ライフサイエンスコーパス: Paracoccus denitrificans

1 ry oxidases from Rhodobacter sphaeroides and Paracoccus denitrificans).

2 t mitochondria, Rhodobacter sphaeroides, and Paracoccus denitrificans).

3 this process has been studied extensively in Paracoccus denitrificans.

4 nters of nitrous oxide reductase (N2OR) from Paracoccus denitrificans.

5 Parabactin was extracted from cultures of Paracoccus denitrificans.

6 ytochromes to the cytochrome c peroxidase of Paracoccus denitrificans.

7 one production by Rhodobacter capsulatus and Paracoccus denitrificans.

8 ration during hypoxia, as does the bacterium Paracoccus denitrificans.

9 ion from previous work with the oxidase from Paracoccus denitrificans.

10 the CuA sites in COX of bovine heart and of Paracoccus denitrificans.

11 uA center in cytochrome c oxidase (COX) from Paracoccus denitrificans.

12 o those of the native CuA center in COX from Paracoccus denitrificans.

13 on (PDB code 1occ) and of the soil bacterium Paracoccus denitrificans (1arl) include a dicopper cente

14 igands to the native type I copper center of Paracoccus denitrificans amicyanin was replaced with the

15 g with antibodies raised against subunits of Paracoccus denitrificans and against synthetic peptides

16 l structures of the cytochrome oxidases from Paracoccus denitrificans and bovine.

17 Cytochrome aa3 from Paracoccus denitrificans and cytochrome ba3 from Thermus

18 between the cytochrome c peroxidase (CCP) of Paracoccus denitrificans and cytochromes c.

19 This is similar to COX from Paracoccus denitrificans and is in contrast to the bovin

20 acter sphaeroides is specifically related to Paracoccus denitrificans and Rc. gelatinosa is related t

21 t is a novel inhibitor of the F1FO-ATPase of Paracoccus denitrificans and related alpha-proteobacteri

22 lly simpler bacterial counterpart (NDH-1) in Paracoccus denitrificans and Thermus thermophilus HB-8 c

23 with structures of Rhodobacter sphaeroides, Paracoccus denitrificans, and bovine CcO derived by crys

24 ic to a bacterium related to R. sphaeroides, Paracoccus denitrificans, and is lethal to R. sphaeroide

25 Atp11p from Candida glabrata and Atp12p from Paracoccus denitrificans, and we show that some features

26 Control strains were Paracoccus denitrificans ATCC 17741(T), P. versutus ATCC

27 in the dimeric cytochrome bc(1) complex from Paracoccus denitrificans by characterizing the kinetics

28 previous papers, cytochrome c peroxidase of Paracoccus denitrificans can accommodate horse cytochrom

29 Cloning and sequencing of the Paracoccus denitrificans ccmG gene indicates that it cod

30 The NADH-quinone oxidoreductase from Paracoccus denitrificans consists of 14 subunits (Nqo1-1

31 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans consists of at least 14 unlike

32 Paracoccus denitrificans contains an unusual arrangement

33 chemical changes in the P(M) intermediate of Paracoccus denitrificans cytochrome c oxidase have been

34 The structure of the P(M) intermediate of Paracoccus denitrificans cytochrome c oxidase was invest

35 es of P(M) and F intermediates of bovine and Paracoccus denitrificans cytochrome c oxidase were inves

36 Paracoccus denitrificans cytochrome C550 is expressed as

37 Paracoccus denitrificans ETF has the identical function,

38 he three-dimensional structures of human and Paracoccus denitrificans ETFs determined by X-ray crysta

39 Our work with the model denitrifying strain Paracoccus denitrificans further shows that ligand-enhan

40 ic quinohemoprotein amine dehydrogenase from Paracoccus denitrificans has been determined at 2.05-A r

41 quinoprotein methylamine dehydrogenase from Paracoccus denitrificans has been refined at 1.75 A reso

42 oxidases, the equivalent tryptophan (W121 in Paracoccus denitrificans) has been identified as the "el

43 ccinate:ubiquinone oxidoreductase (SQR) from Paracoccus denitrificans have been undertaken in the pur

