ライフサイエンスコーパス: photorespiration

1 the import of one glycerate molecule during photorespiration.

2 plasts to faciliate ammonium recovery during photorespiration.

3 nous and monocotyledonous species depends on photorespiration.

4 iratory intermediates, suggesting changes in photorespiration.

5 to elevate CO(2) in BS cells and to minimize photorespiration.

6 ighly expressed in leaves and is involved in photorespiration.

7 likely associated with photosynthesis and/or photorespiration.

8 pe when grown under conditions that suppress photorespiration.

9 lls were grown under conditions that repress photorespiration.

10 ased with increasing CO2 level indicative of photorespiration.

11 an react with O2 instead of CO2 , leading to photorespiration.

12 2 fixation while decreasing losses caused by photorespiration.

13 ly enhancing carbon fixation and suppressing photorespiration.

14 dependence of shoot NO3 (-) assimilation on photorespiration.

15 rough the Calvin-Benson cycle in response to photorespiration.

16 ad of CO2 , leading to the costly process of photorespiration.

17 the Rubisco oxygenase reaction and, in turn, photorespiration.

18 CO2 concentration around Rubisco and reduce photorespiration.

19 oxygenase and the resulting loss of CO(2) by photorespiration.

20 , isobutyrate and propionate metabolism, and photorespiration.

21 In plants, the enzyme participates in photorespiration.

22 fixed carbon and energy in a process termed photorespiration.

23 encodes the mitochondrial SHMT required for photorespiration.

24 nitrogen that would otherwise be lost during photorespiration.

25 the previously characterized role of GGT1 in photorespiration.

26 Since mitochondrial SHMT is crucial to photorespiration, 5-FCL may help prevent 5-CHO-H(4)PteGl

27 Photorespiration, a process that diminishes net photosyn

28 GDC activity is crucial for photorespiration; accordingly, morphological and physiol

29 vin cycle activity associated with increased photorespiration, accumulation of reactive oxygen specie

30 transfer from photorespiration-suppressed to photorespiration-active conditions highlighted the link

31 Conditions that would be unfavorable for photorespiration also inhibited the light-dependent decr

32 nd wheat shoots to conditions that inhibited photorespiration also strongly inhibited nitrate assimil

33 dies suggest that GLU1 plays a major role in photorespiration and also plays a role in primary nitrog

34 photosynthesis depends on the ratio between photorespiration and gross photosynthesis.

35 rs in recycling the ammonia liberated during photorespiration and in exporting the excess redox cofac

36 ating [CO(2)] at Rubisco, thereby decreasing photorespiration and increasing photosynthetic efficienc

37 might be due to its indirect involvement in photorespiration and its numerous enzymatic side activit

38 igation of the metabolic characteristics for photorespiration and other relevant metabolic processes

39 These results indicate the importance of photorespiration and raffinose family oligosaccharide me

40 thway that interacts with photosynthesis and photorespiration and responds to atmospheric CO2 mole fr

41 tive conditions highlighted the link between photorespiration and several other cellular processes, i

42 in part from the inhibitory effect of CO2 on photorespiration and the dependence of shoot NO3 (-) ass

43 discriminates between CO2 and O2, leading to photorespiration and the loss of fixed carbon and nitrog

44 etase were grown in conditions that suppress photorespiration and then transferred for different leng

45 nd a specialized C(4) pathway that minimizes photorespiration and thus increases photosynthetic perfo

46 ght reactions (photosynthesis, Calvin cycle, photorespiration) and carbohydrate metabolism (starch sy

47 tilization effect is larger than the cost of photorespiration, and ecosystem productivity increases l

48 te ammonia produced by nitrate reduction and photorespiration, and GS1 is the major isoform assimilat

49 y, low flux toward amino acid synthesis from photorespiration, and knowledge gaps within nucleotide m

50 consumed in the conversion of CO2 to sugar, photorespiration, and NO3(-) assimilation.

51 onally, increased rates of CO2 assimilation, photorespiration, and plant growth were observed.

52 ries of abundant proteins in photosynthesis, photorespiration, and specific subunits of chlorophyll b

53 olved in the tricarboxylic acid (TCA) cycle, photorespiration, and the degradation of branched-chain

54 nzyme machinery costs through suppression of photorespiration are likely to be offset by the higher f

55 owever, in its absence, significant rates of photorespiration are still possible, indicating that the

56 Though the soluble enzymes involved in photorespiration are well characterized, very few membra

57 Reduced photorespiration at lower temperatures would partly miti

58 s, a low CO2 compensation point, and minimal photorespiration; but it lacks anatomical features analo

59 uence of the induction of photosynthesis and photorespiration by illumination.

60 nvestigations now focus on the regulation of photorespiration by transporters and metabolites.

