ライフサイエンスコーパス: thylakoid membrane

1 ential to the proton motive force across the thylakoid membrane.

2 at the proximity of the stromal face of the thylakoid membrane.

3 rotein is located on the stromal side of the thylakoid membrane.

4 indicate that MSH1 also associates with the thylakoid membrane.

5 place in the amphiphilic environment of the thylakoid membrane.

6 yield at reaction centers in the functional thylakoid membrane.

7 SI) and photosystem II (PSII) located in the thylakoid membrane.

8 arvesting chlorophyll binding protein to the thylakoid membrane.

9 in a well-defined protein environment in the thylakoid membrane.

10 ion retaining its patchy distribution in the thylakoid membrane.

11 bacterial cytoplasmic membrane and the plant thylakoid membrane.

12 ximately 37 proteins that integrate into the thylakoid membrane.

13 was previously localized to the chloroplast thylakoid membrane.

14 ectron transport in one membrane system, the thylakoid membrane.

15 DeltapH but also to the Deltapsi across the thylakoid membrane.

16 d cytb6f complexes in the lipid phase of the thylakoid membrane.

17 hloroplasts, whereas KEA3 is targeted to the thylakoid membrane.

18 ating the supramolecular organization in the thylakoid membrane.

19 t absorption, and pigment binding within the thylakoid membrane.

20 G surface but also to various extents at the thylakoid membrane.

21 c and respiratory electron chains within the thylakoid membrane.

22 lated PSBS (p-PSBS) could be detected in the thylakoid membrane.

23 (6)-ferredoxin/oxidoreductase located in the thylakoid membrane.

24 cted the majority of the two proteins at the thylakoid membrane.

25 okaryotic cytoplasmic membrane and the plant thylakoid membrane.

26 mobility of chlorophyll proteins within the thylakoid membrane.

27 ation of RCIIs was highly reduced within the thylakoid membrane.

28 he photosystems, albeit its abundance in the thylakoid membrane.

29 through several alternative pathways at the thylakoid membrane.

30 ne (OEM), inner envelope membrane (IEM), and thylakoid membrane.

31 cting membrane proteins to either the IEM or thylakoid membrane.

32 egral membrane proteins to either the IEM or thylakoid membrane.

33 nome and cotranslationally inserted into the thylakoid membrane.

34 proton-coupled electron transfer across the thylakoid membrane.

35 lorophyll a/b-binding proteins (LHCP) to the thylakoid membrane.

36 bacterial cytoplasmic membrane and the plant thylakoid membrane.

37 usion showed that the protein resides in the thylakoid membrane.

38 olved in thiol-disulfide biochemistry at the thylakoid membrane.

39 at the chloroplast envelope and HMA8 in the thylakoid membranes.

40 n size, reflecting their role in dismantling thylakoid membranes.

41 TEF30 is associated with the stromal side of thylakoid membranes.

42 he generation of an H(+) gradient across the thylakoid membranes.

43 sion of photosynthetic components in crowded thylakoid membranes.

44 system II (PSII), located in the chloroplast thylakoid membranes.

45 nown about the biogenesis and maintenance of thylakoid membranes.

46 the CD spectra of neoxanthin-deficient plant thylakoid membranes.

47 percomplexes and in different domains of the thylakoid membranes.

48 o quench the singlet oxygen generated in the thylakoid membranes.

49 in the plastid, where it is associated with thylakoid membranes.

50 vicinity of the cytoplasmic membrane and the thylakoid membranes.

51 concentrations at the outer periphery of the thylakoid membranes.

52 dually targeted to plastoglobules as well as thylakoid membranes.

53 the stacked grana regions of photosynthetic thylakoid membranes.

54 duced form during photosynthesis at isolated thylakoid membranes.

55 tically contain grana, cylindrical stacks of thylakoid membranes.

56 s folded proteins across bacterial and plant thylakoid membranes.

57 ons resulted in greater interactions between thylakoid membranes.

58 decrease of photosystem I (PSI) abundance in thylakoid membranes.

59 at they become evenly distributed within the thylakoid membranes.

60 ed for both processes are located within the thylakoid membranes.

61 n to be required for the proper formation of thylakoid membranes.

62 ition, lead to either development or loss of thylakoid membranes.

