ライフサイエンスコーパス: aerogenes

1 reundii, Serratia marcescens, and Klebsiella aerogenes.

2 er cloacae, and one (1%) of 162 Enterobacter aerogenes.

3 nonnutrient agar overlaid with Enterobacter aerogenes.

4 far smaller plaques on a lawn of Klebsiella aerogenes.

5 oli, Klebsiella pneumoniae, and Enterobacter aerogenes.

6 t a locus near the trp cluster in Klebsiella aerogenes.

7 lasmid previously isolated from Enterobacter aerogenes.

8 e glutamate dehydrogenase (gdh) operon in K. aerogenes.

9 e by complementation of a nac mutation in K. aerogenes.

10 ans, as well as Pseudomonas and Enterobacter aerogenes.

11 (21), Acinetobacter spp. (13), Enterobacter aerogenes (11), Citrobacter spp. (10), Pseudomonas spp.

12 freundii, 8 Klebsiella oxytoca, 5 Klebsiella aerogenes, 3 Providencia stuartii, and 2 Morganella morg

13 including Escherichia coli (69), Klebsiella aerogenes (4), Klebsiella oxytoca (3), Klebsiella pneumo

14 %), Serratia marcescens (5.5%), Enterobacter aerogenes (4.4%), Stenotrophomonas maltophilia (4.3%), P

15 Overall, 150 patients with K. aerogenes (46/150 [31%]) or Ecc (104/150 [69%]) BSI were

16 fference) for 6,938 isolates of Enterobacter aerogenes and 13,954 isolates of Enterobacter cloacae te

17 haracterized 8Fe ferredoxin from Peptococcus aerogenes and a Y13C variant of AvFdI could be easily mo

18 9% reduction in S. aureus, P. aeruginosa, K. aerogenes and E.

19 of the method was examined with Enterobacter aerogenes and Enterobacter dissolvens, which did not pro

20 egulation of several operons from Klebsiella aerogenes and Escherichia coli.

21 nes both show the same phenotype; second, K. aerogenes and several other enteric bacteria lack a gene

22 ies were Klebsiella pneumoniae, Enterobacter aerogenes, and Escherichia coli.

23 ine utilization operon (hutUH) of Klebsiella aerogenes, and NAC bound at this site activates transcri

24 hogens Klebsiella pneumonia and Enterobacter aerogenes, and would seem to suggest a subclass of Zn(2+

25 The enteric bacterium Klebsiella aerogenes appears to use at least two pathways to allow

26 icroneedle patch that uses live Enterobacter aerogenes as microengines to actively control drug deliv

27 coli, Citrobacter freundii, and Enterobacter aerogenes, as well as Gram-positive Bacillus subtilis an

28 rename Enterobacter aerogenes to Klebsiella aerogenes, based on whole-genome sequencing (WGS), and t

29 onpolar gltB and a polar gltD mutation of K. aerogenes both show the same phenotype; second, K. aerog

30 K. aerogenes BSI was associated with poor clinical outcomes

31 In a multivariable regression model, K. aerogenes BSI, relative to Ecc BSI, was predictive of po

32 this pathway in both E. coli and Klebsiella aerogenes, but the mechanisms of activation clearly diff

33 For E. aerogenes, categorical agreement between the four diluti

34 The alanine catabolic operon of Klebsiella aerogenes, dadAB, was cloned, and its DNA sequence was d

35 In addition, the E. aerogenes diesterase was tested as a catalyst for the hy

36 red with live or dead bacteria (Enterobacter aerogenes, E. coli, Klebsiella pneumoniae, Pseudomonas a

37 n ranged from 1.1-log to > 8 log (Klebsiella aerogenes, Enterobacter cloaca, Staphylococcus hominis)

38 rin-resistant Escherichia coli, Enterobacter aerogenes, Enterobacter cloacae complex, Klebsiella pneu

39 udied urease system, in which the Klebsiella aerogenes genes are expressed in Escherichia coli, a tra

40 Pasteurella aerogenes has been implicated in reproductive disorders

41 of the related enteric bacterium Klebsiella aerogenes have no defect in the reduction of sulfite to

42 ecies, Serratia marcescens, and Enterobacter aerogenes in most of the trials.

43 or further investigation into the role of P. aerogenes in sow reproductive disorders and its potentia

44 This study aimed to detect P. aerogenes in sow vaginal discharge samples and investiga

45 rophosphodiesterase (GpdQ) from Enterobacter aerogenes is a nonspecific diesterase that enables Esche

46 oli and S. typhimurium, the dad operon of K. aerogenes is activated by the Ntr system, mediated in th

47 Urease from Klebsiella aerogenes is an (alpha beta gamma)3 trimer with each alp

48 Ni2+ binding to UreE from K. aerogenes is an enthalpically favored process but an ent

49 sory protein encoded by ureE from Klebsiella aerogenes is proposed to bind intracellular Ni(II) for t

50 sory protein encoded by ureE from Klebsiella aerogenes is proposed to deliver Ni(II) to the urease ap

51 nt) accounted for 6.1% of the results for E. aerogenes isolates and 6.0% of the results for E. cloaca

52 83 genes in 323 genomic islands unique to K. aerogenes isolates, including putative virulence genes i

53 This study represents the first report of P. aerogenes isolation from sow vaginal discharge in Thaila

54 species (Acinetobacter spp., C. freundii, E. aerogenes, K. pneumoniae, P. aeruginosa, and S. marcesce

55 marcescens, Shigella flexneri, Enterobacter aerogenes, Klebsiella pneumoniae, Yersinia enterocolitic

56 Putative virulence factors in K. aerogenes may account for these differences.

57 pax toxin-positive isolates suggest that P. aerogenes may be an underestimated factor in swine repro

58 and the AmpC beta-lactamases of Enterobacter aerogenes, Morganella morganii, and Citrobacter freundii

59 Citrobacter freundii (n = 4), and Klebsiella aerogenes (n = 2).

60 blotting, using a probe from the Klebsiella aerogenes nac (nacK) gene.