61 a significant role at low light levels, (2) photorespiration can act to dissipate excess energy at h

62 and (13)CO2, supporting the possibility that photorespiration can provide an alternate source of carb

63 -linked proteins functional in 12 processes: photorespiration, citric acid cycle and associated react

64 2O2 levels in plant cells, we focused on the photorespiration-dependent peroxisomal H2O2 production i

65 they are a consequence of the deficiency in photorespiration due to the inability to generate lipoic

66 at they are a consequence of a deficiency in photorespiration due to the reduced lipoylation of the p

67 rtion of total electron transport supporting photorespiration enabled estimation of the bundle sheath

68 s between elevated [CO2 ] and temperature on photorespiration, enzyme systems, carbohydrate productio

69 L) and malate synthase (MLS) are replaced by photorespiration enzymes.

70 In plants, ammonium released during photorespiration exceeds primary nitrogen assimilation b

71 eased isoprenoid emission rates compete with photorespiration for the residual reducing power not inv

72 , very few membrane transporters involved in photorespiration have been identified to date.

73 This previously undescribed role for photorespiration (i) explains several responses of plant

74 s essential for maintaining optimal rates of photorespiration in air; however, in its absence, signif

75 te synthase (Fd-GOGAT) plays a major role in photorespiration in Arabidopsis, as has been determined

76 was characterized to investigate the role of photorespiration in C4 photosynthesis.

77 erns about genetic manipulations to diminish photorespiration in crops.

78 carbon concentration mechanisms and suppress photorespiration in response to inorganic carbon (Ci) li

79 o protein shows that water stress suppresses photorespiration in soybean leaves.

80 orespiration, suggesting the contribution of photorespiration in the protection of photosynthetic pro

81 icating the cytokinin-mediated occurrence of photorespiration in the transgenic plants.

82 low O2 inhibition of photosynthesis and low photorespiration in Udotea.

83 tive amounts of most metabolites involved in photorespiration increased after the onset of light, exh

84 Although photorespiration is a compartmentalized process with enz

85 Photorespiration is an energy-intensive process that rec

86 Photosynthetic carbon assimilation including photorespiration is dynamically regulated during the day

87 Photorespiration is essential for the detoxification of

88 Photorespiration is known to contribute to the decline i

89 complex, GLO-mediated H2O2 production during photorespiration is very high, whereas the affinity of C

90 er viscosity (more costly transport) and low photorespiration (less costly photosynthesis) imply low

91 hypothesized to participate in the steps of photorespiration located in peroxisomes.

92 e absence of ER-ANT1 activity mainly affects photorespiration (maybe solely GDC), whereas basic cellu

93 ate-dependent metabolic processes, including photorespiration, methionine and pantothenate biosynthes

94 genous expression of BASS6 complemented this photorespiration mutant phenotype.

95 Here, we report the effects on growth and photorespiration of overexpressing a cytosolic GS1 isoen

96 However, regulation of photorespiration on the gene level has not been intensiv

97 ncreased H2O2 content but is not involved in photorespiration or amino acid metabolism, demonstrated

98 of hydrogen peroxide released either during photorespiration or as a consequence of biotic and abiot

99 Although no change in photorespiration or dark respiration was observed in the

100 signal for the transcriptional regulation of photorespiration, particularly in the glycine-to-serine

101 ies, we detect a consistent reduction in the photorespiration/photosynthesis ratio in response to the

102 rvational evidence that the reduction of the photorespiration/photosynthesis ratio was ca. 25%.

103 ynthetic C3 glucose contains a signal of the photorespiration/photosynthesis ratio.

104 quantitatively for temperature contrasts (by photorespiration plus viscosity effects) and approximate

105 cell death phenotype of cat2-2 plants under photorespiration-promoting conditions.

106 derable deregulation of the transcription of photorespiration-related genes.

107 wing commitments to secondary metabolism and photorespiration, respectively.

108 activity and specificity for oxygen leads to photorespiration, severely limiting photosynthesis and c

109 ygenation reaction of RubisCO and subsequent photorespiration significantly limit the biomass gains o

110 nthesis and Suc synthesis without increasing photorespiration, starch breakdown did not occur and mal

111 s indicated a cytokinin-induced elevation in photorespiration, suggesting the contribution of photore

112 L. japonicus plants during the transfer from photorespiration-suppressed to photorespiration-active c

113 ocesses including fatty acid beta-oxidation, photorespiration, synthesis of hormones, and homeostasis

114 ese results suggest a major role for GLU1 in photorespiration, the sucrose induction of GLU1 mRNA in

115 AM, despite the potential for suppression of photorespiration through CO2 concentration.

116 be important for fatty acid mobilization and photorespiration through the interaction with oil bodies

117 t C4 photosynthesis in maize is dependent on photorespiration throughout seedling development and sup

118 fixation, more carbohydrates are oxidized by photorespiration to products of the C2 oxidative photosy

119 The contribution of photorespiration to the tolerance of transgenic plants t

120 jor contributing factor for the avoidance of photorespiration under intracellular Ci limitation.

121 Photorespiration was found to be essential for the optim

122 Photorespiration was generally elevated in maize mutant

123 ct in growth and glutamate biosynthesis when photorespiration was repressed by 1% CO2.

124 The effect of antisense constructs on photorespiration was studied in transgenic plants by mea

125 plants and mitochondrial SHMT is central to photorespiration, we examined the impact of an insertion

126 burst and the rate of CO(2) released during photorespiration were both greater in the pmdh mutant co

127 nts, but the negative consequences of severe photorespiration were more pronounced in the absence of

128 ement of At4g17360 and At5g47435 proteins in photorespiration, which is to prevent excessive accumula

129 Specifically there is a restriction in photorespiration with a decrease in the rate of oxidatio