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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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