ライフサイエンスコーパス: light-harvesting

1 of metallaphotocatalysis that are enabled by light harvesting.

2 ation processes that regulate photosynthetic light harvesting.

3 this information to optimize photosynthetic light harvesting.

4 rocesses for directional charge transport or light harvesting.

5 organisms have discovered many solutions for light harvesting.

6 cise blue print of the regulatory network of light harvesting.

7 ay an important role in opto-electronics and light harvesting.

8 g across transformation optics, sensing, and light harvesting.

9 etic landscape and ensuring highly efficient light-harvesting.

10 pt that could efficiently be used to enhance light harvesting?

11 The structure of the RC/YFP-light-harvesting 1 (LH1) complex shows the position of Y

12 h is applied to the 2DES spectroscopy of the Light-Harvesting 2 (LH2) complex of purple bacteria.

13 ta communication, high-speed electronics and light harvesting (8-16) require a thorough understanding

14 ization of DSSCs due to their more favorable light-harvesting abilities and long-term thermal and che

15 further promote the exciton dissociation or light harvesting ability of these PHJs via alternative a

16 ydrogen-evolving catalyst (HEC) exhibit good light-harvesting ability and enhanced photoresponses com

17 ge ordering, tunable porosity, and excellent light-harvesting ability.

18 favorable properties of the polymer, such as light-harvesting ability.

19 d increase the photovoltage, and to improved light harvesting across the visible region.

20 heterostructures shows energy migration and light-harvesting across the interfaces of linearly conne

21 , changes in internal biophysical processes, light-harvesting adaptations (e.g., variations in leaf a

22 al (PEC) water splitting, but limitations in light harvesting and charge collection have necessitated

23 2) O(3-) (x) nanosheets host, which enhances light harvesting and chemical adsorption of CO(2) molecu

24 ox-sensing hub, pivotal to the regulation of light harvesting and cyclic electron transfer that prote

25 nment, which may control the balance between light harvesting and dissipation in vivo.

26 ate transition that regulates photosynthetic light harvesting and electron transfer.

27 s and reduce bandgap, which is beneficial to light harvesting and enhancing short-circuit current den

28 of antenna proteins than vascular plants for light harvesting and for photoprotection.

29 o-acid tryptophans to form networks for both light harvesting and light perception.

30 ion to three leading areas of investigation: light harvesting and nanoscale energy transport, RNA str

31 of materials with promising applications in light harvesting and photocatalysis.

32 Plants must switch rapidly between light harvesting and photoprotection in response to envi

33 their ability to perfectly balance efficient light harvesting and photoprotection.

34 Photosynthetic light harvesting and reaction centre proteins from both

35 Light harvesting and secondary metabolite biosynthetic p

36 chemical processes that depend on plasmonic light harvesting and the transfer of nonequilibrium char

37 erstanding of the impact of heterogeneity on light harvesting and thus how these systems are optimize

38 r cells has a profound influence on both the light harvesting and TTA-UC efficiency.

39 t reactions of photosynthesis, which include light-harvesting and charge separation, take place in th

40 Though the light-harvesting and charge-separation functions of thes

41 e potentially relevant to the development of light-harvesting and electron-transport devices.

42 s is closely related to the understanding of light-harvesting and energy transfer processes that occu

43 egarding the role of specific carotenoids in light-harvesting and photoprotection, obligating the nee

44 roles in photosynthesis, primarily providing light-harvesting and photoprotective energy dissipation

45 le of electronic-nuclear mixing in efficient light-harvesting and the different functionalities of Ch

46 including many involved in nutrient uptake, light harvesting, and nitrogen metabolism.

47 erent nanoscale energy transport, artificial light-harvesting, and nanophotonics.

48 ion), one-dimensional (1D) lamellar network, light-harvesting, and non-toxicity to mention a few.

49 to the large optical cross section of plant light harvesting antenna complexes which capture photons

50 By surveying a range of light harvesting antenna sizes achieved by reduction in

51 sunlight may result in overexcitation of the light-harvesting antenna and the formation of reactive c

52 by reducing the optical cross-section of the light-harvesting antenna by selectively reducing chlorop

53 ductions in the optical cross-section of the light-harvesting antenna can lead to substantial improve

54 At full sunlight the light-harvesting antenna captures photons at a rate near

55 The monomeric photosystem I-light-harvesting antenna complex I (PSI-LHCI) supercompl

56 nas reinhardtii phosphorylates components of light-harvesting antenna complex II (LHCII).

