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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 , with reactivity against both H. capsulatum mycelial and yeast antigens in 30 (68.2%) cases, whereas
4 ine some of the major characteristics of the mycelial and yeast phases.
5 ndividuals had antibodies to the CF yeast or mycelial antigen only, respectively.
6 ial CF testing showed that antibodies to the mycelial antigen serorevert to negative more frequently
7 nalysis of hyphal dimensions showed that the mycelial architecture and the erection of aerial hyphae
8 erentiation and antibiotic production in the mycelial bacteria of the genus Streptomyces.
9             Streptomycetes are multicellular mycelial bacteria that grow as vegetative hyphae, which
10 on genes ftsL and divIC in the gram-positive mycelial bacterium Streptomyces coelicolor A3(2).
11 al mycelium formation and sporulation in the mycelial bacterium Streptomyces coelicolor rely on estab
12 wo antibiotics in Streptomyces coelicolor (a mycelial bacterium).
13 ein (18.34 g/100 g), ergosterol (0.60 mg/g), mycelial biomass (183 mg/g) and total amino acids (58.34
14 content of initial materials, while residual mycelial biomass was affected by mushroom productivity.
15  mating types, resulting in a heterokaryotic mycelial body made up of genetically different nuclei.
16  fluorescent fusion protein localized to the mycelial cell wall.
17  mechanism mediates vegetative fusion within mycelial colonies but has also been repurposed for the f
18 acellular structures, which develop into the mycelial colony.
19 tions, vac7, vac8 and fab1 mutants generated mycelial compartments with more symmetrically distribute
20 anges, which likely limited the capacity for mycelial connections between trees, corresponded with sh
21 Here we test the hypothesis that mycorrhizal mycelial connections provide a direct pathway for transf
22  thaw front providing evidence for potential mycelial connectivity between roots and the permafrost b
23  were clustered separately from the external mycelial cortices and fruiting bodies of Chinese Cordyce
24 entified in the fruiting bodies and external mycelial cortices of Chinese Cordyceps.
25 ies between the fruiting bodies and external mycelial cortices of Chinese Cordyceps.
26 ort to determine genes that are expressed in mycelial cultures of Neurospora crassa over the course o
27                     Yeasts cultures, but not mycelial cultures, release large quantities of a calcium
28  mug/mL in liquid medium with a 5mm diameter mycelial disc of F. verticillioides.
29  was performed with analyses of soil DNA and mycelial DNA.
30 e show that in such circumstances, continual mycelial expansion can only be obtained if internal meta
31 sults from mutational alterations that allow mycelial expression of the con-10'-'hph gene fusion.
32 es and were trans-acting, i.e., they allowed mycelial expression of the endogenous con-10 gene.
33 id profile of the spheroids treated with the mycelial extract was distinct from that of the control a
34 ivity was purified to homogeneity from crude mycelial extracts of S. coelicolor and shown to be BldD.
35                                              Mycelial extracts prepared from S. coelicolor cultures i
36                                          The mycelial extracts were examined for their active ingredi
37 O-sulfate and glycine betaine, were found in mycelial extracts, suggesting that phosphocholine-contai
38 ical examination identified numerous septate mycelial filaments.
39 f fungal hyphae whereas CNF formed a uniform mycelial film over wood particles.
40 ons of these individual steps to the overall mycelial FLU transport rate.
41 orting systems have been shown to facilitate mycelial foraging and long-distance communication in sap
42 at sometimes switch from yeast to pathogenic mycelial form.
43 essentially nonreactive with the surfaces of mycelial forms of the fungus, indicating that neither ep
44 ns, a dimorphic fungus composed of yeast and mycelial forms, is the most common human fungal pathogen
45 nd comparable growth rates of both yeast and mycelial forms.
46 f the molds could be amplified directly from mycelial fragments, while DNA from every yeast colony wa
47 obtained using Aspergillus tamarii NKRC 1229 mycelial fructosyltransferase (m-FTase).
48 37-kDa culture filtrate protein and a 55-kDa mycelial glycoprotein (gp55) exhibited complete N-termin
49 spore dispersal, such as aerial dispersal in mycelial groups and polar tube eversion in the microspor
50 udy explored natural alternatives to inhibit mycelial growth (Aspergilus flavus) and aflatoxin produc
51          The inhibition percentage of fungal mycelial growth (IFMG) of the treated Melia azedarach wo
52 xpression of MtTPS10 in yeast also inhibited mycelial growth and A. euteiches zoospore germination.
