ライフサイエンスコーパス: hyperaccumulation

1 n grown under conditions that favored AdoMet hyperaccumulation.

2 rtmentation of AdoMet as well as the mode of hyperaccumulation.

3 s gene expression, a known hallmark of metal hyperaccumulation.

4 echanisms associated with hypertolerance and hyperaccumulation.

5 vital role in homeostasis of nickel ions in hyperaccumulation.

6 c acid and citric acid involvement in nickel hyperaccumulation.

7 nd whether associated partners may affect Se hyperaccumulation.

8 egrade starch during the night, resulting in hyperaccumulation.

9 ard and reverse genetics for the study of As hyperaccumulation.

10 extremely high level of Cd tolerance and Cd hyperaccumulation.

11 se results demonstrate a role for NAS2 in Zn hyperaccumulation also under near-natural conditions.

12 ever, no correlation was observed between Se hyperaccumulation and ATPS, APR, and SAT activities in s

13 sis pathway, gsh2 mutants exhibited gamma-EC hyperaccumulation and GSH deficiency.

14 le contribution to zinc, cadmium, and nickel hyperaccumulation and hypertolerance were predicted.

15 Mechanisms of Se hyperaccumulation and its adaptive significance appear t

16 derstanding of the mechanisms of heavy metal hyperaccumulation and tolerance and as a source of genes

17 lation and tolerance in plants and algae, Se hyperaccumulation, and ecological and evolutionary aspec

18 of ScATM1, abrogate intra-mitochondrial iron hyperaccumulation, and restore mitochondrial respiratory

19 Diseases characterized by copper hyperaccumulation are currently challenging to identify

20 ing of the traits and mechanisms involved in hyperaccumulation are needed so that phytoextraction can

21 rate that both good biomass yields and metal hyperaccumulation are required to make the process effic

22 ce signalling through ROS and that, as metal hyperaccumulation became effective as a form of elementa

23 tists focused on the mechanisms of Cd and Zn hyperaccumulation but did not take into consideration th

24 kely selection pressure for the evolution of hyperaccumulation, but few have tested the origin(s) of

25 Hence, BSD2 prevents metal hyperaccumulation by exerting negative control over the

26 Arsenic hyperaccumulation can be engineered in A. thaliana by kn

27 1 under the LOB promoter, indicating that BR hyperaccumulation contributes to the lob mutant phenotyp

28 Here we show that a hyperaccumulation effect can allow efficient enrichment

29 The basis of the nutrient-dependent AdoMet hyperaccumulation effect is discussed in relation to hom

30 llow us to alter the expression of candidate hyperaccumulation genes and thus dissect the molecular a

31 Hyperaccumulation has evolved independently in at least

32 ilitated by molecular dissection of plant Zn hyperaccumulation (i.e., the ability of certain plants t

33 lation, but few have tested the origin(s) of hyperaccumulation in a phylogenetic context.

34 To achieve Phe hyperaccumulation in a plant system, we simultaneously d

35 s belong to the same species and that nickel hyperaccumulation in A. serpyllifolium appears to repres

36 However, Se hyperaccumulation in Astragalus is not driven by an over

37 one of the main transporters involved in Cd hyperaccumulation in N. caerulescens and copy number var

38 ot seem to be much ecotypic variation for Zn hyperaccumulation in N. caerulescens.

39 ability of contaminants can sometimes induce hyperaccumulation in normal plants, but may produce unde

40 n of the molecular mechanisms involved in As hyperaccumulation in P. vittata using gametophytes as an

41 eview what is known about evolution of metal hyperaccumulation in plants and describe a population-ge

42 In this work, engineering Cu-hyperaccumulation in plants was approached.

43 our understanding of the evolution of metal hyperaccumulation in plants.

44 ions into the basic mechanisms underlying As hyperaccumulation in plants.

45 on the evolutionary history of selenium (Se) hyperaccumulation in Stanleya (Brassicaceae).

