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1 e sequences indicating members of the genera Chlorobium and Prosthecochloris--anoxygenic photoautotro
2 Aquifex, Chlamydia, Spirochaetes, Cytophaga-Chlorobium, and Planctomycetes, are characterized by thr
3 content and organization was determined for Chlorobium (Cb.) tepidum chlorosomes, the light-harvesti
5 ns of Escherichia coli, and the cruB gene of Chlorobium clathratiforme strain DSM 5477(T) was also he
6 ome is available as a fast electron donor in Chlorobium, it is not necessary to prereduce F(A) and F(
7 als in anaerobically prepared membranes from Chlorobium limicola and Heliobacterium chlorum that rese
8 was subsequently isolated and sequenced from Chlorobium limicola f.sp. thiosulfatophilum strain Tassa
9 concentrations (<5 mM), the Na(+)-PPases of Chlorobium limicola, four other bacteria, and one archae
12 this gene were amplified and sequenced from Chlorobium phaeobacteroides strain 1549, Chlorobium vibr
13 olored, isorenieratene-producing GSB species Chlorobium phaeobacteroides strain DSM 266(T) were heter
16 methyltransferase for BChl c biosynthesis in Chlorobium species, and methylation at the C-20 position
17 as identified by comparative analysis of the Chlorobium tepidum and Chloroflexus aurantiacus genome s
19 this enzyme from the green sulfur bacterium Chlorobium tepidum and determine the role of its two dis
20 ation of chlorosomes isolated from wild-type Chlorobium tepidum and from genetically modified species
21 in whole cells of Chlorobium vibrioforme and Chlorobium tepidum and obtained highly photoactive membr
22 x from two species of green sulfur bacteria (Chlorobium tepidum and Prosthecochloris aestuarii) are c
23 thesis genes from the green sulfur bacterium Chlorobium tepidum and the green nonsulfur bacterium Chl
25 chlorosomes from the green sulfur bacterium Chlorobium tepidum are presented, as well as Stark hole-
26 Chlorosomes of the green sulfur bacterium Chlorobium tepidum comprise mostly bacteriochlorophyll c
27 of the photosynthetic green sulfur bacterium Chlorobium tepidum consist of bacteriochlorophyll (BChl)
29 Chlorosomes of the green sulfur bacterium Chlorobium tepidum have previously been shown to contain
31 of the photosynthetic green sulfur bacteria Chlorobium tepidum is a prototype efficient light-harves
36 plete genome of the green-sulfur eubacterium Chlorobium tepidum TLS was determined to be a single cir
38 derately thermophilic green sulfur bacterium Chlorobium tepidum was found to function as an electron
39 smH, and CsmX) of the green sulfur bacterium Chlorobium tepidum were characterized by cloning and seq
40 ur bacterium Chlorobaculum tepidum (formerly Chlorobium tepidum) can grow on sulfide as the sole elec
43 homogeneity from photoautotrophically grown Chlorobium tepidum, a moderately thermophilic green sulf
44 ents on FMO trimers from the green bacterium Chlorobium tepidum, suggest that real samples exhibit su
45 t similar genome to P. gingivalis is that of Chlorobium tepidum, supporting the previous phylogenetic
46 the cruA gene of the green sulfur bacterium Chlorobium tepidum, was identified in a complementation
47 he bacteriochlorophyll (BChl) a protein from Chlorobium tepidum, which participates in energy transfe
51 of GSH were not found in the green bacteria (Chlorobium thiosulfatophilum and Chloroflexus aurantiacu
52 rongly suggest that CsmA binds the BChl a in Chlorobium-type chlorosomes and further indicate that no
53 te that, although the protein composition of Chlorobium-type chlorosomes is superficially more comple
54 d F(B) to molecular oxygen in whole cells of Chlorobium vibrioforme and Chlorobium tepidum and obtain
55 DNA from the green photosynthetic bacterium Chlorobium vibrioforme complement a heme-requiring Esche
57 rom Chlorobium phaeobacteroides strain 1549, Chlorobium vibrioforme strain 8327d, and C. vibrioforme
58 In this work, the iron-sulfur clusters in Chlorobium vibrioforme were studied using selective ligh
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