63 und either in plastoglobuli or in stroma and thylakoid membranes.

64 tent, as well as poorly developed, unstacked thylakoid membranes.

65 c electron transfer chains, entangled in the thylakoid membranes.

66 localized to the stroma and the periphery of thylakoid membranes.

67 nance of the photosynthetic apparatus in the thylakoid membranes.

68 rentiated plastids that lack photosynthetic (thylakoid) membranes.

69 ynthesis take place in the plant chloroplast thylakoid membrane, a complex three-dimensional structur

70 are concentrated in discrete patches in the thylakoid membranes, about 100-300 nm in diameter and co

71 s realized by subcompartmentalization of the thylakoid membrane, accomplished by the formation of sta

72 photosynthetic activity, disorganization of thylakoid membranes, accumulation of lipid bodies, and a

73 n the electrochemically positive side of the thylakoid membrane activates the kinase domain of Stt7 o

74 ow that SCY1 and ALB3 target directly to the thylakoid membrane and are likely independent of SEC2.

75 required increased proton pumping across the thylakoid membrane and elevated adenosine triphosphate p

76 mported proteins are further targeted to the thylakoid membrane and lumen by the SEC1, TAT, or SRP/AL

77 hat translation invariably initiates off the thylakoid membrane and that ribosomes synthesizing a sub

78 obal distribution of PSI and PSII within the thylakoid membrane and the corresponding location of the

79 chlorophyll molecules that accumulate in the thylakoid membrane and, together with carotenoids, bind

80 MGDG, DGDG, SQDG, and PG establish the thylakoid membranes and are integral constituents of the

81 Here, we studied the lipid composition of thylakoid membranes and chloroplast ultrastructure in is

82 ds on the generation of a pH gradient across thylakoid membranes and on the presence of a protein cal

83 SII core subunits, influences folding of the thylakoid membranes and repair of PSII after photodamage

84 KEA3 localizes to the thylakoid membrane, and allows proton efflux from the th

85 trate that all 3 proteins are located on the thylakoid membrane, and interactome studies indicate tha

86 terial cytoplasmic membrane, the chloroplast thylakoid membrane, and the mitochondrial inner membrane

87 e enzymatic products of AtCPT7 accumulate in thylakoid membranes, and in their absence, thylakoids ad

88 ts mature form, localizes in the chloroplast thylakoid membranes, and is correctly folded with chloro

89 ent Photosystem II 'repair zones' within the thylakoid membranes, and the possible advantages of such

90 imately 55 carbons, which then accumulate in thylakoid membranes; and (2) these polyprenols influence

91 alt and low temperature exhibited comparable thylakoid membrane appression to that of C. reinhardtii

92 membranes indicated that UWO241 altered its thylakoid membrane architecture and reorganized the dist

93 phycobilisome antenna systems for changes in thylakoid membrane architecture under different conditio

94 phycobilisome antenna systems for changes in thylakoid membrane architecture under different conditio

95 e maintenance of photosynthetic function and thylakoid membrane architecture.

96 iency, tolerance to light stress, and impact thylakoid membrane architecture.

97 n addition, 2-dimensional images of a single thylakoid membrane are reported and analyzed to demonstr

98 How thylakoid membranes are formed and maintained is poorly

99 Thylakoid membranes are typical and essential features o

100 Plant photosynthetic (thylakoid) membranes are organized into complex networks

101 and physiological function of an Arabidopsis thylakoid membrane-associated lipase, PLASTID LIPASE1 (P

102 m II (PSII), and cytochrome (Cyt) b6f within thylakoid membranes at the molecular level.

103 ansitions using a lattice-based model of the thylakoid membrane based on existing structural data, de

104 ended the spectrum of FtsH substrates in the thylakoid membranes beyond photosystem II, showing the s

105 rotein in plastids 1), has a crucial role in thylakoid membrane biogenesis and maintenance.

106 orescent VIPP1 spots and suggest a defect in thylakoid membrane biogenesis.

