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1 electronic excitation energy transfer in the photosynthetic reaction center.
2 hemically relevant ferrous iron forms to the photosynthetic reaction center.
3 ates comparable to those observed within the photosynthetic reaction center.
4 oncovalently bound entities of the bacterial photosynthetic reaction center.
5 ht then efficiently direct energy toward the photosynthetic reaction center.
6 sphaeroides funnels excitation energy to the photosynthetic reaction center.
7 ven by the electrical field generated by the photosynthetic reaction center.
8 lographic coordinates of the special pair in photosynthetic reaction center.
9 plings between chromophores in the bacterial photosynthetic reaction center.
10 transfer of electronic excitation toward the photosynthetic reaction center.
11 cceptor moieties in the design of artificial photosynthetic reaction centers.
12 tein that incorporates essential elements of photosynthetic reaction centers.
13 rostatics and influence primary processes in photosynthetic reaction centers.
14 ing energy from sunlight and providing it to photosynthetic reaction centers.
15 Q(A) binding site in Rhodobacter sphaeroides photosynthetic reaction centers.
16 te production of harmful chemical species by photosynthetic reaction centers.
17 ing isoprenoids that are widely exploited by photosynthetic reaction centers.
18 photochemical charge separation unit akin to photosynthetic reaction centers.
19      Anaerobic green sulfur bacteria contain photosynthetic reaction centers analogous to photosystem
20  may store a proton in this way, such as the photosynthetic reaction center and cytochrome c oxidase.
21  body of data for the ET complex between the photosynthetic reaction center and cytochrome c(2).
22 e been previously observed for the bacterial photosynthetic reaction center and indicate that protein
23 ld prove valuable for future analyses of the photosynthetic reaction center and of the roles of BChl
24 le resemblance to the tyrosyl radical of the photosynthetic reaction center and other systems.
25 hanism affects certain reaction rates in the photosynthetic reaction center and therefore may be crit
26 )chlorophylls for the assembly of functional photosynthetic reaction centers and antenna complexes.
27 a-carotene in photosystem II is unique among photosynthetic reaction centers and stems from the very
28 sis indicates that electron transfer between photosynthetic reaction centers and the associated elect
29 tochromes, neuraminidase, hemagglutinin, the photosynthetic reaction center, and annexin.
30      This suggests that the BChl a antennae, photosynthetic reaction centers, and remaining chlorosom
31 imulations of the primary charge transfer in photosynthetic reaction centers are reported.
32                                              Photosynthetic reaction centers are sensitive to high li
33 tes for the primary donor cation radicals of photosynthetic reaction centers based on this criterion.
34 cited primary electron donor P* in bacterial photosynthetic reaction centers (both membrane-bound and
35  in the Q(B) binding pocket of the bacterial photosynthetic reaction center by alanines.
36 elf-assembly methods, a biomimetic bacterial photosynthetic reaction center complex has been construc
37 mber of the early steps of biogenesis of the photosynthetic reaction center complexes in these cyanob
38                                The bacterial photosynthetic reaction center contains bacteriochloroph
39                                              Photosynthetic reaction centers convert excitation energ
40                                              Photosynthetic reaction centers convert light energy int
41                                              Photosynthetic reaction centers convert sunlight into a
42 e contiguous membrane-spanning domain in the photosynthetic reaction center core subunits, which cont
43 charge recombination in native photosystem I photosynthetic reaction centers does occur in the invert
44 , in which the dimeric "special pair" of the photosynthetic reaction center enters a coherent SB-CS s
45 on of cyt c(1) after light activation of the photosynthetic reaction center, especially the dissociat
46                        Successful artificial photosynthetic reaction centers for solar energy convers
47                       The Type I homodimeric photosynthetic reaction center found in anaerobic gram-p
48                  Photosystem II (PS II) is a photosynthetic reaction center found in higher plants wh
49                                       In the photosynthetic reaction center from Rhodobacter sphaeroi
50  The temperature-induced denaturation of the photosynthetic reaction center from Rhodobacter sphaeroi
51 molecular electron transfer reactions in the photosynthetic reaction center from Rhodopseudomonas vir
52                                          The photosynthetic reaction center from the purple bacterium
53                              The core of the photosynthetic reaction center from the purple non-sulfu
54                                              Photosynthetic reaction centers from Rhodobacter sphaero
55                                              Photosynthetic reaction centers from Rhodobacter sphaero
56 tyrosyl radical was investigated in modified photosynthetic reaction centers from Rhodobacter sphaero
57                 Chlorophyll special pairs in photosynthetic reaction centers function as both exciton
58 or the transcript abundance of two important photosynthetic reaction center genes, psbA (encoding the
59 d charge separation process of the bacterial photosynthetic reaction center has been trapped in two D
60                   The evolutionary origin of photosynthetic reaction centers has long remained elusiv
61 hypothesis to account for the development of photosynthetic reaction center holoproteins.
62 nced by reductant and is associated with the photosynthetic reaction center II and the cytochrome b6f
63 Remarkably, the facile reconstitution of the photosynthetic reaction center in the artificial lipid m
64       Photosystem II (PS II) is unique among photosynthetic reaction centers in having secondary elec
65 otential model for the "special pair" of the photosynthetic reaction center is discussed.
