ライフサイエンスコーパス: anaerobic respiration

1 oxides as terminal electron acceptors during anaerobic respiration.

2 ), has a regulatory role in both aerobic and anaerobic respiration.

3 compounds as terminal electron acceptors for anaerobic respiration.

4 ly stage in the regulatory pathway governing anaerobic respiration.

5 sduction system is essential for aerobic and anaerobic respiration.

6 Mn(IV) as terminal electron acceptors during anaerobic respiration.

7 nerals that serve as a source of Fe(III) for anaerobic respiration.

8 bolic dynamics of the switch from aerobic to anaerobic respiration.

9 e as an alternative electron acceptor during anaerobic respiration.

10 on in both cell lines, indicating a shift to anaerobic respiration.

11 riaceae by generating electron acceptors for anaerobic respiration.

12 to proton release into the periplasm during anaerobic respiration.

13 dept at dissipating reducing equivalents via anaerobic respiration.

14 activation of genes involved in aerobic and anaerobic respiration.

15 mic distribution that are mostly involved in anaerobic respiration.

16 c ions as terminal electron acceptors during anaerobic respiration.

17 yclic AMP receptor protein, CRP, to regulate anaerobic respiration.

18 widespread in bacteria and often function in anaerobic respiration.

19 rons directly to Fe(III) in a mineral during anaerobic respiration.

20 (III)] as terminal electron acceptors during anaerobic respiration.

21 similation, methylation, detoxification, and anaerobic respiration.

22 ood about how it regulates genes involved in anaerobic respiration.

23 ase (napFDAGHBC operon product) functions in anaerobic respiration.

24 ther electron acceptors such as fumarate for anaerobic respiration.

25 xpanded by using inflammatory byproducts for anaerobic respiration.

26 showed that the dms operon is induced during anaerobic respiration.

27 g point for defining this organism's complex anaerobic respiration.

28 organisms as a terminal electron acceptor in anaerobic respiration.

29 tation, hydrogen metabolism, and aerobic and anaerobic respiration.

30 erobic biofilms, due, in part, to defects in anaerobic respiration.

31 ent accumulation of toxic NO, a byproduct of anaerobic respiration.

32 ble to use nitrate for both assimilation and anaerobic respiration.

33 regulation of genes involved in aerobic and anaerobic respiration.

34 ion balancing mechanisms during phototrophic anaerobic respiration.

35 hat utilize a fumarate reductase pathway for anaerobic respiration, an important example being the pa

36 s into three putative functional groups: (1) anaerobic respiration and cytokinin-mediated delay in se

37 ns MR-1 has emerged as a good model to study anaerobic respiration and electron transport-linked meta

38 of inducing stimuli by switching the cell to anaerobic respiration and fermentation and by down-regul

39 cells to rely more on fatty acid oxidation, anaerobic respiration and fermentation for ATP productio

40 ession of many genes known to be involved in anaerobic respiration and fermentation was increased und

41 hesis, macromolecular synthesis, and aerobic/anaerobic respiration and fermentation.

42 r controlling many genes involved in aerobic/anaerobic respiration and fermentative metabolism in Esc

43 ssociated with oxidative/nitrosative stress, anaerobic respiration and lactate metabolism.

44 d that CyaC plays a major role in regulating anaerobic respiration and may contribute to additional s

45 s that have been linked to the exhibition of anaerobic respiration and swarming motility were upregul

46 these operons, namely, the ones involved in anaerobic respiration and the Entner-Doudoroff pathway.

47 m smegmatis can switch between fermentation, anaerobic respiration, and aerobic respiration.

48 ative and osmotic stress, defense responses, anaerobic respiration, and cell wall and carbohydrate me

49 phototrophy, scavenging of molecular oxygen, anaerobic respiration, and fermentation.

50 rogram, converts the microbe from aerobic to anaerobic respiration, and induces a dormancy regulon.

51 fting microbial metabolism to less efficient anaerobic respiration, and selectively protecting otherw

52 se, like fumarate reductase, can function in anaerobic respiration but does not constitute a site for

53 Many Tat substrates are involved in anaerobic respiration, but we show that a mutant complet

54 oxidoreductase [QFR]), which participates in anaerobic respiration by E. coli.

55 ic chemical species, and biologically during anaerobic respiration by microbes.

56 As a consequence anaerobic respiration by tetrathionate reduction is like

57 downregulation of the dms operon and loss of anaerobic respiration capability, respectively.

58 ation was dependent on both microaerobic and anaerobic respiration, consistent with the hypothesis th

59 Novel forms of anaerobic respiration continue to be discovered.

60 h, genes for arginine fermentation (arc) and anaerobic respiration (dms), using trimethylamine N-oxid

61 ed genes required for amino acid metabolism, anaerobic respiration, DNA repair, the heat shock respon

62 a-inducible factor HIF-1 is known to promote anaerobic respiration during low oxygen conditions (hypo

63 on of GAPDH and the subsequent inhibition of anaerobic respiration exacerbate ATP depletion selective

64 yanions can serve as an electron acceptor in anaerobic respiration, forming distinct nanoparticles of

65 ence tolerance-associated pathways governing anaerobic respiration, hormone responses, and antioxidan

66 nt ResE, in global regulation of aerobic and anaerobic respiration i B.subtilis.

67 are positive regulators of both aerobic and anaerobic respiration in B. subtilis.

