ライフサイエンスコーパス: mycelial

1 fruiting twice a year, indicating increased mycelial activity and possibly greater decay rates in ec

2 ored on the extracellular plasma membrane of mycelial and spherule-phase cells.

3 ine some of the major characteristics of the mycelial and yeast phases.

4 nalysis of hyphal dimensions showed that the mycelial architecture and the erection of aerial hyphae

5 erentiation and antibiotic production in the mycelial bacteria of the genus Streptomyces.

6 on genes ftsL and divIC in the gram-positive mycelial bacterium Streptomyces coelicolor A3(2).

7 al mycelium formation and sporulation in the mycelial bacterium Streptomyces coelicolor rely on estab

8 wo antibiotics in Streptomyces coelicolor (a mycelial bacterium).

9 content of initial materials, while residual mycelial biomass was affected by mushroom productivity.

10 fluorescent fusion protein localized to the mycelial cell wall.

11 tions, vac7, vac8 and fab1 mutants generated mycelial compartments with more symmetrically distribute

12 were clustered separately from the external mycelial cortices and fruiting bodies of Chinese Cordyce

13 entified in the fruiting bodies and external mycelial cortices of Chinese Cordyceps.

14 ies between the fruiting bodies and external mycelial cortices of Chinese Cordyceps.

15 ort to determine genes that are expressed in mycelial cultures of Neurospora crassa over the course o

16 Yeasts cultures, but not mycelial cultures, release large quantities of a calcium

17 mug/mL in liquid medium with a 5mm diameter mycelial disc of F. verticillioides.

18 was performed with analyses of soil DNA and mycelial DNA.

19 e show that in such circumstances, continual mycelial expansion can only be obtained if internal meta

20 sults from mutational alterations that allow mycelial expression of the con-10'-'hph gene fusion.

21 es and were trans-acting, i.e., they allowed mycelial expression of the endogenous con-10 gene.

22 ivity was purified to homogeneity from crude mycelial extracts of S. coelicolor and shown to be BldD.

23 Mycelial extracts prepared from S. coelicolor cultures i

24 O-sulfate and glycine betaine, were found in mycelial extracts, suggesting that phosphocholine-contai

25 ons of these individual steps to the overall mycelial FLU transport rate.

26 orting systems have been shown to facilitate mycelial foraging and long-distance communication in sap

27 at sometimes switch from yeast to pathogenic mycelial form.

28 essentially nonreactive with the surfaces of mycelial forms of the fungus, indicating that neither ep

29 ns, a dimorphic fungus composed of yeast and mycelial forms, is the most common human fungal pathogen

30 nd comparable growth rates of both yeast and mycelial forms.

31 f the molds could be amplified directly from mycelial fragments, while DNA from every yeast colony wa

32 37-kDa culture filtrate protein and a 55-kDa mycelial glycoprotein (gp55) exhibited complete N-termin

33 spore dispersal, such as aerial dispersal in mycelial groups and polar tube eversion in the microspor

34 ional attributes, including carbon fixation, mycelial growth and nutrient utilization, but this is dr

35 henotype that included significantly reduced mycelial growth and profoundly altered colony morphology

36 hibit significant fitness penalties based on mycelial growth and spore germination, suggesting that i

37 also resulted in reductions in virulence and mycelial growth and, unexpectedly, enhanced conidial pro

38 on of S. parasitica zoospore germination and mycelial growth by two cyclooxygenase inhibitors (aspiri

39 an active chitin synthase-like protein, and mycelial growth is impaired after treatment with a chiti

40 The mycelial growth of Fusarium verticillioides (Sacc.) Nire

41 rast tomography (Q-ACT) we detected that the mycelial growth on the solid agar created multiple surfa

42 Antimicrobial tests for mycelial growth reduction under atmospheric conditions p

43 stationary phase in liquid culture, or from mycelial growth to sporulation on solid media.

