ライフサイエンスコーパス: nitrogen assimilation

1 NA in leaves also suggests a role in primary nitrogen assimilation.

2 thetases (GS) play central roles in cellular nitrogen assimilation.

3 ammonia, a volatile odorant produced during nitrogen assimilation.

4 perate to stimulate chloroplast division and nitrogen assimilation.

5 l. investigate how E. coli robustly controls nitrogen assimilation.

6 eria catabolize allantoin as a mechanism for nitrogen assimilation.

7 metabolic enzymes, and permeases involved in nitrogen assimilation.

8 torespiratory ammonia as well as for primary nitrogen assimilation.

9 CodY in L. monocytogenes in both carbon and nitrogen assimilation.

10 increased expression of enzymes involved in nitrogen assimilation.

11 uctive reactions such as carbon fixation and nitrogen assimilation.

12 ation to developmental changes in carbon and nitrogen assimilation.

13 mulate RN, consistent with limited nighttime nitrogen assimilation.

14 nct physiological roles in the regulation of nitrogen assimilation.

15 -duction proteins, PII and GlnK, involved in nitrogen assimilation.

16 sitive regulator of DAL5, and other genes of nitrogen assimilation.

17 is via NITRATE REDUCTASE (NR), an enzyme of nitrogen assimilation [5].

18 intriguing discovery from this study is that nitrogen assimilation affects the expression of many gen

19 Multiple genes involved in nitrogen assimilation and amino acid metabolism are indu

20 rs play a role in signal transduction during nitrogen assimilation and are required for effective nit

21 microorganisms and contain special traits in nitrogen assimilation and associated processes.

22 very of protein phosphorylation in bacterial nitrogen assimilation and chemotaxis more than 30 years

23 principle, it provides carbon backbones for nitrogen assimilation and evolves CO2 and thus impacts o

24 oss four trophic modes, proteins involved in nitrogen assimilation and light-independent chlorophyll

25 It plays an important role in nitrogen assimilation and metabolism by reversibly regul

26 It plays an important role in nitrogen assimilation and metabolism by reversibly regul

27 nitrite reductase functions both in nitrite nitrogen assimilation and nitrite respiration.

28 Despite the importance of nitrogen assimilation and NO signalling, it remains larg

29 sis, suggesting a tight coordination between nitrogen assimilation and photosynthesis processes.

30 any genes involved in sucrose catabolism and nitrogen assimilation and utilization were also observed

31 to active growth, like lignin biosynthesis, nitrogen assimilation, and defense, were enriched.

32 mproved photosynthesis rates, increased leaf nitrogen assimilation, and enhanced source-to-sink trans

33 in starch biosynthesis, arginine synthesis, nitrogen assimilation, and initial steps in sulfur assim

34 votal players in harmonizing photosynthesis, nitrogen assimilation, and light responses.

35 zed to participate in uric acid degradation, nitrogen assimilation, and nutrient provisioning.

36 ted by iron: biotin uptake and biosynthesis, nitrogen assimilation, and purine biosynthesis.

37 nt with this mechanism, the genes of primary nitrogen assimilation are preferentially expressed in th

38 diator of trans-kingdom signaling, implicate nitrogen assimilation as important for both bacteria and

39 ses genes involved in amino acid metabolism, nitrogen assimilation as well as genes involved in sugar

40 The typical LD acclimation of carbon and nitrogen assimilation as well as redox-related parameter

41 teractions on three target genes involved in nitrogen assimilation: asparagine synthetase (ASN1 and A

42 ased during photorespiration exceeds primary nitrogen assimilation by as much as 10-fold.

43 plays an important role in the regulation of nitrogen assimilation by controlling the uridylylation s

44 nthetase plays an unusually critical role in nitrogen assimilation by H. pylori.

45 he absence of PII, the GlnK protein controls nitrogen assimilation by regulating the activities of th

46 chaea and plants, help coordinate carbon and nitrogen assimilation by regulating the activity of sign

47 ynthesis, while the ggct2;1 mutant increased nitrogen assimilation by severalfold, resulting in a ver

48 nstream transcription factors, transporters, nitrogen assimilation, carbon/nitrogen metabolism, redox

49 two-component sensor systems, phosphate and nitrogen assimilation, chemotaxis, and motility.

