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   1 t may be subject to limitations when testing Enterobacter.                                           
     2 cteria including Pseudomonas, Shewanella and Enterobacter.                                           
  
     4 this test using PB against larger numbers of Enterobacter A total of 143 nonduplicate Enterobacter is
     5 acter cloacae (21), Acinetobacter spp. (13), Enterobacter aerogenes (11), Citrobacter spp. (10), Pseu
     6 ter spp. (6.2%), Serratia marcescens (5.5%), Enterobacter aerogenes (4.4%), Stenotrophomonas maltophi
     7 actam (<1% difference) for 6,938 isolates of Enterobacter aerogenes and 13,954 isolates of Enterobact
     8  selectivity of the method was examined with Enterobacter aerogenes and Enterobacter dissolvens, whic
  
  
  
    12 the human pathogens Klebsiella pneumonia and Enterobacter aerogenes, and would seem to suggest a subc
    13  Escherichia coli, Citrobacter freundii, and Enterobacter aerogenes, as well as Gram-positive Bacillu
    14 c media prepared with live or dead bacteria (Enterobacter aerogenes, E. coli, Klebsiella pneumoniae, 
    15 um cephalosporin-resistant Escherichia coli, Enterobacter aerogenes, Enterobacter cloacae complex, Kl
    16 ium, Serratia marcescens, Shigella flexneri, Enterobacter aerogenes, Klebsiella pneumoniae, Yersinia 
    17 oniae ACT-1, and the AmpC beta-lactamases of Enterobacter aerogenes, Morganella morganii, and Citroba
    18  several bacteria, such as Escherichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa and Salmo
  
  
  
  
    23  Proteus mirabilis, Citrobacter freundii and Enterobacter agglomerans [cyclo(DeltaAla-L-Val) only].  
  
    25 nism include its biochemical similarities to Enterobacter agglomerans, its apparent ability to cause 
    26 es are related to the chromosomal enzymes of Enterobacter and Citrobacter spp. and also mediate resis
  
  
    29 trogenesis by members of the genera Vibrio , Enterobacter , and Citrobacter and by Bacillus stratosph
    30  25% of individual species of Acinetobacter, Enterobacter, and coagulase-negative staphylococci recov
  
    32 eat that CO cannot differentiate Klebsiella, Enterobacter, and Serratia spp., enteric pathogens were 
    33 rial genera, including Salmonella, Yersinia, Enterobacter, and species of the plant pathogen, Erwinia
  
    35 he genera Stenotrophomonas, Pseudomonas, and Enterobacter are responsible for defense suppression.   
  
  
  
    39 m patients were Pseudomonas aeruginosa (22), Enterobacter cloacae (21), Acinetobacter spp. (13), Ente
    40 coli (18.8%), Klebsiella pneumoniae (14.2%), Enterobacter cloacae (9.1%), Acinetobacter spp. (6.2%), 
    41 hogens with interpretive criteria, excluding Enterobacter cloacae (98.3% S) and E. faecalis (86.0% S)
    42 m Staphylococcus aureus, and aac(3)-VIa from Enterobacter cloacae (conferring resistance to kanamycin
  
  
    45 1.9%), Escherichia coli (n = 129, 30.0%) and Enterobacter cloacae (n = 62, 14.4%) were the main Enter
    46   The oxygen-insensitive nitroreductase from Enterobacter cloacae (NR) catalyzes two-electron reducti
    47 linically important enzymes CTX-M-15, KPC-2, Enterobacter cloacae AmpC, Pseudomonas aeruginosa AmpC, 
  
  
  
    51 microbial bacteremia, and seven of these had Enterobacter cloacae and S. marcescens in the same cultu
    52 stant (IC(50), approximately 10,000 nM), and Enterobacter cloacae and Serratia marcescens were highly
    53 L49 antibodies were chemically conjugated to Enterobacter cloacae beta-lactamase (bL), and their abil
    54 nd the increasing clinical importance of the Enterobacter cloacae complex have often been discussed. 
    55 nt Escherichia coli, Enterobacter aerogenes, Enterobacter cloacae complex, Klebsiella pneumoniae, or 
  