57 e individual pigment chromophores present in light-harvesting antenna complexes are introduced, and t

58 Light-harvesting antenna complexes not only aid in the c

59 propose that the N >= 9 carotenoids found in light-harvesting antenna complexes represent a vital com

60 n the aggregation state of the phycobilisome light-harvesting antenna components.

61 ible proteins (Hlips) that are homologous to light-harvesting antenna of plants and algae.

62 The alb3b lines exhibit a truncated light-harvesting antenna phenotype with reduced amounts

63 ion of PSII suggested a constitutively small light-harvesting antenna size relative to other green al

64 we have determined that there is an optimal light-harvesting antenna size that results in the greate

65 ter chlorophyll b levels and correspondingly light-harvesting antenna sizes by light-activated Nab1 r

66 ational control system to dynamically adjust light-harvesting antenna sizes for enhanced photosynthet

67 Therefore, the light-harvesting antenna system of photosystem II in thy

68 getic effects leading to EET optimization of light-harvesting antenna systems while exploring the str

69 toinduced electron transfer from the excited light-harvesting antenna to Eu(III) was investigated.

70 o the lower temperature, the proteins of the light-harvesting antenna were greatly down-regulated and

71 sical behavior of the Eu(III) center and the light-harvesting antenna were studied using cyclic volta

72 Smaller light-harvesting antenna, however, may not exhibit optim

73 der excess light conditions and binds to the light-harvesting antenna, triggering the dissipation of

74 ton transfer components and their associated light-harvesting antenna.

75 We show how light-harvesting antennae can be tuned to maximize power

76 Natural light-harvesting antennae employ a dense array of chromo

77 ains a reaction centre that is surrounded by light-harvesting antennae, which absorb the light and tr

78 implications for the design of bio-inspired light-harvesting antennas and the redesign of natural ph

79 P)-all rigidly linked to each other-serve as light-harvesting antennas as well as electron donors and

80 energy-transfer dynamics and pathways in the light-harvesting antennas of various photosynthetic orga

81 gulation is controlled by the association of light-harvesting antennas with accessory quenchers such

82 racterize molecular systems, such as certain light-harvesting antennas, with cartwheeling charge moti

83 portant and useful design rules for QD-based light harvesting applications using the exciton-surface

84 use much longer energy transfer "wires" for light-harvesting applications in photonic systems.

85 ir use in building multiporphyrin arrays for light-harvesting applications, their use as ligands to f

86 y for the further development of sustainable light-harvesting applications.

87 at the compounds studied may have utility in light-harvesting applications.

88 cyclic molecular systems for electronic and light-harvesting applications.

89 We also applied this catalyst in a light-harvesting artificial leaf platform that concurren

90 earn how to design soft materials containing light-harvesting assemblies and catalysts to generate fu

91 the remarkable efficiency of supramolecular light-harvesting assemblies within photosynthetic organi

92 med into electronic excitation energy of the light-harvesting biomolecular complexes.

93 systems is precise structural control of the light-harvesting building blocks.

94 ayer vesicles to study the impact of MGDG on light harvesting by LHCII.

95 critical test for two contrasting models of light harvesting by photosystem II cores, known as the t

96 functions under NIR excitation at 800 nm: 1) Light harvesting by the UCNP shell containing Nd and sub

97 itivity to static disorder to increase their light-harvesting capability in a number of ways.

