ライフサイエンスコーパス: aerogenes

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

2 far smaller plaques on a lawn of Klebsiella aerogenes.

3 oli, Klebsiella pneumoniae, and Enterobacter aerogenes.

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

5 lasmid previously isolated from Enterobacter aerogenes.

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

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

8 nonnutrient agar overlaid with Enterobacter aerogenes.

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

10 %), Serratia marcescens (5.5%), Enterobacter aerogenes (4.4%), Stenotrophomonas maltophilia (4.3%), P

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Klebsiella aerogenes urease possesses a dinuclear metallocenter in

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

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

66 Klebsiella aerogenes urease uses a dinuclear nickel active site to

67 Klebsiella aerogenes urease uses a dinuclear nickel active site to

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

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

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

71 Klebsiella aerogenes UreE, a metallochaperone that delivers nickel

72 Klebsiella aerogenes UreE, one of four accessory proteins involved

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

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

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

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

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

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