  
    58  structure of the nitroreductase enzyme from Enterobacter cloacae has been determined for the oxidize
  
  
    61 rganisms, intraocular infection secondary to Enterobacter cloacae infection is a devastating disease 
  
  
    64 iae isolates, 3 Escherichia coli isolates, 5 Enterobacter cloacae isolates, 2 S. marcescens isolates,
    65  the x-ray structures of the D305A mutant of Enterobacter cloacae MurA and the D313A mutant of Escher
    66 tured and depicted the Cys-115-PEP adduct of Enterobacter cloacae MurA in various reaction states by 
    67 ablished that Cys115 of Escherichia coli and Enterobacter cloacae MurA is the active site nucleophile
    68 s been determined to be 8.3, by titration of Enterobacter cloacae MurA with the alkylating agent iodo
    69 d the x-ray structure of the C115S mutant of Enterobacter cloacae MurA, which was crystallized in the
    70 ies of the flavin mononucleotide cofactor of Enterobacter cloacae nitroreductase (NR), determined und
  
    72 ed reaction, cephalosporin hydrolysis by the Enterobacter cloacae P99 cephalosporinase (beta-lactam h
    73 dase of Streptomyces sp. R61, a PBP, and the Enterobacter cloacae P99 cephalosporinase, a class C bet
  
  
    76  to react with the class C beta-lactamase of Enterobacter cloacae P99 in two ways, by acylation and b
    77 stants for hydrolysis by beta-lactamase from Enterobacter cloacae P99 indicated kcat values of 476 +/
  
  
  
    81 cts on V/K for the class C beta-lactamase of Enterobacter cloacae P99 suggest an acyl-transfer transi
  
    83 hibited typical class A (TEM-2) and class C (Enterobacter cloacae P99) beta-lactamases in a time-depe
    84 , catalyzed by the class C beta-lactamase of Enterobacter cloacae P99, have been studied in order to 
    85 -2 antibody detected Escherichia coli CMY-2, Enterobacter cloacae P99, Klebsiella pneumoniae ACT-1, a
  
  
  
  
    90     The membrane-bound selenate reductase of Enterobacter cloacae SLD1a-1 is purified in low yield an
  
    92  C beta-lactamase from a clinical isolate of Enterobacter cloacae strain GC1 with improved hydrolytic
    93 fication of a Shiga toxin 1 (Stx1)-producing Enterobacter cloacae strain, M12X01451, from a human cli
    94 nterobacter aerogenes and 13,954 isolates of Enterobacter cloacae tested using a Vitek system; for th
    95 ing the melibiose-H(+) symporter (MelY) from Enterobacter cloacae that had enhanced fermentation on 1
    96 rates higher than the totals were noted with Enterobacter cloacae versus ampicillin-sulbactam, aztreo
  
  
  
   100 inst Escherichia coli, Klebsiella pneumonia, Enterobacter cloacae, Acinetobacter baumannii, and methi
   101  348 Klebsiella pneumoniae, one (<1%) of 890 Enterobacter cloacae, and one (1%) of 162 Enterobacter a
  
  
   104 oci from isolates of Serratia marcescens and Enterobacter cloacae, demonstrating the presence of in-f
   105 y Citrobacter freundii, Clostridium species, Enterobacter cloacae, Enterococcus faecalis, Klebsiella 
   106 fied in the Enterobacteria Escherichia coli, Enterobacter cloacae, Erwinia herbicola, and Salmonella 
   107 ing probes for pathogenic bacteria including Enterobacter cloacae, Escherichia coli J96, Pseudomonas 
   108  isolates of important Gram-negative species-Enterobacter cloacae, Escherichia coli, Klebsiella pneum
   109 several gram-negative bacteria, specifically Enterobacter cloacae, Pseudomonas aeruginosa, and Pantoe
   110 , invasive aspergillosis (20%, 3 of 15), and Enterobacter cloacae, Serratia marcescens, Pneumocystis 
   111 mis, E. coli O157:H7, Klebsiella pneumoniae, Enterobacter cloacae, Shigella dysenteriae, Salmonella e
  
