ライフサイエンスコーパス: gammaproteobacteria

1 resident symbiont Baumannia cicadellinicola (Gammaproteobacteria).

2 gain in the common ancestor of the Beta- and Gammaproteobacteria.

3 cific Zetaproteobacteria and an unclassified Gammaproteobacteria.

4 86 (76%) were positive for bacteria, mainly Gammaproteobacteria.

5 n of active methylamine-utilizing Alpha- and Gammaproteobacteria.

6 tant growth substrate for representatives of Gammaproteobacteria.

7 iched for versatile heterotrophic Alpha- and Gammaproteobacteria.

8 rganisms and could represent a new family of Gammaproteobacteria.

9 cytidine deaminase (CDDL), seen primarily in Gammaproteobacteria.

10 Alphaproteobacteria, Betaproteobacteria and Gammaproteobacteria.

11 ested a strong allergy-protective effect for Gammaproteobacteria.

12 d to metal reduction in Shewanella and other Gammaproteobacteria.

13 ira, Planctomycetes, and SUP05/ARCTIC96BD-19 Gammaproteobacteria.

14 and function are likely conserved throughout gammaproteobacteria.

15 are narrowly distributed to a few orders of Gammaproteobacteria.

16 d may be the reason ZipA is essential in the gammaproteobacteria.

17 highly conserved, especially among beta- and gammaproteobacteria.

18 ividuals, who had a proportional increase of Gammaproteobacteria.

19 labile and stimulated growth of copiotrophic Gammaproteobacteria (Alteromonadaceae and Oceanospirilla

20 Phytoplankton blooms caused an increase of Gammaproteobacteria (Alteromonadaceae, SAR86 and Vibrion

21 Unclassified Gammaproteobacteria and Alphaproteobacteria (Magnetovibr

22 ed by the treatment processes, shifting from Gammaproteobacteria and Betaproteobacteria in RW to Alph

23 ulose synthase operons in representatives of Gammaproteobacteria and Betaproteobacteria.

24 ther primarily because of differences in the Gammaproteobacteria and Epsilonproteobacteria abundances

25 Variations between subjects in levels of Gammaproteobacteria and Erysipelotrichi were directly as

26 acterial phyla shifts from a predominance of Gammaproteobacteria and Firmicutes towards Bacteroidetes

27 Gammaproteobacteria and Firmicutes were consistently enr

28 been restricted to a related cluster within Gammaproteobacteria and have revealed distinctive featur

29 t prominently members of the Flavobacteriia, Gammaproteobacteria and the alphaproteobacterial Roseoba

30 (Alphaproteobacteria, Betaproteobacteria and Gammaproteobacteria) and eukarya (Alveolata, Fungi, Stra

31 the Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, and Deltaproteobacteria classes.

32 olute transporters were Alphaproteobacteria, Gammaproteobacteria, and Deltaproteobacteria, accounting

33 ia, enriched in either Betaproteobacteria or Gammaproteobacteria, and either unicellular Cyanobacteri

34 ella prevented its reliable placement within Gammaproteobacteria, and high bias caused artifacts that

35 rophs, including Pelagibacter, SAR86-cluster Gammaproteobacteria, and marine Euryarchaea.

36 h hydrocarbons resulted in the enrichment of Gammaproteobacteria, and specifically the genera Pseudoa

37 including Actinobacteria, Alpha-, Beta-, and Gammaproteobacteria, and Sphingobacteria.

38 uding Shewanella, Pseudomonas, Psychromonas (Gammaproteobacteria), Arcobacter (Epsilonproteobacteria)

39 Gammaproteobacteria are important gut microbes but only

40 Organisms in the OM60/NOR5 clade of the Gammaproteobacteria are ubiquitous in the world's oceans

41 ) that harbor a community of closely related Gammaproteobacteria as intracellular endosymbionts in th

42 rved among Actinobacteria, Beta-, Delta- and Gammaproteobacteria-as the primary enzyme responsible fo

43 structed the genome of a Chromatiales (class Gammaproteobacteria) bacterium from a metagenomic sequen

44 assemblages were (1) dominated by Alpha- and Gammaproteobacteria, Bacteroidetes, and unclassified Bac

45 cells of Deltaproteobacteria cluster SAR324, Gammaproteobacteria clusters ARCTIC96BD-19 and Agg47, an

46 stimated (e.g. SAR11) or overestimated (e.g. Gammaproteobacteria) common marine taxa.

47 Four phylotypes, one within Gammaproteobacteria (corresponding to "Candidatus Gillia

48 novel, highly divergent marine member of the Gammaproteobacteria, currently without a cultured repres

49 itabine resistance was induced by intratumor Gammaproteobacteria, dependent on bacterial CDDL express

50 microbial taxonomic diversity (P = 0.03) and Gammaproteobacteria (e.g., Enterobacteriaceae; P = 0.04)

51 the sCD14 level; the relative abundances of Gammaproteobacteria, Enterobacteriales, and Enterobacter

52 The relative abundance of Proteobacteria, Gammaproteobacteria, Enterobacteriales, Enterobacteriace

53 liated with the classes Clostridia, Bacilli, Gammaproteobacteria, Epsilonproteobacteria, Bacteroidia,

54 wellia, Cycloclasticus, and other members of Gammaproteobacteria, Flavobacteria, and Rhodobacteria.