98 Instead, the increased light harvesting capacity of PSI is largely due to the m

99 Likewise, the increased light harvesting capacity of PSII upon dephosphorylation

100 The effective light-harvesting capacity of PSII decreases upon NPQ, an

101 haperone essential for the biogenesis of the light harvesting chlorophyll-binding proteins (LHCP), th

102 ast SRP (cpSRP) post-translationally targets light-harvesting chlorophyll a/b-binding proteins (LHCP)

103 Amino acid residues of the light-harvesting chlorophyll a/b-binding proteins involv

104 d redistribution ("state transition") of the light-harvesting chlorophyll proteins between the two ph

105 LHC) protein family, which also includes the light-harvesting chlorophyll-binding proteins of photosy

106 of PCPs have been synthesized with different light harvesting chromophores and transition metal bindi

107 d light-induced phosphorylation in the minor light harvesting complex (LHC) antenna protein LHCB6, wh

108 Abiotic and biotic stresses widely reduce light harvesting complex (LHC) gene expression in higher

109 ed genes, but transcript accumulation of the LIGHT HARVESTING COMPLEX B nuclear genes LHCB1.2 and LHC

110 nd validated by immunoblot analysis were two light harvesting complex binding proteins 1 and 3, Rubis

111 in the oxygen-evolving photosystem II (PSII)-light harvesting complex II (LHCII) supercomplex reveals

112 driven by changes in the phosphorylation of light harvesting complex II (LHCII), which cause a decre

113 Only genes for light harvesting complex proteins displayed a significan

114 een algae by protein subunits called LHCSRs (Light Harvesting Complex Stress Related), homologous to

115 Light harvesting complex stress-related 3 (LHCSR3) is th

116 te genes of chlorophyll biosynthesis and the light harvesting complex.

117 dopsis (Arabidopsis thaliana) belongs to the light-harvesting complex (LHC) protein family, which als

118 ganisms by their photosynthetic pigments and light-harvesting complex (Lhc) proteins, the latter of w

119 uces accumulation of specific members of the light-harvesting complex (LHC) superfamily that contribu

120 on of PsaL and PsaH to PSI, both forming the light-harvesting complex (LHC)II docking site of PSI.

121 purified and spectroscopically characterized light-harvesting complex 2 (LH2) from Rhodobacter sphaer

122 ost in each of the OHPs when residues of the light-harvesting complex chlorophyll-binding motif requi

123 del based on the structure of the main plant light-harvesting complex explains the red-shifted emissi

124 Both trimeric light-harvesting complex II (LHCII) and monomeric LHC pr

125 of Chlamydomonas reinhardtii (Cr) and on Cr light-harvesting complex II (LHCII) in thylakoid lipid b

126 posome technique that incorporates the major light-harvesting complex II (LHCII) into compositionally

127 Plant light-harvesting complex II (LHCII) is the key antenna c

128 e dynamic allocation of a mobile fraction of light-harvesting complex II (LHCII) to photosystem II (P

129 excitation energy transfer (EET) dynamics of light-harvesting complex II (LHCII) with two-dimensional

130 em of photosystem II in thylakoid membranes, light-harvesting complex II (LHCII), has a feedback mech

131 h this, the dynamics were dependent on STN7 (light-harvesting complex II [LHCII] kinase) and TAP38 (L

132 cs of the mixed vibronic Q(y)-Q(x) states of light-harvesting complex II.

133 a model for the energy transfer between the light-harvesting complex LH1 and the reaction center in

134 green light-absorbing protein present in the light-harvesting complex of cyanobacteria and red algae.

135 Members of the light-harvesting complex protein family participate in m

136 r high light by quenching excess energy, and Light-Harvesting Complex Stress Related 1 (LHCSR1) is th

137 stead, a small amount of the protein LHCSR1 (light-harvesting complex stress related 1) is able to in

138 gae, diatoms, and mosses, NPQ depends on the light-harvesting complex stress-related (LHCSR) proteins

139 e photoprotective states and dynamics of the light-harvesting complex stress-related 1 (LHCSR1) prote

140 Accumulation of photoprotective pigments and light-harvesting complex stress-related proteins was not

141 reducing chlorophyll b levels and peripheral light-harvesting complex subunits.

142 uction in photosystem II, the photosystem II light-harvesting complex, and photosystem I.

143 g Complex Stress Related), homologous to the Light Harvesting Complexes (LHC), constituting the anten

144 ling photosystems in which recombinant plant light harvesting complexes are covalently locked with re

145 ed in an application to the phycobiliprotein light harvesting complexes from cryptophyte algae.

