ライフサイエンスコーパス: oil body

1 ecursor backbone, (13R) manoyl oxide, to the oil bodies.

2 in is mainly localized in the surface of the oil bodies.

3 ith histochemical properties consistent with oil bodies.

4 BAP1 protein is involved in the stability of oil bodies.

5 sulted in sterile pollen that lacked visible oil bodies.

6 ps of the two TIPs, and they contained fewer oil bodies.

7 se activity that is associated with purified oil bodies.

8 role in the degradation of storage lipid in oil bodies.

9 m where it is associated with the surface of oil bodies.

10 proteomic analysis was performed on purified oil bodies.

11 h phospholipids in stabilizing reconstituted oil bodies.

12 eosins to stabilize the abundant subcellular oil bodies.

13 s the Brassica oleosin, was localized in the oil bodies.

14 ion technology, which allows extraction with oil bodies.

15 hotorespiration through the interaction with oil bodies and chloroplasts, highlighting a fundamentall

16 Seed oil bodies and floret tapetosomes have been isolated fro

17 e alterations in mesophyll cells, which lack oil bodies and normal plastids.

18 contours and demonstrated internalization of oil bodies and of membrane containing alpha- and delta-t

19 Transgenic plantlets accumulated oil bodies and responded to the abscisic acid biosynthes

20 bcellular triacylglycerol granules in seeds (oil bodies) and floral tapetum (tapetosomes) are stabili

21 h abnormal seed germination, accumulation of oil bodies, and delayed degradation of long-chain fatty

22 mulate more starch, the cytoplasm fills with oil bodies, and lytic vacuoles (LVs) appear smaller in s

23 specialized cell type, and support a role of oil bodies as storage organelles for lipophilic bioactiv

24 One of the identified genes is oil body associated protein1 (obap1), which is transcrib

25 st evidence for the molecular identity of an oil body-associated lipase from plants.

26 YLGLYCEROL ACYLTRANSFERASE1 and the OLEOSIN1 oil body-associated protein, in the adg1suc2 mutant doub

27 ins, caleosin/dioxygenase/steroleosin and LD/oil body-associated proteins, participate in cellular st

28 he average size distribution of pumpkin seed oil bodies at an increasing pH (3, 7.4 and 9) and salt c

29 ring seeds, SSE1 is required for protein and oil body biogenesis, both of which are endoplasmic retic

30 sphonate causes peroxisome clustering around oil bodies but does not affect morphology of other cellu

31 s located on ER membranes in the vicinity of oil bodies, but none were detected on the bulk ER cister

32 Oil bodies can be extracted, isolated and from pumpkins

33 Our evidence indicates that thallus oil body cells, similar to the terpenoid-containing oil

34 OBAP1 protein was detected in the oil body cellular fraction of Arabidopsis embryos.

35 d their embryos have few, big, and irregular oil bodies compared with the wild type.

36 nti-oleosin antibodies, indicating that each oil body contained a mixed population of soybean and rap

37 sing this extraction method about 65% of the oil bodies could be obtained.

38 on at pH 5.0 and then diluting the resulting oil body creams with deionized water.

39 purity and the composition of the recovered oil bodies depends on the molarity of medium used; the u

40 n was targeted to and stably integrated into oil bodies, despite the absence of a soybean partner iso

41 Three natural oil body emulsions of a similar fat content ( approximat

42 Mixtures of the natural oil body emulsions with green tea extracts, aiming to se

43 ies of transgenic rapeseed revealed that all oil bodies examined could be labelled with both the soyb

44 st was prepared by concentrating the aqueous oil body extract with ultrafiltration to a fat content o

45 osins (18 and 24 kDa) were isolated from the oil bodies extracted from soybean seeds and positively c

46 ethod was developed to increase the yield of oil bodies extracted from soybean.