53 chanism, internal recycling processes during mycelial growth and an overall reduced N and P uptake ap
54              Although B. ambifaria inhibited mycelial growth and increased bacterial propagation in t
55 ional attributes, including carbon fixation, mycelial growth and nutrient utilization, but this is dr
56 henotype that included significantly reduced mycelial growth and profoundly altered colony morphology
57 lexible life history strategy combining both mycelial growth and spore dispersal appears to underpin
58 oemulsion could not only effectively inhibit mycelial growth and spore germination of F. graminearum
59 hibit significant fitness penalties based on mycelial growth and spore germination, suggesting that i
60 onstrated that SPI could effectively inhibit mycelial growth and spore germination.
61 eletion mutant shows identical phenotypes on mycelial growth and virulence, as well as similar expres
62 also resulted in reductions in virulence and mycelial growth and, unexpectedly, enhanced conidial pro
63 on of S. parasitica zoospore germination and mycelial growth by two cyclooxygenase inhibitors (aspiri
64 - 4 and 42 +/- 1%, respectively, on C. musae mycelial growth compared to the EERBP extract.
65 th their bacterial cellular dimensions but a mycelial growth habit like fungi, were generally regarde
66 he same configurations decrease P. palmivora mycelial growth in Medicago roots after 24 h.
67 , the green-synthesized AgNPs achieved > 97% mycelial growth inhibition against a spectrum of phytopa
68  an active chitin synthase-like protein, and mycelial growth is impaired after treatment with a chiti
69  tube development, appressoria formation and mycelial growth of C. gloeosporioides, resulting in redu
70            The results demonstrated that the mycelial growth of fungi was completely inhibited after
71                                          The mycelial growth of Fusarium verticillioides (Sacc.) Nire
72            None of these compounds inhibited mycelial growth of P. infestans in vitro Of note, exogen
73 of mefenoxam, 0.24 ppm, did not suppress the mycelial growth of P. irregulare.
74                              Although stable mycelial growth of the heterokaryotic transformant was o
75            Cultivation trials showed optimal mycelial growth on PDA, with sorghum supporting the high
76 rast tomography (Q-ACT) we detected that the mycelial growth on the solid agar created multiple surfa
77 ssential oils of medicinal plants to inhibit mycelial growth rather than synthetic fungicides.
78                      Antimicrobial tests for mycelial growth reduction under atmospheric conditions p
79  stationary phase in liquid culture, or from mycelial growth to sporulation on solid media.
80        The Fo18438 mutants displayed reduced mycelial growth towards B. ambifaria, and the complement
81                                  At 100 ppm, mycelial growth was only reduced by 11.4%, indicating th
82     Moreover, B. cinerea and S. sclerotiorum mycelial growth was reduced in culture media containing
83 e sister group to Saccharomycotina, retained mycelial growth while elaborating two basic ontogenetic
84 cement of MoGSK1 caused significant delay in mycelial growth, complete loss of conidiation and inabil
85 e the MIC is defined on the basis of visible mycelial growth, conidia should germinate and produce sp
86           Among filamentous fungi capable of mycelial growth, het genes play crucial roles by regulat
87  All tested EOs and EEs completely inhibited mycelial growth, sporulation, and mycotoxin production i
88                 During conidial swelling and mycelial growth, the expression of AfSUN1 was strongly i
89          The thin agar film limits excessive mycelial growth, while it often promotes complete sporul
90  isolated mutants that express con-10 during mycelial growth.
91  expressed during conidiation but not during mycelial growth.
92  and the Fo18438 B-lactamase domain restored mycelial growth.
93 group VII), resulting in thin, "transparent" mycelial growth.
94 train was reduced in conidial production and mycelial growth; these effects were most noticeable when
95 GTA to culture media inhibited the growth of mycelial H. capsulatum but had no effect on yeast growth
96                                  Conversely, mycelial H. capsulatum did not produce CBP, a finding th
97       The majority of the isolates exhibited mycelial incompatibility, minimizing the possibility of
98 ot prevent barrage formation associated with mycelial incompatibility.
99 e fractions responsible for up to 61% of the mycelial inhibition of F. jinanense.
