transport chain is compromised, fueling into a

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

135 y challenged to co-ordinate the abundance of electron transport chain protein subunits expressed from

136 The organization of the mitochondrial electron transport chain proteins into supercomplexes (S

137 However, expression levels of the electron transport chain proteins NDUFB8 (complex I), AT

138 16 of 27 identified proteins), in particular electron transport chain proteins.

139 ion. Inhibition of Complexes I and IV of the electron transport chain reduced neurite outgrowth in ZI

140 but were replicated using inhibitors of the electron transport chain respiratory complexes I, III, a

141 and biogenesis by boosting the expression of electron transport chain subunits and of factors essenti

142 ptake induced direct O-GlcNAcylation of many electron transport chain subunits and other mitochondria

143 Other components of the electron transport chain such as the NADH dehydrogenases

144 (2) production, activity of mitoflashes, and electron transport chain supercomplex formation.

145 Q (Q (n) ) is a vital lipid component of the electron transport chain that functions in cellular ener

146 he carbonyl of acetate to the membrane-bound electron transport chain that generates ion gradients dr

147 ocean-associated Margulisbacteria encode an electron transport chain that may support aerobic growth

148 potential gradient that is generated by the electron transport chain to drive the synthesis of ATP(1

149 electron transfer to route their respiratory electron transport chain to insoluble electron acceptors

150 l structure and function, repurposing of the electron transport chain to superoxide production, and N

151 We assembled the entire electron transport chain using the purified soluble doma

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

153 bioenergetic target for the Krebs cycle, the electron transport chain, also becomes altered, generati

154 lycolysis, the tricarboxylic acid cycle, and electron transport chain, are coordinately induced at th

155 in both the tricarboxylic acid cycle and the electron transport chain, can lead to a variety of disor

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

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

158 ncoding enzymes of tricarboxylic acid cycle, electron transport chain, oxidative phosphorylation, ele

159 n such as DOX influence on the mitochondrial electron transport chain, redox cycling, oxidative stres

160 can cause hyper-reduction of the chloroplast electron transport chain, resulting in oxidative damage.

161 By contrast, we show that complex I of the electron transport chain, the malate-aspartate shuttle a

162 P metabolism, glutathione metabolism and the electron transport chain, which belong to the induced ef

163 ression of vital components of mitochondrial electron transport chain, which compromise bioenergetics

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

165 t on the amount of ATP generated through the electron transport chain, with excess ATP going toward t

166 cluding NADPH oxidases and the mitochondrial electron transport chain.

167 Krebs enzyme aconitase and complex IV of the electron transport chain.

168 production by complex I of the mitochondrial electron transport chain.

169 itochondrial translation and assembly of the electron transport chain.

170 on required to support the NQ-driven aerobic electron transport chain.

171 srupt particular iron-sulfur proteins of the electron transport chain.

172 drial proton uncouplers or inhibitors of the electron transport chain.

173 , including the tricarboxylic acid cycle and electron transport chain.

174 termined to interfere with the mycobacterial electron transport chain.

175 itochondrial translation and assembly of the electron transport chain.

176 ining the ability to oxidize NADH within the electron transport chain.

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

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

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

180 ogressively compromised the integrity of the electron transport chain.

181 es, including disorders of the mitochondrial electron transport chain.

182 iration in an interlinked thylakoid membrane electron transport chain.

183 wo benzoquinones as electron carriers in the electron transport chain.

184 produced by complex III of the mitochondrial electron-transport chain were required for macrophage ac

185 le inner-membrane potential generated by the electron-transport chain.

186 harboring wild-type genomes have functional electron transport chains and propagate more vigorously

187 assays narrowly targeting components of the electron transport chains in their native environments.

188 ified the proteins involved in the TM and PM electron transport chains.

189 wastage ('overpotential requirement') across electron-transport chains where rate and power must be m

190 rms a charged centre that sets up two single-electron transport channels.