68 nsduction system is required for aerobic and anaerobic respiration in Bacillus subtilis.

69 sduction system is essential for aerobic and anaerobic respiration in Bacillus subtilis.

70 anscription of genes involved in aerobic and anaerobic respiration in Bacillus subtilis.

71 Here, we further explore the role of anaerobic respiration in colonization using the streptom

72 t RavA-ViaA are functionally associated with anaerobic respiration in Escherichia coli through intera

73 ulating sporulation in Bacillus subtilis and anaerobic respiration in Escherichia coli.

74 ) reductase (Hdr), a key enzyme required for anaerobic respiration in methane-producing archaea.

75 erefore, we examined the spatial profiles of anaerobic respiration in N. gonorrhoeae, using an aniA'-

76 iminase and nitrate reduction) that controls anaerobic respiration in P. aeruginosa.

77 Protection from NO gas, a toxic byproduct of anaerobic respiration in Pseudomonas aeruginosa, is medi

78 was previously implicated in the control of anaerobic respiration in response to the cellular NADH/N

79 Rhodoquinone (RQ) is a required cofactor for anaerobic respiration in Rhodospirillum rubrum, and it i

80 nging to the NapC/NirT family and central to anaerobic respiration in Shewanella sp.

81 e diverse growth modes--aerobic respiration, anaerobic respiration in the dark, and anaerobic photosy

82 haem A biosynthesis, and it is required for anaerobic respiration in this organism.

83 RP and cAMP play a role in the regulation of anaerobic respiration, in addition to their known roles

84 lecule as the terminal electron acceptor for anaerobic respiration, in which process it produces exce

85 use several terminal electron acceptors for anaerobic respiration, including fumarate, nitrate, dime

86 Furthermore, anaerobic respiration is becoming increasing recognized

87 Endogenous S-nitrosylation during anaerobic respiration is controlled by the transcription

88 but can also enhance biofilm formation once anaerobic respiration is initiated.

89 We found that anaerobic respiration occurs predominantly in the substr

90 We probe anaerobic respiration of bacteria in the presence of con

91 ate that one (SO1427-SO1432) is required for anaerobic respiration of DMSO.

92 For example, bacterial anaerobic respiration of ferric iron or the toxic metall

93 ement by up-regulating genes associated with anaerobic respiration of glycerol; supporting this findi

94 ion, anaerobic sulfate/sulfite reduction and anaerobic respiration of organic sulfur.

95 We have investigated anaerobic respiration of the archaeal model organism Hal

96 d that dmsR, dmsA, and dmsD are required for anaerobic respiration on DMSO and TMAO.

97 tion of S. putrefaciens proteins involved in anaerobic respiration on Fe(III) and Mn(IV).

98 -nitrosylation is an obligate concomitant of anaerobic respiration on nitrate in Escherichia coli.

99 ells generate energy by aerobic respiration, anaerobic respiration, or photosynthesis.

100 involved in pyoverdine-mediated iron-uptake, anaerobic respiration, osmotic stress defense, motility,

101 sulfate as a terminal electron acceptor for anaerobic respiration play a central role in the global

102 naquinone, and are necessary for aerobic and anaerobic respiration respectively.

103 e reductase (QFR) participate in aerobic and anaerobic respiration, respectively.

104 [Sb(V)] as a terminal electron acceptor for anaerobic respiration, resulting in the precipitation of

105 e show that a mutant completely deficient in anaerobic respiration retains full virulence in both the

106 like other bacteria that use FNR to regulate anaerobic respiration, Shewanella oneidensis MR-1 uses t

107 including pathways for CO2 and N2 fixation, anaerobic respiration, sulfur oxidation, fermentation an

108 abolism linking anoxygenic photosynthesis to anaerobic respiration that we call 'syntrophic anaerobic

109 x catalyzed the reaction required to support anaerobic respiration, the oxidation of MQ-7.

110 cellular processes ranging from aerobic and anaerobic respiration to catalysis and iron homeostasis.

111 B. multivorans used fermentation rather than anaerobic respiration to gain energy, consistent with th

112 lts clearly establish the genes required for anaerobic respiration using DMSO and TMAO in an archaeon

113 Neisseria gonorrhoeae grows anaerobically by anaerobic respiration using nitrite reductase (Nir) to c

114 that B12 can be synthesized and used during anaerobic respiration using tetrathionate (but not nitra

115 d in the exhibition of swarming motility and anaerobic respiration were upregulated.

116 and extracellular acidification rate (ECAR, anaerobic respiration) were examined in response to isop

117 marate reductase catalyzes the final step of anaerobic respiration when fumarate is the terminal elec

118 ane complex that catalyzes the final step of anaerobic respiration when fumarate is the terminal elec

119 rol with nitrate as the respiratory oxidant (anaerobic respiration), whereas a strain also carrying a

120 They also function catabolically in anaerobic respiration, which involves the use of nitrate

121 r TMAO as the terminal electron acceptor for anaerobic respiration, which is mediated by the molybdoe

122 like function for RavA-ViaA during bacterial anaerobic respiration with fumarate as the terminal elec

123 letion of either cyaA or cyaB did not affect anaerobic respiration with fumarate, dimethyl sulfoxide

124 When arginine fermentation was compared to anaerobic respiration with TMAO, the arc and dms genes w