戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ed pcb gene encoding a photosystem II (PSII) antenna protein.
2 3 peridinin-Chl a/c-binding light-harvesting antenna proteins (AcpPCIs).
3 EL trap to study an important photosynthetic antenna protein, Allophycocyanin (APC).
4 nables the direct analysis of phycobilisomal antenna proteins and report on numerous metabolites from
5 ght on interactions between light harvesting antenna proteins and the PSI core.
6 ient, the organization of the photosystem II antenna proteins and the reversible binding of a specifi
7 nthetic apparatus coupled with remodeling of antenna proteins by dramatic iron-deficiency induction o
8 nthin (Dt); and (3) specific nucleus-encoded antenna proteins, called Light Harvesting Complex Protei
9                               Photosynthetic antenna proteins can be thought of as "programmed solven
10 les and the composition of energy harvesting antenna protein complexes are needed to understand how e
11 conformational and electronic changes at the antenna protein complexes as a response to specific chem
12        Phosphorylation of the photosystem II antenna protein CP29 has been reported to be induced by
13 t-protein complex does contain the PSII core antenna proteins CP47 and CP43, as well as most of their
14 enna complex, the Fenna-Matthews-Olson (FMO) antenna protein from green sulfur bacteria, completely l
15 fer by embedding two variants of the primary antenna protein from purple bacteria, light-harvesting c
16 s I and III of chlorophyll a/b-binding (Cab) antenna proteins from higher plants.
17 membrane-attached Fenna-Matthews-Olson (FMO) antenna protein functions as a "wire" to connect the lar
18 e energy transfer dynamics within individual antenna proteins have been extensively studied over the
19 hin-chlorophyll a/c-binding light-harvesting antenna proteins (iFCPIs) that form a trilayered antenna
20 ation of allophycocyanin (APC), an important antenna protein in cyanobacteria.
21 tase, assemble the split PsaA, and integrate antenna proteins in a non-canonical orientation.
22                      Two chlorophyll-binding antenna proteins in the photosystem II core, CP43 and CP
23  major chlorophyll-binding, light-harvesting antenna proteins in this genus, are present in multiple
24 were found to be well coordinated within the antenna proteins in vivo, arguing against the possibilit
25 in 545 (PE545), the prototypical cryptophyte antenna protein, in its native dimeric form.
26 ssociated core antenna domains and accessory antenna proteins (IsiA, PcbA, PcbC) arose from duplicati
27 ond defect in the mutant, namely in CP26, an antenna protein known to be required for the formation o
28 he PSII subunits (psbA, psbB, and PSBW), the antenna proteins (LHCA1, LHCB1, and LHCB4), the ribulose
29 vestigated the capacity of the photosystem I antenna protein Lhca4 to incorporate far-red absorbing c
30  in the minor light harvesting complex (LHC) antenna protein LHCB6, which was dependent on STN8 kinas
31 eraging, we investigate the purple bacterial antenna protein light harvesting complex 2 (LH2) from Rh
32 ariation in the expression of the minor PSII antenna protein light harvesting complex photosystem II
33  altered in the presence of the fluorescent (antenna) proteins, lumazine protein (LumP) from Photobac
34 nd to CP43, a constitutively expressed Chl a antenna protein of photosystem II.
35  to investigate the mus dynamics of this key antenna protein of plants.
36 SI) of cyanobacteria and plastids, plus core antenna proteins of photosystem II (PSII) from cyanobact
37                                          The antenna proteins of photosystem II have an intriguing du
38  repression of chlorophyll a-containing core antenna proteins of photosystems I and II.
39            Crucially, we reveal that the LH2 antenna protein prevents quenching, even at the high chl
40 ported a single phylogeny in which PSII core antenna proteins (PsbC, PsbB) arose within the cyanobact
41 one iron-stress-induced pcb gene encoding an antenna protein serving photosystem I (PSI)--comparable
42 rometry analysis to be mainly photosystem II antenna proteins, such as LIGHT-HARVESTING COMPLEX B (LH
43            Diatoms contain higher numbers of antenna proteins than vascular plants for light harvesti
44 cteria, RC2 is associated with separate core antenna proteins that are homologous to the core antenna
45 ously known function as one of the core PSII antenna proteins, this work demonstrates that Loop E of
46  light energy transfers through a network of antenna proteins with near-unity quantum efficiency to r