50 f these nitrogen sources is dependent on the nitrogen assimilation control (NAC) protein.

51 The nitrogen assimilation control gene, nac, was detected in

52 entify the nucleotide residues important for nitrogen assimilation control protein (NAC) binding in v

53 The nitrogen assimilation control protein (NAC) binds to a s

54 The nitrogen assimilation control protein (NAC) from Klebsie

55 The nitrogen assimilation control protein (NAC) from Klebsie

56 The nitrogen assimilation control protein (NAC) from Klebsie

57 The nitrogen assimilation control protein (NAC) generally fu

58 The nitrogen assimilation control protein (NAC) is a LysR-ty

59 The nitrogen assimilation control protein (NAC) of Klebsiell

60 otrophy, repression of GDH expression by the nitrogen assimilation control protein (NAC) relieved the

61 he cyclic AMP receptor protein (CRP) and the nitrogen assimilation control protein (NAC), respectivel

62 the Ntr system, mediated in this case by the nitrogen assimilation control protein (NAC).

63 om codBp-lacZ operon fusions showed that the nitrogen assimilation control protein NAC was necessary

64 A negative control mutant of the nitrogen assimilation control protein, NAC, has been iso

65 itrogen regulatory system acting through the nitrogen assimilation control protein, NAC.

66 ptional fusion was strongly repressed by the nitrogen assimilation control protein, NAC.

67 transcription of some operons depends on the nitrogen assimilation control protein, which serves as a

68 S. typhimurium nit mutants are defective in nitrogen assimilation, despite having normal levels of a

69 s displayed inhibition of photosynthesis and nitrogen assimilation during water stress, neither carbo

70 on of genes encoding high substrate affinity nitrogen assimilation enzymes (GS-GOGAT system) was simi

71 r data also suggest that FDX3 is involved in nitrogen assimilation, FDX4 in glycolysis and response t

72 S) has recently been proposed to function in nitrogen assimilation from l-Arg.

73 nt with microbial N(2) fixation, pointing to nitrogen assimilation from soils and not through symbios

74 tional repressor NrpR regulates a variety of nitrogen assimilation genes by 2-oxoglutarate-reversible

75 We demonstrate that the nitrogen assimilation genes encode functional proteins a

76 those encoding TonB-associated transporters, nitrogen assimilation genes, fatty acid catabolism genes

77 roduction concomitant with the enrichment of nitrogen assimilation genes.

78 ich in turn phosphorylates the key enzyme of nitrogen assimilation glutamine synthetase GS2 at two si

79 te reductase, a key enzyme in the process of nitrogen assimilation, has been determined using X-ray d

80 The prominence of polyamine metabolism and nitrogen assimilation highlights the importance of recyc

81 TnrA is a master regulator of nitrogen assimilation in Bacillus subtilis.

82 n catabolite repression, quorum sensing, and nitrogen assimilation in E. coli.

83 suberin biosynthesis, iron transporters, and nitrogen assimilation in endodermal/exodermal cells modu

84 ne synthetase (GS) is the central enzyme for nitrogen assimilation in Escherichia coli and is subject

85 ct PII-like proteins, PII and GlnK, regulate nitrogen assimilation in Escherichia coli.

86 ton-coupled transporters are responsible for nitrogen assimilation in eukaryotes and bacteria through

87 de that glutamine synthetase is critical for nitrogen assimilation in H. pylori and is active under a

88 respiration and also plays a role in primary nitrogen assimilation in leaves, whereas the GLU2 gene m

89 about the genes and pathways responsible for nitrogen assimilation in M. tuberculosis.

90 ed signaling proteins in nature, controlling nitrogen assimilation in organisms ranging from bacteria

91 key processes in eukaryotic cells including nitrogen assimilation in plants by tuning the activity o

92 lineages, suggesting that the regulation of nitrogen assimilation in prasinophytes will differ from

93 e GLU2 gene may play a major role in primary nitrogen assimilation in roots.

