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1 t roots and translocate it to their external mycelium.
2 edistribution of nutrients within the fungal mycelium.
3 the root and is exported to the extraradical mycelium.
4 olites are actively translocated through the mycelium.
5 olony surface into the air to form an aerial mycelium.
6 t culminates with the formation of an aerial mycelium.
7 nt is the lytic dismantling of the substrate mycelium.
8 e whole fruiting process and at the level of mycelium.
9 he haploid nucleus and fitness of the fungal mycelium.
10 in ectomycorrhiza compared with free-living mycelium.
11 rved in in vitro cultures of non-sporulating mycelium.
12 ression in the extraradical and intraradical mycelium.
13 monitoring of cellular metabolism in fungal mycelium.
14 re more highly expressed in the intraradical mycelium.
17 hite and golden enoki (Flammulina velutipes) mycelium and across stages of fruit-body growth of golde
20 es had significantly lower concentrations in mycelium and displayed progressively smaller fold change
21 ified genes differentially expressed between mycelium and fruiting body and 242 proteins in the meval
23 nd proline were predominantly present in the mycelium and have potential for use in food supplementat
25 s food and sex cues to lure nematodes to its mycelium and is triggered to develop specialized trappin
26 Interestingly, tomatine affected only aerial mycelium and not vegetative mycelium, suggesting that th
28 pping the (13)C-labeled UDP-GlcNAc in fungal mycelium and recording its redistribution in hyphae, dir
29 irmaii inhibited > 98% of fungus growth from mycelium and sclerotia, whereas the volatiles generated
30 les of X. szentirmaii cultures on the fungus mycelium and sclerotium inhibition; and evaluate the X.
31 rowth defect but failed to produce an aerial mycelium and showed a significant delay in the productio
33 otoconversion of ergosterol from both fungal mycelium and the cereal matrix, increasing vitamin D2 le
34 tiation involving the formation of an aerial mycelium and the production of pigmented antibiotics.
35 he synthesis of arginine in the extraradical mycelium and the transfer of arginine to the intraradica
36 ate germlings, and subsequent development of mycelium and/or sporulation; fifthly, assessments were c
37 ybrid panel composites based on wood, fungal mycelium, and cellulose nanofibrils (CNF) were developed
40 es Q (COQ) for antroquinonol biosynthesis in mycelium, and polyketide synthase for antrocamphin biosy
41 noreactive component of Coccidioides immitis mycelium- and spherule-phase cell walls, was recently cl
42 like microbial biomass, particularly fungal mycelium, are gaining interest due to their low environm
43 rium Streptomyces coelicolor forms an aerial mycelium as a prerequisite to sporulation, which occurs
44 he biomass, confirming the importance of the mycelium as a reactive network for biomineralization.
45 ed from the extraradical to the intraradical mycelium as arginine, but transferred to the plant witho
46 es and associated vitellogenin by the fungal mycelium as well as by cell-free ethyl acetate fungal ex
47 th chitin-binding domains to functionalize a mycelium-based filter to enhance metal recovery from a C
53 in peroxidases may function principally when mycelium-bound and, therefore, undetectable in culture s
54 vels for gpa1, gpb1 and gpg1 were similar in mycelium, but there was a transient excess of gpb1 durin
55 rangiophore is separated from the supporting mycelium by septa which prevent bulk volume flow between
56 red for nuclear migration through the fungal mycelium, closely resembles the LIS1 protein required fo
57 melanin, or animal melanin, and a compressed mycelium (CMy) coated with PLA (PLA-CMy), after exposure
59 Furthermore, with the rapid expansion of mycelium composite technology, there is a need to increa
60 ses on assessing the environmental impact of mycelium composites for building and construction (MCBs)
67 that these sigma factors, involved in aerial mycelium development and stress response in the actinomy
68 ree distinct phases: growth of the substrate mycelium, development of reproductive structures called
72 entration in absorptive roots, extramatrical mycelium (EMM) biomass, community structure of root-asso
75 celium is outside the root (the extraradical mycelium, ERM) and, because of the dispersed growth patt
76 s salts medium, monazite enhanced growth and mycelium extensively covered rock particle surfaces, pro
78 t contributes to the proper timing of aerial mycelium formation and antibiotic production, and SCO252
79 occurring specifically at the time of aerial mycelium formation and coinciding temporally with the on
80 Production of SapB commences during aerial mycelium formation and depends on most of the genes know
82 genetic peptide that is important for aerial mycelium formation by the filamentous bacterium Streptom
83 Genes required for the initiation of aerial mycelium formation have been termed bld (bald), describi
86 lular signalling in the initiation of aerial mycelium formation in two phylogenetically distant strep
87 indicate that the genetic control of aerial mycelium formation is more complex than previously recog
90 ot occur on medium non-permissive for aerial mycelium formation or in one particular developmental mu
91 from conditioned medium that restores aerial mycelium formation to a mutant of Streptomyces coelicolo
93 mmencing approximately at the time of aerial mycelium formation, and depended on bldG and bldH, but n
94 ession and deletion of cdgB inhibited aerial-mycelium formation, and overexpression also inhibited pr
95 bservations implicate the chaplins in aerial mycelium formation, and suggest that coating of the enve
96 f S. coelicolor, which are blocked in aerial mycelium formation, regain the capacity to erect aerial
97 factors involved in the initiation of aerial mycelium formation, the identification of metabolic defe
101 oints, including those taken prior to aerial mycelium formation; this suggests that whiG may be regul
103 omic analysis of the extracted filtrates and mycelium from 15 blueberry isolates of this endophyte re
106 mulation of plant-fixed carbon in the fungal mycelium grown on oatmeal agar, a greater amount of carb
108 monium and nitrate were beneficial to fungal mycelium growth, cell densities, and sporulation, which
109 f these bacteria cultures on S. sclerotiorum mycelium growth; assess the volatiles of X. szentirmaii
112 Our data demonstrate a high diversity of ECM mycelium in a small (8-cm(3) ) volume of substrate, and
118 ants (interrupted in morphogenesis of aerial mycelium into spores), but was absent from all bld mutan
123 ion into prespore compartments of the aerial mycelium is controlled in part by actin- and tubulin-lik
124 how the nutritional acquisition of the morel mycelium is fulfilled to trigger its fruiting remains un
