ライフサイエンスコーパス: Calvin cycle

1 f enzymes involved in photosynthesis and the Calvin cycle.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 Calvin cycle enzymes and proteins of unknown function we

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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