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1 were also found to accumulate chloroplastic phosphoenolpyruvate carboxylase.
2 ctase, and the CO(2)-anaplerotic pathway via phosphoenolpyruvate carboxylase.
3 a few amino acid positions in the key enzyme phosphoenolpyruvate carboxylase.
4 nthesizing enzymes, pyruvate carboxylase and phosphoenolpyruvate carboxylase.
6 of nuclear SREBP-1a under the control of the phosphoenolpyruvate carboxylase-1 (Pck1) promoter in mic
7 lyase, acetate:CoA ligase (AMP forming), and phosphoenolpyruvate carboxylase activities increased in
8 gether with increases of pyruvate kinase and phosphoenolpyruvate carboxylase activities indicate that
10 und that in respiring root tips, anaplerotic phosphoenolpyruvate carboxylase activity was high relati
12 hat is monitored by the sequential action of phosphoenolpyruvate carboxylase and L-malate dehydrogena
13 in the growth medium stimulated flux through phosphoenolpyruvate carboxylase and malic enzyme, altere
14 er respiratory activity and up-regulation of phosphoenolpyruvate carboxylase and NADP-dependent isoci
15 no acids via posttranslational regulation of phosphoenolpyruvate carboxylase and nitrate reductase.
16 ced, whereas the in vitro activities of both phosphoenolpyruvate carboxylase and Rubisco were increas
17 processes related with the timed actions of phosphoenolpyruvate carboxylase and Rubisco, respectivel
19 ht period when atmospheric CO(2) is fixed by phosphoenolpyruvate carboxylase and stored as malic acid
20 to increase the HCO(-)(3) concentration for phosphoenolpyruvate carboxylase and the C(4) pathway.
21 uvate kinase and in vivo malate synthesis by phosphoenolpyruvate carboxylase and the Krebs cycle were
22 stomatal aperture, malic acid inhibition of phosphoenolpyruvate carboxylase, and enzyme kinetics) wa
23 lic enzyme but not the mesophyll cell marker phosphoenolpyruvate carboxylase, and exhibit thickened w
24 , which suggests that the oxygen-insensitive phosphoenolpyruvate carboxylase becomes a significant co
25 contribute to the regulation of the model C4 phosphoenolpyruvate carboxylase (C4-Pepc) promoter in ma
26 ctron transport (Jmax ), the maximum rate of phosphoenolpyruvate carboxylase carboxylation (Vpmax ),
27 e-enhanced forms of malate dehydrogenase and phosphoenolpyruvate carboxylase cDNAs under the control
28 is was accompanied by a 49% reduction in the phosphoenolpyruvate carboxylase content of leaves (area
32 onectin overexpression induces a doubling of phosphoenolpyruvate carboxylase expression and enhanced
33 f the Entner-Doudoroff pathway (EDP) and the phosphoenolpyruvate carboxylase for intracellularly prol
36 tial role in C4 photosynthesis, the maize C4 phosphoenolpyruvate carboxylase gene (PPCZm1) acquired m
37 alternative oxaloacetate synthesizing enzyme phosphoenolpyruvate carboxylase in M. thermoautotrophicu
39 a gene encoding the CAM-specific isoform of phosphoenolpyruvate carboxylase, increased rapidly in re
40 esis during fasting through the induction of phosphoenolpyruvate carboxylase kinase (PEPCK), fructose
43 em, the calcium-dependent protein kinase and phosphoenolpyruvate carboxylase kinase families are spec
49 kinase (CDPKs), CDPK-related kinases (CRKs), phosphoenolpyruvate carboxylase kinases (PPCKs), PEP car
51 library of promoters to assess the impact of phosphoenolpyruvate carboxylase levels on growth yield a
52 roton-translocating pyrophosphatase (PPase), phosphoenolpyruvate carboxylase, major intrinsic protein
53 encode pyruvate orthophosphate dikinase and phosphoenolpyruvate carboxylase (mesophyll cell specific
58 e observed 2- to 4-fold up-regulation of two phosphoenolpyruvate carboxylase (PEPC) gene transcripts
59 e C(4) plant, Amaranthus edulis, which lacks phosphoenolpyruvate carboxylase (PEPC) in the mesophyll
64 The encoded proteins are similar to other phosphoenolpyruvate carboxylase (PEPC) kinases, in that
66 bolism (CAM), dark CO2 uptake is mediated by phosphoenolpyruvate carboxylase (PEPC), an enzyme that c
67 y limited by the enzymatic rates of Rubisco, phosphoenolpyruvate carboxylase (PEPc), and carbonic anh
69 we have introduced the intact gene of maize phosphoenolpyruvate carboxylase (PEPC), which catalyzes
74 roots (proteoid roots) and the expression of phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) in r
76 the Kranz compartmentation of C4 plants, and phosphoenolpyruvate carboxylase [PEPC; orthophosphate:ox
77 ential to understand how C(4) genes, such as phosphoenolpyruvate carboxylase (PEPC1), are regulated t
79 ogenesis by inhibiting the transcriptions of phosphoenolpyruvate carboxylase (PEPCK) and glucose-6-ph
80 ecreases in O2 evolution after inhibition of phosphoenolpyruvate carboxylases (PEPCs), and increases
81 n enters the TCA cycle via a stage-dependent phosphoenolpyruvate carboxylase/phosphoenolpyruvate carb
83 either NAD-ME or PPDK activity, particularly phosphoenolpyruvate carboxylase (PPC) and PPDK in rNAD-M
84 s effect is reduced production of the enzyme phosphoenolpyruvate carboxylase (PPC) and that adventiti
85 e monophosphate (HMP) pathway flux, elevated phosphoenolpyruvate carboxylase (Ppc) flux, and an incre
86 t the 5'-flanking sequences of the C(4) type phosphoenolpyruvate carboxylase (Ppc) gene from three C(
87 nd the molecular evolution of genes encoding phosphoenolpyruvate carboxylase (PPC), an enzyme require
92 f E. glabrescens accumulated a chloroplastic phosphoenolpyruvate carboxylase protein, albeit at reduc
97 This is the first report of a new type of phosphoenolpyruvate carboxylase that we call PpcA ("A" f
98 e apparent maximum carboxylation activity of phosphoenolpyruvate carboxylase (V(pmaxA)) and CO(2)-sat
100 ate transcript levels for Rubisco, PPDK, and phosphoenolpyruvate carboxylase were assessed and the se
101 ysis of the ppc gene family that encodes the phosphoenolpyruvate carboxylase, which suggests that mem