191 Specifically, the mitochondrial electron transport Complex I, oxidative stress and count

192 0, facilitates the assembly of mitochondrial electron transport complex IV.

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

194 ange couplings, electron transfer rates, and electron transport conductance measurements.

195 iketopyrrolopyrrole-tetrafluorobenzene-based electron transporting copolymer results in single crysta

196 Analysis of the photosynthetic electron transport demonstrated an inhibition of the PSI

197 te, was also determined to better understand electron transport during N-demethylation.

198 ime, and accessing a deeper understanding of electron transport during strong-field interactions.

199 end-products display reduced ATP production, electron transport efficiency, and proliferative capacit

200 Assessment of activities of mitochondrial electron transport enzymes is important for understandin

201 iche of the photosystem II D1 protein impair electron transport (ET) efficiency between quinones and

202 s predict a tight coupling to photosynthetic electron transport (ETR) as a function of temperature, d

203 otosystem II (Y(II)) and the maximum rate of electron transport (ETRmax), and negative with the quant

204 tical tuning algorithm searches for specific electron transport features in gate-defined quantum dot

205 This was essential to maintain mitochondrial electron transport for respiration and pyrimidine synthe

206 contains direct information about the actual electron transport from photosystem II to photosystem I,

207 ers, plastoquinone or plastocyanin, mediates electron transport from stacked grana thylakoids where p

208 tive oxygen species as the result of reverse electron transport fueled by succinate.

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

210 ith Chlamydomonas reinhardtii photosynthetic electron transport: (i) reduction of O(2) to H(2)O throu

211 and QD size distributions for high-mobility electron transport in 1D QDCs.

212 e structures can be suppressed by inhibiting electron transport in a helical way to diminish circular

213 rived from PSII were diverted to alternative electron transport in a rapidly changing light environme

214 via superoxide and superoxide dismutase, by electron transport in chloroplasts and mitochondria, pla

215 thesis that the suppression of mitochondrial electron transport in DS cells is due to high expression

216 osition of the ECSTM probe in order to study electron transport in individual photosystem I (PSI) com

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

218 whether the relative difference in hole and electron transport in solution-processed organic semicon

219 Involvement of mitochondrial electron transport in the activation of evofosfamide and

220 y, irritancy and repellency of mitochondrial electron transport inhibitor of complex I (MET-I) and mi

221 ron optics may be implemented in solids when electron transport is ballistic on the length scale of a

222 ue to the non-functional PSI, photosynthetic electron transport is blocked, which, in turn, leads to

223 hite are gapped(8) and, at low temperatures, electron transport is dominated by surface states.

224 es with topological insulators (TIs) is that electron transport is dominated by the bulk conductance,

225 n of Complex IV is lifted, and mitochondrial electron transport is restored.

226 Electron transport is simulated in a class II condensed

227 and increasing carboxylation (V(cmax) ) and electron-transport (J(max) ) capacities with increasing

228 s of Rubisco carboxylation, V(cmax) , and of electron transport, J(max) ) was reduced in warm-grown s

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

230 In photosynthetic electron transport, large multiprotein complexes are con

231 When used as an electron transport layer (ETL) in MAPbBr(3) based halide

232 currently enhance carrier extraction at both electron transport layer/perovskite and perovskite/hole

233 Using TiO(2) or SnO(2) as an electron transporting layer, a compositionally engineere

234 situated on the anatase TiO(2) surface as an electron-transport layer (ETL) for efficient electron tr

235 The performances of electron-transport-layer (ETL)-free perovskite solar cel

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

237 In metal halide perovskite solar cells, electron transport layers (ETLs) such as TiO(2) dictate

238 rs) as electrodes, hole transporting layers, electron transporting layers and buffer layers in PSCs i

239 the Li-TFSI can modify the interface between electron-transport material (ETM) and perovskite, which

240 ostructured oxides are proposed as excellent electron transport materials (ETMs) for perovskite solar

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

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

243 anine and porphyrin macrocycles as hole- and electron transporting materials.

