ライフサイエンスコーパス: Alcaligenes

1 e-like amidohydrolase (HDAH) from Bordetella/Alcaligenes.

2 ion were the gram negative alkaline tolerant Alcaligenes and gram positive Corynebacterium.

3 ftia and Pseudoperonospora at 30,000 ft; and Alcaligenes and Penicillium at 40,000 ft.

4 ization of a super-integron from Pseudomonas alcaligenes ATCC 55044.

5 ree genes similar to the czc and cnr loci of Alcaligenes eutrophus and the ncc locus of Alcaligenes x

6 ntaining the synthetic operon and the native Alcaligenes eutrophus PHA operon were transformed into E

7 enase (TfdA) in Ralstonia eutropha (formerly Alcaligenes eutrophus) JMP134.

8 tive chemolithoautotroph Ralstonia eutropha (Alcaligenes eutrophus) that fully complements R. solanac

9 coding a homolog to the czcD gene product of Alcaligenes eutrophus, a lysR-type regulatory gene which

10 FlavoHbs from Saccharomyces cerevisiae, Alcaligenes eutrophus, and Escherichia coli share simila

11 various organisms such as Escherichia coli, Alcaligenes eutrophus, and Saccharomyces cerevisiae.

12 ter protein) of Escherichia coli and norA of Alcaligenes eutrophus, respectively.

13 oxybutyrate (BHB) dehydrogenase (BHBDh) from Alcaligenes faecalis (AfBHBDh) as a representative NAD(+

14 Furthermore, outer membrane vesicles from Alcaligenes faecalis also induced intestinal Th17 cells

15 itrite-soaked reduced nitrite reductase from Alcaligenes faecalis have been determined at 1.8-2.0 A r

16 Alcaligenes faecalis proteins were endocytosed by CD4(+)

17 mutants (P80A and P80I) of pseudoazurin from Alcaligenes faecalis S-6 in oxidized and reduced forms a

18 A carbapenem-resistant Alcaligenes faecalis strain was isolated from a surveill

19 nsecticidal protein named AfIP-1A/1B from an Alcaligenes faecalis strain.

20 Alcaligenes faecalis subsp. faecalis NCIB 8687, the beta

21 ii, often referred to as B. avium-like or as Alcaligenes faecalis type II prior to 1995, have also be

22 we reported that colonization of ubiquitous Alcaligenes faecalis was sufficient to induce intestinal

23 ock method is described for fractionation of Alcaligenes faecalis which uses glucose to adjust osmoti

24 s a betaproteobacterium (previously known as Alcaligenes faecalis) that was an early isolate with ars

25 Here, we focused on Alcaligenes faecalis, a Gram-negative bacterium that is

26 To this end, six treatments were studied: Alcaligenes faecalis, Bacillus amyloliquefaciens, CB, PG

27 anders" such as Corynebacterium striatum and Alcaligenes faecalis, typically considered commensals or

28 range of algicidal bacteria (mostly from the Alcaligenes, Flavobacterium/Cytophaga group and Pseudomo

29 genera such as Paracoccus, Pseudomonas, and Alcaligenes have evolved to use DMF as a sole carbon and

30 The functional EPS produced by Pseudomonas alcaligenes Med1 from Central Andean Chilean hot spring

31 wth from 34-44 degrees C) strain Pseudomonas alcaligenes Med1 from Medano hot spring (39.1 degrees C

32 Whole genome of P. alcaligenes Med1 has also been studied in detail to corr

33 ichia adecarboxylata, Comamonas acidovorans, Alcaligenes odorans, Bacillus globigii, and three strain

34 sely resembles Bordetella bronchiseptica and Alcaligenes sp.

35 A crystal structure of the CBAL enzyme from Alcaligenes sp. AL3007 using multiwavelength anomalous d

36 the 4-monochlorobiphenyl degrading bacterium Alcaligenes sp. strain ALP83, was carried out to determi

37 Disseminating bacteria were identified as Alcaligenes species originating from host lymphoid tissu

38 past decade, potential pathogens, including Alcaligenes species, have been increasingly recovered fr

39 nflammation after ILC depletion in mice, and Alcaligenes-specific systemic immune responses were asso

40 ielded the result P. fluorescens/putida) and Alcaligenes spp.

41 d the frequency of correct identification of Alcaligenes spp. by microbiology laboratories affiliated

42 Alcaligenes was sufficient to promote systemic inflammat

43 from Pseudomonas fluorescens and Pseudomonas alcaligenes, we isolated, from both pseudomonads, a thir

44 d-type copper nitrite reductase (wtNiR) from Alcaligenes xylosoxidans (36.5 kDa monomer), the "half-a

45 trosyl complex (5c-NO) of cytochrome c' from Alcaligenes xylosoxidans (AXCP) in which picosecond rebi

46 me c' (RCCP) have been compared to data from Alcaligenes xylosoxidans (AXCP), with the aim of underst

47 ists, as in the microbial cytochrome c' from Alcaligenes xylosoxidans (AxCYTcp), which forms a stable

48 We have isolated and characterised N2OR from Alcaligenes xylosoxidans (AxN2OR) as a homodimer of M(r)

49 tructures of the blue nitrite reductase from Alcaligenes xylosoxidans (AxNiR) are presented in the ox

50 Cu centres for the reduced form of NiR from Alcaligenes xylosoxidans (AxNiR) using X-ray absorption

51 ed in the blue copper nitrite reductase from Alcaligenes xylosoxidans (NCIMB 11015) by a combination

52 The bacterial heme protein Alcaligenes xylosoxidans cytochrome c' (AXCP) forms a no

53 The 5-coordinate ferrous heme of Alcaligenes xylosoxidans cytochrome c' reacts with NO to

54 ce Raman (RR) studies have been conducted on Alcaligenes xylosoxidans cytochrome c', a mono-His ligat

55 gladioli strains, 9 Ralstonia sp. strains, 5 Alcaligenes xylosoxidans strains, 5 Stenotrophomonas mal

56 a 2.2 angstrom cryoEM structure of qNOR from Alcaligenes xylosoxidans, an opportunistic pathogen and

57 identified by the referring laboratories as Alcaligenes xylosoxidans.

58 d NO-bound forms of the reduced protein from Alcaligenes xylosoxidans.

59 f Alcaligenes eutrophus and the ncc locus of Alcaligenes xylosoxidans.

60 ia cepacia, Stenotrophomonas maltophilia, or Alcaligenes xylosoxidans; however, isolation of Candida

61 opportunistic human pathogen Achromobacter (Alcaligenes) xylosoxidans has been recovered with increa

62 notrophomonas maltophilia and Achromobacter (Alcaligenes) xylosoxidans have been increasingly recogni