47 Although oil-body formation per se can occur independently of ole

48 rotubule nucleation domains; the protein and oil body-forming domains; the vacuole-forming ER; the ac

49 In nature, this protein coating protects the oil bodies from environmental stresses and might be util

50 mperature on the properties and stability of oil bodies from pumpkin (Cucurbita) were determined with

51 Oil bodies from pumpkin seeds were extracted, isolated,

52 An aqueous process for the recovery of oil bodies from rapeseed using sodium bicarbonate-based

53 wo were prepared by initially recovering the oil bodies from the extract by centrifugation, either in

54 A plant oil body has a matrix of oils (triacylglycerols) surroun

55 ound peroxisomes clustered around persisting oil bodies in pex6 and pex26 seedlings, suggesting a rol

56 onally equivalent to the subcellular storage oil bodies in plant seeds.

57 ces accumulation of seed storage protein and oil bodies in vegetative and reproductive organs, events

58 of apparent targeting of oleosins via ER to oil bodies in vivo and of possible associated conformati

59 ter (d43) and sedimentation of the resulting oil bodies increased during storage, suggesting they wer

60 detected oleosins on the surface of storage oil bodies inside the maturing microspores.

61 grinding and molarity of the medium used on oil body integrity, purity and storage stability have be

62 Catabolism of fatty acids stored in oil bodies is essential for seed germination and seedlin

63 en tea polyphenols seem to interact with the oil bodies leading to intensive dispersion destabilisati

64 Lipid droplets in plants (also known as oil bodies, lipid bodies, or oleosomes) are well charact

65 c part of the protein is responsible for the oil body localization, which suggests an indirect intera

66 lipase activity that is associated with the oil body membrane.

67 Unlike oleosins associated with oil bodies, none of the membrane-associated oleosins cou

68 Lipid droplets/oil bodies (OBs) are lipid-storage organelles that play

69 Oil bodies (OBs) are seed-specific lipid storage organel

70 examination of Physcomitrella revealed that oil bodies (OBs) were abundant in the photosynthetic veg

71 y cells, similar to the terpenoid-containing oil bodies of modern liverworts, were probably involved

72 drophobic abundant proteins localized in the oil bodies of plant seeds.

73 Apparently, the gametophytic microspore oil-body oleosins share common epitopes at the generally

74 Triacylglycerol (TAG) levels and oil bodies persist in sucrose (Suc)-rescued Arabidopsis

75 ) in the grinding and washing steps produced oil body preparations with the same purity as that resul

76 olecule blocks the breakdown of pre-existing oil bodies resulting in retention of TAG and accumulatio

77 a) were determined with a view to patterning oil body size and structure for future therapeutic inter

78 seed development are a major determinant of oil-body size in desiccation-tolerant seeds.

79 otein fusion was shown to associate with the oil body surface in vivo.

80 eraction of OBAP1 with other proteins in the oil body surface.

81 Caleosin is a Ca(2+)-binding oil-body surface protein.

82 (w/w) significantly improved the quality of oil body suspension to a size more in-line with that see

83 ersely affect the oxidative stability of the oil body suspensions at pH 3 or 7 during storage at 37 d

84 Heat treatment (90 degrees C, 30min) of the oil body suspensions immediately after extraction improv

85 ous extraction method can be used to prepare oil body suspensions with improved long-term stability.

86 curd densely packed and seemed to be rich in oil bodies than any of the four layers.

87 that the seeds of the RNAi plants had fewer oil bodies than the nontransgenic plants.

88 Soybeans contain oil bodies that are coated by a layer of oleosin protein

89 s function appears to be critical to protect oil bodies that are in close proximity to peroxisomes fr

90 l for all four layers where cream had larger oil bodies then upper curd.

91 To assess its role in the degradation of oil-bodies, two independent insertion mutants lacking ca

92 peroxisomal retrotranslocation machinery in oil body utilization.

93 During microscopic analysis, the oil bodies were more intact and in an integrated form at

94 Water extracted oil bodies were spherical for all four layers where crea

95 tural oils (coconut oil, palm oil, and algal oil bodies) were enzymatically converted into fatty alco

96 Plant oils are stored in oleosomes or oil bodies, which are surrounded by a monolayer of phosp

97 The results indicate that interaction of oil bodies with vacuoles is one mechanism that contribut

98 rage vacuole membrane and the interaction of oil bodies with vacuoles.

99 ous 19 kDa rapeseed oleosin) was targeted to oil bodies, with the remainder associated with the micro