61 terminal truncated H144*UreE from Klebsiella aerogenes, Ni2+ binding to the wild-type K. aerogenes Ur

62 The mechanism of action against Enterobacter aerogenes of one of the most efficient of these chemosen

63 loacae, Citrobacter freundii, and Klebsiella aerogenes only) or for third-generation cephalosporin-no

64 We prospectively enrolled patients with K. aerogenes or Enterobacter cloacae complex (Ecc) BSI from

65 lation control protein (NAC) from Klebsiella aerogenes or Escherichia coli (NACK or NACE, respectivel

66 trient agar with live P. aeruginosa, live E. aerogenes, or live S. maltophilia gave good recovery of

67 nt agar prepared with live P. aeruginosa, E. aerogenes, or S. maltophilia offer optimal recovery of A

68 a spp., Pseudomonas aeruginosa, Enterococcus aerogenes, Proteus vulgaris and Enterobacter sakazakii)

69 eria, such as Escherichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa and Salmonella Typhimu

70 urease metallocenter assembly in Klebsiella aerogenes requires the presence of several accessory pro

71 aeruginosa, Escherichia coli, and Klebsiella aerogenes rpoN mutants for a variety of rpoN mutant phen

72 sessed by uptake and digestion of Klebsiella aerogenes, showed that fewer bacteria were taken up by t

73 The G2 strain or Enterobacter aerogenes (Strain EA1) was selected for whole genome seq

74 Klebsiella aerogenes strains with reduced levels of D-amino acid de

75 umifaciens, Salmonella setubal, Enterobacter aerogenes) strains.

76 us demonstrated dose-dependent effects of P. aerogenes supernatant containing pax toxins.

77 lving clinical isolates of E. cloacae and E. aerogenes, susceptibility testing methods with polymyxin

78 , and/or BSI complication) was higher for K. aerogenes than Ecc BSI (32/46 [70%] versus 42/104 [40%];

79 Mutants of Escherichia coli and Klebsiella aerogenes that are deficient in glutamate synthase (glut

80 In Klebsiella aerogenes, the gdhA gene codes for glutamate dehydrogena

81 er aerogenes was recently renamed Klebsiella aerogenes This study aimed to identify differences in cl

82 hage carrying the put control region from K. aerogenes to identify the nucleotide residues important

83 well-founded proposal to rename Enterobacter aerogenes to Klebsiella aerogenes, based on whole-genome

84 flap covering the active site of Klebsiella aerogenes urease but does not play an essential role in

85 ia coli cells that expressed the complete K. aerogenes urease gene cluster with altered forms of ureE

86 n Escherichia coli strains containing the K. aerogenes urease gene cluster with the mutated ureE gene

87 Klebsiella aerogenes urease in a Ni-containing enzyme (two Ni per a

88 Assembly of the Klebsiella aerogenes urease metallocenter requires four accessory p

89 In vivo assembly of the Klebsiella aerogenes urease nickel metallocenter requires the prese

90 UreG from potato and the Klebsiella aerogenes urease operon defective in bacterial ureG were

91 Klebsiella aerogenes urease possesses a dinuclear metallocenter in

92 A mutant form of Klebsiella aerogenes urease possessing Ala instead of His at positi

93 Synthesis of active Klebsiella aerogenes urease requires four accessory proteins to gen

94 Klebsiella aerogenes urease uses a dinuclear nickel active site to

95 Klebsiella aerogenes urease uses a dinuclear nickel active site to

96 In the case of Klebsiella aerogenes urease, a nickel-containing enzyme, metallocen

97 Klebsiella aerogenes urease, a nickel-containing enzyme, provides a

98 aerogenes, Ni2+ binding to the wild-type K. aerogenes UreE protein, and Ni2+ and Zn2+ binding to the

99 Klebsiella aerogenes UreE, a metallochaperone that delivers nickel

100 Klebsiella aerogenes UreE, one of four accessory proteins involved

101 Herein, a Strep-tagged Klebsiella aerogenes UreG (UreG(Str)) and selected site-directed va

102 The plant gene complements the K. aerogenes ureG mutation, demonstrating that it encodes a

103 exin and coumarin are increased after the E. aerogenes VCs exposure.

104 Enterobacter aerogenes VCs lead to growth inhibition and immune respo

105 E. aerogenes VCs negatively regulate auxin response and tra

106 om transcriptional analysis suggests that E. aerogenes VCs trigger hypoxia response, innate immune re

107 osynthesis gene expression in response to E. aerogenes VCs, while MKK3 is the regulator of coumarin b

108 Additionally, MKK1 and MKK3 mediate the E. aerogenes VCs-induced callose deposition.

109 ; P = 0.3) differed between patients with K. aerogenes versus Ecc BSI, respectively.

110 nd bacterial genetics among patients with K. aerogenes versus Enterobacter species bloodstream infect

111 ry protein (Lrp), was cloned from Klebsiella aerogenes W70.

112 The gdhA gene from K. aerogenes was cloned and sequenced, and an insertion mut

113 The linkage of gdhA to trp in K. aerogenes was explained by postulating an inversion of t

114 P. aerogenes was isolated from 40% (8/20) of samples.

115 Enterobacter aerogenes was recently renamed Klebsiella aerogenes This

116 cter isolates (102 E. cloacae complex, 41 E. aerogenes) were tested, including 136 collected from Och