ライフサイエンスコーパス: gamma proteobacteria

1 ally distinct genes in a set of 22 alpha and gamma proteobacteria.

2 onas species and in many polarly flagellated gamma proteobacteria.

3 lular eukaryotes, Bacillus subtilis, and the gamma proteobacteria.

4 ti-sigma factors that are found in alpha and gamma proteobacteria.

5 t delta(13)C taxa, with methane-metabolizing gamma-proteobacteria.

6 (Dam) is widespread and conserved among the gamma-proteobacteria.

7 ative bacteria, NBs are found exclusively in gamma-proteobacteria.

8 ciated DNA binding protein conserved in most gamma-proteobacteria.

9 a bacterial community dominated by beta- and gamma-Proteobacteria.

10 alizing results from bacteriophage infecting gamma-Proteobacteria.

11 dependent growth inhibition (CDI) systems of gamma-proteobacteria.

12 somal fragments but have been limited to the gamma-proteobacteria.

13 of signals may be widespread among beta- and gamma-proteobacteria.

14 d condensation in Escherichia coli and other gamma-proteobacteria.

15 (GSH), the major competing cellular thiol in gamma-proteobacteria.

16 chromosomal segregation and condensation in gamma-proteobacteria.

17 a residue universally conserved in beta- and gamma-proteobacteria.

18 d condensation in Escherichia coli and other gamma-proteobacteria.

19 -dependent genes in alpha-proteobacteria and gamma-proteobacteria.

20 lams that form symbioses with chemosynthetic gamma-proteobacteria.

21 nt represents a new bacterial lineage in the gamma-Proteobacteria.

22 mplexes are phylogenetically conserved among gamma-proteobacteria.

23 en conserved across a broad set of beta- and gamma-Proteobacteria.

24 eudomonas species, although both species are gamma-proteobacteria.

25 tricted to a few groups within the beta- and gamma-Proteobacteria.

26 sting of up to 33 core genes in 16 beta- and gamma-Proteobacteria.

27 atory system which is highly conserved among gamma-proteobacteria.

28 ne bacterial taxa, including both alpha- and gamma-proteobacteria.

29 s that appear to have origins other than the gamma-Proteobacteria.

30 ignificantly greater percentage of the class gamma-proteobacteria (0.07% vs 0.89% of total bacteria,

31 e (APR); in fungi and some cyanobacteria and gamma-proteobacteria, a second activation step, phosphor

32 either Porphyromonas gingivalis or ligature, gamma-proteobacteria accumulate and stimulate host immun

33 the Enterobacteriaceae or in species of the gamma-Proteobacteria agreed well with that of the corres

34 ositions in Hfq form signatures for the beta/gamma proteobacteria, alpha proteobacteria and low GC Gr

35 egulatory system is conserved throughout the gamma-proteobacteria and controls key pathways in centra

36 homologues are present in alpha-, beta-, and gamma-proteobacteria and multiple eukaryotes, including

37 Relative to the genes ancestral to gamma-Proteobacteria and to those genes distributed spor

38 (TF)-binding sites in the genomes of several gamma proteobacteria, and hence describing their transcr

39 anscription factor (TF) binding sites in the gamma-proteobacteria, and have evaluated the statistical

40 genomes of other P. putida strains, in other gamma-Proteobacteria, and in beta- and alpha-Proteobacte

41 ades, such as Actinobacteria, Firmicutes and gamma-Proteobacteria, and shed light on several open que

42 this isolate is the first to be reported for gamma-proteobacteria, and the first instance of a tRNA(L

43 e found only in the Gram-negative alpha- and gamma-proteobacteria, and thus other anaerobic bacteria

44 standing of virulence gene regulation in the gamma Proteobacteria are discussed.

45 gamma-Proteobacteria are produced in the majority of mix

46 cific N2 fixation rates indicates that these gamma-proteobacteria are unlikely to be responsible for

47 acterial classes that are active in the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all o

48 ontrol samples with Alpha-proteobacteria and Gamma-proteobacteria being the predominant classes detec

49 ate lyase is also prominently PHX in enteric gamma-proteobacteria, but not in other prokaryotes.