44 residue in both Saccharomyces cerevisiae and Paracoccus denitrificans have indicated that mutations a

45 of these ligands in supporting the growth of Paracoccus denitrificans in a low-iron environment and t

46 he zinc-specific SBP AztC from the bacterium Paracoccus denitrificans in the zinc-bound and apo-state

47 ATP synthase from the alpha-proteobacterium Paracoccus denitrificans, inhibited by its natural regul

48 Amicyanin from Paracoccus denitrificans is a type 1 copper protein with

49 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of 14 different sub

50 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of 14 different sub

51 e- (NADH-) quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 diff

52 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 subu

53 ating NADH-quinone oxidoreductase (NDH-1) of Paracoccus denitrificans is composed of at least 14 unli

54 We demonstrate that NarK from Paracoccus denitrificans is expressed as a fusion of two

55 esidues (Trp(beta)(57) and Trp(beta)(108) in Paracoccus denitrificans MADH).

56 Paracoccus denitrificans methylamine dehydrogenase (MADH

57 We demonstrated that in the Paracoccus denitrificans NDH-1 subunit, Nqo7 (ND3) direc

58 1-14, encode subunits homologous to those of Paracoccus denitrificans NDH-1, respectively, and are ar

59 Molecular properties of the NQO9 subunit of Paracoccus denitrificans NDH-1, which is predicted to co

60 The enzyme from Paracoccus denitrificans (NorBC) contains two subunits;

61 reported for the homologous D477A mutant of Paracoccus denitrificans or for bovine COX (K(d) = 1-3 m

62 y dependent on haem-iron as a cofactor (e.g. Paracoccus denitrificans) or a Nir that is solely depend

63 dicted from the known processing site of the Paracoccus denitrificans oxidase, does not produce the s

64 ification inhibition in a model denitrifier, Paracoccus denitrificans Pd1222.

65 esolution structure of the related MADH from Paracoccus denitrificans recently reported.

66 The NO reductase from Paracoccus denitrificans reduces NO to N2O (2NO + 2H(+)

67 sis of methylamine dehydrogenase (MADH) from Paracoccus denitrificans requires four genes in addition

68 sis of methylamine dehydrogenase (MADH) from Paracoccus denitrificans requires four genes in addition

69 alculations on the cytochrome c oxidase from Paracoccus denitrificans revealed an unexpected coupling

70 he amino acid sequence of cytochrome c550 of Paracoccus denitrificans strain LMD 52.44 was determined

71 dditionally conserved in Pichia pastoris and Paracoccus denitrificans, suggesting that they are funct

72 In Paracoccus denitrificans, the pathway-specific two-compo

73 The three-dimensional fold of Paracoccus denitrificans TIR is identical to that observ

74 ms from methane-acclimated sludge (including Paracoccus denitrificans) to facilitate electron transfe

75 Threonine 244 in the alpha subunit of Paracoccus denitrificans transfer flavoprotein (ETF) lie

76 based on the biological reduction of N2O by Paracoccus denitrificans using methanol as a carbon/elec

77 of electron transfer flavoprotein (ETF) from Paracoccus denitrificans was determined and refined to a

78 of the Type I copper protein, amicyanin from Paracoccus denitrificans was determined at 1.8 A resolut

79 rystal structure of a new cluster 9 SBP from Paracoccus denitrificans we have called AztC.

80 f this putative accessory factor (AztD) from Paracoccus denitrificans, we have analyzed its transcrip

81 ria (from Bos taurus) and from the bacterium Paracoccus denitrificans, we show that four protons are

82 , also observed in cytochrome c oxidase from Paracoccus denitrificans, were similarly associated with

83 species, such as Rhodobacter sphaeroides and Paracoccus denitrificans, which contain an additional mi

84 ing NADH-quinone oxidoreductase (NDH-1) from Paracoccus denitrificans, which is composed of the NQO1

85 Human and Paracoccus denitrificans wild-type electron transfer fla

86 of the type I copper protein amicyanin from Paracoccus denitrificans with cobalt.

87 Expression in Paracoccus denitrificans yielded no holoprotein.

88 unction, as revealed by the structure of the Paracoccus denitrificans zeta-subunit in complex with AD