2021
DOI: 10.1016/j.jbiosc.2020.12.007
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Efficient production of fungal spores by the combination of reduction of nitrogen source content and embedding of hydrophobic polymer in an agar plate

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Cited by 4 publications
(2 citation statements)
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“…Mycelial morphology and growth phenotypes of fungal isolates can be variably influenced by the composition of culture growth media. Previous work demonstrated that culture media composition can impact the formation of developmental structures in the fungal host, Moura et al (2020) , Sugimoto and Oda (2021) and that these changes coupled with predicted metabolic changes in the fungus could alter endobacterial phenotypes, abundance, and behavior. To determine the effects of culture media composition on endobacterial phenotypes, P. verticillata was grown on four different solid media: (R2A) media which is favorable for bacterial growth, Vogel’s minimal (VM) media for fungi, and two common fungal media, potato dextrose (PD), and malt extract (ME) media which provides a slightly more acidic media environment.…”
Section: Resultsmentioning
confidence: 99%
“…Mycelial morphology and growth phenotypes of fungal isolates can be variably influenced by the composition of culture growth media. Previous work demonstrated that culture media composition can impact the formation of developmental structures in the fungal host, Moura et al (2020) , Sugimoto and Oda (2021) and that these changes coupled with predicted metabolic changes in the fungus could alter endobacterial phenotypes, abundance, and behavior. To determine the effects of culture media composition on endobacterial phenotypes, P. verticillata was grown on four different solid media: (R2A) media which is favorable for bacterial growth, Vogel’s minimal (VM) media for fungi, and two common fungal media, potato dextrose (PD), and malt extract (ME) media which provides a slightly more acidic media environment.…”
Section: Resultsmentioning
confidence: 99%
“…To induce spore production, polypropylene (PP) was mixed with PDA medium and inoculated with the fungal mycelium. The mycelium was gently swept with a sterilized brush, and variable-temperature incubation was applied alternatively between 24 h at 28 °C and 24 h at 4 °C [ 14 ]. Specimens of the dried cultures were deposited at the Herbarium of Guizhou Academy of Agricultural Sciences (Herb.…”
Section: Methodsmentioning
confidence: 99%