ライフサイエンスコーパス: phosphoenolpyruvate carboxylase

1 ctase, and the CO(2)-anaplerotic pathway via phosphoenolpyruvate carboxylase.

2 a few amino acid positions in the key enzyme phosphoenolpyruvate carboxylase.

3 nthesizing enzymes, pyruvate carboxylase and phosphoenolpyruvate carboxylase.

4 were also found to accumulate chloroplastic phosphoenolpyruvate carboxylase.

5 lyase, acetate:CoA ligase (AMP forming), and phosphoenolpyruvate carboxylase activities increased in

6 gether with increases of pyruvate kinase and phosphoenolpyruvate carboxylase activities indicate that

7 und that in respiring root tips, anaplerotic phosphoenolpyruvate carboxylase activity was high relati

8 hat is monitored by the sequential action of phosphoenolpyruvate carboxylase and L-malate dehydrogena

9 in the growth medium stimulated flux through phosphoenolpyruvate carboxylase and malic enzyme, altere

10 er respiratory activity and up-regulation of phosphoenolpyruvate carboxylase and NADP-dependent isoci

11 no acids via posttranslational regulation of phosphoenolpyruvate carboxylase and nitrate reductase.

12 ced, whereas the in vitro activities of both phosphoenolpyruvate carboxylase and Rubisco were increas

13 to increase the HCO(-)(3) concentration for phosphoenolpyruvate carboxylase and the C(4) pathway.

14 uvate kinase and in vivo malate synthesis by phosphoenolpyruvate carboxylase and the Krebs cycle were

15 stomatal aperture, malic acid inhibition of phosphoenolpyruvate carboxylase, and enzyme kinetics) wa

16 lic enzyme but not the mesophyll cell marker phosphoenolpyruvate carboxylase, and exhibit thickened w

17 , which suggests that the oxygen-insensitive phosphoenolpyruvate carboxylase becomes a significant co

18 contribute to the regulation of the model C4 phosphoenolpyruvate carboxylase (C4-Pepc) promoter in ma

19 ctron transport (Jmax ), the maximum rate of phosphoenolpyruvate carboxylase carboxylation (Vpmax ),

20 e-enhanced forms of malate dehydrogenase and phosphoenolpyruvate carboxylase cDNAs under the control

21 is was accompanied by a 49% reduction in the phosphoenolpyruvate carboxylase content of leaves (area

22 Despite the lower phosphoenolpyruvate carboxylase content, there was a 3-f

23 The activation state of phosphoenolpyruvate carboxylase decreased marginally at

24 Overexpression of phosphoenolpyruvate carboxylase enzyme specific activity

25 The phosphoenolpyruvate carboxylase from this organism was p

26 First, the phosphoenolpyruvate carboxylase gene (ppc) from Klebsiel

27 tial role in C4 photosynthesis, the maize C4 phosphoenolpyruvate carboxylase gene (PPCZm1) acquired m

28 alternative oxaloacetate synthesizing enzyme phosphoenolpyruvate carboxylase in M. thermoautotrophicu

29 Carbonic anhydrase and phosphoenolpyruvate carboxylase in vitro activity varied

30 a gene encoding the CAM-specific isoform of phosphoenolpyruvate carboxylase, increased rapidly in re

31 esis during fasting through the induction of phosphoenolpyruvate carboxylase kinase (PEPCK), fructose

32 We have examined the complexity of the phosphoenolpyruvate carboxylase kinase (PPCK) gene famil

33 adian clock-controlled protein kinase called phosphoenolpyruvate carboxylase kinase (PPCK).

34 em, the calcium-dependent protein kinase and phosphoenolpyruvate carboxylase kinase families are spec

35 We report the cloning of phosphoenolpyruvate carboxylase kinase from the Crassula

36 Phosphoenolpyruvate carboxylase kinase is a Ca2+-indepen

37 Surprisingly, phosphoenolpyruvate carboxylase kinase is a member of th

38 Phosphoenolpyruvate carboxylase kinase is an exception t

39 In K. fedtschenkoi, the abundance of phosphoenolpyruvate carboxylase kinase transcripts incre

40 kinase (CDPKs), CDPK-related kinases (CRKs), phosphoenolpyruvate carboxylase kinases (PPCKs), PEP car

41 n for plant CDPKs, CDPK-related kinases, and phosphoenolpyruvate carboxylase kinases.