46 esults give insight into the evolution of Se hyperaccumulation in Stanleya and suggest that Se tolera

47 e organic Se are likely prerequisites for Se hyperaccumulation in Stanleya.

48 t in the epidermal storage cells where metal hyperaccumulation in T. caerulescens occurs.

49 and physiological processes underlying metal hyperaccumulation in T. caerulescens.

50 en suggested to play an important role in Zn hyperaccumulation in T. goesingense.

51 ction in zinc and cadmium hypertolerance and hyperaccumulation in the extremophile plant species Arab

52 ar physiology and molecular biology to Zn/Cd hyperaccumulation in the intact plant, T. caerulescens s

53 ACR3 expression with HAC1 mutation led to As hyperaccumulation in the shoots, whereas combining HAC1

54 onses in plants, is a strong predictor of Ni hyperaccumulation in the six diverse Thlaspi species inv

55 ed a critical role in the evolution of metal hyperaccumulation in the Thlaspi genus.

56 stand the role of free histidine (His) in Ni hyperaccumulation in Thlaspi goesingense, we investigate

57 and molecular basis of nickel (Ni)/zinc (Zn) hyperaccumulation in Thlaspi; however, the molecular sig

58 Metal hyperaccumulation is an uncommon but highly distinctive

59 In mature sbe2a leaves, starch hyperaccumulation is greatest in visibly senescing regio

60 These observations suggest that metal hyperaccumulation is incompatible with defence signallin

61 To investigate whether Se hyperaccumulation is ubiquitous in S. ericoides or restr

62 y was to investigate how plant selenium (Se) hyperaccumulation may affect ecological interactions and

63 een pathogen resistance and Ni tolerance and hyperaccumulation may have played a critical role in the

64 arsenate, consistent with other known metal hyperaccumulation mechanisms in plants.

65 iously characterized maize leaf carbohydrate hyperaccumulation mutants.

66 cled unattached kinetochores, similar to the hyperaccumulation observed of dynamic outer kinetochore

67 This hyperaccumulation occurs because the translation of each

68 h decreased cyclin D1 proteolysis and, thus, hyperaccumulation of active cyclin D1.CDK4 (cyclin-depen

69 The hyperaccumulation of AdoMet was a robust phenomenon when

70 Thus, hyperaccumulation of arf3a and ectopic accumulation of m

71 Hyperaccumulation of As by plants has been identified as

72 in-accumulating regions in leaves due to the hyperaccumulation of carbohydrates.

73 Our study confirmed the hyperaccumulation of Cd and Zn for each metallicolous po

74 Genetic suppressor analysis revealed that hyperaccumulation of copper and cadmium in bsd2 mutants

75 acking superoxide dismutase and also lead to hyperaccumulation of copper ions.

76 tone modifications that are required for the hyperaccumulation of Crb2 at DSBs.

77 cha1Delta strain to high serine resulted in hyperaccumulation of endogenous serine and in turn a sig

78 ncluding the reduction of lignin content and hyperaccumulation of flavonoids and p-coumarate esters.

79 '-hydroxylase (C3'H) lead to reduced lignin, hyperaccumulation of flavonoids, and growth inhibition i

80 nstitutive activation of cAPK suppresses the hyperaccumulation of glycogen in a pho85 mutant.

81 in the increase in phosphate scavenging and hyperaccumulation of glycogen in nutrient-rich condition

82 h defects on a variety of carbon sources and hyperaccumulation of glycogen in rich medium high in Pi.

83 Hyperaccumulation of glycogen in the pho85 strains is in

84 Disruption of PCL8 and PCL10 caused hyperaccumulation of glycogen, activation of glycogen sy

85 ells with disrupted PHO85 genes, we observed hyperaccumulation of glycogen, activation of glycogen sy

86 d levels of metabolites such as glucose-6-P, hyperaccumulation of glycogen, and activation of glycoge

87 ant to inhibition by phosphorylation, caused hyperaccumulation of glycogen.