107 Thylakoid membrane-bound FtsH proteases have a well-char

108 Presumably, the thylakoid membrane-bound FtsH5 and FtsH2 have dual funct

109 sp. PCC 6803 cells contain only rudimentary thylakoid membranes but still a relatively high amount o

110 most abundant lipid in plant photosynthetic thylakoid membranes, but its impact on the functionality

111 , under stress conditions, LCNP protects the thylakoid membrane by enabling sustained NPQ in LHCII, t

112 FLUORESCENCE244 (HCF244) is tethered to the thylakoid membrane by the OHP heterodimer.

113 ication of subcellular components, including thylakoid membranes, carboxysomes and polyribosomes, as

114 eight, elasticity, and viscosity of isolated thylakoid membranes caused by changes in illumination.

115 s, together with the recent elucidation of a thylakoid membrane complex that functions in PSII assemb

116 Other thylakoid membrane complexes accumulated to normal level

117 nt maize FNR proteins localized to different thylakoid membrane complexes on expression in Arabidopsi

118 efects in the supermolecular organization of thylakoid membrane complexes.

119 As a demonstration, we explore the thylakoid membrane components of Chlamydomonas reinhardt

120 The cells harbor thylakoid membranes composed of lipids related to those

121 role of VIPP1 in the biogenesis/assembly of thylakoid membrane core complexes, most likely by supply

122 cpSecA-dependent signal sequence engages the thylakoid membrane cotranslationally.

123 Knowledge of cyanobacterial thylakoid membranes could also be extended to other cell

124 In thylakoid membranes, cpTatC and Hcf106 comprise a large

125 mutants lacking hydrocarbons exhibit reduced thylakoid membrane curvature compared to wild type.

126 identify chromosomal regions associated with thylakoid membrane damage (TMD), plasmamembrane damage (

127 ith disrupted envelope membranes and reduced thylakoid membrane density.

128 increased polyunsaturation of fatty acids on thylakoid membrane digalactosyldiglycerides, indicating

129 t emerge in the periodic geometry of stacked thylakoid membrane disks.

130 Passive ion channels in the thylakoid membrane dissipate the membrane potential (Del

131 ing complex I in separate units in unstacked thylakoid membranes does not require dense protein packi

132 uggested to initiate destacking of appressed thylakoid membranes due to increased electrostatic repul

133 nd directs charge separation (CS) across the thylakoid membrane during photosynthesis.

134 Grana stacking in plant chloroplast thylakoid membranes dynamically responds to the light en

135 etic performance through their modulation of thylakoid membrane dynamics.

136 osynthesis and respiration in an interlinked thylakoid membrane electron transport chain.

137 ography to reveal the native architecture of thylakoid membranes (Engel et al., 2015).

138 monomeric and trimeric LHCII in a realistic thylakoid membrane environment based on the Martini forc

139 rane, FAD4 was primarily associated with the thylakoid membranes facing the stroma.

140 In thylakoid membranes, fast dynamics of protein and pigmen

141 iluting multiple recycling components in the thylakoid membrane following a photodamage event.

142 comprises the signal that links ribosomes to thylakoid membranes for cotranslational integration.

143 g" of Synechocystis sp. PCC 6803 cells, i.e. thylakoid membrane formation and recovery of photosynthe

144 tids (VIPP1) was suggested to play a role in thylakoid membrane formation via membrane vesicles.

145 , and pH homeostasis to plastid division and thylakoid membrane formation.

146 and mobility of photosynthetic complexes in thylakoid membranes from a model cyanobacterium, Synecho

147 Light-dependent [gamma-(33)P]ATP labeling of thylakoid membranes from Chlamydomonas sp. UWO241 exhibi

148 fy the position of cytb6f complexes in grana thylakoid membranes from spinach (Spinacia oleracea).

149 , the stacking of part of the photosynthetic thylakoid membrane generates two main subcompartments: t

150 The long-term adjustment of thylakoid membrane grana diameter positively correlated

151 The thylakoid membrane has a unique lipid composition, consi

152 pe, but the transporter thought to be on the thylakoid membrane has not been identified.

153 vidence that interactions with lipids in the thylakoid membrane have reconstitutive chaperoning activ

154 equence of alterations in the photosynthetic thylakoid membranes helps prepare the plant for the desi

155 The role of natural thylakoid membrane housing of Photosystem I (PSI), the t

156 hPG bilayer membranes that mimic the natural thylakoid membrane housing of PSI is introduced.