244 lity perovskite nanocrystals embedded in the electron-transport molecular matrix, which controls nucl

245 <= 1.3 x 10(-2) S/cm) is enabled by hole and electron transport (mu(e)/mu(h) <= 5.70 x 10(-5) cm(2) V

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

247 controllability over ion-transport networks, electron-transport networks, or both of them.

248 physical phenomena associated with nanoscale electron transport often results in non-trivial spatial

249 Here, the first demonstration of doping in electron transporting organic electrochemical transistor

250 ited a profound suppression of mitochondrial electron transport, oxygen consumption, and ATP generati

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

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

253 In addition to the classical electron transport pathway coupled to ATP synthesis, pla

254 the steady-state rates of the photosynthetic electron transport pathways.

255 tochondrial adenosine triphosphate synthesis/electron transport, pathways downregulated in HFrEF.

256 Our findings show that the electron transport process accompanying exciton formatio

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

258 cytochromes attract much attention for their electron transport properties.

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

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

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

262 s an input for estimating the photosynthetic electron transport rate, which agrees well with two exis

263 ity, yielding deviations in apparent maximal electron transport rates by a factor of 2.

264 Photosynthetic electron transport rates in higher plants and green alga

265 , predawn and midday quantum yields, maximum electron transport rates, water potentials and nitrogen

266 ed to greater F(v) /F(m) values and relative electron transport rates.

267 distant cells are coupled via long-distance electron transport rather than an exchange of chemicals.

268 nalysis suggested that plants underinvest in electron transport relative to carboxylation under eleva

269 he early stages of infection, photosynthetic electron transport remained high, while RuBisCO expressi

270 ementation of the standard liquid-metal drop electron transport setup has been carried out, and this

271 nstrate the implementation of coupled photon-electron transport simulation using inverse transform sa

272 inverse transform sampling in coupled photon-electron transport simulation.

273 efences, and the activity of the respiratory electron transport system in organisms collected on the

274 Under low energy demand, the mitochondrial electron transport system is particularly sensitive to a

275 edox reactions within beta-oxidation and the electron transport system serve as a barometer of substr

276 ion is a byproduct of a transplasma membrane electron transport system that serves to balance the cel

277 Microbes employ a remarkably intricate electron transport system to extract energy from the env

278 in complex that links the Krebs cycle to the electron transport system.

279 located upstream of ATP synthase within the electron transport system.

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

281 The quantized electron transport that is characteristic of the quantum

282 are expected to allow phase-coherent single-electron transport through a topological superconducting

283 lly increased pH-dependent NPQ and decreased electron transport through the cytochrome b (6) f comple

284 ve potential, the cobaloxime linkers promote electron transport through the film as well as function

285 trating the strategy to modulate the rate of electron transport through the incorporation of rapidly

286 ium Shewanella oneidensis MR-1, we show that electron transport through these extracellular conduits

287 Here we study electron transport through this helical network and repo

288 es decrease the ratio of the maximum rate of electron transport to the maximum rate of Rubisco carbox

289 ree key biological processes: carboxylation, electron transport, triose phosphate use (TPU) and an ad

290 re to the electrodes play in determining the electron transport tunnel barrier.

291 ction of DVU2956 revealed DVU2956 influences electron transport via an Hmc complex (high-molecular-we

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

293 lex 1 localizes in mitochondria and disrupts electron transport via NADH photocatalysis.

294 iological semiconductors, the unidirectional electron transport via the p-n junction between function

295 e during dark-to-light transitions, allowing electron transport when the CBBC is not fully activated.

296 ce a rate-limiting diffusion barrier for the electron transport, which is responsible for the capacit

297 own plants is paralleled by increased cyclic electron transport, which positively correlated with NDH

298 e, functional, nonphosphorylating pathway of electron transport, whose operation enhances tolerance t

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

300 As the possibility of electron transport within small biological molecules, su