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1 gene encoding the large subunit of Rubisco (ribulose bisphosphate carboxylase).
2 the large subunit of the CO(2)-fixing enzyme ribulose-bisphosphate carboxylase.
3 used to the transit peptide of ferredoxin or ribulose-bisphosphate carboxylase activase for stromal t
5 ly trapped folding-incompetent conformers of ribulose bisphosphate carboxylase are converted to the n
6 nins GroEL and GroES catalyze the folding of ribulose bisphosphate carboxylase at a rate proportional
7 s in other phototrophic organisms, including ribulose bisphosphate carboxylase (Calvin cycle), citrat
8 nated by the cbbL genes (67%-82%) coding the ribulose-bisphosphate carboxylase large chain in the Cal
9 lycine produced in the oxygenase reaction of ribulose bisphosphate carboxylase-oxygenase is incorpora
10 ration-dependent data on the yield of native ribulose bisphosphate carboxylase/oxygenase (Rubisco) as
12 llowing salinity stress with transcripts for ribulose bisphosphate carboxylase/oxygenase (RuBisCO) su
13 lus neapolitanus fixes CO2 by using a form I ribulose bisphosphate carboxylase/oxygenase (RuBisCO), t
14 o CO(2), raising the CO(2) concentration for Ribulose bisphosphate carboxylase/oxygenase (Rubisco).
15 in the chloroplast and the specificities of ribulose bisphosphate carboxylase/oxygenase (Rubisco).
16 oncentration around the carboxylating enzyme ribulose bisphosphate carboxylase/oxygenase (RuBisCO).
17 the transit peptide of the small subunit of ribulose bisphosphate carboxylase/oxygenase did not affe
18 tration (Cb) using a simple kinetic model of ribulose bisphosphate carboxylase/oxygenase function.
20 nclude changes in photoprotective machinery, ribulose bisphosphate carboxylase/oxygenase kinetics and
21 erized by three unique enzymatic activities: ribulose bisphosphate carboxylase/oxygenase, phosphoribu
24 se of tight-binding inhibitors from dead-end ribulose-bisphosphate carboxylase/oxygenase (Rubisco) co
25 chaperonin-dependent, folding model protein ribulose-bisphosphate carboxylase/oxygenase (RuBisCO), a
27 osynthetic carbon metabolism is initiated by ribulose-bisphosphate carboxylase/oxygenase (Rubisco), w
28 3)(-) to CO(2) for use in carbon fixation by ribulose-bisphosphate carboxylase/oxygenase (RuBisCO).
29 egulated synthesis of both photopigments and ribulose-bisphosphate carboxylase/oxygenase (Rubisco).
30 assist GroEL-mediated refolding of bacterial ribulose-bisphosphate carboxylase/oxygenase but gained t
31 nding protein (CAB) and the small subunit of ribulose bisphosphate carboxylase (RBCS) was also impair
32 ssing are genes for the Calvin cycle enzymes ribulose bisphosphate carboxylase (RuBisCO) and phosphor
35 which induced the aggregation of homodimeric ribulose bisphosphate carboxylase (Rubisco), did not aff
36 in Udotea extracts was equivalent to that of ribulose-bisphosphate carboxylase [Rubisco; 3-phospho-D-
38 tif (another LRE) and the native Arabidopsis ribulose bisphosphate carboxylase small subunit gene RBC
39 rease in chlorophyll a/b-binding protein and ribulose bisphosphate carboxylase small subunit gene tra
40 amily of genes encoding the small subunit of ribulose bisphosphate carboxylase) that are sufficient f
42 carbon, carbon dioxide may be fixed via the ribulose bisphosphate carboxylase, Wood-Ljungdahl pathwa