157 The architecture of thylakoid membranes, however, also provides opportunitie

158 plexes are not constitutively present in the thylakoid membranes; however, in laboratory conditions t

159 Sll0218, on the contrary, resides in the thylakoid membrane in association with a high molecular

160 elle compartments physically attached to the thylakoid membrane in chloroplasts.

161 bout one-half of all proteins that cross the thylakoid membrane in chloroplasts.

162 ystem and to be located predominantly to the thylakoid membrane in cyanobacteria.

163 To understand the biogenesis of the thylakoid membrane in higher plants and to identify auxi

164 s the bacterial cytoplasmic membrane and the thylakoid membrane in plants.

165 During stress or senescence, thylakoid membranes in chloroplasts are disintegrated, a

166 Thylakoid membranes in chloroplasts contain photosynthet

167 Photosynthetic thylakoid membranes in chloroplasts have the remarkable

168 contributed to the reversible disruption of thylakoid membranes in chloroplasts of seedling cotyledo

169 The biogenesis of thylakoid membranes in cyanobacteria is presently not we

170 Thylakoid membranes in dark-maintained fdx5 mutant cells

171 e observations suggest that HetN anchored to thylakoid membranes in heterocysts may serve a function

172 Thylakoid membranes in land plant chloroplasts are organ

173 nobacterial cells and the arrangement of the thylakoid membranes in response to environmental conditi

174 Remodeling of thylakoid membranes in response to illumination is an im

175 sion of solar into chemical energy occurs in thylakoid membranes in the chloroplast.

176 We observed softer thylakoid membranes in the dark that have three-to four

177 We find that the elasticity of the thylakoid membranes increases immediately upon PSII-spec

178 PSI combined with digitonin fractionation of thylakoid membranes indicated that UWO241 altered its th

179 The lipid composition of thylakoid membranes inside chloroplasts is conserved fro

180 topology, we map the molecular landscapes of thylakoid membranes inside green algae cells.

181 (Chlamydomonas reinhardtii), helps maintain thylakoid membrane integrity in the dark.

182 y enzymes, which converts the photosynthetic thylakoid membrane into an intracellular matrix for oxid

183 (proton motive force) across the illuminated thylakoid membrane into electrical potential difference

184 id composition disrupted the organization of thylakoid membranes into granal stacks.

185 Photosystem biogenesis in the thylakoid membrane is a highly complicated process that

186 ng chlorophyll-binding protein (LHCP) in the thylakoid membrane is targeted post-translationally with

187 The chloroplast thylakoid membrane is the site for the initial steps of

188 rowth of cyanobacterial cells, biogenesis of thylakoid membranes is not well understood yet.

189 native organization of PSI in cyanobacterial thylakoid membranes is poorly understood.

190 ergy, yet the development of chloroplast and thylakoid membranes is poorly understood.

191 ity of individual protein complexes in grana thylakoid membranes isolated from Spinacia oleracea.

192 in our experiments), the conductivity of the thylakoid membrane (largely reflecting the activity of t

193 dy-like structures at the origin of multiple thylakoid membrane layers, which appear to coincide with

194 n the center-to-center distances between the thylakoid membrane layers.

195 The role of the extensive folding of thylakoid membranes leading to structural differentiatio

196 bution support the idea that the stacking of thylakoid membranes leads to a division of labor that es

197 rvesting antenna system of photosystem II in thylakoid membranes, light-harvesting complex II (LHCII)

198 Removal of the pH gradient across the thylakoid membrane linked the changes in the amplitudes

199 of transcripts encoding proteins involved in thylakoid membrane lipid recycling suggested more abrupt

200 Thylakoid membrane lipids, comprised of glycolipids and

201 ssion enhances TAG content at the expense of thylakoid membrane lipids, leading to defects in chlorop

202 inations of the three terminal oxidases: the thylakoid membrane-localized cytochrome c oxidase (COX)

203 In unstacked thylakoid membranes, more than 50% of the protein comple

204 light to metabolic energy equivalents in the thylakoid membrane network inside chloroplasts.

205 The thylakoid membrane of chloroplasts and cyanobacteria is

206 the cytoplasmic membrane of bacteria and the thylakoid membrane of chloroplasts.

207 the cytoplasmic membrane of bacteria and the thylakoid membrane of chloroplasts.

208 cytoplasmic membrane of prokaryotes and the thylakoid membrane of chloroplasts.

