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1 was previously localized to the chloroplast thylakoid membrane.
2 ectron transport in one membrane system, the thylakoid membrane.
3 DeltapH but also to the Deltapsi across the thylakoid membrane.
4 d cytb6f complexes in the lipid phase of the thylakoid membrane.
5 hloroplasts, whereas KEA3 is targeted to the thylakoid membrane.
6 ating the supramolecular organization in the thylakoid membrane.
7 G surface but also to various extents at the thylakoid membrane.
8 c and respiratory electron chains within the thylakoid membrane.
9 bacterial cytoplasmic membrane and the plant thylakoid membrane.
10 usion showed that the protein resides in the thylakoid membrane.
11 cted the majority of the two proteins at the thylakoid membrane.
12 okaryotic cytoplasmic membrane and the plant thylakoid membrane.
13 mobility of chlorophyll proteins within the thylakoid membrane.
14 ation of RCIIs was highly reduced within the thylakoid membrane.
15 through several alternative pathways at the thylakoid membrane.
16 olved in thiol-disulfide biochemistry at the thylakoid membrane.
17 ne (OEM), inner envelope membrane (IEM), and thylakoid membrane.
18 cting membrane proteins to either the IEM or thylakoid membrane.
19 egral membrane proteins to either the IEM or thylakoid membrane.
20 and thus triggered by the DeltapH across the thylakoid membrane.
21 bind and target full-length proteins to the thylakoid membrane.
22 ng photosystems I and II) that reside in the thylakoid membrane.
23 be a lipoprotein on the luminal side of the thylakoid membrane.
24 ntinuous with the stroma-side leaflet of the thylakoid membrane.
25 to an overreduced plastoquinone pool in the thylakoid membrane.
26 geable components of AtFtsH complexes in the thylakoid membrane.
27 lorophyll a/b-binding proteins (LHCP) to the thylakoid membrane.
28 ential to the proton motive force across the thylakoid membrane.
29 at the proximity of the stromal face of the thylakoid membrane.
30 rotein is located on the stromal side of the thylakoid membrane.
31 indicate that MSH1 also associates with the thylakoid membrane.
32 place in the amphiphilic environment of the thylakoid membrane.
33 yield at reaction centers in the functional thylakoid membrane.
34 SI) and photosystem II (PSII) located in the thylakoid membrane.
35 arvesting chlorophyll binding protein to the thylakoid membrane.
36 in a well-defined protein environment in the thylakoid membrane.
37 ion retaining its patchy distribution in the thylakoid membrane.
38 bacterial cytoplasmic membrane and the plant thylakoid membrane.
39 ximately 37 proteins that integrate into the thylakoid membrane.
40 o quench the singlet oxygen generated in the thylakoid membranes.
41 in the plastid, where it is associated with thylakoid membranes.
42 vicinity of the cytoplasmic membrane and the thylakoid membranes.
43 concentrations at the outer periphery of the thylakoid membranes.
44 dually targeted to plastoglobules as well as thylakoid membranes.
45 the stacked grana regions of photosynthetic thylakoid membranes.
46 duced form during photosynthesis at isolated thylakoid membranes.
47 tically contain grana, cylindrical stacks of thylakoid membranes.
48 s folded proteins across bacterial and plant thylakoid membranes.
49 ons resulted in greater interactions between thylakoid membranes.
50 decrease of photosystem I (PSI) abundance in thylakoid membranes.
51 at they become evenly distributed within the thylakoid membranes.
52 ed for both processes are located within the thylakoid membranes.
53 n to be required for the proper formation of thylakoid membranes.
54 ition, lead to either development or loss of thylakoid membranes.
55 und either in plastoglobuli or in stroma and thylakoid membranes.
56 m emission observed in intact PSII cores and thylakoid membranes.
57 ansport chains function in the intracellular thylakoid membranes.
58 he chloroplast Tat translocase, cpTatC, into thylakoid membranes.
59 to chloroplasts before being integrated into thylakoid membranes.
60 nsports folded proteins across bacterial and thylakoid membranes.
61 nsports folded proteins across bacterial and thylakoid membranes.
62 ynamic equilibrium with those located in the thylakoid membranes.
63 biosynthesis and storage subcompartments of thylakoid membranes.
