ライフサイエンスコーパス: flax

1 deer, bats) and plants (chestnut, hazelnut, flax).

2 G in PUFA content during seed development in flax.

3 cterization of TAG-synthesizing enzymes from flax.

4 these compounds occur in foods that contain flax.

5 FlaX, a conserved subunit in crenarchaeal archaella, for

6 The bacterial proteins FlaX, A4-fla2, and YidX increased proliferation of CD4(+

7 s from controls, CD4(+) T cells specific for FlaX, A4-fla2, or YidX had a T-helper (Th)1 phenotype; a

8 g/100g of fibre or 10 g/100g of omega-3 oil (flax:algae:menhaden, 8:1:1) or fibre+omega-3 oil (6g/100

9 ied, to our knowledge, for the first time in flax and 11 for the first time in higher plants.

10 s demonstrate that root border-like cells of flax and Arabidopsis are able to perceive an elicitation

11 Cold-pressed hemp, flax and canola seed oils are healthy oils for human con

12 ate the channeling of PUFA from PC to TAG in flax and possibly also in other oleaginous plants that p

13 Films from flax and quince mucilage were found to be more thermally

14 (25:75) (CornSaff; n-6 rich), 4) a blend of flax and safflower oils (60:40) (FlaxSaff; n-6 and short

15 Chia, flax and sesame seeds are well known for the good nutrit

16 t HPLC-MS/MS for the authentication of chia, flax and sesame seeds.

17 llotetraploid cyprinids, allohexaploid false flax, and allooctoploid strawberry.

18 iotics to the seed mucilage films of quince, flax, and basil.

19 or routine authenticity testing of camelina, flax, and hemp oil in food control laboratories.

20 Chia, flax, and sesame seeds are considered superseeds due to

21 Chia, flax, and sesame seeds are well known for their nutritio

22 unoglobulin G, anti-OmpC, anti-A4-Fla2, anti-FlaX, anti-CBir1) and derived the sum of positive antibo

23 esis, transgenic tobacco plants containing a flax AOS cDNA without a chloroplast transit sequence und

24 Induction of the flax AOS gene in transgenic plants with chlor-tetracycli

25 Overexpression of the flax AOS in induced transgenic plants did not increase J

26 tracycline (Tc) led to the expression of the flax AOS mRNA and protein, which resulted in high level

27 cellular fractionation demonstrated that the flax AOS protein and activity were associated with the c

28 However, in wounded tissues overexpressing a flax AOS, levels of JA and the transcript of a pathogene

29 ed when compared to those not expressing the flax AOS.

30 and 12, it is expected that their levels in flax based foods would be low and therefore their presen

31 y latitudes the architecture of domesticated flax became more suitable to fiber production over oil,

32 False flax (Camelina sativa L.), known as camelina, is an anci

33 ve analysis of several oils, including false flax (Camelina sativa) oil stored under different condit

34 In false flax (Camelina sativa), an important hexaploid oilseed c

35 al metabolism in developing embryos of false flax (Camelina sativa).

36 in triacylglycerol (TAG), it is likely that flax contains enzymes that can efficiently transfer ALA

37 s of mucilages, extracted from seven Italian flax cultivars, were evaluated.

38 n vivo experiments showed that co-expressing flax DGAT1-1 and LPCAT1 in the yeast quintuple mutant si

39 nsitive cell-death response triggered by the flax disease resistance protein M1.

40 We identified a small RNA, flaX, downstream of the major flagellin gene flaA.

41 PDAT genes were preferentially expressed in flax embryos.

42 s were used to create 30 vol% unidirectional flax-epoxy composites.

43 mance liquid chromatography) of chia, golden flax, evening primrose, phacelia and fenugreek seeds.

44 Natural fibers, such as flax fiber and their composites, offer a compelling comb

45 reatment on the morphology and properties of flax fibers are reported.

46 Treated flax fibers were used to create 30 vol% unidirectional f

47 oxidation, total volatiles of high n-3 oils (flax, fish, cod liver) were 120-170 mg/kg while low n-3

48 motility structure, the archaellum, contains FlaX, FlaI and FlaH.

49 d flax seed, we tested for their presence in flax food products.

50 FlaX forms a 30 nm ring structure that acts as a scaffol

51 Further seed-specific expression of flax genes in Arabidopsis thaliana indicated that DGAT1,

52 ylglycerol acyltransferases (PDATs) from the flax genome database.

53 Two PEBP family genes in the flax genome, LuTFL1 and LuTFL2, vary in wild and cultiva

54 tion for quantitative traits in this diverse flax germplasm collection.

55 Delphinidin is sporadic in angiosperms, and flax has no known pollination syndrome(s) with functiona

56 nd certain peroxidase genes, suggesting that flax hypolignification is transcriptionally regulated.

57 ound 10,000 years ago several founder crops, flax included, spread to European latitudes.

