ライフサイエンスコーパス: Chlorobium

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

4 completes the biosynthetic pathways for all "Chlorobium chlorophylls."

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

10 etic enzyme EanB from green sulfur bacterium Chlorobium limicola.

11 the enzyme from the closely related organism Chlorobium limicola.

12 s characteristic of the obligate phototrophs Chlorobium phaeobacteroides and C. phaeovibriodes.

13 this gene were amplified and sequenced from Chlorobium phaeobacteroides strain 1549, Chlorobium vibr

14 olored, isorenieratene-producing GSB species Chlorobium phaeobacteroides strain DSM 266(T) were heter

15 Our studies in Chlorobium RCCs show that approaches that employ a singl

16 The Chlorobium RubisCO-like proteins are most closely relate

17 methyltransferase for BChl c biosynthesis in Chlorobium species, and methylation at the C-20 position

18 as identified by comparative analysis of the Chlorobium tepidum and Chloroflexus aurantiacus genome s

19 red to the photosynthetic characteristics of Chlorobium tepidum and Chloroflexus aurantiacus.

20 this enzyme from the green sulfur bacterium Chlorobium tepidum and determine the role of its two dis

21 ation of chlorosomes isolated from wild-type Chlorobium tepidum and from genetically modified species

22 in whole cells of Chlorobium vibrioforme and Chlorobium tepidum and obtained highly photoactive membr

23 x from two species of green sulfur bacteria (Chlorobium tepidum and Prosthecochloris aestuarii) are c

24 thesis genes from the green sulfur bacterium Chlorobium tepidum and the green nonsulfur bacterium Chl

25 in the photosynthetic green sulfur bacterium Chlorobium tepidum and was named bchK.

26 chlorosomes from the green sulfur bacterium Chlorobium tepidum are presented, as well as Stark hole-

27 Chlorosomes of the green sulfur bacterium Chlorobium tepidum comprise mostly bacteriochlorophyll c

28 of the photosynthetic green sulfur bacterium Chlorobium tepidum consist of bacteriochlorophyll (BChl)

29 eating signals among the excitons within the Chlorobium tepidum FMO complex at 77 K.

30 Chlorosomes of the green sulfur bacterium Chlorobium tepidum have previously been shown to contain

31 d from lysates of the green sulfur bacterium Chlorobium tepidum in a single <8 h run.

32 of the photosynthetic green sulfur bacteria Chlorobium tepidum is a prototype efficient light-harves

33 The green sulfur bacterium Chlorobium tepidum is a strict anaerobe and an obligate

34 The Chlorobium tepidum PPA-AT and ADT homologs indeed effici

35 The green sulfur bacterium Chlorobium tepidum produces chlorobactene as its primary

36 The green sulfur bacterium Chlorobium tepidum synthesizes three types of (bacterio)

37 plete genome of the green-sulfur eubacterium Chlorobium tepidum TLS was determined to be a single cir

38 ilic proteins, we subjected the RNase H from Chlorobium tepidum to similar studies.

39 derately thermophilic green sulfur bacterium Chlorobium tepidum was found to function as an electron

40 smH, and CsmX) of the green sulfur bacterium Chlorobium tepidum were characterized by cloning and seq

41 ur bacterium Chlorobaculum tepidum (formerly Chlorobium tepidum) can grow on sulfide as the sole elec

42 (Clostridium difficile, Treponema pallidum, Chlorobium tepidum).

43 In the green sulfur bacterium Chlorobium tepidum, 10 proteins (CsmA, CsmB, CsmC, CsmD,

44 homogeneity from photoautotrophically grown Chlorobium tepidum, a moderately thermophilic green sulf

45 ents on FMO trimers from the green bacterium Chlorobium tepidum, suggest that real samples exhibit su

46 t similar genome to P. gingivalis is that of Chlorobium tepidum, supporting the previous phylogenetic

47 the cruA gene of the green sulfur bacterium Chlorobium tepidum, was identified in a complementation

48 he bacteriochlorophyll (BChl) a protein from Chlorobium tepidum, which participates in energy transfe

49 enome sequence of the green sulfur bacterium Chlorobium tepidum.

50 derately thermophilic green sulfur bacterium Chlorobium tepidum.

51 We identified a putative RNase H from Chlorobium. tepidum and demonstrated that it is an activ

52 of GSH were not found in the green bacteria (Chlorobium thiosulfatophilum and Chloroflexus aurantiacu

53 rongly suggest that CsmA binds the BChl a in Chlorobium-type chlorosomes and further indicate that no

54 te that, although the protein composition of Chlorobium-type chlorosomes is superficially more comple

55 d F(B) to molecular oxygen in whole cells of Chlorobium vibrioforme and Chlorobium tepidum and obtain

56 DNA from the green photosynthetic bacterium Chlorobium vibrioforme complement a heme-requiring Esche

57 ALAD from Chlorobium vibrioforme is shown to form a homo-octameric

58 rom Chlorobium phaeobacteroides strain 1549, Chlorobium vibrioforme strain 8327d, and C. vibrioforme

59 In this work, the iron-sulfur clusters in Chlorobium vibrioforme were studied using selective ligh

60 carbon pathway in the green sulfur bacterium Chlorobium vibrioforme.

61 xes isolated from the green sulfur bacterium Chlorobium vibrioforme.

62 e(II) oxidizers (e.g., Ferrovum, Rhodoferax, Chlorobium) were most abundant in the hypoxic/anoxic zon