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1 metry of light-harvesting complex 2 (LH2) of purple bacteria.
2 s of the light-harvesting complex 2 (LH2) of purple bacteria.
3 comparable to the LH1 antenna complex of the purple bacteria.
4 angement in the light harvesting system 2 of 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 y of the Light-Harvesting 2 (LH2) complex of purple bacteria.
12 erric uptake regulatory) proteins from other purple bacteria.
13  species that span three subdivisions of the 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 en algae and hundreds of genetically reduced purple bacteria.
18  in single light-harvesting complexes LH2 of purple bacteria.
19 ed to those of cytochrome bc1 complexes from purple bacteria and of cytochrome b6f complexes from chl
20 osynthetic species, the other four being the purple bacteria and relatives, the green sulfur bacteria
21 nd gamma subdivisions of the proteobacteria (purple bacteria) and in the Gram-positive bacterium Baci
22 th dependence of absorption in green plants, purple bacteria, and green sulfur bacteria.
23 ion of representatives of the cyanobacteria, purple bacteria, and spirochetes also gave negative resu
24 matium vinosum (formerly Chromatium vinosum) purple bacteria are known to adapt their light-harvestin
25 ing photosynthetic functions in phototrophic purple bacteria are not present in the heliobacteria.
26 hotosynthesis gene trees also indicates that purple bacteria are the earliest emerging photosynthetic
27 ontrast, anoxygenic photosynthesizers (e.g., purple bacteria) are exceedingly rare as intracellular s
28 e focus on the light-harvesting complexes of purple bacteria as a model to illustrate the present und
29 imony and distance analyses further identify purple bacteria as the earliest emerging photosynthetic
30 tris is unique among characterized nonsulfur purple bacteria because of its capacity for anaerobic ph
31 genic cyanobacteria and the oxygen-utilizing purple bacteria, but is absent in many other prokaryotes
32                               Photosynthetic purple bacteria can capture and convert sunlight with a
33 ubstantial levels of GSH were present in the purple bacteria (Chromatium vinosum, Rhodospirillum rubr
34 roteins, light-harvesting (LH) proteins from purple bacteria constitute an ideal object for such a st
35 nthetic chromatophore vesicles found in some purple bacteria constitute one of the simplest light-har
36 The photosynthetic reaction center (RC) from purple bacteria converts light into chemical energy.
37 ructure in the light-harvesting complex 2 of purple bacteria following photoexcitation by creating a
38 structure of the apparatus, as it evolved in purple bacteria, has been constructed through a combinat
39  photosynthetic membranes of land plants and purple bacteria have been previously performed by neutro
40                         The chromatophore of purple bacteria is an intracellular spherical vesicle th
41 tion of the tRNA(Arg)CCUg intron among alpha-purple bacteria is consistent with a recent origin and h
42              The photosynthetic apparatus of purple bacteria is contained within organelles called ch
43 a rings of the light-harvesting complexes of purple bacteria is emphasized.
44  the low light intensities in the habitat of purple bacteria, is suboptimal for steady-state ATP turn
45 y bacteriochlorophyll in reaction centers of purple bacteria, it is clear that changes in Arg180 grea
46 king rings of chlorophyll molecules found in purple bacteria, known as 'light-harvesting system 2'.
47 We studied individual peripheral antennas of purple bacteria (LH2) and single CP chains of 20 nm leng
48 variants of the primary antenna protein from purple bacteria, light-harvesting complex 2 (LH2), toget
49 with the M subunit of the reaction center of purple bacteria, no residues in photosystem II can be cl
50 omposed primarily of Ectothiorhodospira-like purple bacteria or Oscillatoria-like cyanobacteria.
51 sting complex LH1 and the reaction center in purple bacteria photosynthesis.
52                                           In purple bacteria, photosynthesis is carried out on large
53  the monomeric reaction centers in green and purple bacteria, PSI forms trimeric complexes in most cy
54                                 In nonsulfur purple bacteria, redox homeostasis is achieved by the co
55  on the bacterial reaction center (BRC) from purple bacteria, revealing hidden vibronic and excitonic
56 lator is a global transcription regulator in purple bacteria Rhodobacter sphaeroides and Rhodobacter
57 otosynthetic reaction centers (RCs) from the purple bacteria Rhodobacter sphaeroides, Rhodobacter cap
58 ed to probe the redox activity of individual purple bacteria (Rhodobacter sphaeroides).
59 ransfer process in a thriving culture of the purple bacteria, Rhodobacter sphaeroides.
60             Here, we isolated a phototrophic purple bacteria, Rhodobacter strain CZR27, from an arsen
61 l membrane pigment-protein complex, from the purple bacteria Rhodopseudomonas (Rps.) acidophila strai
62 e peripheral light-harvesting complex of the purple bacteria Rhodopseudomonas acidophila strain 10050
63 e similar to homologues among the beta/gamma purple bacteria than to existing cyanobacterial homologu
64                                      In most purple bacteria, the core light-harvesting complex (LH1)
65            For light-harvesting complex 2 of purple bacteria, the inter-ring transfer is 1.5 times sl
66 ein, light harvesting 2 complexes (LH2) from purple bacteria under strong coupling with the light mod
67 ytochrome components of the bc(1) complex in purple bacteria usually report only the sum cyt c(1) + c
68 f Cfx. aurantiacus compared to the RC of the purple bacteria was observed.
69 s synthesized by some species and strains of purple bacteria when growing under what are generally cl