ライフサイエンスコーパス: enterobacteria

1 PS) to elicit antibodies cross-reactive with enterobacteria.

2 of unknown function in Salmonella and other enterobacteria.

3 of the emergence of carbapenemase-producing enterobacteria.

4 he anaerobic fermentation of glucose by many enterobacteria.

5 he nature of the interaction is conserved in enterobacteria.

6 riptional regulation of purine metabolism in enterobacteria.

7 ion against ACA in tmRNAs was seen mostly in enterobacteria.

8 nated by Rho factor, an essential protein in enterobacteria.

9 as a c-di-GMP receptor affecting motility in enterobacteria.

10 olutionary divergence from animal-pathogenic enterobacteria.

11 ci, staphylococci, lactobacilli, yeasts, and enterobacteria.

12 on on the coding strand has been observed in enterobacteria.

13 xposed to either pathogenic or nonpathogenic enterobacteria.

14 linked arthritides follows an infection with enterobacteria.

15 , 4.5-log for yeasts and molds and 2-log for enterobacteria after 20 d of storage.

16 Diverse elements use ssrA; among enterobacteria alone, at least four different integrase

17 demonstrate an antagonistic correlation with enterobacteria and enterococci.

18 concatenation of the core set of TCSTs from enterobacteria and for individual TCST proteins from spe

19 The other group, mostly restricted to Enterobacteria and including Escherichia coli pheL, has

20 that occur in a conserved genomic context in Enterobacteria and is essential in the infection process

21 ible for intracellular formate generation in enterobacteria and other microbes, interacts specificall

22 cquired antibiotic resistance genes found in enterobacteria and pseudomonads are part of small mobile

23 glutamine amidotransferase-QueC homologs in Enterobacteria and Pseudomonas phage, and distant homolo

24 e determinants, its carriage in a variety of enterobacteria, and its presence in both nosocomial and

25 nserved across its entire length in numerous Enterobacteria, and mutational analysis revealed that tw

26 otal anaerobes, aerobes, bifidobacteria, and enterobacteria, and to assay for beta-glucuronidase, nit

27 Type 1 fimbriae of enterobacteria are heteropolymeric organelles of adhesio

28 The core bacteria include Pseudomonas and enterobacteria, both are shared in the sand flies in the

29 as found to be dominated by Lactobacilli and Enterobacteria, both typically facultative anaerobes.

30 QseD is present in all enterobacteria but exists almost exclusively in O157:H7

31 ys show that processing of the model Ag from enterobacteria by mast cells is similar in efficiency to

32 close relatives all infect a broad range of enterobacteria by recognizing a plasmid-encoded conjugal

33 Like Dam in the enterobacteria, CcrM plays a regulatory role in Caulobac

34 We tested a hypothesis that in enterobacteria CheV functions as an additional adaptor l

35 ovora subsp. carotovora, like those of other enterobacteria, consists of flhD and flhC.

36 Comparative genomic analysis revealed that enterobacteria contain eight pairs of core TCSTs.

37 pportunistic infections with FimH-expressing enterobacteria could occur in a setting deprived of opso

38 gmoidoscopy scores (SS) were associated with enterobacteria, desulfovibrios, type E Clostridium perfr

39 hey promote infection by the phytopathogenic enterobacteria Dickeya dadantii and Erwinia amylovora.

40 Like the cells of other enterobacteria, E. coli cells acquire beta-lactam resist

41 ly (OMP) were consistently identified in the Enterobacteria Escherichia coli, Enterobacter cloacae, E

42 Enterobacteria, especially Escherichia coli, are abundan

43 Blochmannia pairs, plus Buchnera and related enterobacteria, estimates of sequence divergence at four

44 temperate double-stranded (ds) phages, like enterobacteria, exhibit significantly high relative abun

45 During flagellum assembly by motile enterobacteria, flagellar axial proteins destined for po

46 lactobacilli) and increase the abundance of enterobacteria including entropathogenic Escherichia col

