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1  MSH was not found in representatives of the Arthrobacter, Agromyces, or Actinomyces genera.
2 he broad-specificity triazine hydrolase from Arthrobacter and Nocardioides spp., is reportedly in the
3 enzoyl-CoA dehalogenation pathway in certain Arthrobacter and Pseudomonas bacterial species contains
4                                Chitinophaga, Arthrobacter, and Renibacterium were common in Brood X,
5 n isotope effects in atrazine degradation by Arthrobacter aurescens TC1 (i) delivered highly characte
6 teny to the Arthrobacter sp. strain FB24 and Arthrobacter aurescens TC1 genomes, but it is approximat
7 t pesticide, atrazine, during cultivation of Arthrobacter aurescens TC1 in chemostat under four diffe
8 n at low dilution/growth rates by the strain Arthrobacter aurescens TC1.
9  (Proteus vulgaris) and chondroitinase ACII (Arthrobacter aurescens), having action patterns previous
10                                           An Arthrobacter beta-galactosidase has homology with the ly
11                Four isolates from the genera Arthrobacter, Brevibacterium, and Microbacterium, which
12 pecies, which we propose to name as follows: Arthrobacter burdickii IIF3SC-B10(T) (= NRRL B-65660(T)
13             All the above data suggests that Arthrobacter can be considered as an excellent PGP rhizo
14 on of the pollutant 4-chlorophenol (4-CP) by Arthrobacter chlorophenolicus A6, this study targeted a
15 ommon member of the Plains bison microbiome, Arthrobacter citreus (BSH(Ac)).
16 NA amplicon sequencing showed that the genus Arthrobacter comprised more than 21% of the total commun
17 it is approximately 1.9 Mb smaller than both Arthrobacter genomes and has a lower G+C content, sugges
18 is reaction in phenylethylamine oxidase from Arthrobacter globiformis (AGAO) has been determined.
19 he activity of the copper amine oxidase from Arthrobacter globiformis (AGAO), with K(i) values betwee
20 ses from Brevibacterium fuscum (Fe-HPCD) and Arthrobacter globiformis (Mn-MndD) that share high seque
21 O), human kidney diamine oxidase (KDAO), and Arthrobacter globiformis amine oxidase (AGAO) to examine
22 ver reoxidation by O(2) of substrate-reduced Arthrobacter globiformis amine oxidase (AGAO) under a wi
23 binant human kidney diamine oxidase (rhDAO), Arthrobacter globiformis amine oxidase (AGAO), and Pichi
24 e (EPAO), pea seedling amine oxidase (PSAO), Arthrobacter globiformis amine oxidase (AGAO), Escherich
25 sis (preprocessed) active site of the enzyme Arthrobacter globiformis amine oxidase (AGAO).
26 otocatechuate 2,3-dioxygenases isolated from Arthrobacter globiformis and Brevibacterium fuscum have
27 ined their toxicity toward the soil bacteria Arthrobacter globiformis and the Collembola Folsomia can
28 rated a lysine residue in the active site of Arthrobacter globiformis CAO (AGAO) by site-directed mut
29 oxyphenylacetate 2,3-dioxygenase (MndD) from Arthrobacter globiformis CM-2 is dependent on manganese
30 ication for apophenylethylamine oxidase from Arthrobacter globiformis has been developed, which avoid
31 mber of mutant forms of choline oxidase from Arthrobacter globiformis have recently been carried out,
32 4-dihydroxyphenylactate 2,3-dioxygenase from Arthrobacter globiformis strain CM-2 (MndD) cloned in Es
33 xidase (DMGO) is a covalent flavoenzyme from Arthrobacter globiformis that catalyzes the oxidative de
34 hylglycine oxidase (DMGO) from the bacterium Arthrobacter globiformis, a bifunctional enzyme that cat
35 is the flavin-dependent choline oxidase from Arthrobacter globiformis, for which structural, mechanis
36 d for wild-type HPAO, the amine oxidase from Arthrobacter globiformis, pea seedling amine oxidase at
37  TPQ in phenylethylamine oxidase (PEAO) from Arthrobacter globiformis, we have identified the C=O str
38 er) with a chloroplast-targeted codA gene of Arthrobacter globiformis, which encodes choline oxidase
39 functional dimethylglycine oxidase (DMGO) of Arthrobacter globiformis.