209 nit pigment-protein complex localized in the thylakoid membrane of cyanobacteria and chloroplasts, me

210 The D1 protein of photosystem II in the thylakoid membrane of photosynthetic organisms is encode

211 cytoplasmic membrane of prokaryotes and the thylakoid membrane of plant chloroplasts.

212 cytoplasmic membrane and is conserved in the thylakoid membrane of plant chloroplasts.

213 a well-characterized protein complex in the thylakoid membrane of Synechocystis sp. PCC 6803 (hereaf

214 e three-dimensional (3D) architecture of the thylakoid membranes of Arabidopsis (Arabidopsis thaliana

215 te NMR spectroscopy on native, heterogeneous thylakoid membranes of Chlamydomonas reinhardtii (Cr) an

216 It is well established that thylakoid membranes of chloroplasts convert light energy

217 For thylakoid membranes of higher plants, a long-standing qu

218 1-containing PGs primarily contribute to the thylakoid membranes of M cells, whereas BS chloroplasts

219 s the bacterial cytoplasmic membrane and the thylakoid membranes of plant chloroplasts.

220 yme embedded in the lipid environment of the thylakoid membranes of plants, algae, and cyanobacteria.

221 The thylakoid membranes of the chloroplast harbor the photos

222 arvesting complex II (LHCII) from the native thylakoid membrane or from aggregates by the use of surf

223 to be linked to the biogenesis of organized thylakoid membrane pairs.

224 marily triggered by a pH gradient across the thylakoid membrane (pH).

225 d light-harvesting complex II (LHCII) at the thylakoid membrane, possibly to allow metabolic channeli

226 exogenously, they were both able to protect thylakoid membranes prepared from Arabidopsis (Arabidops

227 FtsH is the major thylakoid membrane protease found in organisms performin

228 Analysis of thylakoid membrane protein complexes showed that wild-ty

229 ns function in the insertion and assembly of thylakoid membrane protein complexes.

230 SIS AFFECTED MUTANT71 (PAM71) is an integral thylakoid membrane protein involved in Mn(2+) and Ca(2+)

231 an unannotated small Zn finger containing a thylakoid membrane protein of Arabidopsis thaliana (At1g

232 ydomonas reinhardtii mutant lacking CGL71, a thylakoid membrane protein previously shown to be involv

233 RBD1 is an integral thylakoid membrane protein that is enriched in stroma la

234 and it encodes a previously uncharacterized thylakoid membrane protein with thioredoxin-like and bet

235 alysis indicated that Slr1796 is an integral thylakoid membrane protein.

236 07020, which encodes an unannotated integral thylakoid membrane protein.

237 showed a more severe defect with respect to thylakoid membrane proteins and accumulated only 10% of

238 plays a major role in the quality control of thylakoid membrane proteins and in the response of C. re

239 various TMDs derived from different IEM and thylakoid membrane proteins and monitored the subcellula

240 thesis comodulates the expression of several thylakoid membrane proteins that increase both the anten

241 In SCY2 down-regulated seedlings, several thylakoid membrane proteins, including SCY1, ALB3, and T

242 Conversely, when the TMD of the thylakoid membrane proteins, STN8 (State Transition prot

243 was replaced with a TMD derived from various thylakoid membrane proteins, these Arc6(thylTMD) hybrid

244 paralogous kinases phosphorylate subsets of thylakoid membrane proteins.

245 on events are essential for the formation of thylakoid membranes, proteins involved in membrane fusio

246 MD) hybrid proteins could be directed to the thylakoid membrane rather than to the IEM.

247 t composition, and their interactions in the thylakoid membranes remain elusive in different diatoms.

248 ble diffusion of photosynthetic complexes in thylakoid membranes, representative of the reorganizatio

249 The cyanobacterial thylakoid membrane represents a model membrane that can

250 id lumen and some proteins associated to the thylakoid membrane require an N-terminal targeting signa

251 copper-transporting P1B -type ATPase in the thylakoid membrane, required for the maturation of plast

252 st plants the assembly of the photosynthetic thylakoid membrane requires lipid precursors synthesized

253 hotosynthetic electron transfer chain in the thylakoid membranes requires the concerted expression of

254 d electrochemical proton gradient across the thylakoid membrane result in a significant driving force

255 Thylakoid membranes scaffold an assortment of large prot

256 3 assessed the flexibility of cyanobacterial thylakoid membrane sheets and the dependence of the memb

257 I Signal Peptidase 1 (Plsp1) is an integral thylakoid membrane signal peptidase that requires an int

258 oscopy images revealed significantly reduced thylakoid membrane stacking in TEF30-underexpressing cel

259 It is postulated that thylakoid membrane stacking to form grana leads to prote

260 Thylakoid membrane stiffness was also measured using ato

261 f the fluorescence decay components; and (3) thylakoid membrane stiffness.