146 mediated by a reversible phosphorylation of light harvesting complexes II, depending on the redox st

147 Trimers of the PSII light-harvesting complexes (LHCIIs) decreased more than

148 Photosynthetic light-harvesting complexes (LHCs) of higher plants, moss

149 The light-harvesting complexes (LHCs), the de-epoxidation of

150 Like natural light-harvesting complexes (LHCs), the precise arrangeme

151 lity of the antenna rings of chlorophylls in light-harvesting complexes (LHCs).

152 tosystems (PSI and PSII) from the associated light-harvesting complexes (LHCs).

153 plants starts with the capture of photons by light-harvesting complexes (LHCs).

154 ent, accompanied by functional detachment of light-harvesting complexes and interrupted access to pla

155 data have shown that the arrangement of the light-harvesting complexes I (LHCIs) differs substantial

156 ve the ultrafast energy relaxation in single light-harvesting complexes LH2 of purple bacteria.

157 The main light-harvesting complexes of diatoms, known as fucoxant

158 latter half of the article, we focus on the light-harvesting complexes of purple bacteria as a model

159 t resembles the first and the third helix of light-harvesting complexes, including a chlorophyll-bind

160 l energy transfer through extended layers of light-harvesting complexes, mimicking the modular antenn

161 hlorophylls are comparable to those of other light-harvesting complexes, we anticipate that this find

162 tive N >= 9 carotenoids normally utilized in light-harvesting complexes, zeta-carotene does not quenc

163 ins, one of which acts as a quencher for the light-harvesting complexes.

164 nd ATPase while depleted in photosystems and light-harvesting complexes.

165 -absorbing phycourobilin (PUB), within their light-harvesting complexes.

166 modification and assembly of PE into mature light-harvesting complexes.

167 ranslational machinery and downregulation of light harvesting components with increasing light intens

168 kites form an emerging family of exceptional light harvesting compounds.

169 ct transistors (OFETs), solar cells or other light harvesting devices.

170 the hybrid n-PS/Ag layers might be useful in light-harvesting devices and photodetectors, since the o

171 We propose here a new kind of light-harvesting devices using plasmonic nano-antenna gr

172 be applied to the design of novel artificial light-harvesting devices.

173 nomena and can accelerate the fabrication of light-harvesting devices.

174 far is based on a pool of randomly oriented, light-harvesting donor molecules that funnel all excitat

175 s in conjugated polymers and improving their light harvesting efficiency.

176 enic photosynthetic and potentially modulate light harvesting efficiency.

177 was critical to the energy transfer and the light-harvesting efficiency.

178 e reaction centers and drastically undermine light-harvesting efficiency.

179 active and well-defined catalytic sites on a light-harvesting electrode surface.

180 lysis, molecular separation, energy storage, light harvesting, etc.

181 are a key design strategy in photosynthetic light harvesting, expanding the spectral cross-section f

182 ghtly increasing the solvent polarity, these light-harvesting fibres disassemble to spherical structu

183 complex a unique strategy to ensure that its light-harvesting function remains robust in the fluctuat

184 Understanding how photosynthetic light-harvesting functions in the face of these fluctuat

185 phycobilisome linker proteins that stabilize light-harvesting functions.

186 for applications including (photo)catalysis, light harvesting, gas separation and storage, chemosensi

187 ic function of these beats in photosynthetic light-harvesting has been extensively debated.

188 e constructed to demonstrate the function of light harvesting in a polymeric nanostructure.

189 tandem configuration for achieving efficient light harvesting in nonfullerene-based OSCs.

190 l organizing principle giving rise to robust light harvesting in the presence of dynamic light condit

191 Light-harvesting in photosynthesis is accompanied by pho

192 hich provide remarkable efficiencies through light-harvesting in the strongly sub-wavelength device c

193 Light harvesting is a key step in photosynthesis but cre

194 Enhanced light harvesting is an area of interest for optimizing b

195 In oxygenic photosynthesis, light harvesting is regulated to safely dissipate excess

196 Understanding the fundamental processes of light-harvesting is crucial to the development of clean

197 occurring in natural photosynthesis, namely light harvesting (LH), energy transfer (EnT), reductive/

198 ent-binding studies have been performed with LIGHT-HARVESTING-LIKE3 proteins, and the pigment-binding

199 ght, which provides robust regulation of the light-harvesting machinery.

