ライフサイエンスコーパス: symbiosome

1 ne in an organelle-like structure called the symbiosome.

2 ived membrane forming a novel organelle, the symbiosome.

3 a unique plant membrane compartment termed a symbiosome.

4 ome surrounded by a plant membrane to form a symbiosome.

5 nclosed in a specific organelle known as the symbiosome.

6 localized itself to the infection thread and symbiosomes.

7 n plant-derived membrane compartments termed symbiosomes.

8 , forming organelle-like compartments called symbiosomes.

9 cuoles contract, permitting the expansion of symbiosomes.

10 ppears to be essential for the maturation of symbiosomes.

11 brane-derived plant cell compartments called symbiosomes.

12 mall nodules with greatly reduced numbers of symbiosomes.

13 tablishes RSD as a TF implicated directly in symbiosome and bacteroid differentiation and a transcrip

14 d that contained incompletely differentiated symbiosomes and bacteroids.

15 e enclosed in membrane-bound vesicles called symbiosomes and differentiate into bacteroids that are c

16 The nodules and associated symbiosomes are structured for efficient nitrogen fixati

17 However, it blocks symbiosome as well as arbuscule formation, whereas root

18 Both excised and symbiosome-attached patches exhibited a large inward (to

19 However, based on observations with symbiosome-attached patches, the direction of the curren

20 In Medicago truncatula, the symbiosome consists of the symbiosome membrane, a single

21 e and infected cortical cells were devoid of symbiosome-containing bacteroids.

22 dnf1 mutant of M. truncatula, bacteroid and symbiosome development are blocked.

23 ts having defects in rhizobial infection and symbiosome development demonstrated that the MtNIP/LATD

24 expression analysis, we propose that correct symbiosome development in M. truncatula requires the ord

25 Thus, RSD may influence symbiosome development in part by repressing transcripti

26 Here, we describe regulator of symbiosome differentiation (RSD) of Medicago truncatula,

27 ily of plant TFs that is required for normal symbiosome differentiation during nodule development.

28 symbiosis between legumes and rhizobia, the symbiosome encases the intracellular bacteria and receiv

29 ction thread growth, root-nodule number, and symbiosome formation in root nodule cells were severely

30 surface areas of plant cells, vacuoles, and symbiosomes in root nodules of Medicago truncatula and a

31 brane, and is required for the maturation of symbiosomes into functional forms.

32 the establishment of mature nitrogen-fixing symbiosomes, is regulated by osmotic stresses that induc

33 The symbiosome membrane (SM) is a selectively permeable barr

34 nstitutes the major protein component on the symbiosome membrane (SM) of N(2)-fixing soybean nodules.

35 family, is a major component of the soybean symbiosome membrane (SM) that encloses the rhizobium bac

36 ese cells or defects in the formation of the symbiosome membrane during bacterial release.

37 hemical analyses, GmN70 was localized to the symbiosome membrane of infected root nodule cells, sugge

38 nodulin 26 is expressed and targeted to the symbiosome membrane of nitrogen-fixing nodules, where it

39 e ammonium (NH4(+)) channel localized to the symbiosome membrane of soybean root nodules.

40 n the present study, the ion currents of the symbiosome membrane of the model legume Lotus japonicus

41 plasma membrane of nodule cells and also the symbiosome membrane surrounding bacteroids in infected c

42 The host-derived symbiosome membrane surrounding the algae abundantly exp

43 on of this mutant and the host plant-derived symbiosome membrane was disrupted.

44 jN70 are inorganic anion transporters of the symbiosome membrane with enhanced preference for nitrate

45 o truncatula, the symbiosome consists of the symbiosome membrane, a single rhizobium, and the soluble

46 the host cytoplasm and membranes, except the symbiosome membrane, were severely degraded in the faile

47 dulin 26 on Ser-262, which is catalyzed by a symbiosome membrane-associated calcium-dependent protein

48 rin TIP1g from the tonoplast membrane to the symbiosome membrane.

49 zing the enzyme to the cytosolic side of the symbiosome membrane.

50 plasm across the bacterial membranes and the symbiosome membrane.

51 of uninfected cells and infection thread and symbiosome membranes of infected cells.

52 and contained infected cells with disrupted symbiosome membranes, indicating either early senescence

53 The symbiosome of nitrogen fixing root nodules mediates meta

54 ant decrease in average H(+) activity in the symbiosome of up to 75% and a significant reduction in O

55 Symbiosomes remain as individual units and avoid fusion

56 uolar H(+)-ATPase (VHA), which acidifies the symbiosome space down to pH approximately 4.

57 The symbiosome space is enriched with plant-derived proteins

58 MtMATE67-mediated citrate transport into the symbiosome space would increase the solubility and avail

59 d bacteria exists a matrix-filled space (the symbiosome space) that is thought to contain a mixture o

60 d the soluble space between them, called the symbiosome space.

61 ly in root nodules, are localized within the symbiosome space.

62 erved for the wild-type; however, no typical symbiosome structures were formed.

63 ant Phaseolus vulgaris and produced abnormal symbiosome structures.

64 as evolved redundant targeting sequences for symbiosome targeting and that intracellular localization

65 the MtENOD8 protein contains at least three symbiosome targeting domains, including its N-terminal s

66 Within the symbiosomes the bacteria differentiate to bacteroids, th

67 During the maturation of symbiosomes to become N2-fixing organelles, a developmen

68 26 water channels in their native membranes, symbiosomes were isolated from soybean root nodules and

69 o punctate intermediates and subsequently to symbiosomes, with redirection of MtENOD8-SP-GFP from the

70 nclosed in intracellular compartments called symbiosomes within nodules on the root.