66 tructure serve as an antenna conjugated to a photosynthetic reaction center isolated from Rhodobacter
67 he transient ET complexes formed between the photosynthetic reaction center-light harvesting complex
68 most closely resemble the common ancestor of photosynthetic reaction centers, motivating a detailed u
69 oton excitation of the Blastochloris viridis photosynthetic reaction center, observing an ultrafast g
70                                          The photosynthetic reaction center of Heliobacterium modesti
71 ine by aspartic acid at position M210 in the photosynthetic reaction center of Rhodobacter sphaeroide
72 ()) of the primary electron donor (P) in the photosynthetic reaction center of Rhodobacter sphaeroide
73 cytochrome c oxidase, bacteriorhodopsin, the photosynthetic reaction center of Rhodobacter sphaeroide
74       A complex of the modeled LH-I with the photosynthetic reaction center of the same species has b
75 orophylls (the special pair) at the heart of photosynthetic reaction centers of both plants and bacte
76 transfer in the 0.1-10 micros time window in photosynthetic reaction centers of the intact cells of S
77                                              Photosynthetic reaction centers operate in organisms ran
78            Photosystem I (PSI) is one of two photosynthetic reaction centers present in plants, algae
79 levant conformational intermediate states of photosynthetic reaction center protein (RCs) are trapped
80          De novo development of a simplified photosynthetic reaction center protein can clarify pract
81  are strategically placed by the surrounding photosynthetic reaction center protein matrix.
82 erved in both chemical systems as well as in photosynthetic reaction center proteins following photod
83 and to the Mg of bacteriochlorophylls in the photosynthetic reaction center (RC) and many other photo
84                                          The photosynthetic reaction center (RC) from purple bacteria
85 x between cytochrome c(2) (cyt c(2)) and the photosynthetic reaction center (RC) from Rhodobacter sph
86 omplex between cytochrome c(2) (cyt) and the photosynthetic reaction center (RC) from Rhodobacter sph
87 ying concentrations of detergent-solubilized photosynthetic reaction center (RC) from Rhodobacter sph
88  The x-ray crystallographic structure of the photosynthetic reaction center (RC) has proven critical
89 from crystals of the Rhodobacter sphaeroides photosynthetic reaction center (RC) have been collected
90            We present studies on a series of photosynthetic reaction center (RC) mutants created in t
91                                          The photosynthetic reaction center (RC) of green sulfur bact
92                                          The photosynthetic reaction center (RC) of Rhodobacter sphae
93 erties and electron-transfer kinetics in the photosynthetic reaction center (RC) of Rhodobacter sphae
94  primary electron donor (P) in the bacterial photosynthetic reaction center (RC) of Rhodobacter sphae
95 of two distinct metal sites on the bacterial photosynthetic reaction center (RC) protein were probed
96                                The bacterial photosynthetic reaction center (RC) uses light energy to
97 e bacteriopheophytin (H(B)) in the bacterial photosynthetic reaction center (RC).
98 quinone acceptors (Q)-are common features of photosynthetic reaction centers (RC).
99 an be observed in frozen and quinone-blocked photosynthetic reaction centers (RCs) as modification of
100 he special pair (P) to the carotenoid (C) in photosynthetic reaction centers (RCs) from a large famil
101                                              Photosynthetic reaction centers (RCs) from Rhodobacter s
102 pping of cofactor-specific photochemistry in photosynthetic reaction centers (RCs) from Rhodobacter s
103  The interaction of metal ions with isolated photosynthetic reaction centers (RCs) from the purple ba
104               The fusion of hydrogenases and photosynthetic reaction centers (RCs) has proven to be a
105  detailed analysis of reaction mechanisms in photosynthetic reaction centers (RCs) of purple bacteria
106 ironment, light-induced electron transfer in photosynthetic reaction centers (RCs) of the purple bact
107 layers which contain oriented and functional photosynthetic reaction centers (RCs).
108 e 93 to proline mutant of cytochrome c(2) to photosynthetic reaction centers (Rhodobacter sphaeroides
109           Photosystem II (PSII) is the plant photosynthetic reaction center that carries out the ligh
110                        In isolated bacterial photosynthetic reaction centers, the electron transfer f
111 rly identical in both QH*- and the bacterial photosynthetic reaction centers, this electronic differe
112 th electron and proton transfer in bacterial photosynthetic reaction centers to those calculated usin
113 sm that decreases the energy arriving at the photosynthetic reaction centers under high-light conditi
114  in support of nonlinear dynamic behavior of photosynthetic reaction centers under light-activated co
115 etry of 0.6-0.75 cytochrome bc complexes per photosynthetic reaction center was estimated.
116 d waters on the reorganization energy of the photosynthetic reaction center was examined and found to
117  the studies reported, detergent-solubilized photosynthetic reaction center was exchanged into a phos
118 a complexes transfer energy from sunlight to photosynthetic reaction centers where charge separation
119 light energy and transports spatially to the photosynthetic reaction center, while the electron trans
120 bisemiquinone centers have only been done on photosynthetic reaction centers whose function is to red

 
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