58 Ether Reductase were also highly abundant in flax inner stem tissues.

59 the oligomerization, but also essential for FlaX interaction with FlaI, the bifunctional ATPase that

60 nd a strong asymmetry in the terms of trade: flax invested little carbon but gained up to 94% of the

61 The main flax lignan, secoisolariciresinol diglucoside, is stored

62 The flowers of flax (linseed) are blue-hued, ephemeral and self-pollina

63 ini) and its subalpine wildflower host Lewis flax (Linum lewisii) to investigate how climate change m

64 Seed oils of flax (Linum usitatissimum L.) and many other plant speci

65 e polymorphism (SNP) markers in a set of 337 flax (Linum usitatissimum L.) germplasm, phenotyped in f

66 The oil from flax (Linum usitatissimum L.) has high amounts of alpha-

67 ty is given by the developed model system of flax (Linum usitatissimum L.) phloem fibres that can be

68 9 to develop an herbicide tolerance trait in flax (Linum usitatissimum) by precisely editing the 5'-E

69 -1 receptor (TIR) domain-containing NLR from flax (Linum usitatissimum) conferring immunity to the fl

70 Flax (Linum usitatissimum) has a genome in which changes

71 The viscous seed mucilage of flax (Linum usitatissimum) is a mixture of rhamnogalactu

72 The seed oil of flax (Linum usitatissimum) is enriched in ALA, and this

73 ive was to study the mechanisms of action of flax (Linum usitatissimum) phenolic compounds to prevent

74 ps of Arabidopsis (Arabidopsis thaliana) and flax (Linum usitatissimum) release cells known as "borde

75 ermined the inception of gravisensitivity in flax (Linum usitatissimum) roots by clinorotating germin

76 Flax (Linum usitatissimum) stems contain cells showing c

77 ized directly by the resistance protein M in flax (Linum usitatissimum), resulting in effector-trigge

78 The plants were flax (Linum usitatissimum; a C(3) plant) and sorghum (So

79 PA and DHA, ALA-enriched supplements such as flax may have a similar effect, although this hypothesis

80 Although both flax mucilage and zein have excellent film-forming prope

81 The flax mucilage conjugate exhibited thermoplastic and elas

82 The flax mucilage conjugate had a water-holding capacity of

83 y, we explored zein protein conjugation with flax mucilage for packaging material development.

84 Where the flax mucilage undergoes oxidation to form aldehyde group

85 oxic one-pot method for developing the novel flax mucilage/zein conjugate.

86 and 12 have not been detected in commercial flax oil and milled flax seed, we tested for their prese

87 The flax seed cake is a waste product from flax oil extraction.

88 The consumption of either 2.4 or 3.6 g flax oil/d (in capsules) was sufficient to significantly

89 rimental groups receiving 1.2, 2.4, or 3.6 g flax oil/d; 0.6 or 1.2 g fish oil/d; or 1 g sunflower oi

90 acid) had levels of PUFA similar to those of flax oils.

91 y acids (omega-3's), whether from fish oils, flax or supplements, can protect against cardiovascular

92 TFL1 and LuTFL2, vary in wild and cultivated flax over latitudinal range with cultivated flax receivi

93 d to a background of population structure of flaxes over latitude, the LuTFL1 alleles display a level

94 Gravistimulation of flax plants induces gravitropic curvature in non-elongat

95 Thus, in this paper it is proved that flax plants treated with a 0.2% w/v CNF solution after r

96 f leaves obtained from over 1000 mutagenised flax plants, and selected 59 plants whose spectral varia

97 receiving LuTFL1 alleles from northerly wild flax populations.

98 flax over latitudinal range with cultivated flax receiving LuTFL1 alleles from northerly wild flax p

99 archaellar assembly: FlaH binding within the FlaX ring and nucleotide-regulated FlaH binding to FlaI

100 which was earlier shown to be essential for FlaX ring formation and to mediate interaction with FlaI

101 t FlaH assembles as a second ring inside the FlaX ring in vitro.

102 AvrM is a secreted effector protein from flax rust (Melampsora lini) that can internalize into pl

103 the Nudix hydrolase effector AvrM14 from the flax rust fungus (Melampsora lini).

104 um usitatissimum) conferring immunity to the flax rust fungus.

105 We use the fungal 'flax rust' pathogen (Melampsora lini) and its subalpine

106 The flax seed cake is a waste product from flax oil extracti

107 (BCF) were produced by using guar gum (GG), flax seed mucilage (FM) and polyvinyl alcohol (PVA), sup

108 ling the adulteration of camelina, hemp, and flax seed oils with these oils.

109 olysis and glycosidase enzymes in almond and flax seed were most effective for developing a flavone-r

110 enin aglycone after combination with almond, flax seed, or chickpea flour.

111 n detected in commercial flax oil and milled flax seed, we tested for their presence in flax food pro

112 her deglycosylated when mixed with almond or flax seed.

113 we study the aqueous mucilage extracted from flax seeds (Linum usitatissimum) and compare its drag re

114 lum and almond kernels, as well as apple and flax seeds was determined.

115 oducts, rye grains, rye flour, rye bread and flax seeds were extracted by sonication with ethanol/wat

116 d rapidly in sesame seeds and rye but not in flax seeds.

117 in isolated fibres and other portions of the flax stem, together with fibre metabolism characterizati

118 into the growth medium, could be absorbed by flax stems, reinforcing their cell walls formation and,

119 Mutation of flaX substantially reduced motility.

120 In this study, flax technical fibers were treated in supercritical CO(2

121 ed the existence of unique PDAT enzymes from flax that are able to preferentially catalyze the synthe

122 of root border-like cells of Arabidopsis and flax to flagellin22 and peptidoglycan.

123 quence of a natural adaptation of cultivated flax to higher latitudes.

124 omplementation assays, we probed recombinant flax transferase enzymes, previously shown to contribute

125 We conclude that specialized fiber flax types could have formed as a consequence of a natur

126 entally induced heritable changes in certain flax varieties has been shown to be accompanied by chang

127 The inbred flax variety, Stormont Cirrus (Pl), served as the parent

128 The C terminus of FlaX was not only involved in the oligomerization, but a

129 enes N (tobacco), RPS2 (Arabidopsis) and L6 (flax) were used to amplify related sequences from soybea

130 FlaH interacts with the C-terminus of FlaX, which was earlier shown to be essential for FlaX r

131 es, okra, and seeds of basil, fenugreek, and flax, which were identified as SBM-TSF, OKM-TSF, BSM-TSF