ライフサイエンスコーパス: diazotrophic

1 Herbaspirillum seropedicae is a diazotrophic and endophytic bacterium that associates wi

2 unknown multispecies true-moss-cyanobacteria diazotrophic association.

3 A wide range of rhizosphere diazotrophic bacteria are able to establish beneficial a

4 associations with associative and endophytic diazotrophic bacteria.

5 associated genes so far characterized in any diazotrophic bacterial species.

6 at thrive in stratified water and can harbor diazotrophic bacterial symbionts, but does not support e

7 olybdenum for nitrogen fixation in the model diazotrophic bacterium Azotobacter vinelandii.

8 , significant variations are observed in the diazotrophic behavior of these microbes.

9 hrome c oxidase operons and heterotrophic or diazotrophic capabilities.

10 Our characterization of the ETSP diazotrophic community along a gradient from upwelling-i

11 Our results indicate that the diazotrophic community expressing nifH was primarily rep

12 tropical oceans, where they can dominate the diazotrophic community in regions with high inputs of th

13 on based on the growth of the filament under diazotrophic conditions.

14 ubunits for nitrogenase 3 under Mo-deficient diazotrophic conditions.

15 ws growth to accelerate substantially when a diazotrophic culture is switched to ammonia.

16 nd addition of alanine to a nitrogen-fixing (diazotrophic) culture caused partial switch-off of nitro

17 e dominant marine N2 fixers, but unicellular diazotrophic cyanobacteria and bacterioplankton have rec

18 Nitrogen fixation by diazotrophic cyanobacteria is a critical source of new n

19 Colonial diazotrophic cyanobacteria of the genus Trichodesmium ar

20 Unicellular diazotrophic cyanobacteria such as Cyanothece sp. ATCC 5

21 equencing showed a significant selection for diazotrophic cyanobacteria such as Nostoc punctiforme an

22 of genes in Cyanothece and other unicellular diazotrophic cyanobacteria, a comprehensive study of tra

23 n the nitrogen-fixing ability of unicellular diazotrophic cyanobacteria, we analyzed six members of t

24 The unicellular, diazotrophic cyanobacterium Cyanothece sp. ATCC 51142 de

25 erential gene expression in the unicellular, diazotrophic cyanobacterium Cyanothece sp. strain ATCC 5

26 othece sp. strain PCC 7822 is a unicellular, diazotrophic cyanobacterium that can produce large quant

27 hece sp. strain ATCC 51142 is a unicellular, diazotrophic cyanobacterium which demonstrated extensive

28 be Cyanothece sp. ATCC 51142, a unicellular, diazotrophic cyanobacterium with the capacity to generat

29 C by developing a genome-scale model for the diazotrophic cyanobacterium, Cyanothece sp. ATCC 51142.

30 othece sp. strain ATCC 51142, a unicellular, diazotrophic cyanobacterium, demonstrated extensive meta

31 The diazotrophic cyanobacterium, Trichodesmium, is an integr

32 overall hypothesis that naturally occurring diazotrophic endophytes impart growth promotion of the h

33 T1, H1, and P1-2 as a non-Streptomycete, non-diazotrophic, facultative chemolithoautotroph and conclu

34 nfR are required for nitrogenase 3-dependent diazotrophic growth and 15N2 incorporation but not for a

35 ant strains constructed were capable of good diazotrophic growth and also contained FeMo cofactor as

36 Y51F strains were significantly impaired for diazotrophic growth and expression of a nifH-lacZ fusion

37 both nafY and nifX are severely affected in diazotrophic growth and extractable dinitrogenase activi

38 and tungsten (W) oxide nanoparticles on the diazotrophic growth and metals acquisition in pure cultu

39 ced reduction in heterocyst frequency during diazotrophic growth and reduced vegetative cell size com

40 that highlight the significant advantages of diazotrophic growth in the presence of Mo.

41 W specifically inhibited diazotrophic growth in the presence of Mo.

42 mg.L(-1)) TiO(2) NPs have no effects on the diazotrophic growth of A. vinelandii while WO(3) NPs are

43 Stimulation of diazotrophic growth of M. barkeri 227 by V in the absenc

44 of molybdenum, vanadium, and tungsten on the diazotrophic growth of Methanococcus maripaludis.

45 nces between Mo-dependent and Mo-independent diazotrophic growth that highlight the significant advan

46 of anfR, does not appear to be required for diazotrophic growth under Mo- and V-deficient conditions

47 red for fully functional AnfO as measured by diazotrophic growth under Mo- and V-deficient conditions

48 stream of anfK were shown to be required for diazotrophic growth under Mo- and V-deficient conditions

49 F, caused a transient defect in establishing diazotrophic growth, manifested as a strong and prolonge

50 which is required for effective V-dependent diazotrophic growth, was identified.

51 ant showed normal heterocyst development and diazotrophic growth, which could indicate that it is not

52 l-arginine, and was impaired specifically in diazotrophic growth.

53 n-to-MoFe protein ratio required for optimal diazotrophic growth.

54 ar exchange, heterocyst differentiation, and diazotrophic growth.

55 of molecular exchange as filaments adapt to diazotrophic growth.

56 trogen-fixing capacity and, consequently, in diazotrophic growth.

57 of sigD and sigE mutant strains to establish diazotrophic growth.

58 e of aerobic, anaerobic, photosynthetic, and diazotrophic growth.

59 was the same as that found in part in other diazotrophic methanogens and except for the presence of

60 t are encoded within the nif gene cluster of diazotrophic methanogens.

61 Nitrogen-fixing (diazotrophic) microorganisms regulate productivity in di

62 oceans, generating a selective advantage for diazotrophic organisms capable of fixing atmospheric din

63 All diazotrophic organisms sequenced to date encode a molybd

64 In diazotrophic organisms, nitrogenase synthesis and activi

65 ng bacteria ensures widespread selection for diazotrophic phytoplankton that replenish this essential

66 Nitrogen (N) fixation by diazotrophic plankton is the primary source of this cruc

67 ric dinitrogen into bioavailable ammonium in diazotrophic prokaryotes.

68 l Atlantic thus appears to be defined by the diazotrophic response to spatial-temporal variability in

69 In several diazotrophic species of Proteobacteria, P(II) signal tra

70 Ammonia switch-off occurs in diazotrophic species of the methanogenic Archaea as well

71 lasticity in autotrophic, heterotrophic, and diazotrophic strategies supporting microbial communities

72 , CyanoHABs may switch from non-N2 fixing to diazotrophic taxa, with no net improvement in water qual

73 unity succession, with warming favouring non-diazotrophic taxa.

74 tions of N2 fixation and the distribution of diazotrophic Trichodesmium spp. indicate that movement i