ライフサイエンスコーパス: Calvin cycle

1 increase the rate of CO(2) fixation via the Calvin cycle.

2 , to catalyze carbon dioxide fixation in the Calvin Cycle.

3 f enzymes involved in photosynthesis and the Calvin cycle.

4 -bisphosphate carboxylase large chain in the Calvin cycle.

5 % of this CO(2) into cell material using the Calvin cycle.

6 but only 12% of it was reassimilated by the Calvin cycle.

7 n detoxification, malate metabolism, and the Calvin cycle.

8 tained from a detailed computer model of the Calvin cycle.

9 (PRK), a fulcrum for redox regulation of the Calvin cycle.

10 bisco at the heart of carbon fixation in the Calvin cycle.

11 an obstacle for formate assimilation via the Calvin cycle.

12 drogenase, followed by CO(2) fixation by the Calvin cycle.

13 Consistent with decreased Calvin cycle activity and increased PPP and light reacti

14 d reducing power are depleted, resumption of Calvin cycle activity associated with increased photores

15 aeolicus and to the group that comprises the Calvin-cycle aldolases of photosynthetic proteobacteria

16 xport in the light, but the reactions of the Calvin cycle alone are not capable of providing a sustai

17 arboxylase-oxygenase subunit proteins of the Calvin cycle and AMP salvage pathways suggests a strong

18 ioredoxins function in the regulation of the Calvin cycle and associated processes.

19 hate carboxylase/oxygenase) acts without the Calvin cycle and in a previously undescribed metabolic c

20 ved in the assimilation of CO(2) through the Calvin cycle and in chloroplastic glycolysis, are trimet

21 ination of nonpolyploid duplicates), whereas Calvin cycle and light-harvesting complex gene families

22 CO(2) enrichment increased the abundance of Calvin Cycle and nitrogen assimilation metabolites while

23 has been demonstrated for the origin of the Calvin cycle and of the heme and carotenoid biosynthesis

24 in contrast with the traditional view of the Calvin cycle and oxidative pentose phosphate pathway as

25 that MYB99 directs precursor supply from the Calvin cycle and oxidative pentose-phosphate pathway in

26 stis 6803 revealed differences in the use of Calvin cycle and photorespiratory pathway reactions.

27 bon metabolism, with an up-regulation of the Calvin cycle and the photorespiratory pathway in peroxis

28 formed either during photorespiration or the Calvin cycle and thus their isotopic composition may be

29 carboxylation and regeneration phase of the Calvin cycle, and several regulators (e.g., CP12) distri

30 els of genes involved in photosynthesis, the Calvin cycle, and starch degradation in Arabidopsis (Ara

31 profiles suggest that the key enzymes of the Calvin cycle are not repressed under elevated CO(2) in t

32 as organic carbon before being fixed in the Calvin cycle, as expected if the C(4) pathway functions

33 light-independent reaction (analogous to the Calvin cycle) between leuco-methylene blue and the onium

34 ere it plays a key role in regulation of the Calvin cycle by forming a ternary complex with glycerald

35 -application of the toxin with PSK increased Calvin cycle capacity.

36 The Calvin-Benson-Bassham cycle (Calvin cycle) catalyzes virtually all primary productivi

37 including ribulose bisphosphate carboxylase (Calvin cycle), citrate lyase (reverse citric acid cycle)

38 induces a C(4) system in which the C(4) and Calvin cycles co-exist in the same cell and the initial

39 he positive regulation of the cbbI and cbbII Calvin cycle CO2 fixation operons.

40 Proteomic analysis revealed Calvin cycle downregulation by FB1, while co-application

41 thermal optima of enzymes, including the key Calvin Cycle enzyme, Ribulose 1,5 bisphosphate carboxyla

42 Disrupting the activity of the CO2-fixing Calvin cycle enzyme, ribulose 1,5-bisphosphate carboxyla

43 tabacum) plants in which the activity of the Calvin cycle enzyme, sedoheptulose-1,7-bisphosphatase, i

44 Calvin cycle enzymes and proteins of unknown function we

45 ense plants expressing reduced levels of the Calvin cycle enzymes glyceraldehyde-3-phosphate dehydrog

46 increase the production of RuBisCo and other Calvin Cycle enzymes in the cold, but how this is achiev

