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1 y of the Light-Harvesting 2 (LH2) complex of purple bacteria.
2 metry of light-harvesting complex 2 (LH2) of purple bacteria.
3 s of the light-harvesting complex 2 (LH2) of purple bacteria.
4 comparable to the LH1 antenna complex of the purple bacteria.
5  in photosynthetic reaction centers (RCs) of purple bacteria.
6 hototactic response to blue light in certain purple bacteria.
7 e reported for light-harvesting complexes of purple bacteria.
8  intron among 12 additional species of alpha-purple bacteria.
9 n-plant eukaryotes and the alpha-subclass of purple bacteria.
10 ganization in the photosynthetic membrane of purple bacteria.
11 erric uptake regulatory) proteins from other purple bacteria.
12  species that span three subdivisions of the purple bacteria.
13  in single light-harvesting complexes LH2 of purple bacteria.
14 erobic ancestors of modern cyanobacteria and purple bacteria.
15 nship to sequences from among the beta/gamma purple bacteria.
16 e of form II RubisCO obtained from nonsulfur purple bacteria.
17 ed to those of cytochrome bc1 complexes from purple bacteria and of cytochrome b6f complexes from chl
18 osynthetic species, the other four being the purple bacteria and relatives, the green sulfur bacteria
19 nd gamma subdivisions of the proteobacteria (purple bacteria) and in the Gram-positive bacterium Baci
20 ion of representatives of the cyanobacteria, purple bacteria, and spirochetes also gave negative resu
21 matium vinosum (formerly Chromatium vinosum) purple bacteria are known to adapt their light-harvestin
22 ing photosynthetic functions in phototrophic purple bacteria are not present in the heliobacteria.
23 hotosynthesis gene trees also indicates that purple bacteria are the earliest emerging photosynthetic
24 e focus on the light-harvesting complexes of purple bacteria as a model to illustrate the present und
25 imony and distance analyses further identify purple bacteria as the earliest emerging photosynthetic
26 tris is unique among characterized nonsulfur purple bacteria because of its capacity for anaerobic ph
27 genic cyanobacteria and the oxygen-utilizing purple bacteria, but is absent in many other prokaryotes
28 ubstantial levels of GSH were present in the purple bacteria (Chromatium vinosum, Rhodospirillum rubr
29 roteins, light-harvesting (LH) proteins from purple bacteria constitute an ideal object for such a st
30 nthetic chromatophore vesicles found in some purple bacteria constitute one of the simplest light-har
31 The photosynthetic reaction center (RC) from purple bacteria converts light into chemical energy.
32 ructure in the light-harvesting complex 2 of purple bacteria following photoexcitation by creating a
33 structure of the apparatus, as it evolved in purple bacteria, has been constructed through a combinat
34                         The chromatophore of purple bacteria is an intracellular spherical vesicle th
35 tion of the tRNA(Arg)CCUg intron among alpha-purple bacteria is consistent with a recent origin and h
36              The photosynthetic apparatus of purple bacteria is contained within organelles called ch
37 a rings of the light-harvesting complexes of purple bacteria is emphasized.
38  the low light intensities in the habitat of purple bacteria, is suboptimal for steady-state ATP turn
39 y bacteriochlorophyll in reaction centers of purple bacteria, it is clear that changes in Arg180 grea
40 We studied individual peripheral antennas of purple bacteria (LH2) and single CP chains of 20 nm leng
41 with the M subunit of the reaction center of purple bacteria, no residues in photosystem II can be cl
42 omposed primarily of Ectothiorhodospira-like purple bacteria or Oscillatoria-like cyanobacteria.
43                                           In purple bacteria, photosynthesis is carried out on large
44  the monomeric reaction centers in green and purple bacteria, PSI forms trimeric complexes in most cy
45                                 In nonsulfur purple bacteria, redox homeostasis is achieved by the co
46 lator is a global transcription regulator in purple bacteria Rhodobacter sphaeroides and Rhodobacter
47 otosynthetic reaction centers (RCs) from the purple bacteria Rhodobacter sphaeroides, Rhodobacter cap
48 ed to probe the redox activity of individual purple bacteria (Rhodobacter sphaeroides).
49 ransfer process in a thriving culture of the purple bacteria, Rhodobacter sphaeroides.
50 l membrane pigment-protein complex, from the purple bacteria Rhodopseudomonas (Rps.) acidophila strai
51 e peripheral light-harvesting complex of the purple bacteria Rhodopseudomonas acidophila strain 10050
52 e similar to homologues among the beta/gamma purple bacteria than to existing cyanobacterial homologu
53                                      In most purple bacteria, the core light-harvesting complex (LH1)
54 ytochrome components of the bc(1) complex in purple bacteria usually report only the sum cyt c(1) + c
55 f Cfx. aurantiacus compared to the RC of the purple bacteria was observed.
56 s synthesized by some species and strains of purple bacteria when growing under what are generally cl

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