100 ly that, in Streptomyces (a bacterium with a mycelial lifestyle similar to that of filamentous fungi,
101               Zymographic analysis confirmed mycelial localization of the FTase (36 U/g) and lyophili
102 um which are transcriptionally silent in the mycelial (M) phase have recently been cloned and analyze
103 matic, leads to near complete destruction of mycelial microcolonies of a Streptomyces venezuelae ftsZ
104 e with heterogeneous subsurface environments mycelial microorganisms have developed a unique ramified
105  on successful conversion of the saprophytic mycelial (mold) form of this fungus to a parasitic yeast
106 es dermatitidis, for expression in yeast and mycelial morphotypes.
107 ively less due to simultaneous reductions in mycelial N and P contents.
108 ired for the formation of the interconnected mycelial network characteristic of filamentous fungi.
109 s controlling formation of an interconnected mycelial network.
110 hid-infested plants via a common mycorrhizal mycelial network.
111            Mycorrhizal fungi can form common mycelial networks (CMNs) that interconnect plants.
112 findings demonstrate that common mycorrhizal mycelial networks can determine the outcome of multitrop
113 cological amplifiers for fungal and oomycete mycelial networks in soils, extending their potential in
114 ture, and that 'parental nurture' via common mycelial networks may be involved in these processes.
115                                              Mycelial networks of Ceratobasidium cornigerum connectin
116          Fungi form extensive interconnected mycelial networks that scavenge efficiently for scarce r
117                                           In mycelial networks, contaminants were translocated over l
118 s because they form multinucleate, open-pipe mycelial networks, where nutrients, organelles, and chem
119 phanidermatum, were selected as producers of mycelial networks, while Mycobacterium gilvum VM552 serv
120 nt exchange processes across their open-pipe mycelial networks.
121 d transport of the PAH fluorene (FLU) by the mycelial oomycete Pythium ultimum that was grown along t
122  of pre-grown wild-Serbian Ganoderma lucidum mycelial pellets (GLMPs) was evaluated on four different
123 d within the central region of the resulting mycelial pellets and transformed into manganese oxalate
124 ound to influence the morphology of A. niger mycelial pellets.
125  dihydrate which also accumulated within the mycelial pellets.
126 uting to the death of the host trees through mycelial penetration of host tissue, toxin release, inte
127 roliferates within phagolysosomes, while the mycelial phase exists only as a saprophyte in the soil.
128 ble p30 binding activity in either yeast- or mycelial phase extracts, regardless of the source of lab
129 ma capsulatum is its ability to shift from a mycelial phase in the soil to a yeast phase in its human
130                         Genes induced in the mycelial phase included several involved in conidiation,
131                              The saprophytic mycelial phase inhabits moist soil environments; once in
132 was cloned from genomic DNA derived from the mycelial phase of C. immitis by PCR.
133 ing neither conidia nor sexual spores in the mycelial phase, but often producing coiled hyphae.
134 eference antigen (coccidioidin) derived from mycelial-phase Coccidioides immitis and was reactive wit
135 pression of proteins in the spherule and the mycelial phases of C. posadasii with the intent to ident
136                         Root and mycorrhizal mycelial production also decreased substantially.
137                                          The mycelial prokaryote Streptomyces coelicolor A3(2) posses
138 main protein that is required for control of mycelial proliferation and activation of asexual sporula
139 ich both cause constitutive induction of the mycelial proliferation pathway.
140  in the presence of 1000 ng mL(-1) FNP while mycelial quantities of the metabolites decreased with in
141  Here, for the first time, we quantified the mycelial retention of phages in a microfluidic platform
142 e analyzed these IH RNAs relative to control mycelial RNAs using M. oryzae oligoarrays.
143 igh G+C Gram-positive, antibiotic-producing, mycelial soil bacteria.
144               We show that the hyphae of the mycelial soil oomycete Pythium ultimum function as activ
145 dA, spdB, and kilB), which may promote intra-mycelial spread of the plasmid upon its entrance into th
146 ponsible for conjugative plasmid transfer in mycelial Streptomyces Unlike other conjugative systems,
147 mic dynein heavy chain to be absent from the mycelial tip, where it is normally located in wild-type
148  single plasmid gene (tra) for initial inter-mycelial transfer, and involves three additional pIJ101
149 hat its ortholog Ryp1 regulates the yeast to mycelial transition in H. capsulatum.
150 ns, but was specifically associated with the mycelial uptake of Ag NPs.

 
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