64 Q was highly exposed to the luminal space of thylakoid membranes.
65 ltered CydAB sorting between cytoplasmic and thylakoid membranes.
66 r phosphorylation of proteins of chloroplast thylakoid membranes.
67 d proteins across bacterial plasma and plant thylakoid membranes.
68 hery, whereas PAA2 fusions were localized in thylakoid membranes.
69 at the chloroplast envelope and HMA8 in the thylakoid membranes.
70 n size, reflecting their role in dismantling thylakoid membranes.
71 TEF30 is associated with the stromal side of thylakoid membranes.
72 he generation of an H(+) gradient across the thylakoid membranes.
73 sion of photosynthetic components in crowded thylakoid membranes.
74 system II (PSII), located in the chloroplast thylakoid membranes.
75 nown about the biogenesis and maintenance of thylakoid membranes.
76 the CD spectra of neoxanthin-deficient plant thylakoid membranes.
77 percomplexes and in different domains of the thylakoid membranes.
78 rentiated plastids that lack photosynthetic (thylakoid) membranes.
79 are concentrated in discrete patches in the thylakoid membranes, about 100-300 nm in diameter and co
80 s realized by subcompartmentalization of the thylakoid membrane, accomplished by the formation of sta
81 photosynthetic activity, disorganization of thylakoid membranes, accumulation of lipid bodies, and a
82 n the electrochemically positive side of the thylakoid membrane activates the kinase domain of Stt7 o
83 ow that SCY1 and ALB3 target directly to the thylakoid membrane and are likely independent of SEC2.
84 required increased proton pumping across the thylakoid membrane and elevated adenosine triphosphate p
85 mported proteins are further targeted to the thylakoid membrane and lumen by the SEC1, TAT, or SRP/AL
86 hat translation invariably initiates off the thylakoid membrane and that ribosomes synthesizing a sub
87 obal distribution of PSI and PSII within the thylakoid membrane and the corresponding location of the
88 proton electrochemical potential across the thylakoid membrane and thioredoxin-mediated redox modula
89 Here, we studied the lipid composition of thylakoid membranes and chloroplast ultrastructure in is
90 aller in size and possess dramatically fewer thylakoid membranes and grana stacks when compared with
91 ds on the generation of a pH gradient across thylakoid membranes and on the presence of a protein cal
92 etabolic link between the inner envelope and thylakoid membranes and play a role in breakdown of caro
93 SII core subunits, influences folding of the thylakoid membranes and repair of PSII after photodamage
96 terial cytoplasmic membrane, the chloroplast thylakoid membrane, and the mitochondrial inner membrane
97 e enzymatic products of AtCPT7 accumulate in thylakoid membranes, and in their absence, thylakoids ad
98 ts mature form, localizes in the chloroplast thylakoid membranes, and is correctly folded with chloro
99 ent Photosystem II 'repair zones' within the thylakoid membranes, and the possible advantages of such
100 imately 55 carbons, which then accumulate in thylakoid membranes; and (2) these polyprenols influence
101 phycobilisome antenna systems for changes in thylakoid membrane architecture under different conditio
102 phycobilisome antenna systems for changes in thylakoid membrane architecture under different conditio
104 n addition, 2-dimensional images of a single thylakoid membrane are reported and analyzed to demonstr
106 and physiological function of an Arabidopsis thylakoid membrane-associated lipase, PLASTID LIPASE1 (P
108 ended the spectrum of FtsH substrates in the thylakoid membranes beyond photosystem II, showing the s
114 sp. PCC 6803 cells contain only rudimentary thylakoid membranes but still a relatively high amount o
115 , under stress conditions, LCNP protects the thylakoid membrane by enabling sustained NPQ in LHCII, t
116 to each other and remain continuous with the thylakoid membrane by extensions of the half-lipid bilay
117 ported into the stroma and translocated into thylakoid membranes by specific thylakoid translocases.
118 ication of subcellular components, including thylakoid membranes, carboxysomes and polyribosomes, as
119 eight, elasticity, and viscosity of isolated thylakoid membranes caused by changes in illumination.
