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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.
15 ed in which a Rubisco deletion mutant of the photosynthetic bacterium Rhodobacter capsulatus served a
17 orophyll a biosynthesis mutant of the purple photosynthetic bacterium Rhodobacter capsulatus was func
18 acetone carboxylase of the purple nonsulfur photosynthetic bacterium Rhodobacter capsulatus was puri
20 rotein, a transcriptional regulator from the photosynthetic bacterium Rhodobacter capsulatus, were ob
24 ent of rats with lipopolysaccharide from the photosynthetic bacterium Rhodobacter sphaeroides (LPS-RS
25 tudied in isolated reaction centers from the photosynthetic bacterium Rhodobacter sphaeroides by repl
26 ding site of the reaction center (RC) of the photosynthetic bacterium Rhodobacter sphaeroides determi
30 well-characterized reaction center from the photosynthetic bacterium Rhodobacter sphaeroides R-26.
31 it was previously shown that the anoxygenic, photosynthetic bacterium Rhodobacter sphaeroides require
33 r (P) of the reaction center from the purple photosynthetic bacterium Rhodobacter sphaeroides were co
34 f studying energy-generating pathways in the photosynthetic bacterium Rhodobacter sphaeroides, a gene
37 c(2)) and the reaction center (RC) from the photosynthetic bacterium Rhodobacter sphaeroides, that f
38 xpression of photosynthetic complexes in the photosynthetic bacterium Rhodobacter sphaeroides, we hav
39 minolaevulinic acid synthase (ALAS) from the photosynthetic bacterium Rhodobacter sphaeroides, were c
41 The NtrC enhancer binding protein from the photosynthetic bacterium, Rhodobacter capsulatus, is sho
43 arved for nitrogen, non-growing cells of the photosynthetic bacterium Rhodopseudomonas palustris cont
44 uestions we measured metabolic fluxes in the photosynthetic bacterium Rhodopseudomonas palustris grow
47 riophytochromes RpBphP2 and RpBphP3 from the photosynthetic bacterium Rhodopseudomonas palustris work
50 in the cbb(I) region of the nonsulfur purple photosynthetic bacterium Rhodopseudomonas palustris.
53 cently, we have demonstrated that the purple photosynthetic bacterium Rhodospirillum centenum is capa
56 an alpha subunit of the tentoxin-insensitive photosynthetic bacterium Rhodospirillum rubrum F(1) (RrF
57 native nitrogenase from a nifH mutant of the photosynthetic bacterium Rhodospirillum rubrum has been
59 n vivo evidence that the BluB protein of the photosynthetic bacterium Rhodospirillum rubrum is necess
64 The crystal structures of SoxAX from the photosynthetic bacterium Rhodovulum sulfidophilum have b
65 terization of a copA(-) mutant in the purple photosynthetic bacterium Rubrivivax gelatinosus under lo
67 iobacterium chlorum, the recently discovered photosynthetic bacterium that contains a novel form of c
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