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1 e-like amidohydrolase (HDAH) from Bordetella/Alcaligenes.
4 ree genes similar to the czc and cnr loci of Alcaligenes eutrophus and the ncc locus of Alcaligenes x
5 ntaining the synthetic operon and the native Alcaligenes eutrophus PHA operon were transformed into E
7 tive chemolithoautotroph Ralstonia eutropha (Alcaligenes eutrophus) that fully complements R. solanac
8 coding a homolog to the czcD gene product of Alcaligenes eutrophus, a lysR-type regulatory gene which
12 itrite-soaked reduced nitrite reductase from Alcaligenes faecalis have been determined at 1.8-2.0 A r
13 mutants (P80A and P80I) of pseudoazurin from Alcaligenes faecalis S-6 in oxidized and reduced forms a
17 ii, often referred to as B. avium-like or as Alcaligenes faecalis type II prior to 1995, have also be
18 ock method is described for fractionation of Alcaligenes faecalis which uses glucose to adjust osmoti
19 s a betaproteobacterium (previously known as Alcaligenes faecalis) that was an early isolate with ars
20 range of algicidal bacteria (mostly from the Alcaligenes, Flavobacterium/Cytophaga group and Pseudomo
21 ichia adecarboxylata, Comamonas acidovorans, Alcaligenes odorans, Bacillus globigii, and three strain
23 A crystal structure of the CBAL enzyme from Alcaligenes sp. AL3007 using multiwavelength anomalous d
24 the 4-monochlorobiphenyl degrading bacterium Alcaligenes sp. strain ALP83, was carried out to determi
25 Disseminating bacteria were identified as Alcaligenes species originating from host lymphoid tissu
26 past decade, potential pathogens, including Alcaligenes species, have been increasingly recovered fr
27 nflammation after ILC depletion in mice, and Alcaligenes-specific systemic immune responses were asso
29 d the frequency of correct identification of Alcaligenes spp. by microbiology laboratories affiliated
31 from Pseudomonas fluorescens and Pseudomonas alcaligenes, we isolated, from both pseudomonads, a thir
32 d-type copper nitrite reductase (wtNiR) from Alcaligenes xylosoxidans (36.5 kDa monomer), the "half-a
33 trosyl complex (5c-NO) of cytochrome c' from Alcaligenes xylosoxidans (AXCP) in which picosecond rebi
34 me c' (RCCP) have been compared to data from Alcaligenes xylosoxidans (AXCP), with the aim of underst
35 ists, as in the microbial cytochrome c' from Alcaligenes xylosoxidans (AxCYTcp), which forms a stable
36 We have isolated and characterised N2OR from Alcaligenes xylosoxidans (AxN2OR) as a homodimer of M(r)
37 tructures of the blue nitrite reductase from Alcaligenes xylosoxidans (AxNiR) are presented in the ox
38 Cu centres for the reduced form of NiR from Alcaligenes xylosoxidans (AxNiR) using X-ray absorption
39 ed in the blue copper nitrite reductase from Alcaligenes xylosoxidans (NCIMB 11015) by a combination
42 ce Raman (RR) studies have been conducted on Alcaligenes xylosoxidans cytochrome c', a mono-His ligat
43 gladioli strains, 9 Ralstonia sp. strains, 5 Alcaligenes xylosoxidans strains, 5 Stenotrophomonas mal
47 ia cepacia, Stenotrophomonas maltophilia, or Alcaligenes xylosoxidans; however, isolation of Candida
48 opportunistic human pathogen Achromobacter (Alcaligenes) xylosoxidans has been recovered with increa
49 notrophomonas maltophilia and Achromobacter (Alcaligenes) xylosoxidans have been increasingly recogni
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