47 , and most notably missing are genes for the Calvin cycle enzymes ribulose bisphosphate carboxylase (

48 s those for the photosynthetic apparatus and Calvin cycle enzymes, whose expression levels decreased

49 This Calvin cycle flux enabled R. palustris to reoxidize near

50 e so important in modern biochemistry in the Calvin cycle for photosynthesis and the gluconic acid pa

51 lysis of expression patterns of genes in the Calvin cycle from 95 Arabidopsis microarray experiments,

52 In both soybean and Arabidopsis, Calvin cycle gene duplicates exhibit a greater capacity

53 onphotosynthetic heterotrophic bacteria have Calvin cycle genes, and their potential to use CO(2) fix

54 ynthetic pathway and photosynthesis, such as Calvin cycle genes, antioxidant genes involved in chloro

55 Sequenced cyanophage genomes lack Calvin cycle genes, however, suggesting that photosynthe

56 ed to anthocyanins biosynthesis, heat shock, calvin cycle, glycolysis, TCA cycle, mitochondrial elect

57 A. thaliana; (3) light reaction pathway and Calvin cycle in A. thaliana.

58 ation provides spatiotemporal control of the Calvin cycle in cyanobacteria.

59 onditions in addition to inactivation of the Calvin cycle in the dark.

60 tance and decreased gas exchange so that the Calvin cycle in the leaf chloroplasts was no more than 3

61 em II, the light-harvesting complex, and the Calvin cycle) in the cultivated soybean (Glycine max), w

62 molithoautotrophic bacteria that operate the Calvin cycle independent of light must also recycle phos

63 rt here that cyanophages carry and express a Calvin cycle inhibitor, CP12, whose host homologue direc

64 with two types of applications: profiling of Calvin cycle intermediates in (i) dark-adapted and light

65 usly been determined for these gases, or for Calvin-cycle intermediates such as bicarbonate ([Formula

66 Carbon fixation via the Calvin cycle is constrained by the side activity of Rubi

67 however, the converting CO(2) to G3P in the Calvin cycle is low, supported by reduced expression of

68 s led to the long-standing model wherein the Calvin cycle is necessary during photoheterotrophic grow

69 Second, the Calvin cycle is not fully functional, but RubisCO contin

70 (2) The issue of whether the Calvin cycle is present needs to be examined.

71 Thus, the Calvin cycle is still needed to oxidize electron carrier

72 regulations of the metabolite fluxes in the Calvin cycle, is remarkably consistent with the rate-lim

73 esent an alternative evolutionary pathway in Calvin-cycle kinase development.

74 hereas thiamine thizole synthase and CP12, a Calvin Cycle master regulator, were uniformly up-regulat

75 Surprisingly, Calvin cycle mutants of Rs. rubrum, but not of Rp. palus

76 ells and the inability of defined GSH-FDH or Calvin cycle mutants to use methanol as a sole carbon so

77 rimental evidence that such behaviour in the Calvin cycle occurs in vivo as well as in silico.

78 emonstrate that Rs. rubrum and Rp. palustris Calvin cycle phosphoribulokinase mutants that cannot pro

79 proteins of light reactions (photosynthesis, Calvin cycle, photorespiration) and carbohydrate metabol

80 rmation, growth, and fusion of puncta by two Calvin cycle proteins, suggesting that biomolecular cond

81 should be viewed as part of the BS-localized Calvin cycle, rather than a parallel pathway.

82 and larger average gene family size for the Calvin cycle relative to the photosystems.

83 f other CO(2) fixation pathways, such as the Calvin cycle, the reductive acetyl coenzyme A pathway, a

84 anoxygenic phototrophic bacteria require the Calvin cycle to accept electrons when growing with light

85 from glycolate metabolism can be used by the Calvin cycle to recycle reducing power generated in the

86 synthetic energy and reducing power from the Calvin cycle to the de novo synthesis of saturated fatty

87 host homologue directs carbon flux from the Calvin cycle to the pentose phosphate pathway (PPP).

88 to the oxidative pentose phosphate pathway, Calvin cycle, tricarboxylic acid cycle, and amino acid b

89 model (Bartlett et al., 2014) consists of a Calvin cycle typical of C3 plants coupled to an oscillat

90 The Calvin cycle was down-regulated in mature leaves to adju

91 xpression related to antioxidant enzymes and Calvin cycle were quantified.