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1 hemically relevant ferrous iron forms to the photosynthetic reaction center.
2 ates comparable to those observed within the photosynthetic reaction center.
3 oncovalently bound entities of the bacterial photosynthetic reaction center.
4 ht then efficiently direct energy toward the photosynthetic reaction center.
5 sphaeroides funnels excitation energy to the photosynthetic reaction center.
6 ven by the electrical field generated by the photosynthetic reaction center.
7 lographic coordinates of the special pair in photosynthetic reaction center.
8 plings between chromophores in the bacterial photosynthetic reaction center.
9 transfer of electronic excitation toward the photosynthetic reaction center.
10 ing energy from sunlight and providing it to photosynthetic reaction centers.
11 Q(A) binding site in Rhodobacter sphaeroides photosynthetic reaction centers.
12 te production of harmful chemical species by photosynthetic reaction centers.
13 ing isoprenoids that are widely exploited by photosynthetic reaction centers.
14 photochemical charge separation unit akin to photosynthetic reaction centers.
16 may store a proton in this way, such as the photosynthetic reaction center and cytochrome c oxidase.
18 e been previously observed for the bacterial photosynthetic reaction center and indicate that protein
19 ld prove valuable for future analyses of the photosynthetic reaction center and of the roles of BChl
21 hanism affects certain reaction rates in the photosynthetic reaction center and therefore may be crit
22 )chlorophylls for the assembly of functional photosynthetic reaction centers and antenna complexes.
23 a-carotene in photosystem II is unique among photosynthetic reaction centers and stems from the very
24 sis indicates that electron transfer between photosynthetic reaction centers and the associated elect
29 tes for the primary donor cation radicals of photosynthetic reaction centers based on this criterion.
30 cited primary electron donor P* in bacterial photosynthetic reaction centers (both membrane-bound and
32 elf-assembly methods, a biomimetic bacterial photosynthetic reaction center complex has been construc
33 mber of the early steps of biogenesis of the photosynthetic reaction center complexes in these cyanob
38 e contiguous membrane-spanning domain in the photosynthetic reaction center core subunits, which cont
39 charge recombination in native photosystem I photosynthetic reaction centers does occur in the invert
40 on of cyt c(1) after light activation of the photosynthetic reaction center, especially the dissociat
45 The temperature-induced denaturation of the photosynthetic reaction center from Rhodobacter sphaeroi
46 molecular electron transfer reactions in the photosynthetic reaction center from Rhodopseudomonas vir
51 tyrosyl radical was investigated in modified photosynthetic reaction centers from Rhodobacter sphaero
52 or the transcript abundance of two important photosynthetic reaction center genes, psbA (encoding the
53 d charge separation process of the bacterial photosynthetic reaction center has been trapped in two D
56 nced by reductant and is associated with the photosynthetic reaction center II and the cytochrome b6f
57 Remarkably, the facile reconstitution of the photosynthetic reaction center in the artificial lipid m
60 tructure serve as an antenna conjugated to a photosynthetic reaction center isolated from Rhodobacter
61 oton excitation of the Blastochloris viridis photosynthetic reaction center, observing an ultrafast g
63 ine by aspartic acid at position M210 in the photosynthetic reaction center of Rhodobacter sphaeroide
64 ()) of the primary electron donor (P) in the photosynthetic reaction center of Rhodobacter sphaeroide
65 cytochrome c oxidase, bacteriorhodopsin, the photosynthetic reaction center of Rhodobacter sphaeroide
67 orophylls (the special pair) at the heart of photosynthetic reaction centers of both plants and bacte
68 transfer in the 0.1-10 micros time window in photosynthetic reaction centers of the intact cells of S
71 levant conformational intermediate states of photosynthetic reaction center protein (RCs) are trapped
73 and to the Mg of bacteriochlorophylls in the photosynthetic reaction center (RC) and many other photo
75 x between cytochrome c(2) (cyt c(2)) and the photosynthetic reaction center (RC) from Rhodobacter sph
76 omplex between cytochrome c(2) (cyt) and the photosynthetic reaction center (RC) from Rhodobacter sph
77 ying concentrations of detergent-solubilized photosynthetic reaction center (RC) from Rhodobacter sph
78 The x-ray crystallographic structure of the photosynthetic reaction center (RC) has proven critical
79 from crystals of the Rhodobacter sphaeroides photosynthetic reaction center (RC) have been collected
83 erties and electron-transfer kinetics in the photosynthetic reaction center (RC) of Rhodobacter sphae
84 primary electron donor (P) in the bacterial photosynthetic reaction center (RC) of Rhodobacter sphae
85 of two distinct metal sites on the bacterial photosynthetic reaction center (RC) protein were probed
88 an be observed in frozen and quinone-blocked photosynthetic reaction centers (RCs) as modification of
89 he special pair (P) to the carotenoid (C) in photosynthetic reaction centers (RCs) from a large famil
90 pping of cofactor-specific photochemistry in photosynthetic reaction centers (RCs) from Rhodobacter s
91 The interaction of metal ions with isolated photosynthetic reaction centers (RCs) from the purple ba
92 detailed analysis of reaction mechanisms in photosynthetic reaction centers (RCs) of purple bacteria
93 ironment, light-induced electron transfer in photosynthetic reaction centers (RCs) of the purple bact
95 e 93 to proline mutant of cytochrome c(2) to photosynthetic reaction centers (Rhodobacter sphaeroides
98 rly identical in both QH*- and the bacterial photosynthetic reaction centers, this electronic differe
99 th electron and proton transfer in bacterial photosynthetic reaction centers to those calculated usin
100 sm that decreases the energy arriving at the photosynthetic reaction centers under high-light conditi
101 in support of nonlinear dynamic behavior of photosynthetic reaction centers under light-activated co
103 d waters on the reorganization energy of the photosynthetic reaction center was examined and found to
104 the studies reported, detergent-solubilized photosynthetic reaction center was exchanged into a phos
105 a complexes transfer energy from sunlight to photosynthetic reaction centers where charge separation
106 light energy and transports spatially to the photosynthetic reaction center, while the electron trans
107 bisemiquinone centers have only been done on photosynthetic reaction centers whose function is to red
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