88 , lactate or glycerol as a carbon source and hyperaccumulation of glycogen.

89 tion of PKA in a pho85 mutant suppresses the hyperaccumulation of glycogen.

90 Hyperaccumulation of iron in opt3-2 resulted in the form

91 f CYP94B3 function in cyp94b3 mutants causes hyperaccumulation of JA-Ile and concomitant reduction in

92 quantitative mass spectrometry demonstrated hyperaccumulation of Lys63 chains in the insoluble fract

93 f transgenic chloroplasts as bioreactors for hyperaccumulation of membrane proteins for biotechnologi

94 l mutants exhibited reduced levels of JA and hyperaccumulation of OPC-8:0.

95 t incorporates the light requirement and the hyperaccumulation of photoassimilates.

96 poylation of mitochondrial proteins, and the hyperaccumulation of photorespiratory intermediates, gly

97 f different genotypes of annual ryegrass for hyperaccumulation of Pi in their shoots, Gulf and Urugra

98 duction of esterified suberin components and hyperaccumulation of putative suberin precursors in the

99 The latter class of mutations led to hyperaccumulation of repair intermediate Mlh1-Pms1 foci

100 Through genetic analysis we show that hyperaccumulation of Rum1 contributes to re-replication

101 y play an important signaling role in the Se hyperaccumulation of S. pinnata, perhaps by constitutive

102 osensitivity that occurs in conjunction with hyperaccumulation of salicylic acid (SA).

103 mutant's growth defects, suggesting that the hyperaccumulation of salicylic acid is unlikely to be re

104 Detrimental effects of hyperaccumulation of the aromatic amino acid phenylalani

105 ial nutrient for life, but at the same time, hyperaccumulation of this redox-active metal in biologic

106 in CDPK2 deficient parasites results in the hyperaccumulation of this sugar polymer.

107 lso altered so that it largely overrides the hyperaccumulation of transcripts, and as a consequence,

108 rkat T cells, avicin G treatment resulted in hyperaccumulation of ubiquitinated proteins in S. pombe

109 understanding the mechanisms responsible for hyperaccumulation of Zn, Cd, Ni and As by plants.

110 Mapping the trait of Na-hyperaccumulation onto the phylogenetic relationships be

111 metals and thus could be a key player in the hyperaccumulation phenotype expressed in T. caerulescens

112 We therefore conclude that the Ni hyperaccumulation phenotype in T. goesingense is not det

113 ericoidesPR population may contribute to the hyperaccumulation phenotype.

114 uppress the arsenate sensitivity and arsenic hyperaccumulation phenotypes of yeast (Saccharomyces cer

115 The study of these metal hyperaccumulation processes at the cellular level in T.

116 Although Se hyperaccumulation protects plants from herbivory by some

117 Nickel hyperaccumulation reverses this pathogen hypersensitivit

118 Hyperaccumulation tends to negatively affect Se-sensitiv

119 S2-RNAi lines, however, did not reach the Zn hyperaccumulation threshold.

120 and PDF2.3) as possible contributors to the hyperaccumulation/tolerance phenotype.

121 d correlation with Zn(2+), Cd(2+), or Ni(2+) hyperaccumulation/tolerance.

122 us studies have indicated that the Zn and Cd hyperaccumulation trait exhibited by this species involv

123 ility and therefore may contribute to the Se hyperaccumulation trait; however, it is not sufficient t

124 We could not detect Dup hyperaccumulation using mutations in the CRL4(Cdt2) comp

125 o investigate the mechanisms responsible for hyperaccumulation, using natural hyperaccumulators as mo

126 is the key plant characteristic required for hyperaccumulation; vacuolar compartmentalization appears

127 True hyperaccumulation was found in three taxa within the S.

128 Se hyperaccumulation was found to positively correlate with

129 responsible for selenium (Se) tolerance and hyperaccumulation were studied in the Se hyperaccumulato

130 ZNT1 does not directly participate in metal hyperaccumulation within the leaf.