200 homogeneous and heterogeneous catalysts and light harvesting materials, among others.

201 als, surfactants, surface functionalization, light harvesting materials, non-linear optics, charge st

202 Photocatalytic systems that combine light-harvesting materials and catalysts in solution or

203 rmation can be tuned to offer a new class of light-harvesting materials.

204 Visible light harvesting may be enhanced in other conjugated pol

205 Herein, we report a new light-harvesting mixed-ligand Zr(IV)-based metal-organic

206 cations in cellular recognition, plasmonics, light harvesting, model systems for membrane protein ass

207 rameworks (COFs) have emerged as a promising light-harvesting module for artificial photosynthesis an

208 vances and the current status of challenging light-harvesting nanomaterials, such as semiconducting q

209 dering recent advances in the development of light harvesting nanoparticles for solar-to-heat convers

210 ricated by dispersing high concentrations of light harvesting nanoparticles, carbon black and Au nano

211 through composition of stable supramolecular light-harvesting nanotubes enabled by tunable (~4.3-4.9

212 ations, we find that all 18 tryptophans form light-harvesting networks and funnel their excitation en

213 ch, whereby we combined the highly efficient light harvesting of inorganic semiconductors with the hi

214 n vitro system developed here, MGDG controls light harvesting of LHCII by modulating the hydrostatic

215 h as nano-enhanced plasmonics and catalysis, light harvesting, or phase transitions.

216 Light-harvesting pai-conjugated molecules have been demo

217 hts into the underlying principles governing light-harvesting phenomena and can accelerate the fabric

218 roles in many biological processes, such as light harvesting, photoprotection and visual attraction

219 ufQBALMX operon encoding the reaction centre-light-harvesting photosystem complex.

220 ggesting that PhiCpeT may also help assemble light-harvesting phycobiliproteins during infection.

221 ction in energy transfer between the soluble light harvesting phycobilisome complex and membrane-boun

222 cells of DeltarpoZ were not able to increase light-harvesting phycobilisome antenna like CS upon high

223 dissipation of excess energy absorbed by the light-harvesting phycobilisomes (PBS) in cyanobacteria.

224 the extensive pigment diversity within their light-harvesting phycobilisomes enables them to utilize

225 to contain anthocyanin which is an excellent light harvesting pigment needed for the generation of ch

226 ns chlorophyll-a (chl-a), which is the major light harvesting pigment that absorbs light in the blue

227 mily with very diverse members, ranging from light-harvesting pigment-protein complexes to nucleic ac

228 llows for characterization of the density of light harvesting pigments in coral.

229 ng antenna phenotype with reduced amounts of light-harvesting pigments and require a higher light int

230 Phycobilins are light-harvesting pigments of cyanobacteria, red algae, a

231 is group possesses a remarkable diversity of light-harvesting pigments, and most of the group's membe

232 hes in part due to its varied photosynthetic light-harvesting pigments.

233 ,8-diphenyl pyridinium derivative (NPS) as a light-harvesting platform.

234 It is based on light-harvesting polymeric nanoparticles (NPs) encapsula

235 d with the production of reaction centre and light-harvesting polypeptides.

236 al for the assembly of higher molecular mass light-harvesting PORB::PORA complexes and photoprotectio

237 for non-photochemical quenching (NPQ) of the light-harvesting process in most cyanobacteria.

238 ansfer-to-the-trap limitation of the overall light-harvesting process.

239 o their instant light response and efficient light-harvesting properties, precise regulation of biolo

240 triazine and porphyrin faces with promising light-harvesting properties.

241 hesis of axial organic heterostructures with light-harvesting properties.

242 lants and is necessary for the regulation of light harvesting, protection from oxidative stress and a

243 he quantum coherence and exciton dynamics in light-harvesting protein complexes and semiconducting ma

244 In plants, the alignment and assembly of the light-harvesting protein machinery in the green leaf opt

245 MpeY attaches PEB to the light-harvesting protein MpeA in green light, while MpeZ

246 lation, thereby activating the repression of light-harvesting protein synthesis, which is needed to c

247 light supply, which permits accumulation of light-harvesting proteins and efficient light capture.