40 ne oxidase (PEAO) and histamine oxidase from Arthrobacter globiformis.
41             We further show that free-living Arthrobacter induces the surface colonization by scaveng
42 benzoates) were converted by phthalate-grown Arthrobacter keyseri (formerly Micrococcus sp.) 12B to t
43       We developed and validated a multistep Arthrobacter luteus (Alu)-PCR that specifically amplifie
44 erse bacterial hosts, including Escherichia, Arthrobacter, Mycobacterium, Rhodobacter, Staphylococcus
45 with sialidase from Clostridium perfringens, Arthrobacter neurofaciens, or Streptococcus, but not Vib
46 synthesized through sol-gel encapsulation of Arthrobacter nicotianae, a bacterium that selectively ad
47 y-4-oxoquinaldine 2,4-dioxygenase (HOD) from Arthrobacter nitroguajacolicus Ru61a and 1-H-3-hydroxy-4
48 rol microorganisms including actinobacteria (Arthrobacter, Nocardioides and Gaiella) and unclassified
49 e broken by ROS first, while biodegradation (Arthrobacter oryzae and Bacillus sp.) played a relativel
50  the endo-beta-N-acetylglucosaminidases from Arthrobacter protophormiae (Endo-A) and Mucor hiemalis (
51   The endo-beta-N-acetylglucosaminidase from Arthrobacter protophormiae (Endo-A) is of particular int
52                              The enzyme from Arthrobacter protophormiae (Endo-A) was found to be rema
53 f the endo-beta-N-acetylglucosaminidase from Arthrobacter protophormiae (Endo-A) with synthetic sugar
54 undance of beneficial soil bacteria, such as Arthrobacter, rather than decreasing the abundances of p
55 22G/H130Y/D36A/E263Q) of wild-type NylC from Arthrobacter sp. (plasmid pOAD2-encoding enzyme), with a
56         Studies with sarcosine oxidases from Arthrobacter sp. and Pseudomonas sp. show that these het
57 arbamoylsarcosine amidohydrolase (CSHase) of Arthrobacter sp. and YcaC of Escherichia coli, a protein
58 to convert the D-selective hydantoinase from Arthrobacter sp. DSM 9771 into an L-selective enzyme and
59 illus spharericus JS905, Pseudomonas sp. 1A, Arthrobacter sp. JS443, Pseudomonas putida B2) in the pH
60 zoyl-coenzyme A (4-HB-CoA) thioesterase from Arthrobacter sp. strain AU catalyzes the hydrolysis of 4
61 enome has extended regions of synteny to the Arthrobacter sp. strain FB24 and Arthrobacter aurescens
62 es of a p-nitrophenol catabolic pathway from Arthrobacter sp. strain JS443, was cloned and sequenced.
63 oyl-coenzyme A (4-HBA-CoA) thioesterase from Arthrobacter sp. strain SU in the millisecond time domai
64 f the 4-hydroxybenzoyl-CoA thioesterase from Arthrobacter sp. strain SU.
65 hat it was phylogenetically related to other Arthrobacter species.
66 taphylococcus warneri, Flectobacillus major, Arthrobacter stackebrantii, and Flavobacterium sp. and t
67           Our results indicate that isolated Arthrobacter strains present a very high genetic diversi
68                                           55 Arthrobacter strains were isolated and characterized usi
69 brosis patients, with P. aeruginosa and with Arthrobacter, suggesting that formation of hydroxylated
70 piratory activity of carbonate-precipitating Arthrobacter sulfonivorans , isolated from the recently
71                                       In the Arthrobacter thioesterase, each of the four active sites
72 rs that Glu73 is the active site base in the Arthrobacter thioesterase.
73 mis was increased by applying sialidase from Arthrobacter ureafaciens (AUSA) with CAGE on the skin fo
74  was reversed by treatment of the cells with Arthrobacter ureafaciens sialidase, indicating that sial
75 stion studies, treatment with sialidase from Arthrobacter ureafaciens--which hydrolyzed mucin-associa