44 e sister group to Saccharomycotina, retained mycelial growth while elaborating two basic ontogenetic

45 cement of MoGSK1 caused significant delay in mycelial growth, complete loss of conidiation and inabil

46 e the MIC is defined on the basis of visible mycelial growth, conidia should germinate and produce sp

47 Among filamentous fungi capable of mycelial growth, het genes play crucial roles by regulat

48 During conidial swelling and mycelial growth, the expression of AfSUN1 was strongly i

49 The thin agar film limits excessive mycelial growth, while it often promotes complete sporul

50 group VII), resulting in thin, "transparent" mycelial growth.

51 isolated mutants that express con-10 during mycelial growth.

52 expressed during conidiation but not during mycelial growth.

53 train was reduced in conidial production and mycelial growth; these effects were most noticeable when

54 GTA to culture media inhibited the growth of mycelial H. capsulatum but had no effect on yeast growth

55 Conversely, mycelial H. capsulatum did not produce CBP, a finding th

56 The majority of the isolates exhibited mycelial incompatibility, minimizing the possibility of

57 ot prevent barrage formation associated with mycelial incompatibility.

58 ly that, in Streptomyces (a bacterium with a mycelial lifestyle similar to that of filamentous fungi,

59 um which are transcriptionally silent in the mycelial (M) phase have recently been cloned and analyze

60 matic, leads to near complete destruction of mycelial microcolonies of a Streptomyces venezuelae ftsZ

61 e with heterogeneous subsurface environments mycelial microorganisms have developed a unique ramified

62 on successful conversion of the saprophytic mycelial (mold) form of this fungus to a parasitic yeast

63 es dermatitidis, for expression in yeast and mycelial morphotypes.

64 ired for the formation of the interconnected mycelial network characteristic of filamentous fungi.

65 hid-infested plants via a common mycorrhizal mycelial network.

66 Mycorrhizal fungi can form common mycelial networks (CMNs) that interconnect plants.

67 findings demonstrate that common mycorrhizal mycelial networks can determine the outcome of multitrop

68 cological amplifiers for fungal and oomycete mycelial networks in soils, extending their potential in

69 Fungi form extensive interconnected mycelial networks that scavenge efficiently for scarce r

70 In mycelial networks, contaminants were translocated over l

71 phanidermatum, were selected as producers of mycelial networks, while Mycobacterium gilvum VM552 serv

72 d transport of the PAH fluorene (FLU) by the mycelial oomycete Pythium ultimum that was grown along t

73 uting to the death of the host trees through mycelial penetration of host tissue, toxin release, inte

74 roliferates within phagolysosomes, while the mycelial phase exists only as a saprophyte in the soil.

75 ble p30 binding activity in either yeast- or mycelial phase extracts, regardless of the source of lab

76 ma capsulatum is its ability to shift from a mycelial phase in the soil to a yeast phase in its human

77 Genes induced in the mycelial phase included several involved in conidiation,

78 The saprophytic mycelial phase inhabits moist soil environments; once in

79 was cloned from genomic DNA derived from the mycelial phase of C. immitis by PCR.

80 eference antigen (coccidioidin) derived from mycelial-phase Coccidioides immitis and was reactive wit

81 pression of proteins in the spherule and the mycelial phases of C. posadasii with the intent to ident

82 The mycelial prokaryote Streptomyces coelicolor A3(2) posses

83 main protein that is required for control of mycelial proliferation and activation of asexual sporula

84 ich both cause constitutive induction of the mycelial proliferation pathway.

85 e analyzed these IH RNAs relative to control mycelial RNAs using M. oryzae oligoarrays.

86 igh G+C Gram-positive, antibiotic-producing, mycelial soil bacteria.

87 We show that the hyphae of the mycelial soil oomycete Pythium ultimum function as activ

88 dA, spdB, and kilB), which may promote intra-mycelial spread of the plasmid upon its entrance into th

89 mic dynein heavy chain to be absent from the mycelial tip, where it is normally located in wild-type

90 single plasmid gene (tra) for initial inter-mycelial transfer, and involves three additional pIJ101

91 hat its ortholog Ryp1 regulates the yeast to mycelial transition in H. capsulatum.

92 ns, but was specifically associated with the mycelial uptake of Ag NPs.