120 dulation (ESEEM) have been studied in either thylakoid membranes, cellular membranes, or purified pho
122 nt maize FNR proteins localized to different thylakoid membrane complexes on expression in Arabidopsi
126 Leaf chlorophyll fluorescence analysis and thylakoid membrane composition indicated that cyp38 muta
127 versible in whole cells, leaves, or isolated thylakoid membranes containing PSII, in contrast to repo
128 role of VIPP1 in the biogenesis/assembly of thylakoid membrane core complexes, most likely by supply
132 mutants lacking hydrocarbons exhibit reduced thylakoid membrane curvature compared to wild type.
133 identify chromosomal regions associated with thylakoid membrane damage (TMD), plasmamembrane damage (
135 increased polyunsaturation of fatty acids on thylakoid membrane digalactosyldiglycerides, indicating
136 ing complex I in separate units in unstacked thylakoid membranes does not require dense protein packi
139 comprises the signal that links ribosomes to thylakoid membranes for cotranslational integration.
140 g" of Synechocystis sp. PCC 6803 cells, i.e. thylakoid membrane formation and recovery of photosynthe
141 tids (VIPP1) was suggested to play a role in thylakoid membrane formation via membrane vesicles.
143 es light-driven electron transfer across the thylakoid membrane from plastocyanin located in the lume
144 and mobility of photosynthetic complexes in thylakoid membranes from a model cyanobacterium, Synecho
145 fy the position of cytb6f complexes in grana thylakoid membranes from spinach (Spinacia oleracea).
148 equence of alterations in the photosynthetic thylakoid membranes helps prepare the plant for the desi
151 Sll0218, on the contrary, resides in the thylakoid membrane in association with a high molecular
158 diate efficient targeting of proteins to the thylakoid membrane in the absence of the SRP RNA, which
159 in-depth analysis of the architecture of the thylakoid membranes in a unicellular cyanobacterium, Cya
162 contributed to the reversible disruption of thylakoid membranes in chloroplasts of seedling cotyledo
166 nd spatial relationship of plastoglobules to thylakoid membranes in developing, mature, and senescing
167 e observations suggest that HetN anchored to thylakoid membranes in heterocysts may serve a function
168 nobacterial cells and the arrangement of the thylakoid membranes in response to environmental conditi
174 y enzymes, which converts the photosynthetic thylakoid membrane into an intracellular matrix for oxid
177 ng chlorophyll-binding protein (LHCP) in the thylakoid membrane is targeted post-translationally with
179 The diffusion of proteins in chloroplast thylakoid membranes is believed to be important for proc
183 ly, flash oxygen yield analysis performed on thylakoid membranes isolated from the mutant and wild ty
184 h oxygen yield experiments were performed on thylakoid membranes isolated from wild type and the psbo
185 dy-like structures at the origin of multiple thylakoid membrane layers, which appear to coincide with
188 rvesting antenna system of photosystem II in thylakoid membranes, light-harvesting complex II (LHCII)
190 of transcripts encoding proteins involved in thylakoid membrane lipid recycling suggested more abrupt
191 ssion enhances TAG content at the expense of thylakoid membrane lipids, leading to defects in chlorop
192 inations of the three terminal oxidases: the thylakoid membrane-localized cytochrome c oxidase (COX)
198 e that it is also relatively abundant in the thylakoid membrane network, indicating that newly synthe
200 systems transport folded proteins across the thylakoid membrane of chloroplasts and the plasma membra
205 nit pigment-protein complex localized in the thylakoid membrane of cyanobacteria and chloroplasts, me
206 The D1 protein of photosystem II in the thylakoid membrane of photosynthetic organisms is encode
211 a well-characterized protein complex in the thylakoid membrane of Synechocystis sp. PCC 6803 (hereaf
212 e three-dimensional (3D) architecture of the thylakoid membranes of Arabidopsis (Arabidopsis thaliana
214 EC): a multiprotein assembly embedded in the thylakoid membranes of green plants, cyanobacteria, and
215 1-containing PGs primarily contribute to the thylakoid membranes of M cells, whereas BS chloroplasts
218 yme embedded in the lipid environment of the thylakoid membranes of plants, algae, and cyanobacteria.