262 of the light-absorbing centres and a stable thylakoid membrane stiffness.

263 e in the amount of LHCII trimers influencing thylakoid membrane structure and, more indirectly, state

264 we provide an overview of the essentials of thylakoid membrane structure in plants, and consider how

265 erform photosynthesis and respiration in the thylakoid membrane, suggesting that the two processes ar

266 epitope localizes to both the plasma and the thylakoid membranes, suggesting that CopS could be invol

267 localization of two major anionic lipids in thylakoid membranes, sulfoquinovosyldiacylglycerols (SQD

268 nd antenna and by phycobilisomes situated on thylakoid membrane surfaces.

269 recent findings about the plasticity of the thylakoid membrane system in response to different light

270 I repair machinery, which is embedded in the thylakoid membrane system inside chloroplasts.

271 system II (PSII) holocomplex embedded in the thylakoid membrane system inside chloroplasts.

272 Complete restoration of a typical thylakoid membrane system was observed within 24 hours a

273 allowing us to construct a map of the grana thylakoid membrane that reveals nanodomains of colocaliz

274 tosynthetic organisms, cyanobacteria possess thylakoid membranes that house photosystem (PS) I and PS

275 In manganese-depleted spinach thylakoid membranes, the primary donor in PS I, P700, wa

276 rganized, incorporating an array of internal thylakoid membranes, the site of photosynthesis, into ce

277 uinone pool while pumping protons across the thylakoid membrane, thereby increasing the amount of ATP

278 range diffusion of PQ in the protein-crowded thylakoid membrane, thereby optimizing photosynthetic ef

279 oring region of the L2 layer of the SAM lack thylakoid membranes; these appear only at the periphery,

280 medium-chain hydrocarbons in cyanobacterial thylakoid membranes: they regulate redox balance and red

281 um Synechocystis sp PCC 6803, early steps in thylakoid membrane (TM) biogenesis are considered to tak

282 ating a Gram-negative cell wall and internal thylakoid membranes (TMs).

283 ation of photosynthetic complexes within the thylakoid membrane to adapt to changing environmental co

284 the ability to adjust the composition of the thylakoid membrane to optimise the efficiency of electro

285 ide intact and photosynthetically functional thylakoid membranes to be able to understand its structu

286 tii Chlororespiration, which is localized in thylakoid membranes together with the photosynthetic ele

287 than control cells, while complex assembly, thylakoid membrane ultrastructure, and bulk lipid compos

288 Under photosynthetic conditions these thylakoid membranes undergo various dynamical processes

289 We present a direct observation of thylakoid membrane undulatory motion in vivo and show a

290 vestigated PsbS-LHCII interactions in native thylakoid membranes using magnetic-bead-linked antibody

291 K(+)/H(+) antiport across the thylakoid membrane via K+ EXCHANGE ANTIPORTER3 (KEA3) in

292 herefore extrinsically associate with PG and thylakoid membranes via interaction with hydrophilic hea

293 ponent of the proton motive force across the thylakoid membrane was significantly decreased in the ke

294 The grana margins of the thylakoid membrane were found to be the primary site of

295 Thylakoid membranes were still observed in vipp1 mutant

296 s; however, it is quenched to 2 ns in intact thylakoid membranes when PSII reaction centers (RCIIs) a

297 cpSRP recognizes LHCP and delivers it to the thylakoid membrane whereby cpSRP43 plays a central role.

298 was associated with the reduced fluidity of thylakoid membranes, which in turn negatively affects ph

299 of the Photosystem II complex embedded in a thylakoid membrane with realistic composition.

300 fter photobleaching to probe the dynamics of thylakoid membranes within intact chloroplasts.