55 th an unprecedented organization: an unnamed gammaproteobacteria, for which we propose the name Candi

56 The phylogeny of the large bacterial class Gammaproteobacteria has been difficult to resolve.

57 Isolated from coastal Oregon water, Gammaproteobacteria HTCC2148 and HTCC2080 are two member

58 we present the genome sequences of the OM60 Gammaproteobacteria HTCC2148 and HTCC2080.

59 e, Alphaproteobacteria (i.e., Thalassobius), Gammaproteobacteria (i.e., Pseudoalteromonas), Sphingoba

60 A relative abundance of Gammaproteobacteria (ie, Gram-negative facultative bacil

61 The ecology of Gammaproteobacteria in the gut environment is poorly und

62 more, comparative analyses suggest that many Gammaproteobacteria, including all members of the Shewan

63 Most gammaproteobacteria, including Escherichia coli, encode

64 ed by phylogenetically related intracellular gammaproteobacteria, including the opportunistic pathoge

65 ed phylogenies this order does not belong to Gammaproteobacteria; instead, it (and, independently, "M

66 lete sulfide-driven denitrification by SUP05 Gammaproteobacteria is predicted to support inorganic ca

67 The functional role of the gram-negative gammaproteobacteria is supported by in vitro measurement

68 unique member of the OM60/NOR5 clade of the Gammaproteobacteria isolated from coastal seawater of Ka

69 erant, aerobic, methanotrophic member of the Gammaproteobacteria, isolated from coastal seawater.

70 n only the stationary phase in Gram-negative gammaproteobacteria, it is ubiquitous throughout all gro

71 ched for oligotrophic Actinobacteria OM1 and Gammaproteobacteria KI89A clades while nitrate enriched

72 In many gammaproteobacteria, NO controls behavioral responses th

73 ommunities were markedly dominated by select Gammaproteobacteria, notably Escherichia species and Pse

74 and significantly lower generic diversity of gammaproteobacteria on their skin.

75 s a global CCM regulator in some lineages of Gammaproteobacteria operating as a functional replacemen

76 t reduction in the early pioneering bacteria Gammaproteobacteria (P = 0.03) and exhibited a trend for

77 s interaction was positively associated with Gammaproteobacteria (p=0.0010) and negatively associated

78 olitis), there were increased proportions of Gammaproteobacteria (p=0.0011) and lower proportions of

79 ance by Deltaproteobacteria (Desulfobulbus), Gammaproteobacteria (Piscirickettsiaceae), Alphaproteoba

80 with n-hexadecane, and uncultured Alpha- and Gammaproteobacteria populations were enriched in the pol

81 has transferred horizontally across multiple Gammaproteobacteria, potentially driven by pressures to

82 ty of one or more highly conserved proteins; gammaproteobacteria produce two relevant proteins, ribos

83 bacteria KI89A clades while nitrate enriched Gammaproteobacteria SAR86, SAR92 and OM60 clades.

84 The heat shock sigma factors of all gammaproteobacteria sequenced have a histidine at this p

85 ), we identified a potential host-associated Gammaproteobacteria species (Serratia sp.) that was abse

86 Three Gammaproteobacteria species are maternally transmitted.

87 ar patterns are observed in select Beta- and Gammaproteobacteria species.

88 eobacteria yet before the betaproteobacteria/gammaproteobacteria split.

89 gae-dominated reefs had higher abundances of Gammaproteobacteria (such as Alteromonadales, Pseudomona

90 th pilin proteins from other species of soil gammaproteobacteria suggest that these structural differ

91 tarved copepods were Vibrio spp. and related Gammaproteobacteria, suggesting they represent the most

92 Actinobacteria, Bacilli, and many Gammaproteobacteria taxa discriminated birds from mammal

93 phylogenetically unique member of the class Gammaproteobacteria that is only distantly related to it

94 acteria, specifically Betaproteobacteria and Gammaproteobacteria, the likely major players.

95 ransmitted microbes consistently include two Gammaproteobacteria, the obligate mutualists Wiggleswort

96 cession of bacterial classes from Bacilli to Gammaproteobacteria to Clostridia, interrupted by abrupt

97 P103(T) (ATCC BAA-332(T)) is a member of the Gammaproteobacteria utilizing n-alkanes as the sole sour

98 tatively involved in peroxide reduction from gammaproteobacteria were abundant in the VCs, suggesting

99 rom low abundance organisms of the NOR5/OM60 gammaproteobacteria were observed later in the experimen

100 e SUP05 group of uncultured sulfur-oxidizing Gammaproteobacteria, which are abundant in widespread an

101 l five leech species revealed a dominance of gammaproteobacteria, which were distinct from each other