220 arvesting complex II (LHCII) from the native thylakoid membrane or from aggregates by the use of surf
221 multiple systems that target proteins to the thylakoid membranes or thylakoid lumen have been identif
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
229 SIS AFFECTED MUTANT71 (PAM71) is an integral thylakoid membrane protein involved in Mn(2+) and Ca(2+)
230 an unannotated small Zn finger containing a thylakoid membrane protein of Arabidopsis thaliana (At1g
231 ydomonas reinhardtii mutant lacking CGL71, a thylakoid membrane protein previously shown to be involv
232 and it encodes a previously uncharacterized thylakoid membrane protein with thioredoxin-like and bet
235 showed a more severe defect with respect to thylakoid membrane proteins and accumulated only 10% of
236 plays a major role in the quality control of thylakoid membrane proteins and in the response of C. re
237 various TMDs derived from different IEM and thylakoid membrane proteins and monitored the subcellula
238 tress through the degradation of unassembled thylakoid membrane proteins and photodamaged photosystem
239 thesis comodulates the expression of several thylakoid membrane proteins that increase both the anten
240 In SCY2 down-regulated seedlings, several thylakoid membrane proteins, including SCY1, ALB3, and T
242 was replaced with a TMD derived from various thylakoid membrane proteins, these Arc6(thylTMD) hybrid
244 on events are essential for the formation of thylakoid membranes, proteins involved in membrane fusio
245 show that upon Triton X-114 fractionation of thylakoid membranes, PsbQ partitioned in the hydrophobic
247 ble diffusion of photosynthetic complexes in thylakoid membranes, representative of the reorganizatio
249 id lumen and some proteins associated to the thylakoid membrane require an N-terminal targeting signa
250 copper-transporting P1B -type ATPase in the thylakoid membrane, required for the maturation of plast
251 st plants the assembly of the photosynthetic thylakoid membrane requires lipid precursors synthesized
252 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 3 assessed the flexibility of cyanobacterial thylakoid membrane sheets and the dependence of the memb
256 osecond transient absorption measurements on thylakoid membranes show selective formation of a carote
257 nt electron paramagnetic resonance data from thylakoid membranes showed that the mutations affect the
259 oscopy images revealed significantly reduced thylakoid membrane stacking in TEF30-underexpressing cel
261 e in the amount of LHCII trimers influencing thylakoid membrane structure and, more indirectly, state
262 we provide an overview of the essentials of thylakoid membrane structure in plants, and consider how
263 erform photosynthesis and respiration in the thylakoid membrane, suggesting that the two processes ar
264 ng plants are abnormal and largely devoid of thylakoid membranes, suggesting that ClpP4 plays a criti
265 epitope localizes to both the plasma and the thylakoid membranes, suggesting that CopS could be invol
266 ructural coupling between plastoglobules and thylakoid membranes suggests that the lipid molecules co
267 localization of two major anionic lipids in thylakoid membranes, sulfoquinovosyldiacylglycerols (SQD
274 allowing us to construct a map of the grana thylakoid membrane that reveals nanodomains of colocaliz
275 tosynthetic organisms, cyanobacteria possess thylakoid membranes that house photosystem (PS) I and PS
277 rganized, incorporating an array of internal thylakoid membranes, the site of photosynthesis, into ce
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 calizes to the chloroplast stroma and to the thylakoid membrane, to which it is tethered by DNA.
283 than control cells, while complex assembly, thylakoid membrane ultrastructure, and bulk lipid compos
285 vestigated PsbS-LHCII interactions in native thylakoid membranes using magnetic-bead-linked antibody
286 herefore extrinsically associate with PG and thylakoid membranes via interaction with hydrophilic hea
287 ponent of the proton motive force across the thylakoid membrane was significantly decreased in the ke
289 rmore, oxygen-evolving activity in DeltaPsbU thylakoid membranes was highly suppressed in the absence
291 , but the pigment and protein content of the thylakoid membranes were otherwise almost unchanged.
293 s; however, it is quenched to 2 ns in intact thylakoid membranes when PSII reaction centers (RCIIs) a
294 cpSRP recognizes LHCP and delivers it to the thylakoid membrane whereby cpSRP43 plays a central role.
295 was associated with the reduced fluidity of thylakoid membranes, which in turn negatively affects ph
296 tis 6803; PetC1 and PetC2 are located in the thylakoid membrane, while PetC3 is primarily targeted to
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