50 The other, Baumannia cicadellinicola (gamma-Proteobacteria), can produce the remaining two ess

51 active bacteria in the clouds belong to the gamma-Proteobacteria class, among which the Pseudomonas

52 d that the dominant alpha-proteobacteria and gamma-proteobacteria communities in bulk soil and root e

53 In gamma-proteobacteria, CsrA activity is competitively ant

54 gher phylotype abundances were observed from gamma-Proteobacteria, delta-Proteobacteria, Bacteroidete

55 rches have identified 176 representatives in gamma-Proteobacteria, delta-Proteobacteria, Clostridia,

56 HR, 2.63; 95% CI, 1.22-5.32; P = 0.015), and gamma-proteobacteria domination of fecal microbiota (HR,

57 .30; 95% CI, 1.42-31.80; P = 0.016), whereas gamma-proteobacteria domination predicted PCs postengraf

58 Postengraftment PCs and gamma-proteobacteria domination were predictive of morta

59 show that in contrast to other characterised Gamma-proteobacteria, E. coli Sxy is positively autoregu

60 A few species in the class of gamma-proteobacteria encode a cytoplasmic N-glycosylatio

61 Many gamma-proteobacteria encode a functional homologue of Dn

62 w exceptions to this orthodoxy is a group of gamma-proteobacteria flourishing in obligate intracellul

63 , with orthologous data from nine additional gamma-proteobacteria for phylogenetic footprinting.

64 In particular, outgrowth of gamma-proteobacteria has been linked to the etiology of

65 nificant homology to Francisella tularensis (gamma-proteobacteria) have been characterized in several

66 in RNase E homologues in a subfamily of the gamma-proteobacteria, including enzymes from pathogens s

67 ding sites, but CsrA in bacteria outside the gamma-proteobacteria is antagonized by a protein called

68 Proteorhodopsin (PR), found in marine gamma-proteobacteria, is a newly discovered light-driven

69 ound primarily in Escherichia coli and other gamma proteobacteria, it does not appear to be part of a

70 Thus, gamma-Proteobacteria live symbiotically inside beta-Prot

71 nt heterotrophic marine bacteria, alpha- and gamma-Proteobacteria, might hydrolyze DOP outside the cy

72 hain flavodoxin family that is unique to the gamma-proteobacteria, possesses a 22-residue sequence th

73 In both alpha-Proteobacteria and gamma-Proteobacteria, postreplicative formation of N(6)-

74 their PBP-docking regions are restricted to gamma-proteobacteria, providing models for niche-specifi

75 ing sequence between E. coli and a series of gamma proteobacteria ranging from Salmonella to Vibrio.

76 including Actinobacteria, alpha-,beta-, and gamma-proteobacteria, revealing a common role of this Am

77 son of I. loihiensis to the genomes of other gamma-proteobacteria reveals abundance of amino acid tra

78 In E. coli, and probably many other related gamma-proteobacteria, RhlB associates with the essential

79 In the gamma-proteobacteria, small non-coding RNAs (sRNAs) use

80 Homologs of FlgJ produced by the beta- and gamma-proteobacteria, such as Salmonella enterica, Vibri

81 bdus and Photorhabdus spp. are gram negative gamma proteobacteria that form entomopathogenic symbiose

82 chemotaxis operons of many polar-flagellated gamma-proteobacteria that actively promote polar localiz

83 Rok, an analog of H-NS from gamma-proteobacteria that affects chromosome architectur

84 ocarbon plume stimulated deep-sea indigenous gamma-Proteobacteria that are closely related to known p

85 o the Vibrionaceae, a large family of marine gamma-proteobacteria that includes several dozen species

86 of species of non-pathogenic and pathogenic gamma-proteobacteria that infect different hosts, includ

87 ylotypes (one epsilon-proteobacteria and two gamma-proteobacteria) that formed specific associations

88 fic bacterial phylogenetic groups (primarily gamma-proteobacteria) that were rare in ambient waters,

89 In Escherichia coli and some other gamma-Proteobacteria, the alternative sigma factor RpoS

90 cherichia coli and the majority of beta- and gamma-proteobacteria, the fourth step of lipid A biosynt

91 In Escherichia coli and other gamma-proteobacteria, the PhoQ-PhoP two-component signal

92 In the alpha-, beta- and gamma-Proteobacteria, the so-called cytochrome c maturat

93 In Escherichia coli and other gamma-proteobacteria, the transcription factor Crl stimu

94 evolved to become hubs, within lineages like gamma-proteobacteria there is strong tendency to retain

95 en as an electron acceptor, thereby allowing gamma-proteobacteria to synthesize heme in both aerobic

96 s were identified in a variety of alpha- and gamma-proteobacteria, with a significant enrichment in t