47 essing occurs from a number of Gram-negative enterobacteria including Salmonella typhimurium and Esch

48 gen is an exopolysaccharide produced by many enterobacteria, including the majority of Escherichia co

49 toxins are PIN domain endonucleases that, in enterobacteria, inhibit translation by site-specific cle

50 Speciation in enterobacteria involved horizontal gene transfer.

51 can bloom in the inflamed gut; expansion of enterobacteria is a hallmark of microbial imbalance know

52 It appears that cellulose production in enterobacteria is controlled by a two-tiered c-di-GMP-de

53 Respiratory enzyme synthesis in enterobacteria is controlled in response to electron acc

54 understanding how the virulence phenotype in enterobacteria is expressed and regulated.

55 he phage shock protein (Psp) system found in enterobacteria is induced in response to impaired inner

56 ssembly of CoA in Escherichia coli and other enterobacteria is well understood, except for the events

57 Since the alpha gal epitope is found on gut enterobacteria, it has been hypothesized that anti-gal a

58 operate on the chromosomal fis genes of the enterobacteria Klebsiella pneumoniae, Serratia marcescen

59 In enterobacteria like Salmonella, biogenesis of cell surfa

60 relatively conserved, and suggest that these enterobacteria may have maintained their ancient core TC

61 Escherichelin production by colonizing enterobacteria may help human hosts resist opportunistic

62 Pathogenic enterobacteria need to survive the extreme acidity of th

63 d chemical analysis in four plant-associated enterobacteria of the Serratia and Dickeya genera.

64 erving as a rich source of information about enterobacteria on the NIAID established list of Select A

65 ved in c-di-GMP synthesis and degradation in enterobacteria, only a handful of c-di-GMP receptors/eff

66 hese OMP peptides observed are unique to the Enterobacteria order.

67 ate Tetrahymena thermophila, and the viruses Enterobacteria phage Rb49 and Bacteriophage Felix 01.

68 ovel sister clade to the Microvirus genus of Enterobacteria phages.

69 Some strains of enterobacteria possess a mrkD1C allele that is associate

70 Many gram-negative enterobacteria produce surface-associated fimbriae that

71 tructure analysis of the S10 leaders of five enterobacteria (Salmonella typhimurium, Citrobacter freu

72 iocontrol and phytopathogenic strains of the enterobacteria, Serratia and Dickeya.

73 nt high levels of proteobacteria, especially enterobacteria species including E. coli, observed in cl

74 artii and E. rhapontici, as well as in other enterobacteria such as Escherichia coli, Salmonella ente

75 All four enterobacteria tested produce tau and gamma homologs.

76 ere up to 20-fold less efficient in clearing enterobacteria than control WBB6F1 +/+ (+/+) mice or mas

77 Shigella species are invasive enterobacteria that cause dysentery, a severe form of di

78 Salmonellae are enterobacteria that have the unique ability to change th

79 m plays an essential role in the response of enterobacteria to the environment of their mammalian hos

80 In enterobacteria, under non-stress conditions, PspA as a l

81 or the rapid classification of Gram-negative Enterobacteria using on-slide solubilization and trypsin

82 a-Proteobacteria, for example, in genomes of Enterobacteria, Vibrio, and Halomonas species, and in ty

83 of S. typhimurium LT2 genes in eight related enterobacteria was determined using previously completed

84 ells have been shown to phagocytose and kill enterobacteria, we wished to determine whether they coul

85 Total aerobes and enterobacteria were less affected by diet and neosugar.

86 cated in the repression state of AmpR in the enterobacteria, were also shown to play a structural rol

87 sadA; orthologous operons are only found in enterobacteria, whereas other TAAs are not typically ass

88 hE belongs to the flhBAE flagellar operon in Enterobacteria, whose first two members function in Type

89 on genomic comparisons between Eca and other enterobacteria, with particular emphasis on the differen