   113 erial species such as Klebsiella pneumoniae, Enterobacter cloacae, Stenotrophomonas maltophilia, and 
  
  
  
  
  
  
  
  
  
   123 t on four cases of endophthalmitis caused by Enterobacter cloacae: two in patients with acute postope
   124 was examined with Enterobacter aerogenes and Enterobacter dissolvens, which did not produce any signi
   125 a decrease in Clostridium and an increase in Enterobacter, Escherichia/Shigella, and Pseudomonas in s
   126 the Escherichia, Salmonella, Klebsiella, and Enterobacter genera possess only a single LuxR homolog, 
   127 rs of the genera Escherichia, Klebsiella and Enterobacter, genera commonly associated with nosocomial
  
  
  
  
   132 describe the isolation and identification of Enterobacter intermedium from the gallbladder of a patie
   133  of Enterobacter A total of 143 nonduplicate Enterobacter isolates (102 E. cloacae complex, 41 E. aer
  
  
   136 del 1981 (DSM 2032) (desulfolysin [DLY]) and Enterobacter lignolyticus (formerly Enterobacter cloacae
  
   138 hanism consisting of two adjacent genes from Enterobacter lignolyticus, a rain forest soil bacterium 
   139 cteria identified in field-collected H. zea, Enterobacter ludwigii, induced expression of the tomato 
   140 immunized with this alpha-1,3-glucan-bearing Enterobacter (MK7) are protected against cockroach aller
  
  
  
  
  
  
  
  
   149 Enterococcus aerogenes, Proteus vulgaris and Enterobacter sakazakii) bacteria, with decoction present
  
  
   152  vehicle for an emerging foodborne pathogen, Enterobacter sakazakii, resulting in high mortality rate
  
   154 er per os challenge with exogenous bacteria (Enterobacter sp. and Serratia marcescens strain Db11) an
   155 exodon) was hydrolysed and used to cultivate Enterobacter sp. C2361 and Providencia sp. C1112 for the
  
   157 characterized a natural bacterial endophyte, Enterobacter sp. strain PDN3, of poplar trees, that rapi
   158 cticidal activity, and reestablishment of an Enterobacter sp. that normally resides in the midgut mic
  
   160 taphylococci, 1 Enterococcus faecalis, and 1 Enterobacter sp.) on terminal subculture of the AER bott
  
  
  
  
   165 ree hundred sixty-eight patients experienced Enterobacter species bacteremia and received at least 1 
  
  
   168 tation of polymyxin susceptibility tests for Enterobacter species should be undertaken with extreme c
   169 t with P. aeruginosa, Klebsiella species, or Enterobacter species susceptible to one of the marker an
  
  
   172      For polymyxin susceptibility testing of Enterobacter species, close attention must be paid to th
   173 ae (Klebsiella pneumoniae, Escherichia coli, Enterobacter species, etc.), Pseudomonas aeruginosa, and
  
  
  
   177 e, or intra-abdominal fluid cultures growing Enterobacter spp, Serratia spp, or Citrobacter spp were 
  
  
   180 scens, 5/6 with Citrobacter spp., 13/14 with Enterobacter spp., 23/24 with E. coli, 2/3 with K. oxyto
   181 neumoniae, 92.9%; Klebsiella oxytoca, 95.5%; Enterobacter spp., 99.3%; Pseudomonas aeruginosa, 98.9%;
  
   183 rgets (Acinetobacter spp., Citrobacter spp., Enterobacter spp., Escherichia coli/Shigella spp., Klebs
   184 dred consecutive, single patient isolates of Enterobacter spp., Serratia spp., Citrobacter spp., and 
  
   186 s), the second by Proteobacteria (Klebsiella/Enterobacter), the third by Bacteriodetes, and the fourt
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