126 The monotonic mechanical behavior of the mycelium is non-linear both in tension and compression.
128 ytic and redox CAZymes secreted by the morel mycelium is the main force driving the substrate decompo
129 l enters the fungus garden, but where fungal mycelium is too sparse to produce extracellular enzymes
130 abolic differences were observed between the mycelium, juvenile and aged caps, and the stipe, which h
131 stead, the fused cells form a characteristic mycelium, known as the dikaryon, in which haploid nuclei
136 absorption spectroscopy revealed that as the mycelium matured, bioaccumulated copper was transformed
137 cale at which ECM species are distributed as mycelium may be very different from the spatial scale at
139 electron microscopy (SEM) images showed that mycelium modification covered wood particles with a netw
141 It was found that the composites made of mycelium-modified wood and CNF resulted in enhanced phys
142 m was grown on softwood particles to produce mycelium-modified wood which was then hybridized with va
144 rated how excitation wave-fronts behave in a mycelium network colonising an insole and shown that it
145 els: spores vary in their germination times, mycelium networks grow at different rates, and a fractio
146 se medium, was initially inoculated with the mycelium (Neurospora crassa), and following the initial
147 the pressure distribution from an expanding mycelium of a popular plant pathogen, Aspergillus parasi
150 n the free-living partners revealed that the mycelium of L. bicolor produces high concentrations of t
152 st temporarily, allocated to the underground mycelium of mycorrhizal fungi per year, equating to ~36%
154 ver, we report that bioluminescence from the mycelium of Neonothopanus gardneri is controlled by a te
155 s required for nuclear migration through the mycelium of the filamentous fungus Aspergillus nidulans.
157 of Sg bald mutants, which produce no aerial mycelium or spores, was restored in the presence of bldA
158 ult of infection and colonization by haploid mycelium originating from a single basidiospore of C. qu
160 rient conditions, growth, pigment and aerial mycelium production, sporulation and dimorphic transitio
161 transition from vegetative growth to aerial mycelium production, the first stage of morphological de
162 ble to sequence the ITS region from powdered mycelium samples, grocery store mushrooms, and capsules
163 ucted whiK null mutant failed to form aerial mycelium, showing that different alleles of this locus c
164 cted only aerial mycelium and not vegetative mycelium, suggesting that the target(s) of alpha-tomatin
169 pected, many more ECM fungi were detected as mycelium than as ectomycorrhizas in a cube or slice.
171 ucted whiN null mutant failed to form aerial mycelium (the "bald" phenotype) and, as a consequence, w
172 pull an expanding wave of nutrient-absorbing mycelium, the density of which is self-regulated by fusi
173 y a unique biomaterial developed from fungal mycelium, the vegetative part and the root structure of
174 hological and mechanical characterization of mycelium through an integrated experimental and computat
179 e in spores, translocation from intraradical mycelium to ERM, and buffering of intracellular hexose l
180 g have shed light upon the importance of the mycelium-to-yeast transition and the crucial and complex
182 l's cytotoxicity and its effect on the yeast-mycelium transition in Candida albicans, an important vi
183 after nitrate was added to the extraradical mycelium under N-limited growth conditions using hairy r
185 production of ergosterol and the biomass of mycelium varied, as did the effects on the production of
187 ly regulated, increasing sharply when aerial mycelium was present, and reaching a maximum approximate
188 ow that a water extract of Ganoderma lucidum mycelium (WEGL) reduces body weight, inflammation and in
189 laccase-like activity associated with fungal mycelium were found to be efficient in the degradation t
190 n fungi found, except for yeasts and sterile mycelium, were Cladosporium, Alternaria, Penicillium, Ul
192 m in the fruiting body, in contrast with the mycelium where 53.4% of Se-Met and 80.5% of Met is incor
193 the transfer of arginine to the intraradical mycelium, where it is broken down to release N for trans
194 multiscale fiber network-based model for the mycelium which reproduces the tensile and compressive be
195 s Arthromyces produces asexual spores on the mycelium, which may facilitate insect dispersal when gro
196 ization properties, as well as a filamentous mycelium, which may provide mechanical support for miner
197 eling of germinating spores and extraradical mycelium with (13)C(2)-acetate and (13)C(2)-glycerol and
198 s of the fungus resulted in a newly infected mycelium with the same morphology and virus composition