42 library of promoters to assess the impact of phosphoenolpyruvate carboxylase levels on growth yield a

43 roton-translocating pyrophosphatase (PPase), phosphoenolpyruvate carboxylase, major intrinsic protein

44 encode pyruvate orthophosphate dikinase and phosphoenolpyruvate carboxylase (mesophyll cell specific

45 Various isoforms of plant phosphoenolpyruvate carboxylase (PEPC (Ppc)) are control

46 Phosphoenolpyruvate carboxylase (PEPC [Ppc]) has been pr

47 Plant phosphoenolpyruvate carboxylase (PEPc) activity and allo

48 throughout the dark period revealed changing phosphoenolpyruvate carboxylase (PEPC) capacity.

49 e observed 2- to 4-fold up-regulation of two phosphoenolpyruvate carboxylase (PEPC) gene transcripts

50 e C(4) plant, Amaranthus edulis, which lacks phosphoenolpyruvate carboxylase (PEPC) in the mesophyll

51 Phosphoenolpyruvate carboxylase (PEPC) is a "multifacete

52 Phosphoenolpyruvate carboxylase (PEPC) is a crucial enzy

53 Phosphoenolpyruvate carboxylase (PEPC) is a tightly cont

54 Phosphoenolpyruvate carboxylase (PEPC) is a widely distr

55 The encoded proteins are similar to other phosphoenolpyruvate carboxylase (PEPC) kinases, in that

56 Phosphoenolpyruvate carboxylase (PEPC) plays a crucial r

57 bolism (CAM), dark CO2 uptake is mediated by phosphoenolpyruvate carboxylase (PEPC), an enzyme that c

58 y limited by the enzymatic rates of Rubisco, phosphoenolpyruvate carboxylase (PEPc), and carbonic anh

59 The key enzyme for C4 photosynthesis, Phosphoenolpyruvate Carboxylase (PEPC), evolved from non

60 we have introduced the intact gene of maize phosphoenolpyruvate carboxylase (PEPC), which catalyzes

61 uence data from an intron of a nuclear gene, phosphoenolpyruvate carboxylase (PepC).

62 nitial fixation in the light is catalyzed by phosphoenolpyruvate carboxylase (PEPC).

63 roots (proteoid roots) and the expression of phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) in r

64 Maize leaf phosphoenolpyruvate carboxylase [PEPC; orthophosphate:ox

65 the Kranz compartmentation of C4 plants, and phosphoenolpyruvate carboxylase [PEPC; orthophosphate:ox

66 Here we show that the inhibition of phosphoenolpyruvate carboxylase (PEPCase) by 3,3-dichlor

67 ogenesis by inhibiting the transcriptions of phosphoenolpyruvate carboxylase (PEPCK) and glucose-6-ph

68 ecreases in O2 evolution after inhibition of phosphoenolpyruvate carboxylases (PEPCs), and increases

69 n enters the TCA cycle via a stage-dependent phosphoenolpyruvate carboxylase/phosphoenolpyruvate carb

70 Phosphorylation of phosphoenolpyruvate carboxylase plays a key role in the

71 either NAD-ME or PPDK activity, particularly phosphoenolpyruvate carboxylase (PPC) and PPDK in rNAD-M

72 s effect is reduced production of the enzyme phosphoenolpyruvate carboxylase (PPC) and that adventiti

73 e monophosphate (HMP) pathway flux, elevated phosphoenolpyruvate carboxylase (Ppc) flux, and an incre

74 Phosphoenolpyruvate carboxylase (PPC; EC 4.1.1.31) catal

75 f that of all known bacterial and eukaryotic phosphoenolpyruvate carboxylases (PPCs).

76 In all plants, PEPC is phosphorylated by Phosphoenolpyruvate Carboxylase Protein Kinase (PPCK).

77 f E. glabrescens accumulated a chloroplastic phosphoenolpyruvate carboxylase protein, albeit at reduc

78 Maize genes encoding phosphoenolpyruvate carboxylase, pyruvate, orthophosphat

79 ormation of oxaloacetate exclusively via the phosphoenolpyruvate carboxylase reaction.

80 tivity in the anapleurotic (malic enzyme and phosphoenolpyruvate carboxylase) reactions.

81 artment-specific marker enzymes, Rubisco and phosphoenolpyruvate carboxylase, respectively.

82 This is the first report of a new type of phosphoenolpyruvate carboxylase that we call PpcA ("A" f

83 Amounts and expression of phosphoenolpyruvate carboxylase were affected little by

84 ate transcript levels for Rubisco, PPDK, and phosphoenolpyruvate carboxylase were assessed and the se