248 s/molecular mechanics (QM/MM) simulations of light-harvesting proteins from oxygenic (LHCII) and anox

249 ptica to analyze gene sequences for putative light-harvesting proteins in C. meneghiniana, and to elu

250 Rhodopsins are the most abundant light-harvesting proteins.

251 Photosynthesis achieves near unity light-harvesting quantum efficiency yet it remains unkno

252 bithiophene-based 2D CCP-Th exhibits a wide light-harvesting range (up to 674 nm), a optical energy

253 The light-harvesting-reaction center complex (LH1-RC) from t

254 aic reaction centers are embedded throughout light-harvesting regions of the device.

255 This links the protein dynamics to the light-harvesting regulation in plants by the carotenoids

256 Light-harvesting regulation is important for protecting

257 Effectiveness of molecular-based light harvesting relies on transport of excitons to char

258 h separated electrons and holes suitable for light harvesting, results in photoluminescence quenching

259 Coupling the nitrogenase MoFe protein to light-harvesting semiconductor nanomaterials replaces th

260 ramolecular, nanotubular structures in large light-harvesting structures called chlorosomes.

261 The design of optimal light-harvesting (supra)molecular systems and materials

262 minisces the chromophoric arrangement in the light harvesting system 2 of purple bacteria.

263 s was increased by more than 3 times using a light harvesting system.

264 nutricline, which is aided by their superior light-harvesting system and high affinity to iron.

265 acceptor into the NPS-SC4AD co-assembly, the light-harvesting system becomes near-infrared (NIR) emis

266 However, the best practical light-harvesting system could only be discovered by empi

267 nd used as the donor molecule to construct a light-harvesting system in water.

268 pathway for using the output energy from the light-harvesting system to mimic the whole photosyntheti

269 nanotubes in a slipped manner, an artificial light-harvesting system with a two-step sequential Forst

270 aqueous solution, thereby mimicking natural light harvesting systems.

271 ited state energy transfer in photosynthetic light harvesting systems.

272 in photosynthesis but creation of synthetic light-harvesting systems (LHSs) with high efficiencies h

273 nces observed in both natural and artificial light-harvesting systems (such as the Fenna-Matthews-Ols

274 e approach of designing efficient artificial light-harvesting systems and constructing highly emissiv

275 Light-harvesting systems are an important way for captur

276 Potential light-harvesting systems based on dye-doped pi-conjugate

277 ard the construction of efficient artificial light-harvesting systems based on supramolecular peptide

278 pyrrole-based architectures for panchromatic light-harvesting systems for solar-energy conversion.

279 Artificial light-harvesting systems in aqueous media which mimic na

280 Natural light-harvesting systems spatially organize densely pack

281 is crucial for the development of efficient light-harvesting systems, like photocatalytic and photov

282 e, which is essential for the preparation of light-harvesting systems.

283 porphyrin-based nanostructures for potential light-harvesting systems.

284 and informing rational design of artificial light-harvesting systems.

285 coupled exciton dynamics present in natural light-harvesting systems.

286 rface energy transfer process for developing light-harvesting systems.

287 lenge to develop highly efficient artificial light-harvesting systems.

288 similarity with structurally related natural light-harvesting systems.

289 rnerstone of our understanding of artificial light-harvesting systems.

290 ards to applications in opto-electronics and light harvesting; tailored enhancement of such plasmons

291 ent of doped CQWs in LSCs for advanced solar light harvesting technologies.

292 lters and laser resonators(4), for improving light-harvesting technologies(5-7 and for other applicat

293 al for becoming a powerful tool for enhanced light harvesting, the slow-photon effect, a manifestatio

294 MGDG in lipid bilayers switches LHCII from a light-harvesting to a more energy-quenching mode that di

295 r efficiencies of 83% and a small functional light-harvesting unit.During photosynthesis, energy is t

296 hell interfaces and extended long-wavelength light harvesting via spatially indirect interfacial abso

297 cement and introducing future challenges for light harvesting, vibrational spectroscopy, imaging, and

298 , reflection and antireflection, scattering, light harvesting, wave guiding and lensing, camouflage,

299 the level of chlorophyll excited states from light harvesting with the rate of electron transport fro

300 many diverse stimuli in an effort to balance light harvesting with utilizable light energy for carbon