ライフサイエンスコーパス: mycelia

1 xpressed between mycorrhizas and free-living mycelia.

2 ogically active compounds produced in fungal mycelia.

3 bioavailable to bacteria after transport by mycelia.

4 er of FLU bioavailability in the vicinity of mycelia.

5 ily on sand dunes that supported no resident mycelia.

6 with each plant supporting 100-400 m of AMF mycelia.

7 cines afford more protection than those from mycelia.

8 after inoculation of leaflets with S. minor mycelia.

9 ugh transcripts in wild-type S. antibioticus mycelia.

10 d spatially heterogeneous in S. clavuligerus mycelia.

11 conserved, and no transcript was detected in mycelia.

12 nmol/mg dry weight/h, respectively, in young mycelia.

13 e resistant to hygromycin than untransformed mycelia.

14 n C biosynthesis is limited to the substrate mycelia.

15 ed as spherules transformed and matured from mycelia.

16 p, where it is normally located in wild-type mycelia.

17 anges in fruiting phenology imply changes in mycelia activity, with implications for ecosystem functi

18 They could grow slowly as mycelia and could donate nuclei in a sexual cross.

19 ent of the SSPs were secreted by free-living mycelia and five of the 10 most abundant extracellular p

20 GFP and mRFP expression was stable in mycelia and fluorescence was visible in transgenic fruit

21 compartmental movements within the substrate mycelia and includes undetermined steps within the spore

22 fungi suggest that nuclear exchange between mycelia and recombination between heterospecific nuclei

23 tal RNA and double-stranded RNA (dsRNA) from mycelia and RNA from samples enriched for virus particle

24 Ag2) is a major T-cell-reactive component of mycelia and spherule cell walls.

25 due to the simultaneous presence of dynamic mycelia and spores.

26 Considering current trends, the mycelia and the culture media of these mushrooms might b

27 wed anti-inflammatory (absent in S. bellinii mycelia) and a cytotoxicity similar (sometimes superior)

28 splays dramatic polar growth defect, and its mycelia are resistant to cell wall degrading enzymes.

29 estigation a mathematical model representing mycelia as a system of partial differential equations is

30 tin induces PDA1 expression both in cultured mycelia as well as during pathogenesis on pea.

31 However, the question if mycelia-based PAH transport has an effect on PAH biodegr

32 y C. albicans that controls the formation of mycelia but is also a virulence factor.

33 xpression, CcaR was distributed uniformly in mycelia, but became localized distal to the chromosome w

34 CcaR expression was evident in the substrate mycelia, but was completely absent in aerial hyphae.

35 expressed at higher levels in yeast than in mycelia by the same technique.

36 Here, we show that mycorrhizal mycelia can also act as a conduit for signalling between

37 n was isolated from A. fumigatus conidia and mycelia cell wall.

38 The mycelia cultured in low-phosphate (2 mM) medium containe

39 ion, visualizing CcaR within S. clavuligerus mycelia demonstrates a distinct pattern of localization

40 Interestingly, M. perniciosa biotrophic mycelia develop as long-term parasites that orchestrate

41 reen colour reappeared in a small portion of mycelia during mid-exponential growth phase.

42 poor understanding of ectomycorrhizal fungal mycelia (EFM) dynamics.

43 Extramatrical mycelia (EMM) of ectomycorrhizal fungi are important in

44 The addition of mycelia favored biofilm formation and dramatically enhan

45 Here, we investigated the role of mycelia for the translocation of nonessential substances

46 d inability to penetrate the host surface by mycelia-formed appressorium-like structures, consequentl

47 es, and simple structural differentiation of mycelia from submerged fungal cultures.

48 Cultures of mycelia fungi were identified by examining macroscopic a

49 The larger form is produced by mycelia growing in arginine-supplemented medium.

50 es Project 4) medium as well as by submerged mycelia grown in liquid minimal medium.

51 soria development as compared to vegetative (mycelia) growth or during in vivo growth in the insect h

52 Fungal mycelia have a well-established role in nutrient cycling

53 Mycelia have been recently shown to actively transport p

54 Growth of H. capsulatum mycelia in chemically defined minimal medium produced pi

55 This work examines the role of mycelia in enhancing the degradation by attached bacteri

56 rgoes a complex transformation in vivo, with mycelia in the environment producing conidia, which prob

57 ngths to ensure that almost any two mushroom mycelia in the wild can mate, cell fusion is not followe

58 illus fumigatus conidia were allowed to form mycelia in tissue culture media and then harvested for D

59 However, incorporating 5% mushroom mycelia into the bread formula did lower bread's accepta

60 Incorporating 5% mushroom mycelia into the bread formula did not adversely affect

61 As such, host colonization by resident mycelia is thought to outcompete spore infections.

62 if water is available in other zones of the mycelia network.

63 may be hydraulic redistribution of water by mycelia networks.

64 Mushroom mycelia of Antrodia camphorata, Agaricus blazei, Hericiu

65 BAD1 was expressed in yeast but not in mycelia of North American strains of B. dermatitidis, an

66 nged with either spore suspensions or fungal mycelia of Phytophthora parasitica var. nicotianae.

67 incubated in the presence or absence of the mycelia of the oomycetes in both shaking and static cond

68 ional regulators; also, production of aerial mycelia on both rich and poor media is significantly del

69 nding that correlates with the dependence of mycelia on calcium for growth.

70 e of P. ultimum compared to controls without mycelia or FLU.

71 up to 30 times greater than the rate without mycelia, possibly by providing a physical support to bac

72 e transcriptomic analysis during Bailinggu's mycelia, primordia, and fruiting body stages to identify

73 st that bacterial dispersal networks such as mycelia promote the optimized spatial arrangement of mic

74 The highly fluorescent seed culture mycelia quickly lost fluorescence upon inoculation into

75 protein previously identified in T. borchii mycelia revealed a structure comprising the five alpha-h

76 Conversely, P. eryngii mycelia showed anti-inflammatory (absent in S. bellinii

77 S. bellinii mycelia showed higher contents of ergosterol and phenoli

78 y purified RNase P from Aspergillus nidulans mycelia succeeded in cleaving a putative arginine ribosw

79 s resulted in mutants with highly fragmented mycelia that could survive only in media supplemented wi

80 When fusion occurs between fungal mycelia that differ genetically at their het loci, the r

81 evealed that with shaking and the absence of mycelia, the strain VM552 grew by utilizing the bulk of

82 expression were detected 6 h after shifting mycelia to 37 degrees C.

83 ng the temperature-induced transformation of mycelia to yeast.

84 Furthermore, degradation of mycelia-transported FLU by the bacterium Burkholderia sa

85 s with silicon coated glass fibers capturing mycelia-transported FLU guided us to propose a three-ste

86 arly difficult for samples containing fungal mycelia, where processing removes morphological characte

87 differences in the growth rate and produced mycelia, which should be considered in further applicati

88 the Deltacps1 strain showed slower growth of mycelia with delayed and lower spore production than C.