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1 eport of a linear element in the genome of a photosynthetic bacterium.
2 ht-dark cycle influences the metabolism in a photosynthetic bacterium.
3 nd hydrogenase biosynthesis in an anoxygenic photosynthetic bacterium.
5 brivivax gelatinosus CBS, a purple nonsulfur photosynthetic bacterium, can grow photosynthetically us
8 e dismutase from the thermophilic anoxygenic photosynthetic bacterium Chloroflexus aurantiacus was cl
10 is a blue light sensor present in the purple photosynthetic bacterium Ectothiorhodospira halophila, w
12 eroides 2.4.1, the gram-negative facultative photosynthetic bacterium, has been cloned and sequenced.
14 y locked with reaction centres from a purple photosynthetic bacterium, producing macromolecular chime
16 ed in which a Rubisco deletion mutant of the photosynthetic bacterium Rhodobacter capsulatus served a
18 orophyll a biosynthesis mutant of the purple photosynthetic bacterium Rhodobacter capsulatus was func
19 acetone carboxylase of the purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus was puri
21 rotein, a transcriptional regulator from the photosynthetic bacterium Rhodobacter capsulatus, were ob
25 ent of rats with lipopolysaccharide from the photosynthetic bacterium Rhodobacter sphaeroides (LPS-RS
26 tudied in isolated reaction centers from the photosynthetic bacterium Rhodobacter sphaeroides by repl
27 ding site of the reaction center (RC) of the photosynthetic bacterium Rhodobacter sphaeroides determi
30 the crystal structure of cyt bc (1) from the photosynthetic bacterium Rhodobacter sphaeroides in comp
32 relaxation (in the dark) for whole cells of photosynthetic bacterium Rhodobacter sphaeroides lacking
33 well-characterized reaction center from the photosynthetic bacterium Rhodobacter sphaeroides R-26.
34 it was previously shown that the anoxygenic, photosynthetic bacterium Rhodobacter sphaeroides require
36 r (P) of the reaction center from the purple photosynthetic bacterium Rhodobacter sphaeroides were co
37 f studying energy-generating pathways in the photosynthetic bacterium Rhodobacter sphaeroides, a gene
40 c(2)) and the reaction center (RC) from the photosynthetic bacterium Rhodobacter sphaeroides, that f
41 xpression of photosynthetic complexes in the photosynthetic bacterium Rhodobacter sphaeroides, we hav
42 minolaevulinic acid synthase (ALAS) from the photosynthetic bacterium Rhodobacter sphaeroides, were c
44 The NtrC enhancer binding protein from the photosynthetic bacterium, Rhodobacter capsulatus, is sho
46 Here, we identify the MatBAC system from the photosynthetic bacterium Rhodopseudomonas palustris as t
47 arved for nitrogen, non-growing cells of the photosynthetic bacterium Rhodopseudomonas palustris cont
48 uestions we measured metabolic fluxes in the photosynthetic bacterium Rhodopseudomonas palustris grow
51 riophytochromes RpBphP2 and RpBphP3 from the photosynthetic bacterium Rhodopseudomonas palustris work
54 in the cbb(I) region of the nonsulfur purple photosynthetic bacterium Rhodopseudomonas palustris.
57 cently, we have demonstrated that the purple photosynthetic bacterium Rhodospirillum centenum is capa
60 an alpha subunit of the tentoxin-insensitive photosynthetic bacterium Rhodospirillum rubrum F(1) (RrF
61 native nitrogenase from a nifH mutant of the photosynthetic bacterium Rhodospirillum rubrum has been
63 n vivo evidence that the BluB protein of the photosynthetic bacterium Rhodospirillum rubrum is necess
68 The crystal structures of SoxAX from the photosynthetic bacterium Rhodovulum sulfidophilum have b
69 terization of a copA(-) mutant in the purple photosynthetic bacterium Rubrivivax gelatinosus under lo
71 iobacterium chlorum, the recently discovered photosynthetic bacterium that contains a novel form of c
75 tion from an engulfed autonomous unicellular photosynthetic bacterium to a semiautonomous endosymbion
76 e of a light-based strategy evolved in a non-photosynthetic bacterium to exploit scarse water in a de