ライフサイエンスコーパス: oxytoca

1 coli, Klebsiella pneumoniae, and Klebsiella oxytoca.

2 was discovered in both K. pneumoniae and K. oxytoca.

3 d klebicin D gene cluster was detected in K. oxytoca.

4 yclodextrin-specific channel from Klebsiella oxytoca.

5 coli, Klebsiella pneumoniae, and Klebsiella oxytoca.

6 involved in pullulanase export in Klebsiella oxytoca.

7 g isolates of E. coli, K. pneumoniae, and K. oxytoca.

8 The K. oxytoca 11492-1 draft genome contains multiple antibioti

9 bacter spp., 23/24 with E. coli, 2/3 with K. oxytoca, 16/17 with K. pneumoniae, and 0/1 with Proteus

10 (4.3%), Proteus mirabilis (4.0%), Klebsiella oxytoca (2.7%), and Citrobacter freundii (2.0%).

11 tections exceeded 96%, except for Klebsiella oxytoca (92.2%), which achieved 98.3% sensitivity after

12 0%; Klebsiella pneumoniae, 92.9%; Klebsiella oxytoca, 95.5%; Enterobacter spp., 99.3%; Pseudomonas ae

13 In a supplemental study of Klebsiella oxytoca, an organism possessing a chromosomal beta-lacta

14 d that 72% of Klebsiella sp. were Klebsiella oxytoca and 8.7% were K. planticola.

15 for all Klebsiella pneumoniae or Klebsiella oxytoca and E. coli isolates screened and confirmed as E

16 reases in common NICU organisms including K. oxytoca and E. faecalis and increases in common adult or

17 is associated frequently with strains of K. oxytoca and rarely with strains of K. pneumoniae.

18 lla pneumoniae, Escherichia coli, Klebsiella oxytoca, and Citrobacter freundii.

19 ella quintana, Shigella flexneri, Klebsiella oxytoca, and Cryptococcus neoformans.

20 f ESBLs in Klebsiella pneumoniae, Klebsiella oxytoca, and Escherichia coli.

21 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis isolates, including pheno

22 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, and Proteus mirabilis with an ertapenem-suscept

23 Our results show that these reactions in K. oxytoca are catalyzed by a two-component oxygenase (HpxE

24 olated and identified a toxin produced by K. oxytoca as the pyrrolobenzodiazepine tilivalline and dem

25 ost common, and of hyperproduction of the K. oxytoca beta-lactamase, a situation which engenders a le

26 nally discovered in the bacterium Klebsiella oxytoca, but it has recently been shown that mammalian A

27 Klebsiella oxytoca can assimilate nitrate and nitrite by using enzy

28 Klebsiella oxytoca can use nitrate and nitrite as sole nitrogen sou

29 chia coli, Klebsiella pneumoniae, Klebsiella oxytoca, Citrobacter koseri, Citrobacter freundii group,

30 guingly, the OM protein CymA from Klebsiella oxytoca does not depend on TonB but nevertheless mediate

31 urally relevant gene cluster from Klebsiella oxytoca encoding the nitrogen fixation pathway for conve

32 In Klebsiella oxytoca, enzymes required for nitrate assimilation are e

33 d the major pseudopilin GspG from Klebsiella oxytoca: EpsH contains a large beta-sheet in the variabl

34 cal isolates of K. pneumoniae and Klebsiella oxytoca for the presence of bla(KPC) genes.

35 ts, Hcp1, is required for killing Klebsiella oxytoca in vitro and that this activity is mediated by t

36 Finally, we show that K. oxytoca is killed in the host gut in an Hcp1-dependent m

37 tested an additional 43 stock strains of K. oxytoca isolated from newborns by using eight biochemica

38 linical isolates (39 K. pneumoniae and 30 K. oxytoca isolates).

39 r cloacae, Enterococcus faecalis, Klebsiella oxytoca, Klebsiella pneumoniae, and Staphylococcus aureu

40 , Escherichia coli/Shigella spp., Klebsiella oxytoca, Klebsiella pneumoniae, Proteus spp., Pseudomona

41 leotide sequence of the 51,601-bp Klebsiella oxytoca linear plasmid pKO2, and we demonstrate experime

42 combinants of Escherichia coli B, Klebsiella oxytoca M5A1, and Erwinia chrysanthemi EC16.

43 rformed with either panel and isolates of K. oxytoca, MICs of ceftazidime, cefotaxime, and ceftizoxim

44 it the modularity of a refactored Klebsiella oxytoca nitrogen fixation (nif) gene cluster (16 genes,

45 model for a T2SS pseudopilus from Klebsiella oxytoca, obtained by fitting the NMR structure of its ca

46 re of the protelomerase TelK from Klebsiella oxytoca phage varphiKO2, in complex with the palindromic

47 In Klebsiella oxytoca (pneumoniae), enzymes required for nitrate assim

48 cal in amino acid sequence to the Klebsiella oxytoca propanediol dehydratase; this is a much higher i

49 lly includes type II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carotovora (out)

50 Thus, several enzymes in this K. oxytoca purine utilization pathway differ from those in

51 lates of Citrobacter freundii and Klebsiella oxytoca recovered from different patients in a Michigan

52 ergrowth of the enteric bacterium Klebsiella oxytoca results in antibiotic-associated hemorrhagic col

53 rains of Clostridium perfringens, Klebsiella oxytoca, Staphylococcus aureus, and Bacteroides fragilis

54 Klebsiella oxytoca strain 11492-1 was isolated from a perianal swab

55 ySENI and StySGI R-M systems from Klebsiella oxytoca strain M5a1, Salmonella eastbourne, Salmonella e

56 omplex, Klebsiella pneumoniae, or Klebsiella oxytoca that were recovered from sterile-site or urine c

57 coli, Klebsiella pneumoniae, and Klebsiella oxytoca, there is an ever-increasing prevalence of beta-

58 ulE-K putative pilin genes of the Klebsiella oxytoca type II secretion system with the complete comG

59 The enterobacterium Klebsiella oxytoca uses a variety of inorganic and organic nitrogen

60 six isolates of Klebsiella pneumoniae and K. oxytoca were recovered from wild mammals in Australia.

61 milar to the pseudopilin found in Klebsiella oxytoca, while PilA2 is more similar to true pilins foun