94 of excessive nitrogen in generalists but for nitrogen assimilation in specialists.

95 To gain insights into nitrogen assimilation in the ant cuticle we use gut bact

96 ate the role of glutamine synthetase (GS) in nitrogen assimilation in the green alga Chlamydomonas re

97 Nitrogen assimilation in the methanogenic archaeon Metha

98 To explore the metabolic networks for nitrogen assimilation in this bacterium, changes in gene

99 Studies with mutant strains having altered nitrogen assimilation indicated that the decreases in th

100 r bleaching, butterflyfishes exhibit reduced nitrogen assimilation, indicating that coral stress may

101 Nitrogen assimilation into glutamine and glutamate and d

102 This would allow nitrogen assimilation into glutamine to proceed (or not)

103 Nitrogen assimilation is a highly regulated process requ

104 of glutamine synthetase, the key enzyme for nitrogen assimilation, is poorly understood.

105 synthetase (GS), a key enzyme in biological nitrogen assimilation, is regulated in multiple ways in

106 whereas glutamate synthase, a key enzyme in nitrogen assimilation, is repressed.

107 l cofactors relevant for denitrification and nitrogen assimilation like cobalamin, riboflavin, molybd

108 s and redirected to the de novo synthesis of nitrogen assimilation machinery, simultaneously, the pho

109 etic processes, utilization of iron-economic nitrogen assimilation mechanisms, and increased iron upt

110 d genes that may be specifically involved in nitrogen assimilation, metabolism, and the maintenance o

111 increased the abundance of Calvin Cycle and nitrogen assimilation metabolites while suppressing the

112 g C. elegans attraction, we demonstrate that nitrogen assimilation mutants perturb bacterial fitness

113 -NADP(+) and ATP-ADP ratios led to increased nitrogen assimilation, NADP-malate dehydrogenase activat

114 , we have predicted a detailed model for the nitrogen assimilation network in cyanobacterium Synechoc

115 array data, and proposed a new model for the nitrogen assimilation network in WH8102.

116 upon entering phosphate limitation including nitrogen assimilation, oxidative phosphorylation, nucleo

117 on homeostasis, oxidative stress markers and nitrogen assimilation parameters.

118 ive thiols in numerous enzymes composing the nitrogen assimilation pathway and the recently discovere

119 Although bna572 has a functional nitrogen assimilation pathway via glutamate synthase, th

120 o lipid biosynthesis and is regulated by the nitrogen assimilation pathway.

121 Nitrogen assimilation plays a vital role in plant metabo

122 nsistent with temporal niche partitioning of nitrogen assimilation processes over a diel cycle in the

123 formation and bind and modulate a variety of nitrogen assimilation regulators and enzymes.

124 dentify 40 in vivo targets of sigma(54), the nitrogen assimilation sigma factor, and estimate that th

125 f PII phosphorylation that senses carbon and nitrogen assimilation status.

126 sults indicate that ntcA is involved more in nitrogen assimilation than in nitrogen fixation and also

127 modulate the expression of genes involved in nitrogen assimilation, the cyanobacterial PII-interactin

128 pport symbiont functioning and organism-wide nitrogen assimilation through glutamine synthetase/gluta

129 under high temperature, diverting energy to nitrogen assimilation to maintain symbiont population de

130 the cell coordinates protein translation and nitrogen assimilation to optimize cell growth in differe

131 esis is known to be tightly coordinated with nitrogen assimilation, very little is known about the un

132 Host nitrogen assimilation via dipeptide synthesis appears to

133 tion during water stress, neither carbon nor nitrogen assimilation was affected by stress in the tran

134 A major alteration in nitrogen assimilation was observed, with a general reduc

135 mes involved in photosynthesis and inorganic nitrogen assimilation were markedly increased at elevate

136 fluences central carbohydrate metabolism and nitrogen assimilation, whereas bacterial community struc

137 esis (particularly methionine) and sulfur or nitrogen assimilation, whereas many of the underexpresse

138 ribe the complex regulation of P. aeruginosa nitrogen assimilation, which is mediated by a partner-sw

139 s different aspects of metabolism integrates nitrogen assimilation with other metabolic processes.